Aagaard-Tillery, K. M., K. Grove, et al. (2008). “Developmental origins of disease and determinants of chromatin structure: Maternal diet modifies the primate fetal epigenome.” J Mol Endocrinol 41(2): 91–102.
Allen, G. (1978). Thomas Hunt Morgan: The man and his science. Princeton: Princeton University Press.
Amor, D. J., and J. Halliday (2008). “A review of known imprinting syndromes and their association with assisted reproduction technologies.” Hum Reprod 23(12): 2826–2834.
Anway, M. D., A. S. Cupp, et al. (2005). “Epigenetic transgenerational actions of endocrine disruptors and male fertility.” Science 308(5727): 1466–1469.
Anway, M. D., and M. K. Skinner (2008). “Epigenetic programming of the germ line: Effects of endocrine disruptors on the development of transgenerational disease.” Reprod Biomed Online 16(1): 23–25.
Araki, R., Y. Jincho, et al. (2010). “Conversion of ancestral fibroblasts to induced pluripotent stem cells.” Stem Cells 28(2): 213–220.
Ashabranner, B. K. (1988). Always to remember: The story of the Vietnam Veterans Memorial. New York: Putnam.
Atlan, H., and M. Koppel (1990). “The cellular computer DNA: Program or data.” Bull Math Biol 52(3): 335–348.
Au, T. M., A. K. Greenwood, et al. (2006). “Differential social regulation of two pituitary gonadotropin-releasing hormone receptors.” Behav Brain Res 170(2): 342–346.
Bailey, J. A., K. G. Hill, et al. (2009). “Parenting practices and problem behavior across three generations: Monitoring, harsh discipline, and drug use in the intergenerational transmission of externalizing behavior.” Dev Psychol45(5): 1214–1226.
Ballestar, E., M. Esteller, et al. (2006). “The epigenetic face of systemic lupus erythematosus.” J Immunol 176(12): 7143–7147.
Bardi, M., and M. A. Huffman (2002). “Effects of maternal style on infant behavior in Japanese macaques (Macaca fuscata).” Dev Psychobiol 41(4): 364–372.
Bardi, M., and M. A. Huffman (2006). “Maternal behavior and maternal stress are associated with infant behavioral development in macaques.” Dev Psychobiol 48(1): 1–9.
Barker, M., S. Robinson, et al. (1997). “Birth weight and body fat distribution in adolescent girls.” Arch Dis Child 77(5): 381–383.
Bartholdi, D., M. Krajewska-Walasek, et al. (2009). “Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome (SRS): Results from a large cohort of patients with SRS and SRS-like phenotypes.” J Med Genet 46(3): 192–197.
Beadle, G. W., and E. L. Tatum (1941). “Genetic control of biochemical reactions in Neurospora.” Proc Natl Acad Sci USA 27(11): 499–506.
Beck, B., and M. Power (1988). “Correlates of sexual and maternal competence in captive gorillas.” Zoo Biol 7: 339–350.
Beck, S., A. Olek, et al. (1999). “From genomics to epigenomics: A loftier view of life.” Nat Biotechnol 17(12): 1144.
Bellinger, L., and S. C. Langley-Evans (2005). “Fetal programming of appetite by exposure to a maternal low-protein diet in the rat.” Clin Sci (Lond) 109(4): 413–420.
Belshaw, R., V. Pereira, et al. (2004). “Long-term reinfection of the human genome by endogenous retroviruses.” Proc Natl Acad Sci USA 101(14): 4894–4899.
Berletch, J. B., F. Yang, et al. (2010). “Escape from X inactivation in mice and humans.” Genome Biol 11(6): 213.
Bernal, A. J., and R. L. Jirtle (2010). “Epigenomic disruption: The effects of early developmental exposures.” Birth Defects Res A Clin Mol Teratol 88(10): 938–944.
Bettegowda, A., K. Lee, et al. (2007). “Cytoplasmic and nuclear determinants of the maternal-to-embryonic transition.” Reprod Fertil Dev 20(1): 45–53.
Beurton, P. J., R. Falk, et al. (2000). The concept of the gene in development and evolution: Historical and epistemological perspectives. Cambridge, UK: Cambridge University Press.
Bevilacqua, E., R. Brunelli, et al. (2010). “Review and meta-analysis: Benefits and risks of multiple courses of antenatal corticosteroids.” J Matern Fetal Neonatal Med 23(4): 244–260.
Bharadwaj, R., and H. Yu (2004). “The spindle checkpoint, aneuploidy, and cancer.” Oncogene 23(11): 2016–2027.
Bianco, S. D., and U. B. Kaiser (2009). “The genetic and molecular basis of idiopathic hypogonadotropic hypogonadism.” Nat Rev Endocrinol 5(10): 569–576.
Biliya, S., and L. A. Bulla, Jr. (2010). “Genomic imprinting: The influence of differential methylation in the two sexes.” Exp Biol Med (Maywood) 235(2): 139–147.
Bissell, M. J., and M. A. Labarge (2005). “Context, tissue plasticity, and cancer: Are tumor stem cells also regulated by the microenvironment?” Cancer Cell 7(1): 17–23.
Bittel, D. C., N. Kibiryeva, et al. (2005). “Microarray analysis of gene/transcript expression in Angelman syndrome: Deletion versus UPD.” Genomics 85(1): 85–91.
Bjorntorp, P., and R. Rosmond (2000). “Obesity and cortisol.” Nutrition 16(10): 924–936.
Blewitt, M. E., N. K. Vickaryous, et al. (2006). “Dynamic reprogramming of DNA methylation at an epigenetically sensitive allele in mice.” PLoS Genet 2(4): e49.
Blobel, G. (1980). “Intracellular protein topogenesis.” Proc Natl Acad Sci USA 77(3): 1496–1500.
Bodemer, C. W. (1964). “Regeneration and the decline of preformationism in eighteenth century embryology.” Bull Hist Med 38: 20–31.
Bonventre, J. V. (2003). “Dedifferentiation and proliferation of surviving epithelial cells in acute renal failure.” J Am Soc Nephrol 14(Suppl 1): S55–S61.
Booth, A., G. Shelley, et al. (1989). “Testosterone, and winning and losing in human competition.” Horm Behav 23(4): 556–571.
Bradley, R. G., E. B. Binder, et al. (2008). “Influence of child abuse on adult depression: Moderation by the corticotropin-releasing hormone receptor gene.” Arch Gen Psychiatry 65(2): 190–200.
Brand, S. R., S. M. Engel, et al. (2006). “The effect of maternal PTSD following in utero trauma exposure on behavior and temperament in the 9-month-old infant.” Ann N Y Acad Sci 1071: 454–458.
Brenner, S., G. Elgar, et al. (1993). “Characterization of the puffer-fish (Fugu) genome as a compact model vertebrate genome.” Nature 366(6452): 265–268.
Brown, A. S., J. van Os, et al. (2000). “Further evidence of relation between prenatal famine and major affective disorder.” Am J Psychiatry 157(2): 190–195.
Brown, C., and J. Greally (2003). “A stain upon the silence: Genes escaping X inactivation.” Trends Genet 19: 432–438.
Burdge, G. C., M. A. Hanson, et al. (2007). “Epigenetic regulation of transcription: A mechanism for inducing variations in phenotype (fetal programming) by differences in nutrition during early life?” Br J Nutr 97(6): 1036–1046.
Burmeister, S. S., V. Kailasanath, et al. (2007). “Social dominance regulates androgen and estrogen receptor gene expression.” Horm Behav 51(1): 164–170.
Calatayud, F., and C. Belzung (2001). “Emotional reactivity in mice, a case of nongenetic heredity?” Physiol Behav 74(3): 355–362.
Calin, G. A., C. D. Dumitru, et al. (2002). “Frequent deletions and down-regulation of micro-RNA genes miR15 and miR16 at 13q14 in chronic lymphocytic leukemia.” Proc Natl Acad Sci USA 99(24): 15524–15529.
Callinan, P. A., and A. P. Feinberg (2006). “The emerging science of epigenomics.” Hum Mol Genet 15(Suppl 1): R95–R101.
Campbell, K. H., J. McWhir, et al. (1996). “Sheep cloned by nuclear transfer from a cultured cell line.” Nature 380(6569): 64–66.
Capp, J. P. (2005). “Stochastic gene expression, disruption of tissue averaging effects, and cancer as a disease of development.” BioEssays 27(12): 1277–1285.
Carninci, P., and Y. Hayashizaki (2007). “Noncoding RNA transcription beyond annotated genes.” Curr Opin Genet Dev 17(2): 139–144.
Carrell, D. T., and S. S. Hammoud (2010). “The human sperm epigenome and its potential role in embryonic development.” Mol Hum Reprod 16(1): 37–47.
Cassidy, S. B., and D. H. Ledbetter (1989). “Prader-Willi syndrome.” Neurol Clin 7(1): 37–54.
Castle, W. E., F. W. Carpenter, et al. (1906). “The effects of inbreeding, cross-breeding, and selection upon fertility and variability of Drosophila.” Proc Am Acad Arts Sci 41.
Castle, W. E., and S. Wright (1916). “Studies of inheritance in guinea pigs and rats.” Carnegie Inst Wash Publ 241: 163–190.
Cattanach, B. M., C. V. Beechey, et al. (2006). “Interactions between imprinting effects: Summary and review.” Cytogenet Genome Res 113(1–4): 17–23.
Champagne, F. A., and J. P. Curley (2009). “Epigenetic mechanisms mediating the long-term effects of maternal care on development.” Neurosci Biobehav Rev 33(4): 593–600.
Champagne, F., J. Diorio, et al. (2001). “Naturally occurring variations in maternal behavior in the rat are associated with differences in estrogen-inducible central oxytocin receptors.” Proc Natl Acad Sci USA98(22): 12736–12741.
Champagne, F. A, and M. J. Meaney (2001). “Like mother, like daughter: Evidence for non-genomic transmission of parental behavior and stress responsivity.” Prog Brain Res 133: 287–302.
