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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

Mortlock, D.P. and J.W. Innis. 1997. Mutation of Hox a-13 in hand-foot-genital syndrome. Nature Genetics 15: 179-180

Mortlock, D.P. et al. 1996. The molecular basis of hypodactyly (Hd): a deletion in Hox a-13 leads to arrest of digital arch formation. Nature Genetics 13: 284-288

Moskovitz, E. 1987. By the grace of the devil. Rotem, Ramat-Gan, Israel

Muenke M. and P.A. Beachy 2000. Genetics of ventral forebrain development and holoprosencephaly. Current Opinion in Genetics and Development 10: 262-269

Mundlos, S. 1999. Cleidocranial dysplasia: clinical and molecular genetics. Journal of Medical Genetics 36: 177-182

Mundlos, S. et al.1997. Mutations involving the transcription factor CBFAi cause cleiodocranial dysplasia. Cell 89: 773-779

Muragaki, Y. et al. 1996. Altered growth and branching patters in synpolydactyly caused by mutations in Hoxd-13. Science 272: 548-551

Mya-Tu, M. et al. 1962. Tarong pygmies in North Burma. Nature 195: 131-132

Mya-Tu, M. et al. 1966. The Tarons in Burma. Burma Medical Research Institute, Rangoon. Special Report Series No.1

Nanni, L. et al. 1999. The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly. Human Molecular Genetics 8: 2479-2488

Nanni, L. et al. 2001. SHH mutation is associated with solitary median maxillary central incisor: a study of 13 patients and review of the literature. Journal of Medical Genetics 102: 1-10, 2001

Naski, M.C. et al. 1996. Graded activation of fibroblast growth factor receptor 3 by mutations causing achondroplasia and thanatophoric dysplasia. Nature Genetics 13: 233-237

Naski, M.C. et al. 1998. Repression of hedgehog signalling and BMP4 expression in growth plate cartilage by fibroblast growth factor receptor 3. Development 125: 4977-4988

Naudin ten Cate L., C. Vermeij-Keers, D.A. Smit, T.W. Cohen-Overbeek, K.B. Gerssen-Schoorl, T. Dijkhuisen. 1995. intracranial teratoma with multiple fetuses. Pre- and post-natal appearance. Human Pathology 26: 804-807

Neaves, W.B. et al. 1980. Sexual dimorphism of the phallus in spotted hyena (Crocuta crocuta). Journal of Reproduction and Fertility 59: 509-513

Needham, J. 1959. A history of embryology. Cambridge University Press, Cambridge, UK

Netter, A. et al. 1958. Le testicule feminisant. Annales d'endocrinologie 9: 994-1014

Neubert, R. et al. 1999. Developmental model for thalidomide action. Nature 400: 419-420

Newbery, H.J. and C.M. Abbott. 2002. Of mice, men and motor neurons. Trends in Molecular Medicine 8: 88-92

Niccoli, O. 1990. People and prophecy in Renaissance Italy, (trans. L. G. Cochrane.) Princeton University Press, Princeton

Niswander, L. et al. 1993. FGF-4 replaces the apical ectodermal ridge and directs outgrowth and patterning of the limb. Cell 75: 579-587

Nonaka, S. et al. 1998. Randomisation of left-right asymmetry due to loss of nodal cilia generating leftward flow of extraembryonic fluid in mice lacking KIF3B motor protein. Cell 95: 839-847

Noramly, S. and B.A. Morgan. 1998. BMPs mediate lateral inhibition at successive stages in feather tract development. Development 125: 3775-3787

O'Connell, H.E. et al. 1998. Anatomical relationship between urethra and clitoris. Journal of Urology 159: 1892-1897

Olbrich, H. et al. 2002. Mutations in DNAH5 cause primary ciliary dyskinesia and randomisation of left-right asymmetry. Nature Genetics 30: 143-144

Olsen, B.R. et al. 2000. Bone development. Annual Reviews of Cell and Developmental Biology 16: 191-220

On-line Mendelian Inheritance in Man. 2000. OMIM™. McKusick-Nathans Institute for Genetic Medicine, Johns Hopkins University, Baltimore, MD, and National Center for Biotechnology Information, National Library of Medicine, Bethesda, MD

http://www.ncbi.nlm.nih.gov/omim/

Oosterhout, van C. et al. 2003. Inbreeding depression and genetic load of sexually selected traits: how the guppy lost its spots. Journal of Evolutionary Biology 16: 273-281

Oostra, R.-J. et al. 1998a. Congenital anomalies in the teratological collection of the Museum Vrolik in Amsterdam, the Netherlands. I: Syndromes with multiple congenital anomalies. American Journal of Medical Genetics 77: 100-115

Oostra, R.-J. et al. 1998b. Congenital anomalies in the teratological collection of the Museum Vrolik in Amsterdam, the Netherlands. II: Skeletal Dysplasias. American Journal of Medical Genetics 7 7: 116-134

Oostra, R.-J. et al. 1998c. Congenital anomalies in the teratological collection of the Museum Vrolik in Amsterdam, the Netherlands. Ill: Primary field defects, sequences and other complex anomalies. American Journal of Medical Genetics 80: 46-59

Oostra, R.-J. et al. i998d. Congenital anomalies in the teratological collection of the Museum Vrolik in Amsterdam, the Netherlands. IV: Closure defects of the neural tube. American Journal of Medical Genetics 80: 60-73

Oostra, R.-J. et al. 19986. Congenital anomalies in the teratological collection of the Museum Vrolik in Amsterdam, the Netherlands. V: Conjoined and acardiac twins. American Journal of Medical Genetics 80: 74-89

Oro, A.E. and M.P. Scott. 1998. Splitting hairs: dissecting roles of signaling systems in epidermal development. Cell 95: 575-578

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