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April 10, 2026
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"We applaud the burgeoning emphasis on change in regulatory genes as the stuff of morphological evolution... if only because one of us had written a book to argue that the classical, and widely ignored data on evolution by heterochrony should be exhumed and valued as a primary demonstration of regulatory change. We do not see how point mutations in structural genes can lead, even by gradual accumulations, to new morphological designs. Regulatory changes in the timing of complex ontogenetic programs seem far more promisingâand potentially rapid, in conformity with our punctuational predilections. The near identity of humans and chimps for structural genes, and the evidence of major regulatory change indicated by human neoteny provides an important confirmation."
"Mutation: it is the key to our evolution. It is how we have evolved from a single-celled organism into the dominant species on the planet. This process is slow, and normally taking thousands and thousands of years. But every few hundred millennia, evolution leaps forward."
"Anything can happen. How absolutely true. You're exactly the mutant I'm looking for! You're hired."
"Aside from inheriting half of the genome of each of our parents, we are born with a small number of novel mutations that occurred during gametogenesis and postzygotically. Recent genome and exome sequencing studies of parentâoffspring trios have provided the first insights into the number and distribution of these de novo mutations in health and disease, pointing to risk factors that increase their number in the offspring. De novo mutations have been shown to be a major cause of severe early-onset genetic disorders such as intellectual disability, autism spectrum disorder, and other developmental diseases. In fact, the occurrence of novel mutations in each generation explains why these reproductively lethal disorders continue to occur in our population. Recent studies have also shown that de novo mutations are predominantly of paternal origin and that their number increases with advanced paternal age."
"The prevalence of chromosome abnormalities in women facing a single sporadic miscarriage is to be 45%. Approximately 50% to 60% of early spontaneous miscarriages are associated with a chromosomal anomaly of conceptus. Most common abnormality is aneuploidy, with autosomal trisomy accounting for more than 50% of chromosomally abnormal abortuses. A strong family history of recurrent miscarriage or genetic anomaly suggests a parental karyotypic abnormality, and a chromosomal analysis of the affected partner is appropriate in the primary evaluation. Chromosomal analysis of the miscarriage offers an explanation in at least 50% of cases. Parental karyotyping is not predictive of a subsequent miscarriage. Routine karyotyping of couples with recurrent miscarriage is not recommended. Cytogenetic analysis may be performed on products of conception to avoid unnecessary evaluation and treatment and because an aneuploid conceptus indicates a somewhat greater likelihood of success with a subsequent pregnancy (Evidence Level III)."
"What would you do with mutants who were just plain boys and girls and certainly not dangerous? You school them. You develop their skills. So I gave them a teacher, Professor X. Of course, it was the natural thing to do, instead of disorienting or alienating people who were different from us, I made the X-Men part of the human race, which they were. Possibly, radiation, if it is beneficial, may create mutants thatâll save us instead of doing us harm. I felt that if we train the mutants our way, theyâll help us - and not only help us, but achieve a measure of growth in their own sense. And so, we could all live together."
"This was a period when we were experimenting with the atom bomb. People were wondering what the effects would be. Everybody worried âWould we all become mutants? We played around with this âmutation thingâ and I came up with the X-Men, who were associated with radiation and its effects on humanity."
"When an individual acquires great power, the use or misuse of that power is everything. Will it be used for the greater good or will it be used for personal or destructive ends? Now this is a question we must all ask ourselves. Why? Because we are mutants."
"They wish to "cure" us. But I say to you we are the cure! The cure for that infirm, imperfect condition called "Homo sapiens!" They have their weapons... We have ours. We will strike with a vengeance and a fury that this world has never witnessed!"
"It was things like the Teenage Mutant Ninja Turtles, he thought, that made you believe the world was maybe just as well off destroyed."
"I'm either a mutant or a cripple, and I refuse to be a cripple. People pity cripples, but they're afraid of mutants ⌠Fear implies respect."