Champagne, F. A., I. C. Weaver, et al. (2006). “Maternal care associated with methylation of the estrogen receptor-alpha1b promoter and estrogen receptor-alpha expression in the medial preoptic area of female offspring.” Endocrinology 147(6): 2909–2915.
Champoux, M., E. Byrne, et al. (1992). “Motherless mothers revisited: Rhesus maternal behavior and rearing history.” Primates 33: 251–255.
Chang, H. S., M. D. Anway, et al. (2006). “Transgenerational epigenetic imprinting of the male germline by endocrine disruptor exposure during gonadal sex determination.” Endocrinology 147(12): 5524–5541.
Chen, C., J. Visootsak, et al. (2007). “Prader-Willi syndrome: An update and review for the primary pediatrician.” Clin Pediatr (Phila) 46(7): 580–591.
Chen, Z. L., W. M. Yu, et al. (2007). “Peripheral regeneration.” Annu Rev Neurosci 30: 209–233.
Chong, S., N. A. Youngson, et al. (2007). “Heritable germline epimutation is not the same as transgenerational epigenetic inheritance.” Nat Genet 39(5): 574–575, author reply 575–576.
Chow, J. C., Z. Yen, et al. (2005). “Silencing of the mammalian X chromosome.” Annu Rev Genomics Hum Genet 6: 69–92.
Christensen, B. C., E. A. Houseman, et al. (2009). “Aging and environmental exposures alter tissue-specific DNA methylation dependent upon CpG island context.” PLoS Genet 5(8): e1000602.
Christian, J. C., D. Bixler, et al. (1971). “Hypogandotropic hypogonadism with anosmia: The Kallmann syndrome.” Birth Defects Orig Artic Ser 7(6): 166–171.
Chung, L. W., A. Baseman, et al. (2005). “Molecular insights into prostate cancer progression: The missing link of tumor microenvironment.” J Urol 173(1): 10–20.
Chung, Y., C. E. Bishop, et al. (2009). “Reprogramming of human somatic cells using human and animal oocytes.” Cloning Stem Cells 11(2): 213–223.
Cohn, S. A., D. S. Emmerich, et al. (1989). “Differences in the responses of heterozygous carriers of colorblindness and normal controls to briefly presented stimuli.” Vision Res 29(2): 255–262.
Collas, P. (2010). “Programming differentiation potential in mesenchymal stem cells.” Epigenetics 5(6).
Collas, P., and A. M. Hakelien (2003). “Teaching cells new tricks.” Trends Biotechnol 21(8): 354–361.
Cooper, W. N., R. Curley, et al. (2007). “Mitotic recombination and uniparental disomy in Beckwith-Wiedemann syndrome.” Genomics 89(5): 613–617.
Costa, F. F. (2008). “Non-coding RNAs, epigenetics and complexity.” Gene 410(1): 9–17.
Coventry, W. L., S. E. Medland, et al. (2009). “Phenotypic and discordant-monozygotic analyses of stress and perceived social support as antecedents to or sequelae of risk for depression.” Twin Res Hum Genet 12(5): 469–488.
Crespi, B. (2008). “Genomic imprinting in the development and evolution of psychotic spectrum conditions.” Biol Rev Camb Philos Soc 83(4): 441–493.
Crews, D. (2010). “Epigenetics, brain, behavior, and the environment.” Hormones (Athens) 9(1): 41–50.
Cropley, J. E., C. M. Suter, et al. (2006). “Germ-line epigenetic modification of the murine Avy allele by nutritional supplementation.” Proc Natl Acad Sci USA 103(46): 17308–17312.
Currenti, S. A. (2010). “Understanding and determining the etiology of autism.” Cell Mol Neurobiol 30(2): 161–171.
Curtis, H. J. (1965). “Formal discussion of: Somatic mutations and carcinogenesis.” Cancer Res 25: 1305–1308.
Dai, Y., L. Wang, et al. (2006). “Fate of centrosomes following somatic cell nuclear transfer (SCNT) in bovine oocytes.” Reproduction 131(6): 1051–1061.
Daley, G. Q. (2008). “Common themes of dedifferentiation in somatic cell reprogramming and cancer.” Cold Spring Harb Symp Quant Biol 73: 171–174.
Damcott, C. M., P. Sack, et al. (2003). “The genetics of obesity.” Endocrinol Metab Clin North Am 32(4): 761–786.
Deakin, J. E., J. Chaumeil, et al. (2009). “Unravelling the evolutionary origins of X chromosome inactivation in mammals: Insights from marsupials and monotremes.” Chromosome Res 17(5): 671–685.
Dean, F., C. Yu, et al. (2001). “Prenatal glucocorticoid modifies hypothalamo-pituitary-adrenal regulation in prepubertal guinea pigs.” Neuroendocrinology 73(3): 194–202.
De Boo, H. A., and J. E. Harding (2006). “The developmental origins of adult disease (Barker) hypothesis.” Aust N Z J Obstet Gynaecol 46(1): 4–14.
Deeb, S. S. (2005). “The molecular basis of variation in human color vision.” Clin Genet 67(5): 369–377.
Delage, B., and R. H. Dashwood (2008). “Dietary manipulation of histone structure and function.” Annu Rev Nutr 28: 347–366.
Delaval, K., A. Wagschal, et al. (2006). “Epigenetic deregulation of imprinting in congenital diseases of aberrant growth.” BioEssays 28(5): 453–459.
Denenberg, V. H., and K. M. Rosenberg (1967). “Nongenetic Transmission of Information.” Nature 216(5115): 549–550.
de Souza, N. (2010). “Primer: Induced pluripotency.” Nat Methods 7(1): 20–21.
Diamanti-Kandarakis, E., J. P. Bourguignon, et al. (2009). “Endocrine-disrupting chemicals: An Endocrine Society scientific statement.” Endocr Rev 30(4): 293–342.
DiBartolo, P. M., and M. Helt (2007). “Theoretical models of affectionate versus affectionless control in anxious families: A critical examination based on observations of parent-child interactions.” Clin Child Fam Psychol Rev10(3): 253–274.
Diez-Torre, A., R. Andrade, et al. (2009). “Reprogramming of melanoma cells by embryonic microenvironments.” Int J Dev Biol 53(8–10): 1563–1568.
Dobyns, W. B., A. Filauro, et al. (2004). “Inheritance of most X-linked traits is not dominant or recessive, just X-linked.” Am J Med Genet A 129A(2): 136–143.
Dolinoy, D. C., D. Huang, et al. (2007). “Maternal nutrient supplementation counteracts bisphenol A–induced DNA hypomethylation in early development.” Proc Natl Acad Sci USA 104(32): 13056–13061.
Dolinoy, D. C., J. R. Weidman, et al. (2006). “Maternal genistein alters coat color and protects Avy mouse offspring from obesity by modifying the fetal epigenome.” Environ Health Perspect 114(4): 567–572.
Drake, A. J., J. I. Tang, et al. (2007). “Mechanisms underlying the role of glucocorticoids in the early life programming of adult disease.” Clin Sci (Lond) 113(5): 219–232.
Driscoll, D. J., M. F. Waters, et al. (1992). “A DNA methylation imprint, determined by the sex of the parent, distinguishes the Angelman and Prader-Willi syndromes.” Genomics 13(4): 917–924.
Duesberg, P. (2005). “Does aneuploidy or mutation start cancer?” Science 307(5706): 41.
Duesberg, P., R. Li, et al. (2000). “Aneuploidy precedes and segregates with chemical carcinogenesis.” Cancer Genet Cytogenet 119(2): 83–93.
Duesberg, P., R. Li, et al. (2005). “The chromosomal basis of cancer.” Cell Oncol 27(5–6): 293–318.
Duhl, D. M., M. E. Stevens, et al. (1994). “Pleiotropic effects of the mouse lethal yellow (Ay) mutation explained by deletion of a maternally expressed gene and the simultaneous production of agouti fusion RNAs.” Development120(6): 1695–1708.
Duhl, D. M., H. Vrieling, et al. (1994). “Neomorphic agouti mutations in obese yellow mice.” Nat Genet 8(1): 59–65.
Eddy, S. R. (2001). “Non-coding RNA genes and the modern RNA world.” Nat Rev Genet 2(12): 919–929.
Eilertsen, K. J., R. A. Power, et al. (2007). “Targeting cellular memory to reprogram the epigenome, restore potential, and improve somatic cell nuclear transfer.” Anim Reprod Sci 98(1–2): 129–146.
Elgar, G., and T. Vavouri (2008). “Tuning in to the signals: Noncoding sequence conservation in vertebrate genomes.” Trends Genet 24(7): 344–352.
Emack, J., A. Kostaki, et al. (2008). “Chronic maternal stress affects growth, behaviour and hypothalamo-pituitary-adrenal function in juvenile offspring.” Horm Behav 54(4): 514–520.
Emslie, C., and K. Hunt (2008). “The weaker sex? Exploring lay understandings of gender differences in life expectancy: A qualitative study.” Soc Sci Med 67(5): 808–816.
Engert, V., R. Joober, et al. (2009). “Behavioral response to methylphenidate challenge: Influence of early life parental care.” Dev Psychobiol 51(5): 408–416.
Erwin, J. A., and J. T. Lee (2008). “New twists in X-chromosome inactivation.” Curr Opin Cell Biol 20(3): 349–355.
Evanson, N. K., J. G. Tasker, et al. (2010). “Fast feedback inhibition of the HPA axis by glucocorticoids is mediated by endocannabinoid signaling.” Endocrinology 151(10) 4811–4819.
Fassati, A., and N. A. Mitchison (2010). “Testing the theory of immune selection in cancers that break the rules of transplantation.” Cancer Immunol Immunother 59(5): 643–651.
Feinberg, A. P., R. Ohlsson, et al. (2006). “The epigenetic progenitor origin of human cancer.” Nat Rev Genet 7(1): 21–33.
