A 24-year-old Cincinnati man died from a tooth infection earlier this week, due to the fact he was unable to afford the medication needed for treatment. NBC affiliate WLWT reported that Kyle Willis was unable to afford the necessary antibiotics for treatment.

Free MacBook Pro 17 inch i7 2014 Two weeks ago, Willis’ wisdom tooth began to hurt, and a dentist indicated that it should be pulled. However, as he was out of work and without insurance, Willis could not afford to have the tooth pulled. But, when his head began hurting and his face began to swell, he visited the emergency room at University Hospital. “The (doctors) gave him antibiotic and pain medication. But he couldn’t afford to pay for the antibiotic, so he chose the pain meds, which was not what he needed,” his aunt, Bootsy Collins told WLWT. She said she could not believe it when she received the unexpected phone call about her nephew. “I said, ‘What do you mean they’re calling the family?’ (My daughter) said, ‘Mom, the infection (Willis) had in his tooth has gone to his brain.” “People don’t realize that dental disease can cause serious illness,” Dr. Irvin Silverstein, a dentist at the University of California at San Diego, told ABC News. “The problems are not just cosmetic. Many people die from dental disease.” It is difficult, however, for many people to obtain needed dental care, and it is not getting any easier as the economy worsens. According to a Kaiser Family Foundation report in April, 33 percent of those surveyed said they skipped dental care or dental checkups due to inability to pay for them. And, in August, a Commonwealth Fund report indicated that 72 percent of those who lose health insurance when they lose their jobs said that they skip health care and do not fill prescriptions, because they simply cannot afford them. “When people are unemployed or don’t have insurance, where do they go? What do they do?” Silverstein said. “People end up dying, and these are the most treatable, preventable diseases in the world.” Unfortunately, many people believe that “the system” takes care of people in this dilemma, and it just is not true. And, free dental clinics available around the country are not always available to individuals who need them, either because they are not located in their area or because the clinics are overwhelmed and are not accepting new patients, or force patients to wait months for treatment. Silverstein, who operates three free dental clinics in the San Diego area, confirmed this problem with ABC News. Willis was a father, with a six-year-old daughter, as well as an aspiring paralegal. NBC,affiliate,WLWT,reported,that,Kyle,Willis,was,unable,to,afford,the,necessary,antibiotics,for,treatment,medication,needed,for,treatment,he,was,unable,to,afford,the

Is a parent enabling their son by giving him money, if his son did graduate from a 4-year college or university paid for or not paid for by his parents? Is a parent enabling their son by giving him money, if his son did not graduate from a 4-year college or university? Is a parent enabling their son by giving him money, if his son dropped out of a 4-year university on good academic standing during the second semester of his sophomore year (after getting a divorce from his ex-wife), with the major of Electrical Engineering?

     Is a parent enabling their son by giving him money, if his son did graduate from a 4-year college or university paid for or not paid for by his parents?  

     Is a parent enabling their son by giving him money, if his son did not graduate from a 4-year college or university?  

     Is a parent enabling their son by giving him money, if his son dropped out of a 4-year university on good academic standing during the second semester of his sophomore year (after getting a divorce from his ex-wife), with the major of Electrical Engineering?

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The Problems Created by the APA

  Mark R. Rowe

8/17/14

     What is wrong with the American Psychiatric Association?  Why do the people that sit on the board of directors and attempt to make psychiatry larger than it it?  Psychiatry is such a large entity that it is equivalent to the size of some smaller religions of the world.

      Do we need to drug our children on a wide scale basis, as this is promoted in American media in the form of television, radio, and internet advertisements attempting to sell drugs.

      Recently I saw a public awareness advertisement on the side of a city bus that read:  "1 in 4 people suffer from a mental illness."  Is the APA really that dumb to assume that if they were to post "awareness" statements like this, people would believe that 25 per cent of all people have some type of mental illness?  I am sorry but people smart and not stupid.  See, the problem here, is that, psychiatrists during the 1940's finally had a chemical substance that could create a profound psychological effect on the human mind.  This chemical substance is a drug known to many by its acronym, LSD or D-Lysergic Acid.  LSD was discovered by Alexander Hofmann, a scientist working in Switzerland in 1943.

     Before the year 1943, psychiatrists were physicians that were not respected in the general field of medicine.  Psychiatry was merely a trial and error pseudo scientific discipline of medicine during the years before 1943.

      Psychiatrists could now synthesize real symptoms of schizophrenia and of other psychotic mental disorders with the prescription and administering of LSD to psychiatric patients.  These mimicked schizophrenic symptoms were believed to reduce the sum total of the quantity of hallucinations caused by Schizophrenia, and that LSD could regulate or attempt to regulate when hallucinations triggered by schizophrenia, (not by LSD) would occur for the psychiatric patient, thus giving psychiatrists and psychotherapists a ballpark time frame to use therapeutic measures to treat the patient.

     When psychiatrists first began administering LSD to psychiatric patients, psychiatrists had a low success rate for the reduction of psychotic symptoms, but as new drug research progressed and with government run behavior modification programs such as, MK-Ultra and the Phoenix Program, psychiatry began to establish itself as a more credible discipline of medicine. 

Phases of the Human Genome Project Based on the insights gained from the yeast and worm studies, the Human Genome Project employed a two-phase approach to tackle the human genome sequence (IHGSC, 2001). The first phase, called the shotgun phase, divided human chromosomes into DNA segments of an appropriate size, which were then further subdivided into smaller, overlapping DNA fragments that were sequenced. The Human Genome Project relied upon the physical map of the human genome established earlier, which served as a platform for generating and analyzing the massive amounts of DNA sequence data that emerged from the shotgun phase. Next, the second phase of the project, called the finishing phase, involved filling in gaps and resolving DNA sequences in ambiguous areas not obtained during the shotgun phase. Figure 1 shows the exponential increase in DNA sequence information deposited in the High-Throughput Genomic Sequences (HTGS) division of GenBank by the end of the shotgun phase. Indeed, the shotgun phase yielded 90% of the human genome sequence in draft form. The shotgun phase of the Human Genome Project itself consisted of three steps: Obtaining a DNA clone to sequence Sequencing the DNA clone Assembling sequence data from multiple clones to determine overlap and establish a contiguous sequence

The Human Genome Project was a 13-year-long, publicly funded project initiated in 1990 with the objective of determining the DNA sequence of the entire euchromatic human genome within 15 years. In its early days, the Human Genome Project was met with skepticism by many people, including scientists and nonscientists alike. One prominent question was whether the huge cost of the project would outweigh the potential benefits. Today, however, the overwhelming success of the Human Genome Project is readily apparent. Not only did the completion of this project usher in a new era in medicine, but it also led to significant advances in the types of technology used to sequence DNA.

Initial Principles and Goals of the Human Genome Project
From its inception, the Human Genome Project revolved around two key principles (International Human Genome Sequencing Consortium, 2001). First, it welcomed collaborators from any nation in an effort to move beyond borders, to establish an all-inclusive effort aimed at understanding our shared molecular heritage, and to benefit from diverse approaches. The group of publicly funded researchers that eventually assembled was known as International Human Genome Sequencing Consortium (IHGSC). Second, this project required that all human genome sequence information be freely and publicly available within 24 hours of its assembly. This founding principle ensured unrestricted access for scientists in academia and in industry, and it provided the means for rapid and novel discoveries by researchers of all types. At any given time, approximately 200 labs in the United States were funded by either the National Institutes of Health or the U.S. Department of Energy to support these efforts. In addition, more than 18 different countries from across the globe had contributed to the Human Genome Project by the time of its completion.
Just as the Human Genome Project revolved around two key principles, it also started with two early goals: (1) building genetic and physical maps of the human and mouse genomes, and (2) sequencing the smaller yeast and worm genomes as a test run for sequencing the larger, more complex human genome (IHGSC, 2001). When the yeast and worm efforts proved successful, the sequencing of the human genome proceeded with full force.

Phases of the Human Genome Project

Based on the insights gained from the yeast and worm studies, the Human Genome Project employed a two-phase approach to tackle the human genome sequence (IHGSC, 2001). The first phase, called the shotgun phase, divided human chromosomes into DNA segments of an appropriate size, which were then further subdivided into smaller, overlapping DNA fragments that were sequenced. The Human Genome Project relied upon the physical map of the human genome established earlier, which served as a platform for generating and analyzing the massive amounts of DNA sequence data that emerged from the shotgun phase. Next, the second phase of the project, called the finishing phase, involved filling in gaps and resolving DNA sequences in ambiguous areas not obtained during the shotgun phase. Figure 1 shows the exponential increase in DNA sequence information deposited in the High-Throughput Genomic Sequences (HTGS) division of GenBank by the end of the shotgun phase. Indeed, the shotgun phase yielded 90% of the human genome sequence in draft form.
The shotgun phase of the Human Genome Project itself consisted of three steps:
Obtaining a DNA clone to sequence
Sequencing the DNA clone
Assembling sequence data from multiple clones to determine overlap and establish a contiguous sequence

The approach used by the members of the IHGSC was called the hierarchical shotgun method, because the team members systematically generated overlapping clones mapped to individual human chromosomes, which were individually sequenced using a shotgun approach (Figure 2). The clones were derived from DNA libraries made by ligating DNA fragments generated by partial restriction enzyme digestion of genomic DNA from anonymous human donors into bacterial artificial chromosome vectors, which could be propagated in bacteria.
When possible, the DNA fragments within the library vectors were mapped to chromosomal regions by screening for sequence-tagged sites (STSs), which are DNA fragments, usually less than 500 base pairs in length, of known sequence and chromosomal location that can be amplified using polymerase chain reaction (PCR). Library clones were also digested with the restriction enzyme HindIII, and the sizes of the resulting DNA fragments were determined using agarose gel electrophoresis. Each library clone exhibited a DNA fragment "fingerprint," which could be compared to that of all other library clones in order to identify overlapping clones. Fluorescence in situ hybridization (FISH) was also used to map library clones to specific chromosomal regions. Collectively, the STS, DNA fingerprint, and FISH data allowed the IHGSC to generate contigs, which consisted of multiple overlapping bacterial artificial chromosome (BAC) library clones spanning each of the 24 different human chromosomes (i.e., 22 autosomes and the X and Y chromosomes).

Next, individual BAC clones selected for DNA sequence analysis were further fragmented, and the smaller genomic DNA fragments were subcloned into vectors to generate a BAC-derived shotgun library. The inserts were sequenced using primers matching the vector sequence flanking the genomic DNA insert, and overlapping shotgun clones were used to generate a DNA sequence spanning the entire BAC clone. A summary of this step is shown in Figure 3. The members of the IHGSC agreed that each center would obtain an average of fourfold sequence coverage, with no clone having less than threefold coverage. The term "shotgun" comes from the fact that the original BAC clone was randomly fragmented and sequenced, and the raw DNA sequence data was then subjected to computational analyses to generate an ordered set of DNA sequences that spanned the BAC clone.

Before the IHGSC had completed the first phase of the Human Genome Project, a private biotechnology company called Celera Genomics also entered the race to sequence the human genome. Led by Dr. Craig Venter, Celera proclaimed that it would sequence the entire human genome within three years. As outlined in Figure 4, Celera used two independent data sets together with two distinct computational approaches to determine the sequence of the human genome (Venter et al., 2001). The first data set was generated by Celera and consisted of 27.27 million DNA sequence reads, each with an average length of 543 base pairs, derived from five different individuals. The second data set was obtained from the publicly funded Human Genome Project and was derived from the BAC contigs (called bactigs); here, Celera "shredded" the Human Genome Project DNA sequence into 550-base-pair sequence reads representing a total of 16.05 million sequence reads. The company then used a whole-genome assembly method and a regional chromosome assembly method to sequence the human genome.