"It is a generally accepted assumption that sporadic pregnancy losses occurring before an embryo has developed represent a âphysiologicalâ phenomenon, which prevents conceptions affected by serious structural malformations or chromosomal aberrations incompatible with life from progressing to viability. This concept is supported by clinical studies in which embryoscopy was used to assess fetal morphology prior to removal by uterine evacuation. Fetal malformations were observed in 85% of cases presenting with early clinical miscarriage. The same study also demonstrated that 75% of the fetuses had an abnormal karyotype. Fetal chromosomal aneuploidies arising from non-inherited and non-disjunctional events are common. Indeed, in a recent study using comparative genomic hybridization to study the chromosomal complement of all blastomeres in preimplantation human embryos, more than 90% were found to have at least one chromosomal abnormality in one or more cells. The clinical implications of minor, mosaic and possibly âtransientâ aneuploidies remain unclear. However, while most fetuses with severe developmental defects will die in utero some aneuploidies can be compatible with survival to term. The most commonly encountered is trisomy 21, although 80% of affected embryos perish in utero or in the neonatal period. In most cases, the extra chromosome is of maternal origin and caused by a malsegregation event in the first meiotic division. The risk of this increases with maternal age and may be considered to be a biological rather than pathological phenomenon. Although fetal chromosomal aberrations may be identified in 29% to 60% of cases in women with RM, the incidence decreases as the number of miscarriages increases suggesting other mechanisms as a cause of the miscarriage in RM couples with multiple losses."
"I declare that The Beatles are mutants. Prototypes of evolutionary agents sent by God, endowed with a mysterious power to create a new human species, a young race of laughing freemen."
"The X-Men, created by Jewish American comics legends Stan Lee and Jack Kirby in 1963, is a team of mutants, a class of human being first introduced as people that âpossess an extrapowerâŚone which ordinary humans do not!!â (EUX1 #1: 8ii). Especially after the introduction of the mutant-hunting robot Sentinels in X-Men #14 (Nov. 1965, EUX1), Marvel Comicsâ mutants have been increasingly inscribed with allegorical Otherness. They have been subject to many of the prejudices that have historically plagued marginalized minorities, including, among other things, forced and voluntary segregation, slurs, persecution, and genocidal campaigns, and, conspiracy theories about their aims as a group."
"Most miscarriages occur because the fetus isn't developing as expected. About 50 percent of miscarriages are associated with extra or missing chromosomes. Most often, chromosome problems result from errors that occur by chance as the embryo divides and grows â not problems inherited from the parents."
"It's 1987, do you know what your children are? Paid for by citizens in support of the Mutant Registration Act."
"Sometimes something can go wrong at the point of conception and the foetus receives too many or not enough chromosomes. The reasons for this are often unclear, but it means the foetus will not be able to develop normally, resulting in a miscarriage. This is very unlikely to recur. It does not necessarily mean there's any problem with you or your partner."
"The most common cause of pregnancy loss is a problem with the chromosomes that would make it impossible for the fetus to develop normally."
"We conclude â unexpectedly â that there is little evidence for the neo-Darwinian view: its theoretical foundations and the experimental evidence supporting it are weak, and there is no doubt that mutations of large effect are sometimes important in adaptation. We hasten to add, however, that we are not "macromutationists" who believe that adaptations are nearly always based on major genes. The neo-Darwinian view could well be correct. ⌠We hope to encourage evolutionists to reexamine this neglected question and to provide evidence to settle it."
"But, be that as it may, is this variation, or variations, beneficial to humanity in their environment? According to Lois Gresh and Robert Weinberg, the X-men do have âhelpful mutations..." This point is demonstrated numerous times in the adventures of the X-Men, where team members use their mutant powers to help them survive dangerous situations where normal humans would be killed instantlyâ (Gresh and Weinberg 2002, 135). What Gresh and Weinberg have overlooked, however, is that these âdangerous situationsâ came after the genetic variation, not before. Most of the battles the X-Men fight are either against other mutants-- such as Magneto and the Brotherhood of Evil Mutants, who have a more violent response to human oppression of mutants-- or against anti-mutant hate groups, such as the Sentinels or Friends of Humanity, whose only goal is to wipe out all mutants. All of these âdangerous situationsâ come up in response to the X-Menâs genetic variation, meaning that this variation cannot be an adaptive response to an environment. Of course, under the theory of evolution by natural selection, every mutation need not necessarily be useful."
