Книга Мутанты - Арман Мари Леруа
Шрифт:
Интервал:
Закладка:
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