Fishman, L., and J. H. Willis (2006). “A cytonuclear incompatibility causes anther sterility in Mimulus hybrids.” Evolution 60(7): 1372–1381.
Forterre, P. (2001). “Genomics and early cellular evolution. The origin of the DNA world.” C R Acad Sci Ser III 324(12): 1067–1076.
Forterre, P. (2002). “The origin of DNA genomes and DNA replication proteins.” Curr Opin Microbiol 5(5): 525–532.
Fowden, A. L., C. Sibley, et al. (2006). “Imprinted genes, placental development and fetal growth.” Horm Res 65(Suppl 3): 50–58.
Fox Keller, E. (1999). “Elusive locus of control in biological development: Genetic versus developmental programs.” Exp Zool 285(3): 283–290.
Fox Keller, E. (2000). The century of the gene. Cambridge: Harvard University Press.
Francis, D. D., F. A. Champagne, et al. (1999). “Maternal care, gene expression, and the development of individual differences in stress reactivity.” Ann N Y Acad Sci 896: 66–84.
Francis, D. D., F. C. Champagne, et al. (2000). “Variations in maternal behaviour are associated with differences in oxytocin receptor levels in the rat.” J Neuroendocrinol 12(12): 1145–1148.
Francis, D., J. Diorio, et al. (1999). “Nongenomic transmission across generations of maternal behavior and stress responses in the rat.” Science 286(5442): 1155–1158.
Francis, D. D., and M. J. Meaney (1999). “Maternal care and the development of stress responses.” Curr Opin Neurobiol 9(1): 128–134.
Francis, R. C. (1992). “Sexual lability in teleosts: Developmental factors.” Q Rev Biol 67(1): 1–18.
Francis, R. C., B. Jacobson, et al. (1992). “Hypertrophy of gonadotropin releasing hormone-containing neurons after castration in the teleost, Haplochromis burtoni.” J Neurobiol 23(8): 1084–1093.
Francis, R. C., K. Soma, et al. (1993). “Social regulation of the brain-pituitary-gonadal axis.” Proc Natl Acad Sci USA 90: 7794–7798.
Frank, S. A., and M. A. Nowak (2004). “Problems of somatic mutation and cancer.” BioEssays 26(3): 291–299.
Frank, U. (2007). “The evolution of a malignant dog.” Evol Dev 9(6): 521–522.
French, M., M. Venu, et al. (2009). “Non-identical Kallmann’s syndrome in otherwise identical twins.” Endocr Abstr 19:46.
Fulka, J., Jr., and H. Fulka (2007). “Somatic cell nuclear transfer (SCNT) in mammals: The cytoplast and its reprogramming activities.” Adv Exp Med Biol 591: 93–102.
Galvan, A., F. S. Falvella, et al. (2010). “Genome-wide association study in discordant sibships identifies multiple inherited susceptibility alleles linked to lung cancer.” Carcinogenesis 31(3): 462–465.
Ganesan, A., L. Nolan, et al. (2009). “Epigenetic therapy: Histone acetylation, DNA methylation and anti-cancer drug discovery.” Curr Cancer Drug Targets 9(8): 963–981.
Gatenby, R. A., and T. L. Vincent (2003). “An evolutionary model of carcinogenesis.” Cancer Res 63(19): 6212–6220.
Gaudet, F., J. G. Hodgson, et al. (2003). “Induction of tumors in mice by genomic hypomethylation.” Science 300(5618): 489–492.
Georgantas, R. W., III, R. Hildreth, et al. (2007). “CD34+ hematopoietic stem-progenitor cell microRNA expression and function: A circuit diagram of differentiation control.” Proc Natl Acad Sci USA 104(8): 2750–2755.
Gibson, G. (2007). “Human evolution: thrifty genes and the Dairy Queen.” Curr Biol 17(8): R295–R296.
Gilbert, S. F. (1991). Developmental biology, 3rd ed. Sunderland, MA: Sinauer.
Gilbert, S. F., and S. Sarkar (2000). “Embracing complexity: Organicism for the 21st century.” Dev Dyn 219(1): 1–9.
Goldberg, J., W. R. True, et al. (1990). “A twin study of the effects of the Vietnam War on posttraumatic stress disorder.” JAMA 263(9): 1227–1232.
Grace, K. S., and K. D. Sinclair (2009). “Assisted reproductive technology, epigenetics, and long-term health: A developmental time bomb still ticking.” Semin Reprod Med 27(5): 409–416.
Greenfield, E. A., and N. F. Marks (2010). “Identifying experiences of physical and psychological violence in childhood that jeopardize mental health in adulthood.” Child Abuse Negl 34(3): 161–171.
Griffiths, P., and R. D. Gray (1994). “Developmental systems and evolutionary explanation.” J Phil 91: 277–304.
Griffiths, P., and E. Neumann-Held (1999). “The many faces of the gene.” BioScience 49(8): 656–662.
Gross, K. L., and J. A. Cidlowski (2008). “Tissue-specific glucocorticoid action: A family affair.” Trends Endocrinol Metab 19(9): 331–339.
Gross-Sorokin, M. Y., S. D. Roast, et al. (2006). “Assessment of feminization of male fish in English rivers by the Environment Agency of England and Wales.” Environ Health Perspect 114(Suppl 1): 147–151.
Guerriero, G. (2009). “Vertebrate sex steroid receptors: Evolution, ligands, and neurodistribution.” Ann N Y Acad Sci 1163: 154–168.
Gurdon, J. B., and D. A. Melton (2008). “Nuclear reprogramming in cells.” Science 322(5909): 1811–1815.
Hales, C. N., and D. J. P. Barker (2001). “The thrifty phenotype hypothesis: Type 2 diabetes.” Br Med Bull 60(1): 5–20.
Hamelin, C. E., G. Anglin, et al. (2006). “Genomic imprinting in Turner syndrome: Effects on response to growth hormone and on risk of sensorineural hearing loss.” J Clin Endocrinol Metab 91(8): 3002–3010.
Hannes, R.-P., D. Franck, et al. (1984). “Effects of rank-order fights on whole-body and blood concentrations of androgens and corticosteroids in the male swordtail (Xiphophorus helleri).” Z Tierpsychol 65: 53–65.
Haque, F. N., Gottesman, I. I., et al. (2009). “Not really identical: Epigenetic differences in monozygotic twins and implications for twin studies in psychiatry.” Am J Med Genet C Semin Med Genet 151C(2): 136–141.
Harlow, H. F., M. K. Harlow, et al. (1971). “From thought to therapy: Lessons from a primate laboratory.” Am Sci 50: 538–549.
Harlow, H. F., and R. R. Zimmerman (1959). “Affectional responses in the infant monkey.” Science 136: 421–431.
Hatchwell, E., and J. M. Greally (2007). “The potential role of epigenomic dysregulation in complex human disease.” Trends Genet 23(11): 588–595.
Hayashi, T., A. G. Motulsky, et al. (1999). “Position of a ‘green-red’ hybrid gene in the visual pigment array determines colour-vision phenotype.” Nat Genet 22(1): 90–93.
Hayes, T. B., A. A. Stuart, et al. (2006). “Characterization of atrazine-induced gonadal malformations in African clawed frogs (Xenopus laevis) and comparisons with effects of an androgen antagonist (cyproterone acetate) and exogenous estrogen (17[.beta]-estradiol): Support for the demasculinization/feminization hypothesis.” Environ Health Perspect 114(Suppl 1): 134–141.
Henderson, I. R., and S. E. Jacobsen (2007). “Epigenetic inheritance in plants.” Nature 447(7143): 418–424.
Hendriks-Jansen, H. (1996). Catching ourselves in the act: Situated activity, integrative emergence, evolution, and human thought. Cambridge, MA: MIT Press.
Hendrix, M. J., E. A. Seftor, et al. (2007). “Reprogramming metastatic tumour cells with embryonic microenvironments.” Nat Rev Cancer 7(4): 246–255.
Hess, C. T. (2009). “Monitoring laboratory values: Vitamin B1, vitamin B6, vitamin B12, folate, calcium, and magnesium.” Adv Skin Wound Care 22(6): 288.
Hinney, A., C. I. Vogel, et al. (2010). “From monogenic to polygenic obesity: Recent advances.” Eur Child Adolesc Psychiatry 19(3): 297–310.
Hipkin, L. J., I. F. Casson, et al. (1990). “Identical twins discordant for Kallmann’s syndrome.” J Med Genet 27: 198–199.
Hipp, J., and A. Atala (2008). “Sources of stem cells for regenerative medicine.” Stem Cell Rev 4(1): 3–11.
Hisamuddin, I. M., and V. W. Yang (2006). “Molecular genetics of colorectal cancer: An overview.” Curr Colorectal Cancer Rep 2(2): 53–59.
Hobbes, T. (1651/1996). Leviathan, ed. R. Tuck. New York: Cambridge University Press.
Hoch, S. L. (1998). “Famine, disease, and mortality patterns in the parish of Borshevka, Russia, 1830–1912.” Popul Stud (Camb) 52(3): 357–368.
Hochedlinger, K., R. Blelloch, et al. (2004). “Reprogramming of a melanoma genome by nuclear transplantation.” Genes Dev 18(15): 1875–1885.
Holliday, R. (1996). “Endless quest.” BioEssays 18(1): 3–5.
Holliday, R. (2006). “Epigenetics: A historical overview.” Epigenetics 1(2): 76–80.
Horvitz, H. R., and J. E. Sulston (1980). “Isolation and genetic characterization of cell-lineage mutants of the nematode Caenorhabditis elegans.” Genetics 96(2): 435–454.
Hsiao, Y. W., K. W. Liao, et al. (2008). “Interactions of host IL-6 and IFN-gamma and cancer-derived TGF-beta1 on MHC molecule expression during tumor spontaneous regression.” Cancer Immunol Immunother 57(7): 1091–1104.