"Family entertainment? Bollocks. What they want is filth: people doing things to each other with chainsaws during tupperware parties, babysitters being stabbed with knitting needles by gay presidential candidates, vigilante groups strangling chickens, armed bands of theatre critics exterminating mutant goats. Where's the fun in pictures? Oh, well, there we are. Here's the theme music. Goodnight."
"One way to further improve the estimate of the abortion rate is to account for at least some of the occult abortions that are not detected by high-sensitivity comes from studies comparing aneuploidy in very young embryos (cleavage stage and blastocysts) to conceptuses that spontaneously aborted after a pregnancy had been clinically detected. At the early embryo stages, monosomy (missing one homolog from one or more of the 23 pairs of homologous chromosomes) and trisomies (a extra chromosome at one or more of the 23 pairs of homologous chromosomes) were found to be equally common. But among conceptuses that survive to clinical detection, and then abort, essentially no autosomal monosomies were observed (<<1%). This repeated finding demonstrates that all autosomal monosomic conceptuses spontaneously abort before a pregnancy can be detected by elevated levels of hCG, i.e., prior to implantation. As a consequence, for every observed aborted conceptus that carried one or more trisomies after clinical detection, there must have been one occult aborted conceptus due to one or more monosomies. At least 50% of aborted fetuses are karyotypically abnormal and at least 60% of these carry one or more trisomies. There are therefore at least 0.5*0.6* = 0.3 occult abortions due to monosomy for every detected post-implantation abortion. In Fig. 3, I have added these additional occult abortions to the total."
"6.2 Genetic factors The finding of an abnormal parental karyotype should prompt referral to a clinical geneticist. Genetic counselling offers the couple a prognosis for the risk of future pregnancies with an unbalanced chromosome complement and the opportunity for familial chromosome studies. Reproductive options in couples with chromosomal rearrangements include proceeding to a further natural pregnancy with or without a prenatal diagnosis test, gamete donation and adoption. Preimplantation genetic diagnosis has been proposed as a treatment option for translocation carriers. Since preimplantation genetic diagnosis necessitates that the couple undergo in vitro fertilisation to produce embryos, couples with proven fertility need to be aware of the financial cost as well as implantation and live birth rates per cycle following in vitro fertilisation/preimplantation genetic diagnosis. Furthermore, they should be informed that they have a higher (50â70%) chance of a healthy live birth in future untreated pregnancies following natural conception than is currently achieved after preimplantation genetic diagnosis/in vitro fertilisation (approximately 30%). Preimplantation genetic screening with in vitro fertilisation treatment in women with unexplained recurrent miscarriage does not improve live birth rates. Preimplantation genetic screening in conjunction with in vitro fertilisation has been advocated as a treatment option for women with recurrent miscarriage, the rationale being that the identification and transfer of what are thought to be genetically normal embryos will lead to a live birth. The live birth rate of women with unexplained recurrent miscarriage who conceive naturally is significantly higher than currently achieved after preimplantation genetic screening/in vitro fertilisation (20â30%)."
"I'm telling you, with everything we know, about science, about the makeup of the human body, what happened in that classroom is impossible. That kid attracted an arc of electricity from thirty feet away, and not just from the Jacob's Ladder, I mean, after a second it was like it was coming out of the whole⌠building."
"We're stumbling around in a very dark age basically trying not to kill each other. So it hurts me when you say "So what?" Because you are not just different, Jeremy, I think you have a mind that we won't evolve to for like thousands of years â you're maybe the man of the future right here and now."
"People love a nice shot of an orange sunrise over the islands in Casco Bay, of waves crashing on the rocks in front of Portland Head Light, or of seagulls fighting over rotten bait. But the time tested crowd favorite is a picture of a mutant lobster. Theyâre actually a lot more common than one might think, sometimes they come up with multiple claws, sometimes theyâre different colors, and sometimes theyâre so riddled with shell disease that theyâre almost unrecognizable."
