Онлайн книга «Мутанты»
|
Kenyon, C. et al. 1993. АС. elegans mutant that lives twice as long as wild type. Nature 366: 461-464 Kere, J. et al. 1996. X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by a mutation in a novel transmembrane protein. Nature Genetics 13: 409-416 Kingdon-Ward, F. 1924. From China to Hkamti Long. Edward Arnold, London Kingdon-Ward, F. 1937. Plant hunter's paradise. Jonathan Cape, London Kirk, G.S. 1974. The nature of the Greek myths. Penguin, Harmondsworth, UK Knussmann, R. et al. 1992. Relations between sex hormone level and characteristics of hair and skin in healthy young men. American Journal of Physical Anthropology 88: 59-67 Kobelt, G.L. 1844. The female sex organs in humans and some mammals (trans. H.E Bernays) in Lowry, T.P. (1978) The classic clitoris, historical contributions to scientific sexuality. Nelson-Hall, Chicago Kohn, M. 1995. The race gallery: the return of racial science. Jonathan Cape, London Kollar, E.J. and C. Fisher. 1980. Tooth induction in chick epithelium: expression of quiescent genes for enamel synthesis. Science 207: 993-995 Komori et al. 1997. Targeted disruption of Cbfa1 results in a complete lack of bone formation owing to maturational arrest of osteoblasts. Cell 89: 755-764 Kondo, S. et al. 2001. The medaka rS-3 locus required for scale development encodes ectodysplasin-A receptor. Current Biology 7: 1201-1206 Kondo, T. et al. 1997. Of fingers, toes, and penises. Nature 390: 29 Koren, Y. and E. Negev. 2003. im Herzen waren wir Riesen. Econ, Munich Kornak, U. et al. 2000. Mutations in the а3 subunit of the vacuolar H+-ATPase cause infantile malignant osteopetrosis. Human Molecular Genetics 9: 2059-2063 Kostic, D. and M.R. Capecchi. 1994. Targeted disruptions of the murine HoxA-4 and HoxA-6 genes result in homeotic transformations of components of the vertebral column. Mechanisms of Development 46: 231-247 Kremer, H. et al. 1995. Male pseudohermaphroditism due to a homozygous missense mutation of the luteinising hormone receptor gene. Nature Genetics 9: 160-164 Krude, H. et al. 1998. Severe early onset obesity, adrenal insufficiency and red hair pigmentation caused by РОМС mutations in humans. Nature Genetics 19: 155-157 Kruglyak, L. and D.A. Nickerson. 2001. Variation is the spice of life. Nature Genetics 27: 234-236 Krzisnik, C. et al. 1999. The 'Little People' of the Island of Krk – Revisited. Etiology of hypopituitarism revealed. Journal of Endocrine Genetics 1: 9-19 Kuester and Happle. 1984. The inheritance of common baldness. Two В or not two B? Journal of the American Academy of Dermatology 11: 921-926 Laara, E. and P. Rantakallio. 1996. Body size and mortality in women: a 29-year follow up of 12,000 pregnant women in northern Finland. Journal of Epidemiology and Community Health 50: 408-414 Lahr, M.M. 1996. The evolution of modern human diversity: a study in cranial variation. Cambridge University Press Lamb, T.M. et al. 1993. Neural induction by the secreted polypeptide noggin. Science 262: 713-718 Lammer, E.J. et al. 1985. Retinoicacid embryopathy. New England Journal of Medicine 313: 837-841 Landucci, L. 1542, 1927. A Florentine diary from 1450 to 1516 by Luca Landucci, continued by an anonymous writer till 1542 with notes by lodoco del Badia (trans. A. de Rosen Jervis). J.M. Dent & Sons, London Lanza, R.P. et al. 2000. Extension of cell life-span and telomere length in animals cloned from senescent somatic cells. Science 288: 665-668 Laqueur, T.W. 1989. 'Amor Veneris, vel Dulcedo Appeleteur' pp.90-131 in M. Feher (ed.) Zone 5. Fragments for a history of the human body, part 3. Zone, N.Y. Laqueur, T.W. 1990. Making sex, body and gender from the Greeks to Freud. Harvard University Press, Cambridge. Mass. Laue, L.L. et al. 1996. Compound heterozygous mutations of the luteinising hormone receptor gene in Leydig cell hypoplasia. Molecular Endocrinology 10: 987-997 Lawrence, P. 1992. The making of a fly. Blackwell. London Laycock, J. and P. Wise. 1996. Essential Endocrinology. (3rd ed.) Oxford University Press Lazner, E. et al. 1999. Osteopetrosis and osteoporosis: two sides of the same coin. Human Molecular Genetics 8: 1839-1846 Le Guyader, H. 1998. Etienne Geoffroy Saint-Hilaire (1772-1844): un naturalist visionnaire. Belin, Paris Le Mouellic, H. et al. 1992. Homeosis in the mouse induced by a null mutation in the HOX-3.1 gene. Cell 69: 251-264 Le Roith, D. et al. 2001. What is the role of circulating IGF? Trends in Endocrinology and Metabolism 12: 48-52 Lee, C.-K. et al. 1999. Gene expression profile of aging and its retardation by caloric restriction. Science 285: 1390-1393 Lee, H.W. et al. 1998. Essential role of mouse telomerase in highly proliferative organs. Nature 392: 569-574 Lee, P.A. and S.R Witchel. 1997. The influence of estrogen on growth. Current opinion in pediatrics 9: 431-436 Lenz, W. 1962. Thalidomide and congenital abnormalities. Lancet 1: 45 Leroi, A.M. 2001. Molecular signals versus the loi de balancement. Trends in Ecology and Evolution. 16: 24-29 Leroi, A.M. et al. 2003. Cancer selection. Nature Cancer Reviews 3: 226-231 Lettice, L.A. et al. 2002. Disruption of a long-range cis-acting regulator for Shh causes preaxial Polydactyly. Proceedings of the National Academy of Sciences; USA 99: 7548-7553 Levin, M. et al. 1995. A molecular pathway determining left-right asymmetry in chick embryogenesis. Cell 82: 803-814 Levin, M. et al. 1996. Laterality defects in conjoined twins. Nature 384: 321 Lewandoski, M. et al. 2000. Fgf8 signalling from the AER is essential for normal limb development. Nature Genetics 26: 460-463 Lewis, E. 1978. A gene complex controlling segmentation in Drosophila. Nature 27: 565-570 |