Hunt, D. M., A. J. Williams, et al. (1993). “Structure and evolution of the polymorphic photopigment gene of the marmoset.” Vision Res 33(2): 147–154.
Ikeda, D., and S. Watabe (2004). “[Fugu genome: The smallest genome size in vertebrates].” Tanpakushitsu Kakusan Koso 49(14): 2235–2241.
Ingber, D. E. (2002). “Cancer as a disease of epithelial-mesenchymal interactions and extracellular matrix regulation.” Differentiation 70(9–10): 547–560.
Jablonka, E. (2004). “The evolution of the peculiarities of mammalian sex chromosomes: An epigenetic view.” BioEssays 26: 1327–1332.
Jablonka, E., and M. J. Lamb (2002). “The changing concept of epigenetics.” Ann N Y Acad Sci 981: 82–96.
Jablonka, E., and G. Raz (2009). “Transgenerational epigenetic inheritance: Prevalence, mechanisms, and implications for the study of heredity and evolution.” Q Rev Biol 84(2): 131–176.
Jacobs, G. H. (1998). “A perspective on color vision in platyrrhine monkeys.” Vision Res 38(21): 3307–3313.
Jacobs, G. H. (2008). “Primate color vision: a comparative perspective.” Vis Neurosci 25(5–6): 619–633.
Jacobs, G. H., and J. F. Deegan II (2003). “Cone pigment variations in four genera of New World monkeys.” Vision Res 43(3): 227–236.
Jameson, K. A., S. M. Highnote, et al. (2001). “Richer color experience in observers with multiple photopigment opsin genes.” Psychon Bull Rev 8(2): 244–261.
Jobling, S., R. Williams, et al. (2006). “Predicted exposures to steroid estrogens in U.K. rivers correlate with widespread sexual disruption in wild fish populations.” Environ Health Perspect 114(Suppl 1): 32–39.
Johnsen, H., K. Malene Krag, et al. (2009). “Cancer stem cells and the cellular hierarchy in haematological malignancies.” Eur J Cancer 45: 194–201.
Jones, J. R., C. Skinner, et al. (2008). “Hypothesis: Dysregulation of methylation of brain-expressed genes on the X chromosome and autism spectrum disorders.” Am J Med Genet A 146A(17): 2213–2220.
Jones, P. A., and S. B. Baylin (2007). “The epigenomics of cancer.” Cell 128(4): 683–692.
Jordan, G., and J. D. Mollon (1993). “A study of women heterozygous for colour deficiencies.” Vision Res 33(11): 1495–1508.
Jorgensen, A. L., J. Philip, et al. (1992). “Different patterns of X inactivation in MZ twins discordant for red-green color-vision deficiency.” Am J Hum Genet 51(2): 291–298.
Joyce, P. R., S. A. Williamson, et al. (2007). “Effects of childhood experiences on cortisol levels in depressed adults.” Aust N Z J Psychiatry 41(1): 62–65.
Junien, C., and P. Nathanielsz (2007). “Report on the IASO Stock Conference 2006: Early and lifelong environmental epigenomic programming of metabolic syndrome, obesity and type II diabetes.” Obes Rev8(6): 487–502.
Just, E. E. (1939). The biology of the cell surface. Philadelphia: Blakison’s.
Kaitz, M., H. R. Maytal, et al. (2010). “Maternal anxiety, mother-infant interactions, and infants’ response to challenge.” Infant Behav Dev 33(2): 136–148.
Kaminsky, Z., A. Petronis, et al. (2008). “Epigenetics of personality traits: An illustrative study of identical twins discordant for risk-taking behavior.” Twin Res Hum Genet 11(1): 1–11.
Kapoor, A., A. Kostaki, et al. (2009). “The effects of prenatal stress on learning in adult offspring is dependent on the timing of the stressor.” Behav Brain Res 197(1): 144–149.
Kapoor, A., J. Leen, et al. (2008). “Molecular regulation of the hypothalamic-pituitary-adrenal axis in adult male guinea pigs after prenatal stress at different stages of gestation.” J Physiol 586(Pt 17): 4317–4326.
Kapoor, A., and S. G. Matthews (2008). “Prenatal stress modifies behavior and hypothalamic-pituitary-adrenal function in female guinea pig offspring: Effects of timing of prenatal stress and stage of reproductive cycle.” Endocrinology 149(12): 6406–6415.
Kapoor, A., S. Petropoulos, et al. (2008). “Fetal programming of hypothalamic-pituitary-adrenal (HPA) axis function and behavior by synthetic glucocorticoids.” Brain Res Rev 57(2): 586–595.
Kato, T. (2009). “Epigenomics in psychiatry.” Neuropsychobiology 60(1): 2–4.
Kato, T., K. Iwamoto, et al. (2005). “Genetic or epigenetic difference causing discordance between monozygotic twins as a clue to molecular basis of mental disorders.” Mol Psychiatry 10(7): 622–630.
Katz, L. A. (2006). “Genomes: Epigenomics and the future of genome sciences.” Curr Biol 16(23): R996–R997.
Kenny, P. A., and M. J. Bissell (2003). “Tumor reversion: Correction of malignant behavior by microenvironmental cues.” Int J Cancer 107(5): 688–695.
Kenny, P. A., G. Y. Lee, et al. (2007). “Targeting the tumor microenvironment.” Front Biosci 12: 3468–3474.
Kim, J. B., H. Zaehres, et al. (2008). “Pluripotent stem cells induced from adult neural stem cells by reprogramming with two factors.” Nature 454(7204): 646–650.
Kim, K. C., S. Friso, et al. (2009). “DNA methylation, an epigenetic mechanism connecting folate to healthy embryonic development and aging.” J Nutr Biochem 20(12): 917–926.
Kimball, J. W. (2010). Kimball’s biology pages. http://users.rcn.com/jkimball.ma.ultranet/BiologyPages/.
King, N. E., and J. D. Mellen (1994). “The effects of early experience on adult copulatory behavior in zoo-born chimpanzees (Pan troglodytes.”) Zoo Biol 13: 51–59.
Kinoshita, T., Y. Ikeda, et al. (2008). “Genomic imprinting: A balance between antagonistic roles of parental chromosomes.” Semin Cell Dev Biol 19(6): 574–579.
Kirschner, M., J. Gerhart, et al. (2000). “Molecular ‘vitalism.’” Cell 100(1): 79–88.
Ko, J. M., J. M. Kim, et al. (2010). “Influence of parental origin of the X chromosome on physical phenotypes and GH responsiveness of patients with Turner syndrome.” Clin Endocrinol (Oxf) 73(1): 66–71.
Kochanska, G., R. A. Barry, et al. (2009). “Early attachment organization moderates the parent-child mutually coercive pathway to children’s antisocial conduct.” Child Dev 80(4): 1288–1300.
Koornneef, M., C. J. Hanhart, et al. (1991). “A genetic and physiological analysis of late flowering mutants in Arabidopsis thaliana.” Mol Gen Genet 229(1): 57–66.
Kraemer, S. (2000). “The fragile male.” BMJ 321(7276): 1609–1612.
Kulesa, P. M., J. C. Kasemeier-Kulesa, et al. (2006). “Reprogramming metastatic melanoma cells to assume a neural crest cell-like phenotype in an embryonic microenvironment.” Proc Natl Acad Sci USA103(10): 3752–3757.
Lanctot, C., T. Cheutin, et al. (2007). “Dynamic genome architecture in the nuclear space: Regulation of gene expression in three dimensions.” Nat Rev Genet 8(2): 104–115.
Lander, E. S., L. M. Linton, et al. (2001). “Initial sequencing and analysis of the human genome.” Nature 409(6822): 860–921.
Lanza, R. P., J. B. Cibelli, et al. (2000). “Cloning of an endangered species (Bos gaurus) using interspecies nuclear transfer.” Cloning 2(2): 79–90.
Laprise, S. L. (2009). “Implications of epigenetics and genomic imprinting in assisted reproductive technologies.” Mol Reprod Dev 76(11): 1006–1018.
Laugharne, J., A. Janca, et al. (2007). “Posttraumatic stress disorder and terrorism: 5 years after 9/11.” Curr Opin Psychiatry 20(1): 36–41.
Leeming, R. J., and M. Lucock (2009). “Autism: Is there a folate connection?” J Inherit Metab Dis 32(3): 400–402.
Lewis, A., and W. Reik (2006). “How imprinting centres work.” Cytogenet Genome Res 113(1–4): 81–89.
Li, Y., Y. Dai, et al. (2006). “Cloned endangered species takin (Budorcas taxicolor) by inter-species nuclear transfer and comparison of the blastocyst development with yak (Bos grunniens) and bovine.” Mol Reprod Dev 73(2): 189–195.
Li, Y., Y. Dai, et al. (2007). “In vitro development of yak (Bos grunniens) embryos generated by interspecies nuclear transfer.” Anim Reprod Sci 101(1–2): 45–59.
Lightman, S. L. (2008). “The neuroendocrinology of stress: A never ending story.” J Neuroendocrinol 20(6): 880–884.
Lillycrop, K. A., E. S. Phillips, et al. (2005). “Dietary protein restriction of pregnant rats induces and folic acid supplementation prevents epigenetic modification of hepatic gene expression in the offspring.” J Nutr 135(6): 1382–1386.
Lillycrop, K. A., J. L. Slater-Jefferies, et al. (2007). “Induction of altered epigenetic regulation of the hepatic glucocorticoid receptor in the offspring of rats fed a protein-restricted diet during pregnancy suggests that reduced DNA methyltransferase-1 expression is involved in impaired DNA methylation and changes in histone modifications.” Br J Nutr 97(6): 1064–1073.
Liu, D., J. Diorio, et al. (1997). “Maternal care, hippocampal glucocorticoid receptors, and hypothalamic-pituitary-adrenal responses to stress.” Science 277(5332): 1659–1662.