In the whole-genome assembly method (also called the whole-genome random shotgun method), Celera generated a massive shotgun library derived from its own DNA sequence data combined with the "shredded" Human Genome Project DNA sequence data, which together corresponded to a total of 43.32 million sequence reads (Venter et al., 2001). Celera used computational methods and sophisticated algorithms to identify overlapping DNA sequences and to reconstruct the human genome by generating a set of scaffolds (Figure 5).

In contrast, with the regional chromosome assembly approach (also called the compartmentalized shotgun assembly method), Celera organized its own data and the Human Genome Project sequence data into the largest possible chromosomal segments, followed by shotgun assembly of the sequence data within each segment (Venter et al., 2001); this approach was similar to the hierarchical shotgun approach used by the IHGSC. The first step of the regional assembly approach involved separating Celera reads that matched Human Genome Project reads from those that were distinct from the public sequence data. Of the 27.27 million Celera reads, 21.38 million matched a Human Genome Project bactig, and 5.89 million did not match the public sequence data. These reads were assembled into Celera-specific or Human Genome Project-specific scaffolds, which were then combined and analyzed using whole-gene assembly algorithms. The resulting bactig data were again "shredded" to permit unbiased assembly of the combined sequence data.

Celera's whole-genome and regional chromosome assembly methods were independent of each other, permitting direct comparison of the data. Celera found that the regional chromosome assembly method was slightly more consistent than the whole-genome assembly method. Using these complementary approaches, Celera generated data that was in strong agreement with that of the IHGSC.

In February 2001, drafts of the human genome sequence were published simultaneously by both groups in two separate articles (IHGSC, 2001; Venter et al., 2001). Due to technical advances in DNA sequencing methods and a productive level of synergy between the two groups, they tied at the finish line, and both projects were completed ahead of schedule.
A Quick Lesson in DNA Sequencing
As previously mentioned, the IHGSC and Celera used different approaches to determine the sequence of the human genome. However, they used the same general method for the DNA sequencing step (Hood & Galas, 2003). This method uses DNA polymerase, the same enzyme used in DNA replication, to produce DNA sequence information. As shown in Figure 6a, DNA polymerase binds to a single-stranded DNA template and adds DNA bases to the 3′ end of the complementary DNA strand it synthesizes. DNA polymerase requires an existing primer with a free 3′ end to which it adds new DNA bases in a 5′ to 3′ manner, and it moves along the template strand in a 3′ to 5′ direction.

Researchers from both the IHGSC and Celera combined the DNA template they were interested in sequencing with DNA polymerase, a single-stranded DNA primer, free deoxynucleotide bases (dATP, dCTP, dGTP, and dTTP), and a sparse mixture of fluorescently labeled dideoxynucleotide bases (ddATP, ddCTP, ddGTP, and ddTTP) that were each labeled with a different color and would terminate new DNA strand synthesis once incorporated into the end of a growing DNA strand. The mixture was first heated to denature the template DNA strand; this was followed by a cooling step to allow the DNA primer to anneal. Following primer annealing, the polymerase synthesized a complementary DNA strand. The template would grow in length until a dideoxynucleotide base (ddNTP) was incorporated; the conditions were such that this occurred at random along the length of the newly synthesized DNA strands. In the end, the researchers were left with a mixture of newly synthesized DNA strands that differed in length by a single nucleotide, and that were labeled at their 3′ end with the color of the ddNTP-associated dye molecule

In order to determine the sequence of the newly synthesized, color-coded DNA strands, researchers needed a way to separate them based on their size, which differed by only one DNA nucleotide. To accomplish this, they electrophoresed the DNA through a gel matrix that permitted single-base differences in size to be easily distinguished. Small fragments run more quickly through the gel, and larger fragments run more slowly (Figure 6c). By putting the entire mixture into a single well of the gel, a laser can be used to scan the DNA bands as they move through the gel and determine their color; this data can be used to generate a sequence trace (also called an electropherogram), showing the color and signal intensity of each DNA band that passes through the gel (Figure 6d). The color of each band represents the final 3′ base incorporated at that position, and by reading from the bottom to the top of the gel, one can determine the sequence of the newly synthesized DNA strand from the 5′ to the 3′ end.

From Rough Draft to Final Form
As stated earlier, after the completion of the draft phase of the Human Genome Project, the IHGSC pursued the second phase of the project: the finishing phase (IHGSC, 2004). During this phase, the researchers filled in gaps and resolved DNA sequences in ambiguous areas that were not solved during the shotgun phase. The finishing phase yielded 99% of the human genome in final form. The final form of the human genome contained 2.85 billion nucleotides, with a predicted error rate of 1 event per 100,000 bases sequenced. Furthermore, the IHGSC reduced the number of gaps by 400-fold; only 341 gaps out of 147,821 gaps remained. The remaining gaps were associated with technically challenging chromosomal regions. Although the earlier draft publications had predicted as many as 40,000 protein-encoding genes, the finishing phase reduced this estimate to between 20,000 and 25,000 protein-encoding genes. Future challenges identified by the IHGSC during this phase included the identification of polymorphisms as a platform for understanding genetic links to human disease, the identification of functional elements within the genome (genes, proteins, elements involved in gene regulation, and structural elements), and the identification of gene and protein "modules" that act in concert with one another.


From Digital Information to Molecular Medicine

One particularly striking finding of the Human Genome Project research is that the human nucleotide sequence is nearly identical (99.9%) between any two individuals. However, a single nucleotide change in a single gene can be responsible for causing human disease. Because of this, our knowledge of the human genome sequence has also contributed immensely to our understanding of the molecular mechanisms underlying a multitude of human diseases. Furthermore, a merging of cytogenetic approaches with the human genome sequence will continue to propel our understanding of human disease to an entirely new level. Thus, although it was met with skepticism at its inception, the Human Genome Project will certainly be heralded as one of the most important scientific endeavors of our time.
Unfortunately, the initial hope of accelerating the discovery of new treatments for disease was not necessarily accomplished by the Human Genome Project. With the sequence of the human genome in hand, we have learned that it requires more than just knowledge of the order of the base pairs in our genome to cure human disease. Current efforts are therefore focused on understanding the protein products that are encoded by our genes. When a gene is mutated, the corresponding protein is most often defective. The emerging field of proteomics aims to understand how protein function and expression are altered in human disease states. Furthermore, investigators are also turning their attention to the expansive regions of our genome devoid of traditional protein-encoding genes. We have already started to reap the benefits of our knowledge of the human genome, and future data-mining efforts will most certainly uncover many more exciting and unexpected links to human disease.


Summary

Within a span of only 13 years, an amalgam of public and private researchers was able to successfully complete the Human Genome Project. Although these scientists used a number of different methods in their work, they nonetheless obtained the same results. In doing so, the researchers not only silenced their critics, but they also beat their own estimated project timeline by two entire years. Perhaps even more importantly, these scientists inspired an ongoing revolution in our fight against human disease and provided a new vision of the future of medicine, although that future has yet to be fully realized.

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Some of the accomplishments of Great Britain

1596-1606 marks the 10 year time period that Great Britain completed the last phases of their means to exploit, colonize, cheat, steal, lie, and enslave an entire continent, for the sake of the love of money for over 300 years. Mark,Rowe,David,Rowe,Nina,Dougherty,Clifford,Dougherty,Anita,Ferguson,Virginia,Ferguson,William,Jones,Frederick,Jones,Charles,Rowe,Jacqueline,Kennedy,Esther,Rowe,Ralph,Rowe,Judy,Garland,Ethel,Kennedy,Robert,John,Kennedy,international,affairs,world,economic,domination,and,control,policy,makers,decisions,for,material,gain,persuasion,of,the,masses,Did,you,know,that,the,NSA,can,track,the,location,of,your,phone,even,when,it,is,turned,off,and,the,batteries,have,been,removed,This,admission,went,largely,unnoticed,in,a,Washington,Post,report,entitled,NSA,growth,fueled,by,need,to,target,terrorists,In,the,article,writer,Dana,Priest,details,how,teams,of,NSA,employees,stationed,around,the,globe,are,dedicated,to,tracking,phones,in,real,time,By,September,2004,a,new,NSA,technique,enabled,the,agency,to,find,cellphones,even,when,they,were,turned,off,JSOC,troops,called,this,The,Find,and,it,gave,them,thousands,of,new,targets,including,members,of,a,burgeoning,al,Qaeda,sponsored,insurgency,in,Iraq,according,to,members,of,the,unit,At,the,same,time,the,NSA,developed,a,new,computer,linkup,called,the,Real,Time,Regional,Gateway,into,which,the,military,and,intelligence,officers,could,feed,every,bit,of,data,or,seized,documents,and,get,back,a,phone,number,or,list,of,potential,targets,It,also,allowed,commanders,to,see,on,a,screen,every,type,of,surveillance,available,in,a,given,territory,The,technique,by,which,the,NSA,can,wiretap,cellphones,even,when,they,are,turned,off,and,powered,down,is,most,likely,being,performed,with,the,complicity,of,telecommunications,companies,who,have,proven,friendly,to,NSA,snooping,Trojan,horse,programs,disguised,behind,routine,system,updates,are,the,likely,method,through,which,the,NSA,gains,direct,access,to,millions,of,Americans,cellphones,and,other,devices,you,may,recall,the,fact,that,Verizon,and,ATT,notably,did,not,sign,the,collective,letter,asking,the,government,to,allow,affected,companies,to,release,information,on,government,requests,for,data,writes,Tim,Cushing,given,this,background,its,not,unimaginable,that,Verizon,and,ATT,would,accommodate,the,NSA,and,FBI,if,it,wished,to,use,their,update,systems,to,push,these,trojans,as,we,have,also,previously,highlighted,terms,of,agreement,for,many,of,the,apps,you,download,to,your,smartphone,now,use,your,microphone,to,listen,to,you,and,your,camera,to,take,pictures,of,you,without,your,knowledge,the,notion,of,the,federal,government,tracking,your,location,via,your,cellphone,is,particularly,prescient,given,yesterdays,report,concerning,the,DHS,funded,mesh,network,system,that,seattle,police,eventually,intend,to,roll,out,across,the,city,but,have,temporarily,been,forced,to,deactivate,due,to,a,privacy,outcry,aruba,networks,company,behind,the,system,of,wifi,hubs,which,can,record,the,last,thousands,locations,of,cellphones,belonging,to,anyone,in,the,coverage,area,bragged,in,their,promotional,material,that,the,grid,could,track,rogue,or,unassociated,devices,In,other,words,even,if,you,do,not,allow,your,phone,to,connect,to,such,wifi,networks,they,can,still,access,your,device,record,its,current,and,historical,location,as,well,as,download,private,information,from,your,apps,and,other,settings,ILLUMINATI,illuminetai,illuminati,a,name,given,by,the,Ante,Nicene,Church,Fathers,to,those,who,submitted,to,Christian,baptism,Greek,phi,omega,tau,os,illumination,They,were,called,Illuminati,,phi,omega,tau,os,of,illuminated,ones,on,the,assumption,that,those,who,were,instructed,for,baptism,in,the,Apostolic,faith,had,received,the,grace,of,illumination,in,an,enlightened,understanding,Clement,of,Alexandria,speaks,thus,of,such,baptismal,light,This,is,the,one,grace,of,illumination,that,our,characters,are,not,the,same,as,before,our,washing.,And,since,knowledge,springs,up,with,illumination,shedding,its,beams,around,the,mind,the,moment,we,hear,we,who,were,untaught,become,disciples,This,work,is,called,illumination,by,which,that,holy,light,of,salvation,is,beheld,that,is,by,which,we,see,God,clearly,,Among,the,societies,subsequently,adoption,the,name,century,and,appearing,in,France,as,the,Guerinets,during,the,period,by,a,secret,society,founded,by,Adam,Weishaupt,professor,of,canon,law,at,Ingolstadt,on,May,the,early,were,the,sixteenth,religion,with,,rationalism,,Frederick,Bronkema,,combating,Alumbrados,the ,Alombrados,a,mystical,existing,in,Spain,or,sect,1,1776,the,aim,fostering,a‚illuminati      