"We hypothesize that the increased risk of spontaneous abortion with male age is a consequence of an increasing frequency of chromosomal anomalies in the spermatozoa with male age, which in turn increases the risk of spontaneous abortion. The influence of male age on the proportion of spermatozoa carrying a chromosomal anomaly or with damaged DNA has been documented in several groups of men. It may well result, in part, from the continuous replication of stem cell chromosomes from puberty onward; indeed, male stem cells have undergone about 150 chromosomal replications at the age of 20 years and about 600 by the age of 40 years. The chromosomal anomalies found in spontaneous abortions include autosomal trisomies, present in about 50 percent of abortuses with chromosomal anomalies, monosomy X (present in about 20 percent), and triploidy (16 percent). The remaining 12 percent correspond mainly to tetraploidy and structural anomalies of the chromosomes. The two most frequent anomalies sometimes have a paternal origin: Autosomal trisomies stem from nondisjunction during spermatogenesis in 10â20 percent or more of cases and, in monosomy X, the missing chromosome is most often the paternal one. Moreover, sperm chromosome aneuploidy may play a role in the etiology of recurrent pregnancy loss."
"There was a world of mutants, men and women who were more than normal men and women, persons who had certain human talents and certain human understandings which the normal men and women of the world had never known, or having known, could not utilize in their entirety, unable to use intelligently all the mighty powers which lay dormant in their brains."
"The people finally know. They've been told about the mutants. And they hated the mutants. Of course, they hated them. They hated them because the existence of the mutants makes them second-class humans, because they are Neanderthalers suddenly invaded by a bow and arrow people."
"Genetic bases of defective chromosome content or structure In a biological sense, genetic defects leading to abortion may originate from two partners: The conceptus and the uterus. From the conceptus side, it is well established that chromosomal anomalies lead to implantation defects. However, they occur mostly stochastically; to be the genetic cause of a recurrent loss, a genetic defect leading to systematic chromosome anomalies has to be found, as nicely reviewed recently by Kurahashi and coworkers. Abnormal chromosome structure may originate from defects in the checkpoint mechanisms that constitute a quality control factory of the cell, which is able to detect meiosis anomalies and is called Spindle Assembly Checkpoint (SAC), constituted by pro teins such as Mad1, Mad2, Bub1, Bub3, BubR1, and Mps1. A very recent study addressed this question on the general issue of defective reproduction performance, by screening two candidate genes, aurora kinase B (AURKB) and synaptonemal complex protein 3 (SYCP3). In the AURKB gene, the authors identified low frequency (0.5%) non synonymous variants (c. 155C.T, c. 236T.C, and c. 880G.A) inducing the changes p.A52V, p.I79T, and p.A294T in the polypeptidic chain, respectively. 236T >C and 880G >A were associated with antecedents of pregnancy losses. This preliminary study is one of those that pave the way toward evaluating genes playing a role in the quality of the meiotic progression. Two other genes have been investigated to this respect in miscarriage, BUB1 and MAD2. The authors showed firstly that as generally assumed, half the embryos from spontaneous miscarriages have an abnormal karyotype. By western blotting, the authors quantified the two proteins and estimated that they were under expressed in pathological cases. The authors also isolated chorionic villi where they targeted BUB1 and MAD2 expression by short hairpin RNA (shRNA) and showed that this induces an abnormal karyotype at a ~ sixfold increased frequency, compared to controls (indicating that mitotic defects can also be induced when these genes are dysfunctional). The role of MAD2 in such defects was independently confirmed by another study on trisomic abortuses. Clearly, therefore, anomalies in spindle assembly can lead to aneuploidies, and infertilities in the most severe cases, such as in the case of the recently identified mutation of the cohesin STAG3, leading to premature ovarian failure, but less severe mutations in the SAC genes could lead to variants that have more subtle effects. There is clearly space for studying this aspect of spindle stability on a wider basis than what has been performed up to now in the context of recurrent miscarriage."
"Robert Anton Wilson is the unacknowledged elephant in our cultural living room: a direct and indirect influence on popular books, movies, TV shows, music, games, comics, and commentary. ⌠Wilson is a primary source for the ironic style of conspiracism, a sensibility that treats alleged cabals not as intrigues to be exposed or lies to be debunked but as a bizarre mutant mythos to be mined for laughs, metaphors, and social insights."
"Of all creatures, only the Binder had bested the Lord of Hellwell. Then the gods had come to challenge his power. They had been puny in the early days, struggling to discipline their mutant powers with drugs, hypnosis, meditation, neurosurgery â forging them into Attributes â and across the ages, those powers had grown. Four of them had entered Hellwell, only four, and his legions had not been able to repel them."
