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Hayashizaki, Y. et al. 1989. Thyroid-stimulating hormone (TSH) deficiency caused by a single base substitution in the CAGYC region of the β-subunit. EMBO Journal 8: 2291-2296 Headon, D.J. and P.A. Overbeek. 1999. Involvement of a novel Tnf receptor homologue in hair follicle induction. Nature Genetics 22: 370-374 Healy, E. et al. 2001. Functional variation of MC1R alleles from red-haired individuals. Human Molecular Genetics. 10: 2397-2402 Heijmans, B.T. et al. 2000. Common gene variants, mortality and extreme longevity in humans. Experimental Gerontology 35: 865-877 Hennessy, R.J. and C.B. Stringer. 2002. Geometric morphometric study of the regional variation of modern human craniofacial form. American Journal of Physical Anthropology 117: 37-48 Herdt, G. 1994. Mistaken sex: culture, biology and the third sex in New Guinea, in G. Herdt (ed.) Third sex, third gender. Zone Books. Cambridge, Mass. Heron, T.M. 1986. Boruwlaski, the little count. Durham, UK Hertel, C. 2001. Hairy issues: Portraits of Petrus Gonsalus and his family in Archduke Ferdinand II's Kunstkammer and their contexts. Journal of the History of Collections 13: 1-22 Hinchliffe, J.R. and D.R.Johnson. 1980. The development of the vertebrate limb. Claredon Press, Oxford Holekamp, K.E. et al. 1996. Rank and reproduction in female spotted hyenas. Journal of Reproduction and Fertility 108: 229-237 Holliday, R. 1989. Food, reproduction and longevity: is the extended lifespan of calorie-restricted animals an evolutionary adaptation? Bioessays 10: 125-127 Holly, J.M.P. et al. 1999. Growth hormone, IGF-1 and cancer. Less intervention to avoid cancer? More intervention to prevent cancer? Journal of Endocrinology 162: 321-330 Horan,. G.S. et al. 1994. Homeotic transformation of cervical vertebrae in Hoxa-4 mutant mice. Proceedings of the National Academy of Sciences, USA. 91: 12644-12648 Horan, G.S. et al. 1995a. Compound mutants for the paralogous Hoxa-4, Hoxb-4, and Hoxc-4 genes show more complete homeotic transformations and a dose dependent increase in the number of vertebrae transformed. Genes and Development 9: 1667-1677 Horan, G.S. et al. 1995b. Mutations in paralogous Hox genes result in overlapping homeotic transformations of the axial skeleton-evidence for unique and redundant function. Developmental Biology 169: 359-372 Houssay, E. 1937. De la nature, des causes, des différences des monstres. Editions Hippocrates, Paris Hu, D. and J.A. Helms. 1999. The role of sonic hedgehog in normal and abnormal craniofacial morphogenesis. Development 126: 4873-4884 Huelsken J. et al. 2001. Beta-catenin controls hair follicle morphogenesis and stem cell differentiation in the skin. Cell 105: 533-545 Hummel, K.P. 1958. The inheritance and expression of Disorganization, an unusual mutation in the mouse. Journal of Experimental Zoology 137: 389-423 Hummel, K.P. 1959. Developmental anomalies in mice resulting from action of the gene Disorganization, a semi-dominant lethal. Pediatrics 23: 212-221 Ianakiev, P. et al. 2000. Acheiropodia is caused by a g~nomic deletion in C70rf2 the human orthologue of the Lmbr1 gene. American Journal of Human Genetics 68: 38-45 Imperato-McGinley, J. et al. 1974. Steroid 5-alpha-reductase deficiency in man: an inherited form of male pseudohermaphroditism. Science 186: 1213-1215 Imperato-McGinley, J. et al. 1991. A cluster ofmale pseudohermaphrodites with 5-alpha-reductase deficiency in Papua New Guinea. Clinical Endocrinology 34: 293-298 Incardona, J.P. 1998. The teratogenic Veratrum alkaloid cyclopamine inhibits sonic hedgehog signal transduction. Development 125: 3553-3562 International Sequencing Consortium. 2001. Initial sequencing and analysis of the human genome. Nature 409: 860-921 Irving, J. 1862. The drowned women of Wigton, a romance of the Covenant. Porteous and Hislop, Glasgow Isaac, A. et al. 2000. FGF and genes encoding transcription factors in early limb specification. Mechanisms of Development 93: 41-48 Iwai, T. 1907. A statistical study on the polymastia of the Japanese. Lancet 2: 753-4 Jackson, I.J. 1997. Homologous pigmentation mutations in human, mouse and other model organisms. Human Molecular Genetics 6: 1613-1624 Jackson, W.P.U. 1951. Osteo-dental dysplasia (Cleidocranial dysostosis) 'The Arnold Head'. Acta Medica Scandinavica 139: 293-295 Janin, J. 1829. (1998) Une femme à deux têtes. S. Pestel (ed.) La collection electronique de la Biblioteque Municipale de Lisieux: http://ourworld.Compuserve.com/homepages/bibhhlisieux/ Jarvik, G.P. et al. 1994. Non-mendelian transmission in a human developmental disorder: Split Hand / Split Foot. American Journal of Human Genetics 55: 710-713 Jeannotte, L. et al. (1993) Specification of axial identity in the mouse: role of the Hoxa5 (Hox1.3) gene. Genes and Development 7: 2085-2096 Jenkins, P. 1998. Cancer in acromegaly. Trends in Endocrinology and Metabolism 9: 360-366 Johanson, D. and B. Edgar. 1996. From Lucy to language. Orion, London Joseph, R. and P. Godson. 1988. Peace at last for tragic Rita: white outcase in black skin. Sunday Times Johannesburg). 28 August, p. 12 Jost, A. 1946-47. Recherches sur la différenciation sexuellede l'етbryоп de lapin (Troisieme Partie). Archives d'anatomie microscopique et de morphologie expérimental 36: 271-315 Jung, H.-S. et al. 1998. Local inhibitory action of BMPs and their relationships with activators in feather formation: implications for periodic patterning. Developmental Biology 196: 11-23 Kappler, С. 1980. Monstres, demons et merveilles a la fin du Moyen age. Payot, Paris Kaufman, M.H. and K.S. O'Shea. 1978. induction of monozygotic twinning in the mouse. Nature 276: 707-708 Keith, A. 1911. An inquiry into the nature of the skeletal changes in acromegaly Lancet 1: 993-1002 |