Мутанты - Арман Мари Леруа
Шрифт:
Интервал:
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
Поделиться книгой в соц сетях:
Обратите внимание, что комментарий должен быть не короче 20 символов. Покажите уважение к себе и другим пользователям!