Loat, C. S., K. Asbury, et al. (2004). “X inactivation as a source of behavioural differences in monozygotic female twins.” Twin Res 7(1): 54–61.
Loh, R., D. Hayes, et al. (2006). “The immunohistochemical characterization of devil facial tumor disease (DFTD) in the Tasmanian Devil (Sarcophilus harrisii).” Vet Pathol 43(6): 896–903.
Lorthongpanich, C., C. Laowtammathron, et al. (2008). “Development of interspecies cloned monkey embryos reconstructed with bovine enucleated oocytes.” J Reprod Dev 54(5): 306–313.
Lotem, J., and L. Sachs (2002). “Epigenetics wins over genetics: Induction of differentiation in tumor cells.” Semin Cancer Biol 12(5): 339–346.
Lu, J., G. Getz, et al. (2005). “MicroRNA expression profiles classify human cancers.” Nature 435(7043): 834–838.
Lumey, L. H. (1998). “Reproductive outcomes in women prenatally exposed to undernutrition: A review of findings from the Dutch famine birth cohort.” Proc Nutr Soc 57(1): 129–135.
Lumey, L. H., and A. D. Stein (1997). “In utero exposure to famine and subsequent fertility: The Dutch Famine Birth Cohort Study.” Am J Public Health 87(12): 1962–1966.
Lyon, M. F. (1961). “Gene action in the X-chromosome of the mouse (Mus musculus L.).” Nature 190(4773): 372–373.
Lyon, M. F. (1971). “Possible mechanisms of X chromosome inactivation.” Nat New Biol 232(34): 229–232.
Lyon, M. F. (1989). “X-chromosome inactivation as a system of gene dosage compensation to regulate gene expression.” Prog Nucleic Acid Res Mol Biol 36: 119–130.
Lyon, M. F. (1995). “The history of X-chromosome inactivation and relation of recent findings to understanding of human X-linked conditions.” Turk J Pediatr 37(2): 125–140.
Lyssiotis, C. A., R. K. Foreman, et al. (2009). “Reprogramming of murine fibroblasts to induced pluripotent stem cells with chemical complementation of Klf4.” Proc Natl Acad Sci USA 106(22): 8912–8917.
Maestripieri, D. (2003). “Similarities in affiliation and aggression between cross-fostered rhesus macaque females and their biological mothers.” Dev Psychobiol 43(4): 321–327.
Maestripieri, D. (2005). “Early experience affects the intergenerational transmission of infant abuse in rhesus monkeys.” Proc Natl Acad Sci USA 102(27): 9726–9729.
Maienschein, J. (2008). “Epigenesis and preformationism.” Stanford encyclopedia of philosophy, ed. E. N. Zalta. Stanford, CA: Stanford University.
Martin, D. I., J. E. Cropley, et al. (2008). “Environmental influence on epigenetic inheritance at the Avy allele.” Nutr Rev 66(Suppl 1): S12–S14.
Martin, D. I., R. Ward, et al. (2005). “Germline epimutation: A basis for epigenetic disease in humans.” Ann N Y Acad Sci 1054: 68–77.
Masip, M., A. Veiga, et al. (2010). “Reprogramming with defined factors: From induced pluripotency to induced transdifferentiation.” Mol Hum Reprod 16(11): 856–868.
Mastroeni, D., A. McKee, et al. (2009). “Epigenetic differences in cortical neurons from a pair of monozygotic twins discordant for Alzheimer’s disease.” PLoS One 4(8): e6617.
Mattick, J. (2003). “Challenging the dogma: The hidden layer of non-protein-coding RNAs in complex organisms.” BioEssays 25: 930–939.
Mattick, J. S., and I. Makunin (2006). “Non-coding RNA.” Hum Mol Genet 15: R17–R29.
McCallum, H. (2008). “Tasmanian devil facial tumour disease: Lessons for conservation biology.” Trends Ecol Evol 23(11): 631–637.
McClellan, J., and M. C. King (2010). “Genetic heterogeneity in human disease.” Cell 141(2): 210–217.
McCormack, K., M. M. Sanchez, et al. (2006). “Maternal care patterns and behavioral development of rhesus macaque abused infants in the first 6 months of life.” Dev Psychobiol 48(7): 537–550.
McGowan, P. O., A. Sasaki, et al. (2009). “Epigenetic regulation of the glucocorticoid receptor in human brain associates with childhood abuse.” Nat Neurosci 12(3): 342–348.
Mcmillen, I. C., and J. S. Robinson (2005). “Developmental origins of the metabolic syndrome: Prediction, plasticity, and programming.” Physiol Rev 85(2): 571–633.
Meaney, M. J., M. Szyf, et al. (2007). “Epigenetic mechanisms of perinatal programming of hypothalamic-pituitary-adrenal function and health.” Trends Mol Med 13(7): 269–277.
Meder, A. (1993). “The effect of familiarity, age, dominance and rearing on reproductive success of captive gorillas.” In International studbook for the gorilla, ed. R. Kirchshofer, 227–236. Frankfurt, Frankfurt Zoological Garden.
Michaud, E. J., M. J. van Vugt, et al. (1994). “Differential expression of a new dominant agouti allele (Aiapy) is correlated with methylation state and is influenced by parental lineage.” Genes Dev 8(12): 1463–1472.
Milnes, M. R., D. S. Bermudez, et al. (2006). “Contaminant-induced feminization and demasculinization of nonmammalian vertebrate males in aquatic environments.” Environ Res 100(1): 3–17.
Miltenberger, R. J., R. L. Mynatt, et al. (1997). “The role of the agouti gene in the yellow obese syndrome.” J Nutr 127(9): 1902S–1907S.
Mintz, B., and K. Illmensee (1975). “Normal genetically mosaic mice produced from malignant teratocarcinoma cells.” Proc Natl Acad Sci USA 72(9): 3585–3589.
Monroy, A. (1986). “A centennial debt of developmental biology to the sea urchin.” Biol Bull 171: 509–519.
Morak, M., H. K. Schackert, et al. (2008). “Further evidence for heritability of an epimutation in one of 12 cases with MLH1 promoter methylation in blood cells clinically displaying HNPCC.” Eur J Hum Genet 16(7): 804–811.
Moreira de Mello, J. C., E. S. de Araujo, et al. (2010). “Random X inactivation and extensive mosaicism in human placenta revealed by analysis of allele-specific gene expression along the X chromosome.” PLoS One 5(6): e10947.
Morgan, H., H. G. Sutherland, et al. (1999). “Epigenetic inheritance at the agouti locus in the mouse.” Nat Genet 23: 314–318.
Moss, L. (1992). “A kernel of truth? On the reality of the genetic program.” Phil Sci Assoc Proc 1992: 335–348.
Murchison, E. P., C. Tovar, et al. (2010). “The Tasmanian devil transcriptome reveals Schwann cell origins of a clonally transmissible cancer.” Science 327(5961): 84–87.
Murgia, C., J. K. Pritchard, et al. (2006). “Clonal origin and evolution of a transmissible cancer.” Cell 126(3): 477–487.
Murphy, S. K., and R. L. Jirtle (2003). “Imprinting evolution and the price of silence.” BioEssays 25(6): 577–588.
Namekawa, S. H., J. L. VandeBerg, et al. (2007). “Sex chromosome silencing in the marsupial male germ line.” Proc Natl Acad Sci USA 104(23): 9730–9735.
Nathans, J. (1999). “The evolution and physiology of human color vision: Insights from molecular genetic studies of visual pigments.” Neuron 24(2): 299–312.
Nathans, J., T. P. Piantanida, et al. (1986). “Molecular genetics of inherited variation in human color vision.” Science 232(4747): 203–210.
Nathans, J., D. Thomas, et al. (1986). “Molecular genetics of human color vision: The genes encoding blue, green, and red pigments.” Science 232(4747): 193–202.
Neel, J. V. (1962). “Diabetes mellitus: A ‘thrifty’ genotype rendered detrimental by ‘progress’?” Am J Hum Genet 14: 353–362.
Neel, J. V. (1999). “The ‘thrifty genotype’ in 1998.” Nutr Rev 57(5 Pt 2): S2–9.
Nelson, C. M., and M. J. Bissell (2006). “Of extracellular matrix, scaffolds, and signaling: Tissue architecture regulates development, homeostasis, and cancer.” Annu Rev Cell Dev Biol 22: 287–309.
Neugebauer, R., H. W. Hoek, et al. (1999). “Prenatal exposure to wartime famine and development of antisocial personality disorder in early adulthood.” JAMA 282(5): 455–462.
Newman, S. A. (2009). “E. E. Just’s ‘independent irritability’ revisited: The activated egg as excitable soft matter.” Mol Reprod Dev 76(10): 966–974.
Nicholson, J. M., and P. Duesberg (2009). “On the karyotypic origin and evolution of cancer cells.” Cancer Genet Cytogenet 194(2): 96–110.
Niemann, H., X. C. Tian, et al. (2008). “Epigenetic reprogramming in embryonic and foetal development upon somatic cell nuclear transfer cloning.” Reproduction 135(2): 151–163.
Nijhout, H. F. (1990). “Metaphors and the role of genes in development.” BioEssays 12(9): 441–446.
Nobrega, M. A., Y. Zhu, et al. (2004). “Megabase deletions of gene deserts result in viable mice.” Nature 431(7011): 988–993.
O’Brien S. J., D. E. Wildt, et al. (1983). “The cheetah is depauperate in genetic variation.” Science 221(4609): 459–462.
Ohno, S. (1969). “The preferential activation of maternally derived alleles in development of interspecific hybrids.” Wistar Inst Symp Monogr 9: 137–150.
Okano, H. (2009). “Strategies toward CNS-regeneration using induced pluripotent stem cells.” Genome Inform 23(1): 217–220.
Otani, K., A. Suzuki, et al. (2009). “Effects of the ‘affectionless control’ parenting style on personality traits in healthy subjects.” Psychiatry Res 165(1–2): 181–186.