Dr. Johnathan Corrigan Wells Ph. D., Sun Myung Moon, The Unification Church, and Artificial Human Intelligent Design

Jonathan Wells
Born John Corrigan Wells
1942 (age 71–72)
USA
Alma mater University of California, Berkeley, Unification Theological Seminary, Yale University
Occupation Author
Known for Intelligent design advocate and anti-evolution activist
Title Senior Fellow, Discovery Institute
Religion Unification Church

John Corrigan "Jonathan" Wells (born 1942) is an American molecular biologist, author and advocate of intelligent design.  Wells joined the Unification Church in 1974, and subsequently wrote that the teachings of church founder Sun Myung Moon, his own studies at the Unification Theological Seminary and his prayers convinced him to devote his life to "destroying Darwinism." The term Darwinism is often used by intelligent design proponents to refer to the scientific consensus on evolution.  He gained a PhD in religious studies at Yale University in 1986, then became Director of the Unification Church’s inter-religious outreach organization in New York City. In 1989, he studied the University of California, Berkeley, where he earned a PhD in molecular and cellular biology in 1994. He became a member of several scientific associations and was published in academic journals.

In his book Icons of Evolution: Science or Myth? (2000), Wells said that a number of examples used to illustrate biology textbooks were grossly exaggerated, distorted the truth, or were patently false; he said that this shows that evolution conflicts with the evidence, and so argued against its teaching in public education.  Some reviewers of Icons of Evolution have said the Wells misquoted experts cited as sources and took minor issues out of context, basing his argument on a flawed syllogism.  Wells's views on evolution have been rejected by the scientific community.

Wells was born in New York City in 1942 and grew up in New Jersey, and was brought up as a Protestant Christian. He studied geology at Princeton University, where he dropped out in his junior year. Following a brief stint as a taxi driver, he was drafted into the United States Army and spent two years serving in Germany. After his discharge in 1966, he attended University of California, Berkeley, where he publicly refused to report for reserve duty. This resulted in him being arrested and being incarcerated for eighteen months at the Leavenworth military prison. Upon his release, Wells returned to Berkeley where he completed his studies with a major in geology and physics and a minor in biology.

In 1974, Wells joined the Unification Church of the United States.  He graduated from the church's Unification Theological Seminary in 1978 with a master's degree in religious education.  Wells continued his studies at Yale University, earning a PhD in religious studies in 1986, focusing on historical reactions to Darwinism.  During this time he wrote extensively on Unification theology and taught at the Unification Theological Seminary.  Wells was on the Board of Trustees of the Unification Theological Seminary until resigning in 1997 to return to teaching.  He also acted as the director of the International Religious Foundation, a Unification Church affiliated organization which sponsors interdenominational conferences.

Wells has written on the subject of marriage within the Unification Church and has been called a "Unification Church marriage expert" by church sources.  Wells defended Unification Church theology against what he said were unfair criticisms made in 1977 by the National Council of Churches.

In 1994, Wells earned another PhD in molecular and cellular biology at UC Berkeley.  After receiving his doctorate, he worked at a position he described as "a post-doctoral research biologist at Berkeley, writing articles critical of Darwinism." Shortly after that Wells joined former UC Berkeley law professor Phillip E. Johnson, father of the intelligent design movement, at the Discovery Institute.  He now serves as a fellow at the Discovery Institute's Center for Science and Culture, the hub of the intelligent design movement, and at the International Society for Complexity, Information, and Design, which also promotes intelligent design.

Of his student days at Unification Theological Seminary (1976–78), Wells said, "One of the things that Father [Reverend Sun Myung Moon] advised us to do at UTS was to pray to seek God's plan for our lives." He later described that plan: "To defend and articulate Unification theology especially in relation to Darwinian evolution."

Wells stated that his religious doctoral studies at Yale, which were paid for by the Unification Church, focused on the "root of the conflict between Darwinian evolution and Christian doctrine" and encompassed the whole of Christian theology within a focus of Darwinian controversies.  He said:

...I learned (to my surprise) that biblical chronology played almost no role in the 19th- century controversies, since most theologians had already accepted geological evidence for the age of the earth and re-interpreted the days in Genesis as long periods of time. Instead, the central issue was design.

Wells said that "destroying Darwinism" was his motive for studying Christian theology at Yale and going on to seek his second PhD at Berkeley, studying biology and in particular embryology.

Father's [Rev. Moon's] words, my studies, and my prayers convinced me that I should devote my life to destroying Darwinism, just as many of my fellow Unificationists had already devoted their lives to destroying Marxism. When Father chose me (along with about a dozen other seminary graduates) to enter a Ph.D. program in 1978, I welcomed the opportunity to prepare myself for battle.

Wells's statement and others like it are viewed by the scientific community as evidence that Wells lacks proper scientific objectivity and mischaracterizes evolution by ignoring and misrepresenting the evidence supporting it while pursuing an agenda promoting notions supporting his religious beliefs in its stead.

He has written articles for the Discovery Institute, WorldNetDaily, Origins & Design, and other sympathetic publications attacking evolution and defending intelligent design.  In 1997, he presented a paper entitled "Evolution by Design" at the Unification Church sponsored International Conference on the Unity of the Sciences in Washington, D.C.

In 1999, Wells debated with the New Mexicans for Science and Reason.  He was one of the contributors to Natural History magazine's 2002 debate between intelligent design advocates and evolution supporters.[36] In 2005, he debated Massimo Pigliucci on the PBS talk show Uncommon Knowledge.  Pigliucci said that Wells "clearly lied" during his debates and misrepresented his agenda and science, as well as not understanding some of the theories he tries to attack.

Wells is one of the signatories of the Discovery Institute's "A Scientific Dissent From Darwinism," a petition which the intelligent design movement uses to promote intelligent design by attempting to cast doubt on evolution.  He is also the author of "Ten questions to ask your biology teacher about evolution" for high school students, which is published by the Discovery Institute.  The National Center for Science Education has issued a list of answers to the questions.
    Wells is best known for his 2000 book Icons of Evolution, in which he discusses ten examples which he says show that many of the most commonly accepted arguments supporting evolution are invalid.  The book is rejected by many members of the scientific community and has received much criticism by those opposed to his views.  There have been 12 detailed reviews of Icons, from scholars familiar with the subject matter, which have come to the consensus that the book's claims are a politically motivated extreme exaggeration and misrepresentation of a scattering of minor issues.  Scholars quoted in the work have accused Wells of purposely misquoting them and misleading readers.  Biology Professor Jerry Coyne wrote of Icons, "Wells's book rests entirely on a flawed syllogism: ... textbooks illustrate evolution with examples; these examples are sometimes presented in incorrect or misleading ways; therefore evolution is a fiction."

Kansas evolution hearings
Main article: Kansas evolution hearings
In 2005, Wells participated in the Kansas evolution hearings, which were boycotted by mainstream scientists. There Wells testified:

I became convinced that the Darwinian theory is false because it conflicts with the evidence. ... I think the earth is probably four-and-a-half billion or so years old. But I'll tell you this, I used to-- I would have said, a few years ago, I'm convinced it's four-and-a-half billion years old. But the truth is I have not looked at the evidence. And I have become increasingly suspicious of the evidence that is presented to me and that's why at this point I would say probably it's four-and-a-half billion years old, but I haven't looked at the evidence. ... There are already scientists-- respected scientists in this country who do experiments on things that most people consider supernatural, such as prayer. When Newton proposed the theory of gravitation it was dismissed as supernaturalism because it was action at a distance. What constitutes supernaturalism in today's science may very well not be supernatural in tomorrow's science.
     Prior to the evolution hearings, in December 2000 after the Pratt County, Kansas, school board revised its tenth-grade biology curriculum at the urging of intelligent design proponents to include material that encourages students to question the theory of evolution, The Pratt Tribune published a letter from Jerry Coyne challenging Wells's characterization in an article of his work on peppered moths, saying that his article appended to the Pratt standards was misused and being mischaracterized:

Creationists such as Jonathan Wells claim that my criticism of these experiments casts strong doubt on Darwinism. But this characterization is false. ... My call for additional research on the moths has been wrongly characterized by creationists as revealing some fatal flaw in the theory of evolution. ... It is a classic creationist tactic (as exemplified in Wells' book, "Icons of Evolution") to assert that healthy scientific debate is really a sign that evolutionists are either committing fraud or buttressing a crumbling theory.
     The Politically Incorrect Guide to Darwinism and Intelligent Design
In 2006, Wells published his second major book, The Politically Incorrect Guide to Darwinism and Intelligent Design, which was part of a series published by Regnery Publishing. The book was praised by Tom Bethell, author of The Politically Incorrect Guide to Science,[56] but was described by Dr. Reed A. Cartwright of The Panda's Thumb weblog as being "not only politically incorrect but incorrect in most other ways as well: scientifically, logically, historically, legally, academically, and morally."  Cartwright also edited a chapter-by-chapter critique of the book.   A quote from the book linking evolution to eugenics, abortion and racism appeared on Starbucks paper cups in 2007.

Main article: AIDS denialism
In 1991, Wells and his mentor Phillip E. Johnson signed an open letter which said in full:

It is widely believed by the general public that a retrovirus called HIV causes the group [of] diseases called AIDS. Many biochemical scientists now question this hypothesis. We propose that a thorough reappraisal of the existing evidence for and against this hypothesis be conducted by a suitable independent group. We further propose that critical epidemiological studies be devised and undertaken.
     Wells and Johnson have been criticized, along with others, for their questioning of the scientific and medical consensus that HIV causes AIDS.  In the Washington University Law Review, critics Matthew J. Brauer, Barbara Forrest, and Steven G. Gey faulted Wells, Johnson, and others for denying the HIV/AIDS connection and promoting denialism via a petition designed to garner publicity but without any scientific support.

