Рейтинговые книги
Читем онлайн Мутанты. О генетической изменчивости и человеческом теле. - Арман Мари Леруа

Шрифт:

-
+

Интервал:

-
+

Закладка:

Сделать
1 ... 69 70 71 72 73 74 75 76 77 ... 87

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

Orr, H.T. 2000. A proposed mechanism of ALS fails the test in vivo. Nature Neuroscience 5: 287-288

Ortega-Ortiz, J.G. and B. Villa-Ramirez. 2000. Polydactyly and other features of the manus of the vaquita, Phocoena sinus. Marine Mammal Science 16: 277-286

Pare, A. 1573 (1971). Des monstres. J. Ceard (ed.) Droz, Geneva

Pare, A. 1573 (1982). On monsters and marvels (trans. J. L. Pallister) Chicago University Press, Chicago

Park, K. and L. Daston. 1981. Unnatural conceptions: the study of monsters in sixteenth and seventeenth century France and England. Past and Present 92: 20-54

Parkes, T.L. et al. 1998. Extension of Drosophila lifespan by over expression of human SOD1 in motorneurons. Nature Genetics 19: 171-174

Partridge, L. and D. Gems. 2002. Mechanisms of ageing: public or private? Nature Reviews Genetics 3: 165-175

Patronek, G.J. et al. 1997. Comparative longevity of pet dogs and humans: implications for gerontology research. Journal of Gerontology 52A: B171-178

Pearson, K. et al. 1913. A monograph on albinism in man. 3 V. text; 3 V. plates. Draper's company research memoirs, Biometric series X. Dulau & Co. London

Pearson, K. 1908. On the inheritance of the deformity known as split-foot or lobster claw. Biometrika 6: 69-79

Pearson, K. 1913. Notes on the Honduras piebald. Biometrika 9: 330-331

Perrett, D.I. et al. 1994. Facial shape and judgments of female attractiveness. Nature 368: 239-242

Perriton, C. et al. 2002. Sonic hedgehog signalling from the urethral epithelium controls external genital development Developmental Biology 247: 26-46

Piccolo, S. et al. 1996. Dorsoventral patterning in Xenopus: inhibition of ventral signals by direct binding of Chord in to BMP-4. Cell 86: 589-598

Pinto-Correa, C. 1997. The ovary of Eve: egg and sperm and preformationism. Chicago University Press, Chicago

Pletcher, S.D. et al. 2002. Genome-wide transcript profiles in aging and calorically restricted Drosophila melanogaster. Current Biology 30: 712-723

Posel, D. 2001. Race as common sense: racial classification in twentieth century South Africa. African Studies Review 44: 87-113

Posner, G. L. and J. Ware. 1986. Mengele: the complete story. Futura, London

Power, C. and S. Matthews. 1997. Origins of health inequalities in a national population sample. Lancet 350: 1584-1589

Qu, S. et al. 1998. Mutations in mouse Aristaless-like4 cause Strong's luxoid polydactyly. Development. 125: 2711-2721

Quance, E. 1977. Alexander Graham Bell, human inheritance, and the eugenics movement. Research Bulletin of the National Historic Parks and Sites Branch, Parks Canada. No. 62

Quigley, C.A. et al. 1992. Complete deletion of the androgen receptor gene: definition of the null phenotype of the androgen insensitivity syndrome and determination of carrier status. Journal of Clinical Endocrinology and Metabolism 74: 932-933

Ramesar, R.S. et al. 1996. Mapping of the gene for cleidocranial dysplasia in the historical Cape Town (Arnold) kindred and evidence for locus homogeneity. Journal of Medical Genetics 33: 511-514

Ramirez-Solis et al. 1993. Hoxb-4 (Hox-2.6) mutant mice show homeotic transformation of a cerivical rudiment and defects in the closure of the sternal rudiments. Cell 73: 279-294

Rana, B.K. et al. 1999. High polymorphism at the human melanocortin 1 receptor locus. Genetics 151: 1547-1557

Rancourt et al. 1995. Genetic interaction between Hoxb-5 and Hoxb-6 is revealed by nonallelic noncomplementation. Genes and Development 9: 108-122

Reaume, A.G. et al. 1996. Motor neurons in Cu/Zn superoxide dismutase-deficient mice develop normally but exhibit enhanced cell death after axonal injury. Nature Genetics 13: 43-47

Reed, Т.Е. and J.V. Neel. 1959. Huntington's chorea in Michigan. American Journal of Human Genetics 11: 107-635

Reeves, R.H. et al. 2001. Too much of a good thing: mechanisms of gene action in Down syndrome. Trends in Genetics 17: 83-241

Reichert, H. and A. Simeone. 2001. Developmental genetic evidence for a monophyletic origin of the bilaterian brain. Philosophical Transactions of the Royal Society В 356: 1533-1544

Reynolds, A.J. et al. 1999. Trans-gender induction of hair follicles. Nature 402: 46-47

Ricklefs, R.E. and C.E. Finch. 1995. Ageing: a natural history. Scientific American, N.Y.

Riddle, R.D. et al. 1993. Sonic hedgehog mediates the Polarizing Activity of the ZPA. Cell 75: 1401-1416

Robbins, L.S. et al. 1993. Pigmentation phenotypes of variant extension locus alleles result from point mutations that alter MSH receptor function. Cell 72: 827-834

Roberts, R.S. 1974. The making of a Rhodesian myth. Rhodesian History 5: 89-91

Robins, A.H. 1991. Biological perspectives on human pigmentation. Cambridge University Press, Cambridge, UK

Rodriguez, J.M. 1870. Descripcion de un monstruo cuadruple, nacido en Durango el ano de 1860. Gaceta Medica de Mexico 5: 33-48

Roessler, E. et al. 1996. Mutations in the human sonic hedgehog gene cause holoprosencephaly. Nature Genetics 14: 357-360

Root, A. 1998. Editorial: does growth hormone have a role in the management of children with nongrowth hormone deficient short stature and intrauterine growth retardation? Journal of Clinical Endocrinology and Metabolism 83: 1067-1069

Rose, M.R. 1984. Laboratory evolution of postponed senescence in Drosophila melanogaster. Evolution 38: 1004-1010

Rose, M.R. 1991. Evolutionary biology of ageing. Oxford University Press, N.Y.

Rosen, D.R. et al. 1993. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Nature 362: 59-62

Rosenbaum, S. et al. 1985. A survey of heights and weights of adults in Great Britain. Annals of Human Biology 12: 115-127

Rosenbloom, A.L. and J.G. Guevara-Aguirre. 1998. Lessons from the genetics of Laron syndrome. Trends in Endocrinology and Metabolism 9: 27-83

Rosenburg, N.A. et al. 2002. Genetic structure of human populations. Science 298: 2381-2385

Rosenfeld, R.G. et al. 1994. Growth hormone (GH) insensitivity due to primary GH deficiency. Endocrine Reviews 15: 369-390

Rousseau, F. et al. 1994. Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia. Nature 371: 252-254

1 ... 69 70 71 72 73 74 75 76 77 ... 87
На этой странице вы можете бесплатно читать книгу Мутанты. О генетической изменчивости и человеческом теле. - Арман Мари Леруа бесплатно.
Похожие на Мутанты. О генетической изменчивости и человеческом теле. - Арман Мари Леруа книги

Оставить комментарий