Ou, L., X. Wang, et al. (2010). “Is iPS cell the panacea?” IUBMB Life 62(3): 170–175.
Owen, C. M., and J. H. Segars, Jr. (2009). “Imprinting disorders and assisted reproductive technology.” Semin Reprod Med 27(5): 417–428.
Oyama, S. (1985). The ontogeny of information: Developmental systems and evolution. Cambridge, UK: Cambridge University Press. Painter, R. C., C. Osmond, et al. (2008). “Transgenerational effects of prenatal exposure to the Dutch famine on neonatal adiposity and health in later life.” BJOG 115(10): 1243–1249.
Painter, R. C., T. J. Roseboom, et al. (2005). “Adult mortality at age 57 after prenatal exposure to the Dutch famine.” Eur J Epedemiol 20(8): 673–676.
Pardo, P. J., A. L. Pérez, et al. (2007). “An example of sex-linked color vision differences.” Color Res Appl 32(6): 433–439.
Parikh, V. N., T. Clement, et al. (2006). “Physiological consequences of social descent: Studies in Astatotilapia burtoni.” J Endocrinol 190(1): 183–190.
Passier, R., and C. Mummery (2003). “Origin and use of embryonic and adult stem cells in differentiation and tissue repair.” Cardiovasc Res 58(2): 324–335.
Pathak, S., and A. S. Multani (2006). “Aneuploidy, stem cells and cancer.” EXS 96: 49–64.
Patton, G. C., C. Coffey, et al. (2001). “Parental ‘affectionless control’ in adolescent depressive disorder.” Soc Psychiatry Psychiatr Epidemiol 36(10): 475–480.
Pearse, A. M., and K. Swift (2006). “Allograft theory: Transmission of devil facial-tumour disease.” Nature 439(7076): 549.
Pembrey, M. E., L. O. Bygren, et al. (2006). “Sex-specific, male-line transgenerational responses in humans.” Eur J Hum Genet 14(2): 159–166.
Petronis, A. (2001). “Human morbid genetics revisited: relevance of epigenetics.” Trends Genet 17(3): 142–146.
Pezer, Z., and D. Ugarkovic (2008). “Role of non-coding RNA and heterochromatin in aneuploidy and cancer.” Semin Cancer Biol 18(2): 123–130.
Pigliucci, M. (2010). “Genotype-phenotype mapping and the end of the ‘genes as blueprint’ metaphor.” Phil Trans Royal Soc B 365(1540): 557–566.
Pollard, K. S., S. R. Salama, et al. (2006). “An RNA gene expressed during cortical development evolved rapidly in humans.” Nature 443(7108): 167–172.
Popova, B. C., T. Tada, et al. (2006). “Attenuated spread of X-inactivation in an X-autosome translocation.” Proc Natl Acad Sci USA 103(20): 7706–7711.
Portin, P. (2009). “The elusive concept of the gene.” Hereditas 146(3): 112–117.
Porton, I., and K. Niebrugge (2002). The changing role of handrearing in zoo-based primate breeding programs. In Developments in primatology, Progress and prospects: Nursery rearing of nonhuman primates in the 21st century, ed. G. P. Sackett, G. C. Ruppenthal, and K. Elias, 21–31. New York: Springer.
Prentice, A. M., B. J. Hennig, et al. (2008). “Evolutionary origins of the obesity epidemic: Natural selection of thrifty genes or genetic drift following predation release?” Int J Obes (Lond) 32(11): 1607–1610.
Prins, G. S. (2008). “Endocrine disruptors and prostate cancer risk.” Endocr Relat Cancer 15(3): 649–656.
Provine, W. B. (1986). Sewall Wright and evolutionary biology. Cambridge, MA: MIT Press.
Ptak, C., and A. Petronis (2010). “Epigenetic approaches to psychiatric disorders.” Dialogues Clin Neurosci 12(1): 25–35.
Puri, D., J. Dhawan, et al. (2010). “The paternal hidden agenda: Epigenetic inheritance through sperm chromatin.” Epigenetics 5(5). Rakyan, V., M. Blewitt, et al. (2002). “Metastable epialleles in mammals.” Trends Genet 18: 348–353.
Rakyan, V. K., S. Chong, et al. (2003). “Transgenerational inheritance of epigenetic states at the murine Axin(Fu) allele occurs after maternal and paternal transmission.” Proc Natl Acad Sci USA 100(5): 2538–2543.
Rakyan, V. K., J. Preis, et al. (2001). “The marks, mechanisms and memory of epigenetic states in mammals.” Biochem J 356(Pt 1): 1–10.
Rassoulzadegan, M., V. Grandjean, et al. (2006). “RNA-mediated non-Mendelian inheritance of an epigenetic change in the mouse.” Nature 441(7092): 469–474.
Rassoulzadegan, M., V. Grandjean, et al. (2007). “Inheritance of an epigenetic change in the mouse: A new role for RNA.” Biochem Soc Trans 35(3): 623–625.
Ravelli, A. C., J. H. van der Meulen, et al. (1998). “Glucose tolerance in adults after prenatal exposure to famine.” Lancet 351(9097): 173–177.
Ravelli, G. P., Z. A. Stein, et al. (1976). “Obesity in young men after famine exposure in utero and early infancy.” N Engl J Med 295(7): 349–353.
Reik, W. (1989). “Genomic imprinting and genetic disorders in man.” Trends Genet 5(10): 331–336.
Reik, W., M. Constancia, et al. (2003). “Regulation of supply and demand for maternal nutrients in mammals by imprinted genes.” J Physiol 547(Pt 1): 35–44.
Reik, W., W. Dean, et al. (2001). “Epigenetic reprogramming in mammalian development.” Science 293: 1089–1092.
Renn, S. C., N. Aubin-Horth, et al. (2008). “Fish and chips: Functional genomics of social plasticity in an African cichlid fish.” J Exp Biol 211(Pt 18): 3041–3056.
Revollo, J. R., and J. A. Cidlowski (2009). “Mechanisms generating diversity in glucocorticoid receptor signaling.” Ann N Y Acad Sci 1179: 167–178.
Rheinberger, H.-J. (2008). “Gene.” Stanford encyclopedia of philosophy. Stanford, CA: Stanford University.
Richards, E. J. (2006). “Inherited epigenetic variation—revisiting soft inheritance.” Nat Rev Genet 7(5): 395–401.
Riggs, A. D. (2002). “X chromosome inactivation, differentiation, and DNA methylation revisited, with a tribute to Susumu Ohno.” Cytogenet Genome Res 99(1–4): 17–24.
Rodriguez-Carmona, M., L. T. Sharpe, et al. (2008). “Sex-related differences in chromatic sensitivity.” Vis Neurosci 25(3): 433–440.
Roemer, I., W. Reik, et al. (1997). “Epigenetic inheritance in the mouse.” Curr Biol 7: 277–280.
Rogers, E. J. (2008). “Has enhanced folate status during pregnancy altered natural selection and possibly autism prevalence? A closer look at a possible link.” Med Hypotheses 71(3): 406–410.
Roseboom, T. J., S. de Rooij, et al. (2006). “The Dutch famine and its long-term consequences for adult health.” Early Hum Dev 82(8): 485–491.
Roseboom, T. J., J. H. van der Meulen, et al. (1999). “Blood pressure in adults after prenatal exposure to famine.” J Hypertens 17(3): 325–330.
Roseboom, T. J., J. H. van der Meulen, et al. (2000a). “Coronary heart disease after prenatal exposure to the Dutch famine, 1944–45.” Heart 84(6): 595–598.
Roseboom, T. J., J. H. van der Meulen, et al. (2000b). “Plasma lipid profiles in adults after prenatal exposure to the Dutch famine.” Am J Clin Nutr 72(5): 1101–1106.
Ross, H. E., and L. J. Young (2009). “Oxytocin and the neural mechanisms regulating social cognition and affiliative behavior.” Front Neuroendocrinol 30(4): 534–547.
Ross, J., D. Roeltgen, et al. (2006). “Cognition and the sex chromosomes: Studies in Turner syndrome.” Horm Res 65(1): 47–56.
Rothwell, N. J., and M. J. Stock (1981). “Regulation of energy balance.” Annu Rev Nutr 1: 235–256.
Ruppenthal, G. C., G. L. Arling, et al. (1976). “A 10-year perspective of motherless-mother monkey behavior.” J Abnorm Psychol 85(4): 341–349.
Ryan, S., S. Thompson, et al. (2002). “Effects of hand-rearing on the reproductive success of western lowland gorillas in North America.” Zoo Biol 21: 389–401.
Sales, K. M., M. C. Winslet, et al. (2007). “Stem cells and cancer: An overview.” Stem Cell Rev 3(4): 249–255.
Sanjayan, M. A., and K. Crooks (1996). “Skin grafts and cheetahs.” Nature 381(6583): 566.
Santos, F., and W. Dean (2004). “Epigenetic reprogramming during early development in mammals.” Reproduction 127(6): 643–651.
Sapp, J. (2009). “‘Just’ in time: Gene theory and the biology of the cell surface.” Mol Reprod Dev 76(10): 903–911.
Schickel, R., B. Boyerinas, et al. (2008). “MicroRNAs: Key players in the immune system, differentiation, tumorigenesis and cell death.” Oncogene 27(45): 5959–5974.
Schier, A. F. (2007). “The maternal-zygotic transition: Death and birth of RNAs.” Science 316(5823): 406–407.
Schubeler, D. (2009). “Epigenomics: Methylation matters.” Nature 462(7271): 296–297.
Schulz, W. A., and J. Hatina (2006). “Epigenetics of prostate cancer: Beyond DNA methylation.” J Cell Mol Med 10(1): 100–125.
Schulze-Tanzil, G. (2009). “Activation and dedifferentiation of chondrocytes: Implications in cartilage injury and repair.” Ann Anat 191(4): 325–338.