Wells, Jonathan (1985). "Inertial force as a possible factor in mitosis". BioSystems (Amsterdam: Elsevier) 17 (4): 301–315. doi:10.1016/0303-2647(85)90046-2. ISSN 0303-2647. PMID 3902112.
Larabell, Carolyn A.; Rowning, Brian A.; Wells, Jonathan; Wu, Mike; Gerhart, John C. (April 1996). "Confocal microscopy analysis of living Xenopus eggs and the mechanism of cortical rotation" (PDF). Development (Cambridge: The Company of Biologists) 122 (4): 1281–1289. OCLC 15088415. PMID 8620855. Retrieved 2013-12-12.
Rowning, Brian A.; Wells, Jonathan; Wu, Mike; Gerhart, John C.; Moon, Randall T.; Larabell, Carolyn A. (February 18, 1997). "Microtubule-mediated transport of organelles and localization of β-catenin to the future dorsal side of Xenopus eggs". Proceedings of the National Academy of Sciences of the United States of America (Washington, D.C.: National Academy of Sciences) 94 (4): 1224–1229. doi:10.1073/pnas.94.4.1224. ISSN 0027-8424. PMC 19772. PMID 9037034. Retrieved 2008-07-16.
Books
Wells, Jonathan (1988). Charles Hodges' Critique of Darwinism: An Historical-Critical Analysis of Concepts Basic to the 19th Century Debate. illustrations by Jody F. Sjogren. Lewiston, NY: Edwin Mellen Press. ISBN 0-88946-671-8. LCCN 87031222. OCLC 16924943.
—— (2000). Icons of Evolution: Science or Myth?: Why Much of What We Teach About Evolution is Wrong. Washington, D.C.: Regnery Publishing. ISBN 0-89526-276-2. LCCN 00062544. OCLC 44768911.
—— (2006). The Politically Incorrect Guide to Darwinism and Intelligent Design. Washington, D.C.: Regnery Publishing. ISBN 978-1-596-98013-6. LCCN 2008270992. OCLC 70870578.
Dembski, William A.; Wells, Jonathan (2008). How to be an Intellectually Fulfilled Atheist (or not) (1st ed.). Wilmington, DE: ISI Books. ISBN 978-1-933-85984-2. LCCN 2008934995. OCLC 232128215.
——; —— (2008). Dembski, William A., ed. The Design of Life: Discovering Signs of Intelligence in Biological Systems. Dallas, TX: Foundation for Thought and Ethics. ISBN 978-0-980-02130-1. LCCN 2009281462. OCLC 183624199.
Wells, Jonathan (2011). The Myth of Junk DNA (1st ed.). Seattle, WA: Discovery Institute Press. ISBN 978-1-936-59900-4. LCCN 2011925471. OCLC 739090951.

Wells, Jonathan (November 2004). "Using Intelligent Design Theory to Guide Scientific Research" (PDF). Progress in Complexity, Information and Design (Princeton, NJ: International Society for Complexity, Information, and Design). 3.1.2. ISSN 1555-5089. OCLC 315922913. Retrieved 2008-07-16.
Gishlick, Alan D. (November 23, 2006). "Icon 4 — Haeckel's Embryos". National Center for Science Education. Berkeley, CA: National Center for Science Education. Retrieved 2008-12-17.
Wells, Jonathan. "Darwinism: Why I Went for a Second Ph.D.". True Parents Organization. Denver, CO. Retrieved 2013-12-12.
Forrest, Barbara (March 2000). "Barbara Forrest's Letter to Simon Blackburn". In Dembski, William A. "The Rise and Fall of Baylor University's Michael Polanyi Center". DesignInference.com. William Dembski. Retrieved 2013-12-12. "As I stated earlier, Johnson, Dembski, and their associates have assumed the task of destroying 'Darwinism,' 'evolutionary naturalism,' 'scientific materialism,' 'methodological naturalism,' 'philosophical naturalism,' and other 'isms' they use as synonyms for evolution." Quoted in "Rebuttal to Reports by Opposing Expert Witnesses" (PDF) by William A. Dembski (May 14, 2005).
Wells, Jonathan. "INTRODUCTION to ICONS of EVOLUTION: Science or Myth? Why much of what we teach about evolution is wrong". Icons of Evolution. Seattle, WA: Discovery Institute. Retrieved 2013-12-12. "Biological evolution is the theory that all living things are modified descendants of a common ancestor that lived in the distant past. It claims that you and I are descendants of ape-like ancestors, and that they in turn came from still more primitive animals.
[...]
...much of what we teach about evolution is wrong. This fact raises troubling questions about the status of Darwinian evolution. If the icons of evolution are supposed to be our best evidence for Darwin's theory, and all of them are false or misleading, what does that tell us about the theory? Is it science, or myth?"
Coyne, Jerry (April 12, 2001). "Creationism by stealth". Nature (Book review) (London: Nature Publishing Group) 410: 745–46. doi:10.1038/35071144. Retrieved 2006-12-24.
Wells, Jonathan (June 12, 2002). "Critics Rave Over Icons of Evolution: A Response to Published Reviews". Center for Science and Culture. Seattle, WA: Discovery Institute. Retrieved 2007-08-13. "Several of them grossly exaggerate or distort the truth, while others are patently false. Yet they are found year after year in almost all textbooks dealing with evolutionary theory, and they invariably accompany other material promoting that theory. When someone points out that the textbook examples misrepresent the facts, Darwinists don't rush to correct them. Instead, they rush to defend them."
Forrest & Gross 2004, p. 98. Reviews specifically cited include those by David Ussery, Massimo Pigliucci, Kevin Padian and Alan Gishlick.
Humburg, Burt (August 26, 2006). "The Politically Incorrect Guide to Darwinism and Intelligent Design Review: Why Should Words Have Meanings? (Chapter 1)". In Cartwright, Reed A. The Panda's Thumb (Blog). Houston, TX: The TalkOrigins Foundation, Inc. Retrieved 2007-02-04. "In order to advance his thesis, Wells has to convey the idea that 'Darwinism' pits itself against traditional Christianity: to allow pupils to learn it is to give them up to atheism, decadence, liberalism and to lose the culture war.
Note that Wells does not wage war against evolution. In fact, he is at pains to make it (somewhat) clear that he wages war against 'Darwinism', which in context might sound like the sort of thing any sensible Christian would want to guard against. Unfortunately, Wells isn't exactly clear what he means by Darwinism as opposed to evolution.
[...]
Easily, one of the prominent faults of Wells’s screed is a pervasive confusion between terms. Words, like 'Darwinism' and 'Traditional Christianity', seem to mean whatever Wells wants them to mean for that specific sentence. In many cases words are used without regard for his own stated definitions and usually without regard to usage elsewhere in his book. There are several possible reasons for this confusion in terms. First, Wells confusion may be by design. I have argued elsewhere that creationists intend to confuse their audiences when they argue. Second, if you review the acknowledgements page, you’ll read how Wells used many authors to help him prepare this text. It is possible that Wells's editorship was so insufficient that he allowed a term that makes up part of the book's very title to have a flexible meaning. My suspicion is that there was both disparity between the understanding of key terms by different authors as well as an intention to confuse."
Cashill 2005, p. 174
Wells, Jonathan. "Jonathan Wells Then". The Politically Incorrect Guide to Darwinism and Intelligent Design. Seattle, WA: The Discovery Institute. Retrieved 2008-07-16.
Numbers 2006, p. 381
"Board of Trustees". True Parents Organization. Denver, CO. Retrieved 2013-12-12.
Antal, Chris (February 2000). "New Hope for Dialogue with National Council of Churches of Christ". True Parents Organization. Denver, CO. Retrieved 2013-12-12.
"CULTIVATING FRIENDS REV. MOON HOSTS RELIGIOUS SCHOLARS". Philadelphia Daily News. November 21, 1985.[verification needed]
Wells, Jonathan. "Marriage and the Family: the Unification Blessing". True Parents Organization. Denver, CO. Retrieved 2013-12-12.
Lanham, Cheryl Wetzstein (September 1994). "True Subject and Object, Not Men and Women". Unification News (Letter to the editor (reprint)) (New York: Holy Spirit Association for the Unification of World Christianity). ISSN 1061-0871. Retrieved 2013-12-12.
"Unificationist Photos from 1997 and 1998". True Parents Organization. Denver, CO. Retrieved 2013-12-12.
"Jonathan Wells, Senior Fellow - CSC". Discovery Institute. Seattle, WA: Discovery Institute. Retrieved 2013-12-12.
"Society Fellows". International Society for Complexity, Information, and Design. Princeton, NJ: International Society for Complexity, Information, and Design. Retrieved 2013-12-12.
"Intelligent Design and Peer Review". American Association for the Advancement of Science. Washington, D.C. Archived from the original on 2007-03-07. Retrieved 2013-12-12.
Wells Hits a Home Run at Harvard
Panelists Discuss Validity Of Evolutionary Theory
Why I Won't Debate Creationists
Wells and Palumbi debate
"Dr. Jonathan Wells Returns to UTS". The Cornerstone (Barrytown, NY: Unification Theological Seminary). May–June 1997. ISSN 0197-5196. Retrieved 2013-12-12.
Andrew, Stephen (January 15, 2006). "Know Your Creationists". Daily Kos (Blog). Berkeley, CA: Kos Media, LLC. OCLC 59226519. Retrieved 2013-12-12.
Wilkins, John S. (March 30, 2004). "Mything the point: Jonathan Wells' bad faith". The Panda's Thumb (Blog). Houston, TX: The TalkOrigins Foundation, Inc. Retrieved 2014-01-18.
Myers, PZ (January 24, 2007). "Jonathan Wells knows nothing about development, part I". Pharyngula (Blog). ScienceBlogs LLC. Retrieved 2014-01-18.
Myers, PZ (January 25, 2007). "Jonathan Wells knows nothing about development, part II". Pharyngula (Blog). ScienceBlogs LLC. Retrieved 2014-01-18.
Myers, PZ (November 3, 2006). "PZ Myers is such a LIAR!". Pharyngula (Blog). ScienceBlogs LLC. Retrieved 2014-01-18.
Smith, Tara C. (January 31, 2007). "Whereby Jon Wells is smacked down by an undergrad in the Yale Daily News". Aetiology (Blog). ScienceBlogs LLC. Retrieved 2014-01-18.
"Article Database". Discovery Institute. Seattle, WA: Discovery Institute. Retrieved 2013-12-12. List of articles written by Jonathan Wells.
Wells, Jonathan. "Evolution by Design". True Parents Organization. Denver, CO. Retrieved 2013-12-12.
"The C-Files: Jonathan Wells". New Mexicans for Science and Reason. Peralta, NM: New Mexicans for Science and Reason. Retrieved 2008-05-17.
Milner, Richard; Maestro, Vittorio, eds. (April 2002). "Intelligent Design?". Natural History (Research Triangle Park, NC: Natural History Magazine, Inc.). Retrieved 2013-12-12.
Robinson, Peter (host); Massimo, Pigliucci; Wells, Jonathan (January 14, 2005). "MONKEY BUSINESS: Evolution and Intelligent Design". Uncommon Knowledge. Stanford, CA: Hoover Institution. PBS. KTEH. Retrieved 2008-07-17.
Pigliucci 2002, pp. 44–45
Pennock, Robert T. (September 2003). "Creationism and Intelligent Design" (PDF). Annual Review of Genomics and Human Genetics (Palo Alto, CA: Annual Reviews) 4: 143–163. doi:10.1146/annurev.genom.4.070802.110400. PMID 14527300. Retrieved 2008-07-16.
Chang, Kenneth (February 21, 2006). "Few Biologists but Many Evangelicals Sign Anti-Evolution Petition". The New York Times. Retrieved 2008-05-05.
"A Scientific Dissent From Darwinism" (PDF). Discovery Institute. Seattle, WA: Discovery Institute. Retrieved 2008-05-05.
"10 Questions, and Answers, About Evolution". The New York Times. August 23, 2008. Retrieved 2008-09-17.
"'A Teacher on the Front Line'". National Center for Science Education. Berkeley, CA: National Center for Science Education. August 24, 2008. Retrieved 2008-09-06.
"10 Answers to Jonathan Wells's '10 Questions'". National Center for Science Education. Berkeley, CA: National Center for Science Education. October 17, 2008. Retrieved 2008-02-19.
"Scientist Exposes Evolution’s Weaknesses in Politically Incorrect Book About Darwinism and Intelligent Design". Center for Science and Culture. Seattle, WA: Discovery Institute. August 2, 2006. Retrieved 2013-12-12.
Padian, Kevin; Gishlick, Alan D. (March 2002). "The Talented Mr. Wells". The Quarterly Review of Biology (Chicago: University of Chicago Press) 77 (1): 33–37. doi:10.1086/339201.
Gishlick, Alan D. (October 19, 2008). "Why much of what Jonathan Wells writes about evolution is wrong". National Center for Science Education. Berkeley, CA: National Center for Science Education. Retrieved 2013-12-12.
Matzke, Nick. "Icon of Obfuscation". TalkOrigins Archive. Houston, TX: The TalkOrigins Foundation, Inc. Retrieved 2013-12-12.
Scott, Eugenie C. (June 2001). "Fatally Flawed Iconoclasm". Science (Book review) (Washington, D.C.: American Association for the Advancement of Science) 292 (5525): 2257–2258. doi:10.1126/science.1060716. Retrieved 2007-05-17.
Pigliucci 2002, pp. 252–264
Forrest & Gross 2004, p. 105
Weisenberg, Richard (December 16, 2000). "Challenging ideas against teaching of evolution". The Philadelphia Inquirer (Letter to the editor) (Interstate General Media). p. A16. Retrieved 2013-12-12. Letter in response to "Let's Change Science Standards And Let Students Do Real Science" by Jonathan Wells (December 11, 2000).
Forrest & Gross 2004, p. 111. Quoting Dr. Bruce Grant, Professor of Biology at College of William & Mary: "But should we blame Ms Rider for her outrage upon learning that moths were glued to trees? No. Instead I blame Dr Wells, who wrote the article she cites as her source of information. While he has done no work on industrial mechanism, he has written an opinion about that work. To one outside the field, he passes as a scholar, complete with Ph.D. Unfortunately, Dr Wells is intellectually dishonest. . . . He lavishly dresses his essays in quotations from experts (including some from me) which are generally taken out of context, and he systematically omits relevant details to make our conclusions seem ill founded, flawed, or fraudulent."
Coyne, Jerry (December 6, 2000). "Criticism of moth study no challenge to evolution". The Pratt Tribune (Letter to the editor) (Pratt, KS: GateHouse Media). Retrieved 2013-12-12. "Creationists such as Jonathan Wells claim that my criticism of these experiments casts strong doubt on Darwinism. But this characterization is false. ... My call for additional research on the moths has been wrongly characterized by creationists as revealing some fatal flaw in the theory of evolution. ... It is a classic creationist tactic (as exemplified in Wells' book, 'Icons of Evolution') to assert that healthy scientific debate is really a sign that evolutionists are either committing fraud or buttressing a crumbling theory."
"Kansas Evolution Hearings: Jonathan Wells, Bruce Simat, Giuseppe Sermonti, and Ralph Seelke". TalkOrigins Archive (Transcript from the Kansas evolution hearings). Houston, TX: The TalkOrigins Foundation, Inc. Retrieved 2013-12-12.
Bethell, Tom (September 1, 2006). "'Politically Incorrect' Series Takes on Darwinism and Intelligent Design". Human Events (Washington, D.C.: Eagle Publishing, Inc.). ISSN 0018-7194. Retrieved 2013-12-12.
Cartwright, Reed A., ed. (August 19, 2006). "The Politically Incorrect Guide to Darwinism and Intelligent Design Review". The Panda's Thumb (Blog). Houston, TX: The TalkOrigins Foundation, Inc. Retrieved 2006-11-04.
Rosen, Rebecca (May 16, 2009). "Starbucks stirs things up with controversial quotes". The Denver Post (MediaNews Group). Retrieved 2009-03-29.
"The Group". VirusMyth: A Rethinking AID$ Website. Hilversum, Netherlands: Robert Laarhoven. Retrieved 2013-12-12.
Quittman, Beth (September 8, 2006). "Undercover at the Discovery Institute". Seattlest (Blog) (New York: Gothamist LLC). Retrieved 2008-07-17. Wells' "personal peculiarities include membership in the Moonies and support for AIDS reappraisal - the theory that the HIV is not the primary cause of AIDS."
"Aids 'denialism' gathers strange bedfellows". The Vancouver Sun (Vancouver, BC: Postmedia Network Inc.). June 17, 2006. Retrieved 2008-07-17.