"The world has arisen in some way or another. How it originated is the great question, and Darwin's theory, like all other attempts to explain the origin of life, is thus far merely conjectural. I believe he has not even made the best conjecture possible in the present state of our knowledge."
"An example of such emergent phenomena is the origin of life from non-living chemical compounds in the oldest, lifeless oceans of the earth. Here, aided by the radiation energy received from the sun, countless chemical materials were synthesized and accumulated in such a way that they constituted, as it were, a primeval âsoup.â In this primeval soup, by infinite variations of lifeless growth and decay of substances during some billions of years, the way of life was ultimately reached, with its metabolism characterized by selective assimilation and dissimulation as end stations of a sluiced and canalized flow of free chemical energy."
"Q: Strange, isn't it, Jean-Luc? Everything you know... your entire civilization... it all begins right here in this little pond of goo. It's appropriate somehow, isn't it? Too bad you didn't bring a microscope -- this is quite fascinating. Here they go... the amino acids are moving closer... closer...closer...Ohhhh! Nothing happened! You see what you've done?"
"You know, my brothers, the nature of our business. The child you see before you, thanks to a talisman stolen from the powers of Earth, is able to take possession of the Blue Bird and thus to snatch from us the secret which we have kept since the origin of life... Now we know enough of Man to entertain no doubt as to the fate which he reserves for us once he is in possession of this secret. That is why it seems to me that any hesitation would be both foolish and criminal... It is a serious moment; the child must be done away with before it is too late..."
"Believing the first cell originated by chance is like believing a tornado ripping through a junkyard full of airplane parts could produce a Boeing 747."
"Life could spread from planet to planet or from stellar system to stellar system, carried on meteors."
"It is as though a puzzle could be put together simply by shaking its pieces."
"The fine-tuning of the universe, about which cosmologists make such a to-do, is both complex and specified and readily yields design. So too, Michael Behe's irreducibly complex biochemical systems readily yield design. The complexity-specification criterion demonstrates that design pervades cosmology and biology. Moreover, it is a transcendent design, not reducible to the physical world. Indeed, no intelligent agent who is strictly physical could have presided over the origin of the universe or the origin of life."
"It is mere rubbish thinking, at present, of origin of life; one might as well think of origin of matter. â"
"The elegant study... is consistent with the themes of modern cognitive neuroscience. Every aspect of thought and emotion is rooted in brain structure and function, including many psychological disorders and, presumably, genius. The study confirms that the brain is a modular system comprising multiple intelligences, mostly nonverbal."
"The biggest single obstacle to the full use of mathematics in real neuroscience is the sheer difficulty of the relevant mathematics. The brain is far more complex than today's computers; therefore to understand it, one must use even more sophisticated mathematics than the average research engineer is familiar with. Because of this difficulty, a few "middle men" have presented oversimplified description of biology to the engineers, and oversimplified descriptions of the engineering to the biologists. These oversimplifications have often led to considerable misunderstanding and justified mistrust."
"As we approach the 21st century, neuroscience is the crown jewel of medical progress. The molecular mechanisms encoded in the human genome are being carefully analyzed. Gene therapy is a practical reality."
"Although many philosophers used to dismiss the relevance of neuroscience on grounds that what mattered was âthe software, not the hardwareâ, increasingly philosophers have come to recognize that understanding how the brain works is essential to understanding the mind."
"There was another major phase of split-brain research where we studied the patients as a way of getting at the other questions very much alive in neuroscience, everything from questions about visual midline overlap to spatial attention and resource allocations. At this point the split-brain patients provided a way of examining cortical-subcortical relationships, and other matters."
"The Society for Neuroscience is the world's largest gathering of scientists. It drew nearly 23,000 researchers to San Diego in late 1995, and it is almost impossible to cover single-handedly."
"Neuroscience has contributed so much in just a few decades to how we think about human nature and how we know ourselves."
"There are three levels of self to consider: the proto, the core, and the autobiographical. The first two are shared with many, many other species, and they are really coming out largely of the brain stem and whatever there is of cortex in those species."
"It now seems beyond question that the traditional account of depression as a chemical imbalance in the brain is simply wrong."