Schwanzel-Fukuda, M., K. L. Jorgenson, et al. (1992). “Biology of normal luteinizing hormone-releasing hormone neurons during and after their migration from olfactory placode.” Endocr Rev 13(4): 623–634.
Seckl, J. R. (2004). “Prenatal glucocorticoids and long-term programming.” Eur J Endocrinol 151(Suppl 3): U49–U62.
Seckl, J. R. (2008). “Glucocorticoids, developmental ‘programming’ and the risk of affective dysfunction.” Prog Brain Res 167: 17–34.
Seckl, J. R., and M. C. Holmes (2007). “Mechanisms of disease: Glucocorticoids, their placental metabolism and fetal ‘programming’ of adult pathophysiology.” Nat Clin Pract Endocrinol Metab 3(6): 479–488.
Seckl, J. R., and M. J. Meaney (2006). “Glucocorticoid ‘programming’ and PTSD risk.” Ann N Y Acad Sci 1071: 351–378.
Serbin, L. A., and J. Karp (2004). “The intergenerational transfer of psychosocial risk: Mediators of vulnerability and resilience.” Annu Rev Psychol 55: 333–363.
Shi, W., A. Krella, et al. (2005). “Widespread disruption of genomic imprinting in adult interspecies mouse (Mus) hybrids.” Genesis 43(3): 100–108.
Shire, J. G. (1989). “Unequal parental contributions: Genomic imprinting in mammals.” New Biol 1(2): 115–120.
Shively, C. A., T. C. Register, et al. (2009). “Social stress, visceral obesity, and coronary artery atherosclerosis: Product of a primate adaptation.” Am J Primatol 71(9): 742–751.
Shuldiner, A. R., and K. M. Munir (2003). “Genetics of obesity: More complicated than initially thought.” Lipids 38(2): 97–101.
Shyue, S. K., D. Hewett-Emmett, et al. (1995). “Adaptive evolution of color vision genes in higher primates.” Science 269(5228): 1265–1267.
Siddle, H. V., A. Kreiss, et al. (2007). “Transmission of a fatal clonal tumor by biting occurs due to depleted MHC diversity in a threatened carnivorous marsupial.” Proc Natl Acad Sci USA 104(41): 16221–16226.
Sikela, J. M. (2006). “The jewels of our genome: The search for the genomic changes underlying the evolutionarily unique capacities of the human brain.” PLoS Genet 2(5): e80.
Simmons, R. A. (2007). “Developmental origins of diabetes: The role of epigenetic mechanisms.” Curr Opin Endocrinol Diabetes Obes 14(1): 13–16.
Singh, S. M., and R. O’Reilly (2009). “(Epi)genomics and neurodevelopment in schizophrenia: Monozygotic twins discordant for schizophrenia augment the search for disease-related (epi)genomic alterations.” Genome 52(1): 8–19.
Skinner, M. K., M. Manikkam, et al. (2010). “Epigenetic transgenerational actions of environmental factors in disease etiology.” Trends Endocrinol Metab 21(4): 214–222.
Skuse, D. H., R. S. James, et al. (1997). “Evidence from Turner’s syndrome of an imprinted X-linked locus affecting cognitive function.” Nature 387(6634): 705–708.
Smith, C. (1947). “The effects of wartime starvation in Holland on pregnancy and its product.” Am J Obst Gynecol 53: 599–608.
Smith, F. M., L. J. Holt, et al. (2007). “Mice with a disruption of the imprinted Grb10 gene exhibit altered body composition, glucose homeostasis, and insulin signaling during postnatal life.” Mol Cell Biol27(16): 5871–5886.
Smithies, O. (2005). “Many little things: one geneticist’s view of complex diseases.” Nat Rev Genet 6(5): 419–425.
Snell, G. D., and S. Reed (1993). “William Ernest Castle, pioneer mammalian geneticist.” Genetics 133(4): 751–753.
Song, B. S., S. H. Lee, et al. (2009). “Nucleologenesis and embryonic genome activation are defective in interspecies cloned embryos between bovine ooplasm and rhesus monkey somatic cells.” BMC Dev Biol 9:44.
Soto, A. M., and C. Sonnenschein (2004). “The somatic mutation theory of cancer: Growing problems with the paradigm?” BioEssays 26(10): 1097–1107.
Soto, A. M., and C. Sonnenschein (2010). “Environmental causes of cancer: Endocrine disruptors as carcinogens.” Nat Rev Endocrinol 6(7): 363–370.
Speakman, J. R. (2006). “Thrifty genes for obesity and the metabolic syndrome—time to call off the search?” Diab Vasc Dis Res 3(1): 7–11.
Speakman, J. R. (2008). “Thrifty genes for obesity, an attractive but flawed idea, and an alternative perspective: The ‘drifty gene’ hypothesis.” Int J Obes (Lond) 32(11): 1611–1617.
Stein, A. D., A. C. Ravelli, et al. (1995). “Famine, third-trimester pregnancy weight gain, and intrauterine growth: The Dutch Famine Birth Cohort Study.” Hum Biol 67(1): 135–150.
Stein, Z., and M. Susser (1975). “The Dutch famine, 1944–1945, and the reproductive process. II. Interrelations of caloric rations and six indices at birth.” Pediatr Res 9(2): 76–83.
Stein, Z., M. Susser, et al. (1972). “Nutrition and mental performance.” Science 178: 706–713.
Stocum, D. L. (2002). “Regenerative biology and medicine.” J Musculoskelet Neuronal Interact 2(3): 270–273.
Stocum, D. L. (2004). “Amphibian regeneration and stem cells.” Curr Top Microbiol Immunol 280: 1–70.
Stokes, T. L., B. N. Kunkel, et al. (2002). “Epigenetic variation in Arabidopsis disease resistance. Genes Dev 16(2): 171–182.
Stokes, T. L., and E. J. Richards (2002). “Induced instability of two Arabidopsis constitutive pathogen-response alleles.” Proc Natl Acad Sci USA 99(11): 7792–7796.
Stoltz, K., P. E. Griffiths, et al. (2004). “How biologists conceptualize genes: An empirical study.” Stud Hist Phil Biol Biomed Sci 35: 647–673.
Storz, G., S. Altuvia, et al. (2005). “An abundance of RNA regulators.” Annu Rev Biochem 74: 199–217.
Stouder, C., and A. Paoloni-Giacobino (2010). “Transgenerational effects of the endocrine disruptor vinclozolin on the methylation pattern of imprinted genes in the mouse sperm.” Reproduction 139(2): 373–379.
Strahl, B. D., and C. D. Allis (2000). “The language of covalent histone modifications.” Nature 403(6765): 41–45.
Straube, W. L., and E. M. Tanaka (2006). “Reversibility of the differentiated state: Regeneration in amphibians.” Artif Organs 30(10): 743–755.
Suay, F., A. Salvador, et al. (1999). “Effects of competition and its outcome on serum testosterone, cortisol and prolactin.” Psychoneuroendocrinology 24(5): 551–566.
Suijkerbuijk, K. P., E. van der Wall, et al. (2007). “[Epigenetic processes in malignant transformation: The role of DNA methylation in cancer development].” Ned Tijdschr Geneeskd 151(16): 907–913.
Sun, Y. H., S. P. Chen, et al. (2005). “Cytoplasmic impact on cross-genus cloned fish derived from transgenic common carp (Cyprinus carpio) nuclei and goldfish (Carassius auratus) enucleated eggs.” Biol Reprod 72(3): 510–515.
Susser, M., and B. Levin (1999). “Ordeals for the fetal programming hypothesis. The hypothesis largely survives one ordeal but not another.” BMJ 318(7188): 885–886.
Swarbrick, M. M., and C. Vaisse (2003). “Emerging trends in the search for genetic variants predisposing to human obesity.” Curr Opin Clin Nutr Metab Care 6(4): 369–375.
Szyf, M., I. C. Weaver, et al. (2005). “Maternal programming of steroid receptor expression and phenotype through DNA methylation in the rat.” Front Neuroendocrinol 26(3–4): 139–162.
Taft, R. J., M. Pheasant, et al. (2007). “The relationship between non-protein-coding DNA and eukaryotic complexity.” BioEssays 29(3): 288–299.
Takahashi, K., K. Okita, et al. (2007). “Induction of pluripotent stem cells from fibroblast cultures.” Nat Protoc 2(12): 3081–3089.
Taylor, P. D., and L. Poston (2007). “Developmental programming of obesity in mammals.” Exp Physiol 92(2): 287–298.
ten Berge, D., W. Koole, et al. (2009). “Wnt signaling mediates self-organization and axis formation in embryoid bodies.” Cell Stem Cell 3(5): 508–515.
Thomas, C. A. J. (1971). “The genetic organization of chromosomes.” Annu Rev Genet 5: 237–256.
Thongphakdee, A., S. Kobayashi, et al. (2008). “Interspecies nuclear transfer embryos reconstructed from cat somatic cells and bovine ooplasm.” J Reprod Dev 54(2): 142–147.
Tiberio, G. (1994). “MZ female twins discordant for X-linked diseases: A review.” Acta Genet Med Gemellol (Roma) 43(3–4): 207–214.
Tobi, E. W., L. H. Lumey, et al. (2009). “DNA methylation differences after exposure to prenatal famine are common and timing-and sex-specific.” Hum Mol Genet 18(21): 4046–4053.
Tokumoto, Y., S. Ogawa, et al. (2010). “Comparison of efficiency of terminal differentiation of oligodendrocytes from induced pluripotent stem cells versus embryonic stem cells in vitro.” J Biosci Bioeng109(6): 622–628.
Tovee, M. J. (1993). “Colour vision in New World monkeys and the single-locus X-chromosome theory.” Brain Behav Evol 42(2): 116–127.
Trosko, J. E. (2009). “Review paper. Cancer stem cells and cancer nonstem cells: From adult stem cells or from reprogramming of differentiated somatic cells.” Vet Pathol Online 46(2): 176–193.