Cashill, Jack (2005). Hoodwinked: How Intellectual Hucksters Have Hijacked American Culture. Nashville, TN: Nelson Current. ISBN 1-59555-011-9. LCCN 2005006138. OCLC 58386577.
Forrest, Barbara; Gross, Paul R. (2004). Creationism's Trojan Horse: The Wedge of Intelligent Design. Oxford; New York: Oxford University Press. ISBN 0-19-515742-7. LCCN 2002192677. OCLC 50913078.
Numbers, Ronald L. (2006) [Originally published 1993; Berkeley: University of California Press]. The Creationists: From Scientific Creationism to Intelligent Design (Expanded ed.). Cambridge, MA: Harvard University Press. ISBN 0-674-02339-0. LCCN 2006043675. OCLC 69734583.
Pigliucci, Massimo (2002). Denying Evolution: Creationism, Scientism, and the Nature of Science. Sunderland, MA: Sinauer Associates. ISBN 0-87893-659-9. LCCN 2002005190. OCLC 49530100.

Jonathan Wells biography from the Discovery Institute
Articles by Wells from the Discovery Institute
Articles by Wells from the Access Research Network
"Icons of Evolution FAQs" from talk.origins
Wells's testimony at the Kansas evolution hearings
"Icons of Evolution? – Why much of what Jonathan Wells writes about evolution is wrong" by Alan D. Gishlick
"10 Answers to Jonathan Wells's '10 Questions'" from National Center for Science Education
Chapter by chapter analysis of Wells's The Politically Incorrect Guide to Darwinism and Intelligent Design by Dr. Reed A. Cartwright, The Panda's Thumb.

The people who tried to play God

     The Human Genome Project began the first phases of it construction during the year 1987 and was completed in the year 2001.  The founders and all the employees of this biotechnological project are all bunch of devil worshiping racist eugenicist pigs that can also be defined as Nazi World War 2 scientists who thought that they could play God with God’s creation when in fact they are not God and are only a collection of scientists and engineers attempting to disturb and alter the most basic and fundamental properties of human biology such as tampering with the human germ line that will only result in more and more anger from God (with each passing day of the Human Genome Project’s existence), manifested by God in the form of more and more weather catastrophes, drought, spread of disease, epidemics, famine and plagues.      

     There is no evidence to accurately correlate this cause and effect relationship, but to defy God in this manner surely qualifies to Him to be angry at his creation and at the God defying works of altering, synthesizing, sterilizing the weak and disabled, modifying human gene frequencies, and the cloning of plants, animals and human beings.  

     

