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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

Lewis, T. and D. Embleton. 1908. Split-hand and split-foot deformities, their types, origin, and transmission. Biometrika 6: 26-58

Li, J. et al. 1997. Dinucleotide repeat in the 3' flanking region provides a clue to the molecular evolution of the Duffy gene. Human Genetics 99: 573-577

Liceti, F. 1634. De monstrorum natura caussis et differentiis. Padua

Licht, P. et al. 1992. Hormonal correlates of 'masculinisation' in female spotted hyenas (Crocuta crocuta). 2. Maternal and fetal steroids. Journal of reproduction and fertility 95: 463-474

Lickert, H. et al. 2002. Formation of multiple hearts in mice following deletion of beta-catenin in the embryonic endoderm. Developmental Cell 3: 171-181

Lifton, R.J. 1986. The Nazi doctors: medical killing and the psychology of genocide. Macmillan, London

Lindroth, S. 1983. The two faces of Linnaeus. in T. Fdingsmyr (ed.) Linnaeus: the man and his work. University of California Press, Berkeley

Linnaeus, C. 1758, 1939. Systema naturae. 10th edition. British Museum, London

Linnaeus, C. 1761. Fauna svecica. Stockholm

Lloyd, A.T. 1986. Pussy Cat, Pussy Cat, where have you been? Natural History 95(7): 46-52

Logrofio, R. et al. 1997. Heteropagus conjoined twins due to fusion of two embryos: report and review. American Journal of Medical Genetics 73: 239-243

Lopez-Bermejo, A. et al. (2000). Genetic defects of the growth hormone-insulin-like growth factor axis. Trends in Endocrinology and Metabolism 11: 39-49

Lufkin, T. et al. 1991. Disruption of the Hox-1.6 (Hoxal) homeobox gene results in defects in a region corresponding to its rostral domain of expression. Cell 66: 1105-1119

Lupu, F. et al. 2001. Roles of growth hormone and insulin-like growth factor 1 in mouse postnatal growth. Developmental Biology 229: 141-162

McBride,W.B. 1961. Thalidomide and congenital abnormalities. Lancet 11: 1358

McEwan, C. et al. 1997. (eds) Patagonia: natural history, prehistory and ethnography at the uttermost ends of the earth. British Museum, London

Mackenbach, J.P. 1991. Narrowing inequalities in children's height. Lancet 338: 764

McLachlan, J. 1994. Medical embryology: Addison-Wesley, Wokingham

McLaren, A. 1990. What makes a man a man? Nature 346: 216-217

McMahon J.A. et al. 1998. Noggin-mediated antatonism of BMP signalling is required for growth and patterning of the neural tube and somite. Genes and Development 12: 1438-1452

McMullen, G. and K. Pearson. 1913. On the inheritance of the deformity known as split-foot or lobster-claw. Biometrika 9: 381-390

McPherron, A.C. and S.J. Lee. 1997. Doubling muscle in cattle due to mutations in the myostatin gene. Proceedings of the National Academy of Sciences, USA 94: 12457-12461

McPherron, A.C. et a 1.1997. Regulation of skeletal muscle mass in mice by a new TGF-Beta superfamily member. Nature 387: 83-90

Maden, M. 1999. Heads or tails? Retinoic acid will decide. Bioessays 21: 809-812

Maeder, T. 1998. A few hundred people turned to bone. The Atlantic, February, (two parts)

Manoiloff, E.O. 1931. A rare case of hereditary hexadactylism. American Journal of Physical Anthropology 15: 503-508

Manouvrier-Hanu S. et al. 1999. Genetics of limb anomalies in humans. Trends in Genetics 15: 409-417

Mansholt, U.J. 1987. The increase in the height of Dutchmen and the attraction of tennis. Nederlands Tijdschrift voor Geneeskunde 131: 376

Mark, M. et al. 1993. Two rhombomeres are altered in Hoxa-I mutant mice. Development 119: 319-338

Maroteaux,P. 1995. Toulouse-Lautrec's diagnosis. Nature Genetics II: 362

Maroteaux, P. and M. Lamy. 1965. The malady of Toulouse-Lautrec. JAMA, Journal of the American Medical Association 191: 111-113

Marshall, H.K. and H.I. Harder. 1958. Testicular feminising syndrome in male pseudohermaphrodite: report of two cases in identical twins. Obstetrics and Gynecology 12: 284-293

Martin, E. 1880. Histoire des monstres. C. Reinwald, Paris

Martin, G. and J. Oshima. 2000. Lessons from human progeroid syndromes. Nature 408: 263-266

Martinez-Frias, M.-L. 1993. Another way to interpret the description of the Monster of Ravenna of the sixteenth century. American Journal of Medical Genetics 49: 362

Mascie-Taylor, C.G.N. and J.L. Boldsen. 1985. Regional and social analysis of height variation in a contemporary British sample. Annals of Human Biology 12: 315-324

Mathon, N.F. et al. 2001. Lack of replicative sensecence in normal rodent glia. Science 291: 872-875

Mayor, A. 2000. The first fossil hunters. Princeton University Press, Princeton, N.J.

Medawar, P.B. 1952. An unsolved problem in biology. H. K. Lewis. London

Melanchthon, P. and M. Luther. 1523 (1823). Interpretation of two horrible monsters [Deuttung tier czwo grewlichï Figuren, etc.]

Merimee, T.J. et al. 1981. Dwarfism in the pygmy. New England Journal of Medicine 305: 965-968

Merimee, T.J. et al. 1987. Insulin-like growth factors in pygmies: the role of puberty in determining final stature. New England Journal of Medicine 316: 906-911

Merke, F. 1993. History and iconography of endemic goitre and cretinism. MTP Press, Lancaster

Merlo, G.R. et al. 2002. Mouse model of split hand / foot malformation type 1. Genesis 33: 97-101

Meyers, E.N. and G.R. Martin. 1999. Differences in left-right axis pathways in mouse and chick: functions of FGF8 and SHH. Science 285: 403-406

Miller, R. and S. Austad. 1999. Large animals in the fast lane. Science 285: 199

Mills, A.A. et al. 1999. p63 is a P53 homologue required for limb and epidermal morphogenesis. Nature 398: 708-713

Mittwoch, U. 1973. Genetics of sex differentiation. Academic Press, N.Y.

Monreal, A.W. 1999. Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia. Nature Genetics 22: 366-369

Montaigne, M. de. 1580 (1958). Essays (trans. J.M. Cohen). Penguin Books, Harmondsworth, UK

Montaigne, M. de. 1603 (1998). Florio's translation of Montaigne's essays. B. R. Schneider (ed.), Renascence Editions, University of Oregon

Moon, A.M. and M.R. Capecchi. 2000. Fgf8 is required for outgrowth and patterning of the limbs. Nature Genetics 26: 455-459

Morin, A. 1996. La teratologic de Geoffroy Saint-Hilaire à nos jours. Bulletin de l'Association des Anatomistes 80: 17-31

Morishima, A. et al. 1995. Aromatase deficiency in male and female siblings caused by a novel mutation and the physiological role of estrogens. Journal of clinical endocrinology and metabolism 80: 3689-3698

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