Tu, S. M., S. H. Lin, et al. (2002). “Stem-cell origin of metastasis and heterogeneity in solid tumours.” Lancet Oncol 3(8): 508–513.
Tweedell, K. (2008). New paths to pluripotent stem cells.” Curr Stem Cell Res Ther 3:151–162.
Tyrka, A. R., L. Wier, et al. (2008). “Childhood parental loss and adult hypothalamic-pituitary-adrenal function.” Biol. Psychiat. 63(12): 1147–1154.
Uhm, S. J., M. K. Gupta, et al. (2007). “Expression of enhanced green fluorescent protein in porcine-and bovine-cloned embryos following interspecies somatic cell nuclear transfer of fibroblasts transfected by retrovirus vector.” Mol Reprod Dev 74:1538–1547.
Urnov, F. D., and A. P. Wolffe (2001). “Above and within the genome: Epigenetics past and present.” J Mammary Gland Biol Neoplasia 6(2): 153–167.
VandeBerg, J. L., P. G. Johnston, et al. (1983). “X-chromosome inactivation and evolution in marsupials and other mammals.” Isozymes Curr Top Biol Med Res 9: 201–218.
Van Speybroeck, L., D. De Waele, et al. (2002). “Theories in early embryology.” Ann N Y Acad Sci 981: 7–49.
Ventolini, G., R. Neiger, et al. (2008). “Incidence of respiratory disorders in neonates born between 34 and 36 weeks of gestation following exposure to antenatal corticosteroids between 24 and 34 weeks of gestation.” Am J Perinatol 25(2): 79–83.
Verriest, G., and A. Gonella (1972). “An attempt at clinical determination by means of surface colours of the convergence points in congenital and acquired defects of colour vision.” Mod Probl Ophthalmol11: 205–212.
Virtanen, H. E., E. Rajpert-De Meyts, et al. (2005). “Testicular dysgenesis syndrome and the development and occurrence of male reproductive disorders.” Toxicol Appl Pharmacol 207(2, Suppl): 501–505.
Voisey, J., and A. van Daal (2002). “Agouti: From mouse to man, from skin to fat.” Pigment Cell Res 15(1): 10–18.
Vos, J. G., E. Dybing, et al. (2000). “Health effects of endocrine-disrupting chemicals on wildlife, with special reference to the European situation.” Crit Rev Toxicol 30(1): 71–133.
Waddington, C. (1935/1946). How animals develop. London: George Allen &Unwin.
Waddington, C. (1962). New patterns in genetics and development. New York: Columbia University Press.
Waddington, C. (1968). “The basic ideas of biology.” In Towards a theoretical biology, ed. C. Waddington. Vol. 1: Prolegomena, 1–32. Edinburgh: Edinburgh University Press.
Wadhwa, P. D., C. Buss, et al. (2009). “Developmental origins of health and disease: Brief history of the approach and current focus on epigenetic mechanisms.” Semin Reprod Med 27(5): 358–368.
Wagschal, A., and R. Feil (2006). “Genomic imprinting in the placenta.” Cytogenet Genome Res 113(1–4): 90–98.
Walker, B. R., and R. Andrew (2006). “Tissue production of cortisol by 11ß-hydroxysteroid dehydrogenase type 1 and metabolic disease.” Ann N Y Acad Sci 1083: 165–184.
Warner, M. J., and S. E. Ozanne (2010). “Mechanisms involved in the developmental programming of adulthood disease.” Biochem J 427(3): 333–347.
Waterland, R. A., and K. B. Michels (2007). “Epigenetic epidemiology of the developmental origins hypothesis.” Annu Rev Nutr 27(1): 363–388.
Waterland, R. A., M. Travisano, et al. (2007). “Diet-induced hypermethylation at agouti viable yellow is not inherited transgenerationally through the female.” FASEB J 21(12): 3380–3385.
Watson, J. D. (1968). The double helix: A personal account of the discovery of the structure of DNA. New York: Atheneum.
Watson, J. D., and F. H. Crick (1953a). “Genetical implications of the structure of deoxyribonucleic acid.” Nature 171(4361): 964–967.
Watson, J. D., and F. H. Crick (1953b). “Molecular structure of nucleic acids; a structure for deoxyribose nucleic acid.” Nature 171(4356): 737–738.
Weaver, A., R. Richardson, et al. (2004). “Response to social challenge in young bonnet (Macaca radiata) and pigtail (Macaca nemestrina) macaques is related to early maternal experiences.” Am J Primatol62(4): 243–259.
Weaver, I. C. (2009). “Shaping adult phenotypes through early life environments.” Birth Defects Res C Embryo Today 87(4): 314–326.
Weaver, I. C., N. Cervoni, et al. (2004). “Epigenetic programming by maternal behavior.” Nat Neurosci 7(8): 847–854.
Weaver, I. C., F. A. Champagne, et al. (2005). “Reversal of maternal programming of stress responses in adult offspring through methyl supplementation: Altering epigenetic marking later in life.” J Neurosci25(47): 11045–11054.
Weaver, I. C., M. J. Meaney, et al. (2006). “Maternal care effects on the hippocampal transcriptome and anxiety-mediated behaviors in the offspring that are reversible in adulthood.” Proc Natl Acad Sci USA103(9): 3480–3485.
Weksberg, R., C. Shuman, et al. (2005). “Beckwith-Wiedemann syndrome.” Am J Med Genet C Semin Med Genet 137C(1): 12–23.
Weksberg, R., and J. A. Squire (1996). “Molecular biology of Beckwith-Wiedemann syndrome.” Med Pediatr Oncol 27(5): 462–469.
Wells, J. C. (2009). “Ethnic variability in adiposity and cardiovascular risk: The variable disease selection hypothesis.” Int J Epidemiol 38(1): 63–71.
White, S. A., T. Nguyen, et al. (2002). “Social regulation of gonadotropin-releasing hormone.” J Exp Biol 205(Pt 17): 2567–2581.
Whitlock, K. E., N. Illing, et al. (2006). “Development of GnRH cells: Setting the stage for puberty.” Mol Cell Endocrinol 254–255: 39–50.
Williams, C. A., H. Angelman, et al. (1995). “Angelman syndrome: Consensus for diagnostic criteria. Angelman Syndrome Foundation.” Am J Med Genet 56(2): 237–238.
Wilmut, I., A. E. Schnieke, et al. (1997). “Viable offspring derived from fetal and adult mammalian cells.” Nature 385(6619): 810–813.
Wilson, B. D., M. M. Ollmann, et al. (1995). “Structure and function of ASP, the human homolog of the mouse agouti locus.” Hum Mol Genet 4(2): 223–230.
Witchel, S. F., and D. B. DeFranco (2006). “Mechanisms of disease: Regulation of glucocorticoid and receptor levels—impact on the metabolic syndrome.” Nat Clin Pract Endocrinol Metab 2(11): 621–631.
Wohlfahrt-Veje, C., K. M. Main, et al. (2009). “Testicular dysgenesis syndrome: Foetal origin of adult reproductive problems.” Clin Endocrinol (Oxf) 71(4): 459–465.
Wolff, G. L. (1996). “Variability in gene expression and tumor formation within genetically homogeneous animal populations in bioassays.” Fundam Appl Toxicol 29(2): 176–184.
Wolff, G. L., R. L. Kodell, et al. (1998). “Maternal epigenetics and methyl supplements affect agouti gene expression in Avy/a mice.” FASEB J 12(11): 949–957.
Wolff, G. L., D. W. Roberts, et al. (1986). “Prenatal determination of obesity, tumor susceptibility, and coat color pattern in viable yellow (Avy/a) mice. The yellow mouse syndrome.” J Hered 77(3): 151–158.
Wolfram, S. (2002). A new kind of science. Champagn, IL: Wolfram Media.
Wong, A. H., Gottesman, I. I., et al. (2005). “Phenotypic differences in genetically identical organisms: The epigenetic perspective.” Hum Mol Genet 14(Spec 1): R11–R18.
Wright, S. (1916). “An intensive study of the inheritance of color and other coat characters in guinea pigs with special reference to graded variation.” Carnegie Inst Wash Publ 241: 59–160.
Wright, S. (1927). “The effects in combination of the major color factors of the guinea pig.” Genetics 12: 530–569.
Wroe, S., C. McHenry, et al. (2005). “Bite club: Comparative bite force in big biting mammals and the prediction of predatory behaviour in fossil taxa.” Proc Biol Sci 272(1563): 619–625.
Yan, S. Y., M. Tu, et al. (1990). “Developmental incompatibility between cell nucleus and cytoplasm as revealed by nuclear transplantation experiments in teleost of different families and orders.” Int J Dev Biol 34(2): 255–266.
Yehuda, R., A. Bell, et al. (2008). “Maternal, not paternal, PTSD is related to increased risk for PTSD in offspring of Holocaust survivors.” J Psychiatr Res 42(13): 1104–1111.
Yehuda, R., and L. M. Bierer (2007). “Transgenerational transmission of cortisol and PTSD risk.” Prog Brain Res 167: 121–135.
Yehuda, R., S. M. Engel, et al. (2005). “Transgenerational effects of posttraumatic stress disorder in babies of mothers exposed to the World Trade Center attacks during pregnancy.” J Clin Endocrinol Metab90(7): 4115–4118.
Ying, S. Y., D. C. Chang, et al. (2008). “The microRNA (miRNA): Overview of the RNA genes that modulate gene function.” Mol Biotechnol 38(3): 257–268.
Youngson, N. A., and E. Whitelaw (2008). “Transgenerational epigenetic effects.” Annu Rev Genomics Hum Genet 9(1): 233–257.
Zeisel, S. H. (2009). “Importance of methyl donors during reproduction.” Am J Clin Nutr 89(2): 673S–677S.
Zilberman, D., and S. Henikoff (2005). “Epigenetic inheritance in Arabidopsis: Selective silence.” Curr Opin Genet Dev 15(5): 557–562.