Bioengineering and eugenics

     In the mid-1990s, embryologist Jacques Cohen pioneered a promising new technique for helping infertile women have children. His technique, known as cytoplasmic transfer, was intended to "rescue" the eggs of infertile women who had undergone repeated, unsuccessful attempts at in vitro fertilization, or IVF. It involved injecting the cytoplasm found inside the eggs of a fertile donor, into the patient's eggs.
When the first baby conceived through cytoplasmic transfer was born in 1997, the press instantly hailed Cohen's technique as yet another technological miracle. But four years later, the real story has proven somewhat more complicated. Last year, Cohen and his colleagues at the Institute for Reproductive Medicine and Science of St. Barnabas, a New Jersey fertility clinic, set off alarm bells among bioethicists with the publication of a paper detailing the genetic condition of two the 17 cytoplasmic-transfer babies born through the clinic to date. The embryologists reported that they had endowed the children with extra bits of a special type of genetic material, known as mitochondrial DNA, or mtDNA, which came with the cytoplasm transferred from the donor eggs to the patient's.
     That meant the resulting children had three genetic parents: mother, father, and mtDNA donor. It also meant that female children would transmit their unorthodox combination of mitochondrial DNA to their own offspring (mtDNA is passed down only through eggs), with unknown implications. In effect, Cohen had created the first bioengineered babies. As Cohen's group noted, their experiment was "The first case of human [inheritable] genetic modification resulting in normal, healthy children."
     Just how normal those children will turn out to be is anybody's guess. At a recent meeting in Europe, the New Jersey researchers reported that one of the children conceived through cytoplasmic transfer has been diagnosed with "pervasive developmental disorder," a catch-all term for symptoms that range from mild delays in speech to autism. Cohen's group maintained that it is extremely unlikely that cytoplasmic transfer and the resulting mishmash of mtDNA is to blame.
     But geneticists have only begun to trace the connections between mtDNA and a host of diseases ranging from strange metabolic ailments to diabetes and Lou Gehrig's disease, and some experts argued that the child's disorder may well be caused by a mismatch between the donor and mother's mtDNA. As Jim Cummins, a molecular biologist at Murdoch University in Western Australia, put it: "To deliberately create individuals with multiple mitochondrial genotypes without knowing the consequences is really a step into the dark."
     Welcome to the murky world of "reprogenetics," as Princeton biologist Lee Silver has dubbed the merger between the science of genetics and the fertility industry. While much of the nation's attention has been focused on human cloning, a possibility that is still largely theoretical, a massive, uncontrolled experiment in bioengineering humans is well underway in the Wild West of American fertility clinics, as Cohen and his colleagues have demonstrated. Indeed, there has been more debate over---and far more research into---the implications of bioengineered corn than of bioengineered humans.
     Now, many bioethicists believe that Cohen's experiment with cytoplasmic transfer was just one more small step towards a world in which eugenics is another name for making babies. Today, any couple with several thousand dollars to spare can choose the sex of their offspring, while parents who are carriers for certain genetic disorders can undergo IVF and have the resulting embryos genetically tested to ensure their children are free of disease. Tomorrow, parents may be able to enhance their offspring with designer genes. One day, the fertility industry's efforts to help couples conceive could bring society to the brink of altering the genetic heritage of the species.
     All that currently stands in the way of parents bent on practicing homegrown eugenics are the ethics of individual fertility specialists and the technical hurdles. Most fertility doctors have the best of intentions, to help patients get pregnant, and to avoid transmitting debilitating disease. And it is by no means certain that science will ever be able to offer parents the option of bioengineering their offspring.
     All the same, the pace of the technology is dizzying. A year ago, scientists at the Oregon Regional Primate Research Center announced the birth of the first genetically engineered primate, named ANDi (for "inserted DNA" spelled backwards), a rhesus monkey whose cells contained the gene that makes jellyfish glow in the dark. The experiment was something of a flop; ANDi does not glow. (Rodents implanted with the gene do.) But imagine that one day science does acquire the skills to make "designer babies," that the connections between genes and complex traits such as intelligence or musical ability are finally known. While only the weirdest of parents would to want to genetically engineer offspring with jellyfish genes, others would undoubtedly jump at the chance to "customize" their children with a sparkling personality, brains, and beauty.
     One need not be deeply religious or oppose abortion to be troubled by the prospect of a society in which, as bioethicist Alexander Capron puts it, "the wanted child becomes the made-to-order child."
     One near-term possibility that many parents, if given the opportunity, will want to weed out embryos carrying genetic traits for a host of non-lethal conditions, like baldness, shyness, short stature, or homosexuality. Fertility specialists are already getting requests from prospective parents who want to know if they can be assured their embryos won't turn out to be hyperactive or gay. Today, Tom Sawyer and Huck Finn would have been diagnosed with attention-deficit disorder and medicated. Tomorrow, they might not be allowed out of the petri dish.
     Yet thanks largely to abortion politics and our collective squeamishness about intruding on the individual's right to become a parent, the nation has few mechanisms in place for controlling the pace of this new technology, ensuring the safety of patients, or even talking about the ethics of such experiments.
     Since 1998, the Food and Drug Administration (FDA) has argued that genetically manipulated embryos are a "biological product," and therefore subject to regulation, just like medical devices and drugs. But because of a quirk in federal law, the FDA's authority in this sphere is far from certain.
     Last summer, FDA sent warning letters to six fertility centers threatening "enforcement action," and asserting its regulatory power over "therapy involving the transfer of genetic material by means other than the union of [sperm and egg.]" Cohen's clinic at St. Barnabas chose to stop performing cytoplasmic transfer. But at least two other recipients scoffed at the agency's threat: Panos Zavos, an embryologist at a Kentucky fertility clinic, and Brigitte Boisselier, the scientific director of Clonaid, the clinic set up by a group known as the Raelians, who believes human beings were genetically engineered by aliens. Both have announced their intentions to clone a human being.
     Both also disputed the FDA's authority, and several bioethicists and legal scholars had to agree that the FDA could not prevent them from tinkering with human bioengineering. "It's a stretch for the FDA," says R. Alta Charo, a legal scholar and bioethicist at the University of Wisconsin, and former member of President Bill Clinton's Bioethics Advisory Committee.
     When the state of Virginia approved the opening of the nation's first IVF clinic in Norfolk, Va., in 1980, anti-abortionists protested by the hundreds. Abortion opponents were concerned that fertility doctors would be playing God with babies' lives, and that they would discard or experiment on imperfect embryos before implantation. They also feared that couples would be inclined to abort abnormal fetuses.
     Charles Dean Jr., president of the Norfolk chapter of the anti-abortion Virginia Society for Human Life, told The Washington Post, perhaps somewhat presciently, "There was no proper study of the medical, moral, legal and scientific merits [of IVF]. Meanwhile, we're charging off into the darkness, and I feel it's a tragedy and a disgrace."
     In fact, there had been two decades of research in animals on IVF, and the protesters failed to block the Norfolk clinic from producing its first test-tube baby a year later. But abortion foes did manage to take their case to the federal government. After Louise Brown, the first test-tube baby, was born in England in 1978, and the potential for the new technology became apparent, researchers at the Norfolk clinic, along with several other American scientists, applied for federal funds for embryo research.
     The anti-abortion movement, however, intervened and successfully lobbied the government to ban federal funding in the field. The ban did little to address the protesters' core concerns about the implications and use of new reproductive technology. In fact, one could argue that it only made the situation worse.
     As it turned out, fertility doctors didn't need federal money. With millions of American couples unable to conceive, doctors and embryologists found a lucrative market for the end products of their work, which could legally continue so long as it involved no federal funds.
     Financed entirely with private money, the burgeoning fertility industry emerged without a framework for deliberating the ethics of the technology. It also was not bound by any of the requirements that would have come with federally regulated research funds to adequately test new techniques for safety and efficacy before putting them into widespread use.
     Not surprisingly, the industry boomed. In 1985, there were 30 fertility clinics in the U.S. A decade later, there were more than 300. More than one million couples seek fertility treatment each year, and spend more than $3 billion in pursuit of babies. Fees for IVF, the simplest procedure offered, vary between $5,000 and $15,000, with another $2,000 to $3,000 for fertility drugs. A new technology, called pre-implantation genetic diagnosis, or PGD, allows parents who are carriers for certain recessive genetic disorders, like cystic fibrosis and hemophilia, to screen embryos before they are transferred to the mother's womb. PGD can add several thousand dollars to the bill.
     With so much money at stake, the market for fertility services is highly competitive, but without government regulation or oversight, the infertility business has become a bit like the dietary supplement industry. There are lots of miraculous claims but not much data to back them up---and tremendous financial incentive to push the envelope with radical new products.
     For instance, not all clinics are equally adept at producing babies. Clinic success rates have improved steadily over the last few years, from an average of 17 percent in 1992 for women under 40, to nearly 30 percent in 1999, the most recent year for which figures are available. But these rates vary wildly, from as low as 14 percent to as high as 60 percent.
     And babies, of course, are what patients are paying for---usually out of their own pockets, because most insurers do not cover IVF treatment. Clinics have strong financial incentives to inflate their pregnancy rates, or at least to persuade prospective patients that their chances of getting pregnant are high. The largest clinics have substantial advertising budgets, and they market heavily to primary care physicians, who refer patients to clinics, with lavish dinners and seminars in exotic locales.
     The fertility industry's self-promotion has gone largely unchallenged, either by the media or the scientific community. While the press has hailed each new development as a godsend for desperate would-be parents, with headlines such as "Amazing Medical Breakthrough" and "New Hope for Infertile Couples," medical researchers who may doubt the validity of these claims have for the most part remained mute. That's because the ban on federal funding for embryo research has made objective analysis of new techniques nearly impossible, and have left infertile couples the unwitting participants in a vast experiment of largely untested technology.
     Scientific development in the field has fallen not to high-caliber, federally funded embryologists, but instead to the clinics themselves, which use profits from patients to conduct research. The technology has proceeded with minimal government oversight and peer review, and in the opinion of many biologists, has suffered in quality as a result. "There is no real hard-core scientific background on the part of many of the individuals who are doing this work," says Jonathan Van Blerkom, a leading embryologist at the University of Colorado. Clinics focus their efforts almost exclusively on increasing pregnancy rates, often with little regard for the basic biology and potential consequences to patients and babies.
     In the early 1990s, for example, clinics were trumpeting an alphabet soup of new techniques, with names like GIFT, for gamete intra-fallopian transfer, and ZIFT, for zygote intra-fallopian transfer. Both involved surgery, and were used on hundreds of patients, only to be abandoned when clinicians figured out they did not improve pregnancy rates and other techniques proved more helpful.
     "Co-culture," the practice of mixing reproductive tissue taken from animals with the culture medium was widely used to incubate embryos, with little regard for the possibility that animal tissue might contain contaminants, such as the infectious agent that causes mad cow disease. Without quantitative results to guide the field, such untested techniques as co-culture are often adopted on faith.
     In most cases, patients and potential offspring were unharmed, but not always. Take, for example, "assisted hatching" a technique that involves creating a tiny hole in the outer covering of an embryo just before transferring it to the mother's womb. Many fertility specialists believe that assisted hatching helps embryos implant properly in the womb and boosts pregnancy rates, although they have little hard evidence for this. Assisted hatching also may increase the risk of conjoined, or Siamese, twins. But there are no statistics available to pin down the risk, because most families choose to abort, and clinics are reluctant to publish such results.
     Then there's intra-cytoplasmic sperm injection (ICSI), a procedure that was hailed in the mid-90s as a breakthrough in male infertility. ICSI does indeed allow men with few or feeble sperm to become fathers. An embryologist draws a single sperm into a micro-needle and then injects it directly into the mother's egg, rather than simply mixing sperm and eggs in a petri dish, as in normal IVF.
     To date, several thousand American babies have been born thanks to the steady hands of embryologists. Yet the technology's long-term safety is still unclear. "ICSI is almost certainly going to increase the likelihood of male infertility in the offspring," says Murdoch University's Jim Cummins. Since ICSI is only ten years old, there's no way to settle the question until ICSI boys grow up.
     In the meantime, ICSI children may be vulnerable to birth defects. In November 1997, The British Medical Journal published a controversial study that found that ICSI babies were 200 percent more likely to have a major birth defect than babies conceived naturally, and 50 percent more likely to have a minor defect. Some critics argue that this study suffers from statistical flaws, but a variation on the technology, known as second-day ICSI, heightens the risk of such chromosomal abnormalities as Down's syndrome, and clinics have stopped using it.
     Even when techniques pose a clear danger to offspring, clinics are loath to abandon them as long as they boost pregnancy rates. The most glaring example is the practice of transferring multiple embryos to a woman's womb. Since 1980, according to the National Center for Health Statistics, the number of twins born per year has risen 67 percent. The rate of triplets and higher-order birth multiples has soared from 37 per 100,000 live births in 1980 to 184 per 100,000 in 1999. The increase is due almost entirely, according to federal statisticians, to fertility treatments. Only 20 percent of triplets and higher-order multiples are conceived naturally. (Most extremely high-order multiples, like the McCaughey septuplets, occur when the woman is given fertility drugs and her doctor fails to recognize how many eggs she has produced.)
     The risks to multiples and their mother are substantial, and so is the cost. Women pregnant with multiples are more likely than those with singletons to suffer premature delivery, toxemia (a potentially fatal form of high blood pressure), and hemorrhage. Their infants are vulnerable to cerebral palsy, learning disabilities, blindness, developmental delays, and mental retardation, largely because they are often born prematurely. While there are no national statistics on the cost of multiples, a recent study, published in The Journal of Maternal and Fetal Medicine, found that the average charge per triplet pregnancy at one New York City hospital was nearly $190,000. Other studies have shown that triplets can cost as much as 400 times a standard singleton pregnancy and delivery.
     "Data on higher-order gestations have been known for years," says Van Blerkom. But fertility clinics have been unwilling to do anything about it he says, for fear they would cut their pregnancy rates. "Have you ever seen a fertility specialist stand next to a couple with their premature quads and say, ŒThis is a disaster for these patients. I think we blew it?'" says Van Blerkom. "Most people in the field were content to let selective terminations at week 13 or 14 clean up the problem."
     Under pressure from insurance companies, who often refuse to pay for IVF but wind up footing the bill for multiple births, the American Society for Reproductive Medicine finally issued guidelines last year aimed at reducing the chances of multiples. From the outside, the guidelines seem self-evident: For younger patients, ASRM recommended transferring at most two embryos to the mother's womb; older women, whose embryos are less likely to implant in the uterus and begin developing, can receive as many as five.
     But for clinics, the dual pressures of profitability and desperate patients have made such seemingly obvious precautions difficult to follow. "We're under pressure to have high pregnancy rates," complains one clinic doctor. "The problem is we've never had any way of knowing what was the right number of embryos to transfer."
     European fertility specialists, who are often required by law to transfer no more than one or two embryos to a single patient, don't seem to have the same trouble. They use research conducted by Van Blerkom and others in the late 1990s showing how to select the most viable embryos and reduce the number that is transferred to the mother. But choosing embryos requires painstaking attention, often at odd hours of the night, and American fertility clinics have been reluctant to invest in technologists who can perform it.
     Without federal funding for studies, or oversight from a government body like the FDA, reproductive medicine has had little outside incentive to make such changes as bringing down the rate of multiple births. "We've got the worst system you could possibly come up with," says Dr. Lawrence Udoff, a fertility specialist and director of the pre-implantation genetics program at the University of Maryland at Baltimore. "There are people in this business who are a lot better at marketing than they are at replicating their results. The patient ends up footing the bill for procedures that are untested."
     The industry trade group, the American Society for Reproductive Medicine, argues that fertility doctors are doing nothing different from any other specialist. "Reproductive medicine starts from the same regulatory basis as every other kind of medicine," says ASRM spokesman, Sean Tipton. If a heart surgeon thinks a new way of tying off an artery might work, she simply does it. If the patient lives, she tries it again. Eventually, she may take a retrospective look at her cases and compare the outcomes of those who received the new method versus the old.
     It is also true, however, that the history of medicine is littered with examples of doctors unquestioningly adopting new treatments long before they have been evaluated, only to abandon them when they turn out to be ineffective---or worse. More than 30,000 women with breast cancer received high dose chemotherapy with bone-marrow transplants in the 1980s and 90s. At least 9,000 died from the treatment before researchers finally performed clinical trials, which ultimately demonstrated that high dosage is no better than standard chemotherapy regimens.
     The deeper question, of course, is why we allow uncontrolled experimentation on human subjects in any branch of medicine. But the issue is particularly pressing for reproductive technologies, especially now that fertility centers are wading into the uncharted waters of the gene pool.
     Embryologists have already experimented with transferring the nucleus of an older woman's egg into a young donor's egg from which the nucleus has been removed, a technique that is similar to the method used to create Dolly, the sheep. Another fertility team successfully split a human embryo into several identical copies, a trick that could one day help infertile women who produce very few eggs. But it could also make possible such Dorian Gray scenarios as multiple identical embryos being thawed and then born several years apart, or a woman giving birth to herself.
     In the mid-1990s, embryologist Jacques Cohen pioneered a promising new technique for helping infertile women have children. His technique, known as cytoplasmic transfer, was intended to "rescue" the eggs of infertile women who had undergone repeated, unsuccessful attempts at in vitro fertilization, or IVF. It involved injecting the cytoplasm found inside the eggs of a fertile donor, into the patient's eggs.
When the first baby conceived through cytoplasmic transfer was born in 1997, the press instantly hailed Cohen's technique as yet another technological miracle. But four years later, the real story has proven somewhat more complicated. Last year, Cohen and his colleagues at the Institute for Reproductive Medicine and Science of St. Barnabas, a New Jersey fertility clinic, set off alarm bells among bioethicists with the publication of a paper detailing the genetic condition of two the 17 cytoplasmic-transfer babies born through the clinic to date. The embryologists reported that they had endowed the children with extra bits of a special type of genetic material, known as mitochondrial DNA, or mtDNA, which came with the cytoplasm transferred from the donor eggs to the patient's.
     That meant the resulting children had three genetic parents: mother, father, and mtDNA donor. It also meant that female children would transmit their unorthodox combination of mitochondrial DNA to their own offspring (mtDNA is passed down only through eggs), with unknown implications. In effect, Cohen had created the first bioengineered babies. As Cohen's group noted, their experiment was "The first case of human [inheritable] genetic modification resulting in normal, healthy children."
     Just how normal those children will turn out to be is anybody's guess. At a recent meeting in Europe, the New Jersey researchers reported that one of the children conceived through cytoplasmic transfer has been diagnosed with "pervasive developmental disorder," a catch-all term for symptoms that range from mild delays in speech to autism. Cohen's group maintained that it is extremely unlikely that cytoplasmic transfer and the resulting mishmash of mtDNA is to blame.
     But geneticists have only begun to trace the connections between mtDNA and a host of diseases ranging from strange metabolic ailments to diabetes and Lou Gehrig's disease, and some experts argued that the child's disorder may well be caused by a mismatch between the donor and mother's mtDNA. As Jim Cummins, a molecular biologist at Murdoch University in Western Australia, put it: "To deliberately create individuals with multiple mitochondrial genotypes without knowing the consequences is really a step into the dark."
     Welcome to the murky world of "reprogenetics," as Princeton biologist Lee Silver has dubbed the merger between the science of genetics and the fertility industry. While much of the nation's attention has been focused on human cloning, a possibility that is still largely theoretical, a massive, uncontrolled experiment in bioengineering humans is well underway in the Wild West of American fertility clinics, as Cohen and his colleagues have demonstrated. Indeed, there has been more debate over---and far more research into---the implications of bioengineered corn than of bioengineered humans.
     Now, many bioethicists believe that Cohen's experiment with cytoplasmic transfer was just one more small step towards a world in which eugenics is another name for making babies. Today, any couple with several thousand dollars to spare can choose the sex of their offspring, while parents who are carriers for certain genetic disorders can undergo IVF and have the resulting embryos genetically tested to ensure their children are free of disease. Tomorrow, parents may be able to enhance their offspring with designer genes. One day, the fertility industry's efforts to help couples conceive could bring society to the brink of altering the genetic heritage of the species.
     All that currently stands in the way of parents bent on practicing homegrown eugenics are the ethics of individual fertility specialists and the technical hurdles. Most fertility doctors have the best of intentions, to help patients get pregnant, and to avoid transmitting debilitating disease. And it is by no means certain that science will ever be able to offer parents the option of bioengineering their offspring.
     All the same, the pace of the technology is dizzying. A year ago, scientists at the Oregon Regional Primate Research Center announced the birth of the first genetically engineered primate, named ANDi (for "inserted DNA" spelled backwards), a rhesus monkey whose cells contained the gene that makes jellyfish glow in the dark. The experiment was something of a flop; ANDi does not glow. (Rodents implanted with the gene do.) But imagine that one day science does acquire the skills to make "designer babies," that the connections between genes and complex traits such as intelligence or musical ability are finally known. While only the weirdest of parents would to want to genetically engineer offspring with jellyfish genes, others would undoubtedly jump at the chance to "customize" their children with a sparkling personality, brains, and beauty.
     One need not be deeply religious or oppose abortion to be troubled by the prospect of a society in which, as bioethicist Alexander Capron puts it, "the wanted child becomes the made-to-order child."
     One near-term possibility that many parents, if given the opportunity, will want to weed out embryos carrying genetic traits for a host of non-lethal conditions, like baldness, shyness, short stature, or homosexuality. Fertility specialists are already getting requests from prospective parents who want to know if they can be assured their embryos won't turn out to be hyperactive or gay. Today, Tom Sawyer and Huck Finn would have been diagnosed with attention-deficit disorder and medicated. Tomorrow, they might not be allowed out of the petri dish.
     Yet thanks largely to abortion politics and our collective squeamishness about intruding on the individual's right to become a parent, the nation has few mechanisms in place for controlling the pace of this new technology, ensuring the safety of patients, or even talking about the ethics of such experiments.
     Since 1998, the Food and Drug Administration (FDA) has argued that genetically manipulated embryos are a "biological product," and therefore subject to regulation, just like medical devices and drugs. But because of a quirk in federal law, the FDA's authority in this sphere is far from certain.
     Last summer, FDA sent warning letters to six fertility centers threatening "enforcement action," and asserting its regulatory power over "therapy involving the transfer of genetic material by means other than the union of [sperm and egg.]" Cohen's clinic at St. Barnabas chose to stop performing cytoplasmic transfer. But at least two other recipients scoffed at the agency's threat: Panos Zavos, an embryologist at a Kentucky fertility clinic, and Brigitte Boisselier, the scientific director of Clonaid, the clinic set up by a group known as the Raelians, who believes human beings were genetically engineered by aliens. Both have announced their intentions to clone a human being.
     Both also disputed the FDA's authority, and several bioethicists and legal scholars had to agree that the FDA could not prevent them from tinkering with human bioengineering. "It's a stretch for the FDA," says R. Alta Charo, a legal scholar and bioethicist at the University of Wisconsin, and former member of President Bill Clinton's Bioethics Advisory Committee.
     When the state of Virginia approved the opening of the nation's first IVF clinic in Norfolk, Va., in 1980, anti-abortionists protested by the hundreds. Abortion opponents were concerned that fertility doctors would be playing God with babies' lives, and that they would discard or experiment on imperfect embryos before implantation. They also feared that couples would be inclined to abort abnormal fetuses.
     Charles Dean Jr., president of the Norfolk chapter of the anti-abortion Virginia Society for Human Life, told The Washington Post, perhaps somewhat presciently, "There was no proper study of the medical, moral, legal and scientific merits [of IVF]. Meanwhile, we're charging off into the darkness, and I feel it's a tragedy and a disgrace."
     In fact, there had been two decades of research in animals on IVF, and the protesters failed to block the Norfolk clinic from producing its first test-tube baby a year later. But abortion foes did manage to take their case to the federal government. After Louise Brown, the first test-tube baby, was born in England in 1978, and the potential for the new technology became apparent, researchers at the Norfolk clinic, along with several other American scientists, applied for federal funds for embryo research.
     The anti-abortion movement, however, intervened and successfully lobbied the government to ban federal funding in the field. The ban did little to address the protesters' core concerns about the implications and use of new reproductive technology. In fact, one could argue that it only made the situation worse.
     As it turned out, fertility doctors didn't need federal money. With millions of American couples unable to conceive, doctors and embryologists found a lucrative market for the end products of their work, which could legally continue so long as it involved no federal funds.
     Financed entirely with private money, the burgeoning fertility industry emerged without a framework for deliberating the ethics of the technology. It also was not bound by any of the requirements that would have come with federally regulated research funds to adequately test new techniques for safety and efficacy before putting them into widespread use.
     Not surprisingly, the industry boomed. In 1985, there were 30 fertility clinics in the U.S. A decade later, there were more than 300. More than one million couples seek fertility treatment each year, and spend more than $3 billion in pursuit of babies. Fees for IVF, the simplest procedure offered, vary between $5,000 and $15,000, with another $2,000 to $3,000 for fertility drugs. A new technology, called pre-implantation genetic diagnosis, or PGD, allows parents who are carriers for certain recessive genetic disorders, like cystic fibrosis and hemophilia, to screen embryos before they are transferred to the mother's womb. PGD can add several thousand dollars to the bill.
     With so much money at stake, the market for fertility services is highly competitive, but without government regulation or oversight, the infertility business has become a bit like the dietary supplement industry. There are lots of miraculous claims but not much data to back them up---and tremendous financial incentive to push the envelope with radical new products.
     For instance, not all clinics are equally adept at producing babies. Clinic success rates have improved steadily over the last few years, from an average of 17 percent in 1992 for women under 40, to nearly 30 percent in 1999, the most recent year for which figures are available. But these rates vary wildly, from as low as 14 percent to as high as 60 percent.
     And babies, of course, are what patients are paying for---usually out of their own pockets, because most insurers do not cover IVF treatment. Clinics have strong financial incentives to inflate their pregnancy rates, or at least to persuade prospective patients that their chances of getting pregnant are high. The largest clinics have substantial advertising budgets, and they market heavily to primary care physicians, who refer patients to clinics, with lavish dinners and seminars in exotic locales.
     The fertility industry's self-promotion has gone largely unchallenged, either by the media or the scientific community. While the press has hailed each new development as a godsend for desperate would-be parents, with headlines such as "Amazing Medical Breakthrough" and "New Hope for Infertile Couples," medical researchers who may doubt the validity of these claims have for the most part remained mute. That's because the ban on federal funding for embryo research has made objective analysis of new techniques nearly impossible, and have left infertile couples the unwitting participants in a vast experiment of largely untested technology.
     Scientific development in the field has fallen not to high-caliber, federally funded embryologists, but instead to the clinics themselves, which use profits from patients to conduct research. The technology has proceeded with minimal government oversight and peer review, and in the opinion of many biologists, has suffered in quality as a result. "There is no real hard-core scientific background on the part of many of the individuals who are doing this work," says Jonathan Van Blerkom, a leading embryologist at the University of Colorado. Clinics focus their efforts almost exclusively on increasing pregnancy rates, often with little regard for the basic biology and potential consequences to patients and babies.
     In the early 1990s, for example, clinics were trumpeting an alphabet soup of new techniques, with names like GIFT, for gamete intra-fallopian transfer, and ZIFT, for zygote intra-fallopian transfer. Both involved surgery, and were used on hundreds of patients, only to be abandoned when clinicians figured out they did not improve pregnancy rates and other techniques proved more helpful.
     "Co-culture," the practice of mixing reproductive tissue taken from animals with the culture medium was widely used to incubate embryos, with little regard for the possibility that animal tissue might contain contaminants, such as the infectious agent that causes mad cow disease. Without quantitative results to guide the field, such untested techniques as co-culture are often adopted on faith.
     In most cases, patients and potential offspring were unharmed, but not always. Take, for example, "assisted hatching" a technique that involves creating a tiny hole in the outer covering of an embryo just before transferring it to the mother's womb. Many fertility specialists believe that assisted hatching helps embryos implant properly in the womb and boosts pregnancy rates, although they have little hard evidence for this. Assisted hatching also may increase the risk of conjoined, or Siamese, twins. But there are no statistics available to pin down the risk, because most families choose to abort, and clinics are reluctant to publish such results.
     Then there's intra-cytoplasmic sperm injection (ICSI), a procedure that was hailed in the mid-90s as a breakthrough in male infertility. ICSI does indeed allow men with few or feeble sperm to become fathers. An embryologist draws a single sperm into a micro-needle and then injects it directly into the mother's egg, rather than simply mixing sperm and eggs in a petri dish, as in normal IVF.
     To date, several thousand American babies have been born thanks to the steady hands of embryologists. Yet the technology's long-term safety is still unclear. "ICSI is almost certainly going to increase the likelihood of male infertility in the offspring," says Murdoch University's Jim Cummins. Since ICSI is only ten years old, there's no way to settle the question until ICSI boys grow up.
     In the meantime, ICSI children may be vulnerable to birth defects. In November 1997, The British Medical Journal published a controversial study that found that ICSI babies were 200 percent more likely to have a major birth defect than babies conceived naturally, and 50 percent more likely to have a minor defect. Some critics argue that this study suffers from statistical flaws, but a variation on the technology, known as second-day ICSI, heightens the risk of such chromosomal abnormalities as Down's syndrome, and clinics have stopped using it.
     Even when techniques pose a clear danger to offspring, clinics are loath to abandon them as long as they boost pregnancy rates. The most glaring example is the practice of transferring multiple embryos to a woman's womb. Since 1980, according to the National Center for Health Statistics, the number of twins born per year has risen 67 percent. The rate of triplets and higher-order birth multiples has soared from 37 per 100,000 live births in 1980 to 184 per 100,000 in 1999. The increase is due almost entirely, according to federal statisticians, to fertility treatments. Only 20 percent of triplets and higher-order multiples are conceived naturally. (Most extremely high-order multiples, like the McCaughey septuplets, occur when the woman is given fertility drugs and her doctor fails to recognize how many eggs she has produced.)
     The risks to multiples and their mother are substantial, and so is the cost. Women pregnant with multiples are more likely than those with singletons to suffer premature delivery, toxemia (a potentially fatal form of high blood pressure), and hemorrhage. Their infants are vulnerable to cerebral palsy, learning disabilities, blindness, developmental delays, and mental retardation, largely because they are often born prematurely. While there are no national statistics on the cost of multiples, a recent study, published in The Journal of Maternal and Fetal Medicine, found that the average charge per triplet pregnancy at one New York City hospital was nearly $190,000. Other studies have shown that triplets can cost as much as 400 times a standard singleton pregnancy and delivery.
     "Data on higher-order gestations have been known for years," says Van Blerkom. But fertility clinics have been unwilling to do anything about it he says, for fear they would cut their pregnancy rates. "Have you ever seen a fertility specialist stand next to a couple with their premature quads and say, This is a disaster for these patients. I think we blew it?'" says Van Blerkom. "Most people in the field were content to let selective terminations at week 13 or 14 clean up the problem."
     Under pressure from insurance companies, who often refuse to pay for IVF but wind up footing the bill for multiple births, the American Society for Reproductive Medicine finally issued guidelines last year aimed at reducing the chances of multiples. From the outside, the guidelines seem self-evident: For younger patients, ASRM recommended transferring at most two embryos to the mother's womb; older women, whose embryos are less likely to implant in the uterus and begin developing, can receive as many as five.
     But for clinics, the dual pressures of profitability and desperate patients have made such seemingly obvious precautions difficult to follow. "We're under pressure to have high pregnancy rates," complains one clinic doctor. "The problem is we've never had any way of knowing what was the right number of embryos to transfer."
     European fertility specialists, who are often required by law to transfer no more than one or two embryos to a single patient, don't seem to have the same trouble. They use research conducted by Van Blerkom and others in the late 1990s showing how to select the most viable embryos and reduce the number that is transferred to the mother. But choosing embryos requires painstaking attention, often at odd hours of the night, and American fertility clinics have been reluctant to invest in technologists who can perform it.
     Without federal funding for studies, or oversight from a government body like the FDA, reproductive medicine has had little outside incentive to make such changes as bringing down the rate of multiple births. "We've got the worst system you could possibly come up with," says Dr. Lawrence Udoff, a fertility specialist and director of the pre-implantation genetics program at the University of Maryland at Baltimore. "There are people in this business who are a lot better at marketing than they are at replicating their results. The patient ends up footing the bill for procedures that are untested."
     The industry trade group, the American Society for Reproductive Medicine, argues that fertility doctors are doing nothing different from any other specialist. "Reproductive medicine starts from the same regulatory basis as every other kind of medicine," says ASRM spokesman, Sean Tipton. If a heart surgeon thinks a new way of tying off an artery might work, she simply does it. If the patient lives, she tries it again. Eventually, she may take a retrospective look at her cases and compare the outcomes of those who received the new method versus the old.
     It is also true, however, that the history of medicine is littered with examples of doctors unquestioningly adopting new treatments long before they have been evaluated, only to abandon them when they turn out to be ineffective or worse. More than 30,000 women with breast cancer received high dose chemotherapy with bone-marrow transplants in the 1980s and 90s. At least 9,000 died from the treatment before researchers finally performed clinical trials, which ultimately demonstrated that high dosage is no better than standard chemotherapy regimens.
     The deeper question, of course, is why we allow uncontrolled experimentation on human subjects in any branch of medicine. But the issue is particularly pressing for reproductive technologies, especially now that fertility centers are wading into the uncharted waters of the gene pool.
     Embryologists have already experimented with transferring the nucleus of an older woman's egg into a young donor's egg from which the nucleus has been removed, a technique that is similar to the method used to create Dolly, the sheep. Another fertility team successfully split a human embryo into several identical copies, a trick that could one day help infertile women who produce very few eggs. But it could also make possible such Dorian Gray scenarios as multiple identical embryos being thawed and then born several years apart, or a woman giving birth to herself.
     In hindsight, perhaps the anti-abortion activists who feared the emergence of technology like IVF were right to step back and question the larger implications. While few Americans would begrudge infertile couples the babies that have been produced through IVF, the issues now being raised by genetic engineering are not ones to be taken lightly, and a national consensus can only be arrived at through vigorous public debate.
     Some of that debate emerged in 2000, when Lisa and Jack Nash briefly made the news when their son Adam was born in Colorado. The Nashes already had one child, six-year-old Molly, who was born with a rare genetic bone marrow disease that would kill her unless she received a transplant from someone with the identical tissue type. Both Lisa and Jack were carriers for Fanconi anemia, a genetic disorder, leaving them with a one-in-four chance of having another affected child each time Lisa got pregnant.
     The Nashes elected, instead, to conceive 15 embryos and subject them to PGD, or pre-implantation genetic diagnosis. A single cell was taken from each embryo and tested for the presence of the genetic mutation that causes Fanconi anemia. Then the Nashes went a step further, and had the embryos checked to see which one carried a tissue type that matched their daughter, Molly's.
     Adam was born in Denver in August. In September, doctors in Minnesota performed a stem cell transplant on Molly, using blood taken at birth from Adam's umbilical cord and his bone marrow. Today, the Nashes have two healthy children. Faced with the same situation, many American parents would undoubtedly choose the same course.
     At the same time, the Nash case raises the unsettling possibility of parents bearing children not to love and cherish them, but for the purpose of harvesting their tissue. And what about parents who simply want their kids to be like them, genetic warts and all? Consider the deaf lesbian couple in Washington, D.C., who recently sought a sperm donor who was also congenitally deaf, so they could be assured of a deaf child. Such desires might seem reasonable if not for the fact that any parent who deafened a hearing baby would be charged with child abuse.
     Under the current political landscape, the nation has little control over what it deems acceptable. Americans may one day decide that it is perfectly all right to genetically engineer children with blue skin or webbed feet or any other trait that parents see fit. In the meantime, current practices in the fertility industry could use some oversight.
     Thus far, however, the only legislative response to worrisome reproductive technologies has been to ban them and accuse their practitioners of "playing God," an argument that appeals to conservative constituents but will in the short term, at least, prove futile. Says former bioethics committee member Charo, "As soon as you have absolute prohibitions you run into constitutional challenges."
     Over the long term, banning certain technologies, such as reproductive cloning, may well be advisable, but reining in the pace of reprogenetics now is going to take a network of regulatory solutions. First on the list: Update the FDA's decades-old charter. In recent years, Congress has generally sided with business against the agency, beating back its efforts to rein in the herbal medicine industry, for example. But legislators have already signaled their distaste for reproductive cloning, and the balance of power is likely to shift when it comes to giving the FDA regulatory control over reprogenetics.
     The FDA, along with the U.S. Department of Health and Human Services (HHS), jointly oversee the protection of human subjects in clinical trials, which are required to demonstrate safety and efficacy before new drugs or medical devices can be licensed for market. Most of the time, companies put their products through rigorous testing in animals long before proceeding to human experimentation. Applying the same standards to human embryo experiments would compel fertility clinics to perform similar tests before subjecting patients to new reprogenetic technologies. It would also entail the creation of specialized review boards with the expertise to evaluate human reproductive experiments.
     Tweaking tort law would also impose greater discipline on fertility doctors and would-be human genetic engineers. Current malpractice law rests on the idea of negligence, which means that plaintiffs must demonstrate that a doctor failed to provide care in accordance with accepted standards. In fast-moving, innovative arenas of medicine, such as fertility, there is no established or accepted "standard of care." Not surprisingly, fertility patients almost never sue, in part because they can't find lawyers to take their cases.
     One solution, says Charo, is to stop using negligence as the standard for reproductive medicine, and impose strict liability instead. If the patient or child suffers a bad outcome, the clinic is liable, and patients could, in effect, sue for wrongful life.
     England also offers a model for creating boundaries for thornier issues bordering on eugenics. A decade after the birth of the first test-tube baby, Parliament created a licensing board, the Human Fertilization and Embryology Authority (HFEA), which has kept a tight lid on burgeoning genetic technologies since 1991---to the dismay of some would-be patients and clinic directors.
     In a recent case before the HFEA, for example, a family with four boys that had lost their young daughter in a fire asked to be allowed to choose female embryos for IVF. HFEA refused, fearing that sex selection for purposes other than to prevent a sex-linked disease, such as hemophilia, would push British society toward eugenics, or at least widespread sex-selection. A national licensing board like the HFEA would probably prove unworkable in this country, but the U.S. would do well to create an advisory panel for reproductive technologies that would provide a public forum for what are now individual decisions with huge social consequences.
     Finally, anti-abortion activists need to recognize that federal involvement in embryo research is critical for limiting the risks posed by genetic engineering of the future and improving the current outcomes for families desperately seeking to have a child.
     Tens of thousands of embryos are discarded by fertility clinics each year because embryologists are not allowed to work on them using federal dollars. If conservatives wish to ban the creation of embryos for the purpose of research, they should focus their formidable political power on allowing research on embryos created in the hopes of producing a child.
     Funding such science would certainly bring a higher level of rigor to the field and increased oversight of human experimentation. The nation is already sliding down a slippery slope toward the age of reprogenetics. Our only hope of slowing the pace is to apply the brakes of regulation.