The question of heterogeneity in Marfan syndromepp228 - 229 Harry Dietz, Uta Francke, Heinz Furthmayr, Clair Francomano, Anne De Paepe, Richard Devereux, Francesco Ramirez
& Reed Pyeritz doi:10.1038/ng0395-228 References|PDF
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Reply to "The question of heterogeneity in Marfan syndrome"pp230 - 231 Catherine Boileau, Claudine Junien, Gwenaëlle Collod, Guillaume Jondeau, Olivier Dubourg, Jean-Pierre Bourdarias, Catherine Bonaïti-Pellié, Jean Frézal
& Pierre Maroteaux doi:10.1038/ng0395-230 References|PDF
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Immune surveillance in colorectal carcinomapp231 - 232 Pauline Branch, David C. Bicknell, Andrew Rowan, Walter F. Bodmer
& Peter Karran doi:10.1038/ng0395-231 References|PDF
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Effect on splicing of a silent FGFR2 mutation in Crouzon syndromepp232 - 233 Xiang Li, Woo-Jin Park, Reed E. Pyeritz
& Ethylin Wang Jabs doi:10.1038/ng0395-232 References|PDF
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Genomic imprinting of Mash2, a mouse gene required for trophoblast developmentpp235 - 242 François Guillemot, Tamara Caspary, Shirley M. Tilghman, Neal G. Copeland, Debra J. Gilbert, Nancy A. Jenkins, David J. Anderson, Alexandra L. Joyner, Janet Rossant
& András Nagy doi:10.1038/ng0395-235 Abstract + references|PDF
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Gene transfer and expression in progeny after intravenous DNA injection into pregnant micepp243 - 248 Makoto Tsukamoto, Takahiro Ochiya, Sho Yoshida, Takashi Sugimura
& Masaaki Terada doi:10.1038/ng0395-243 Abstract + references|PDF
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Mutation of the MXI1 gene in prostate cancerpp249 - 255 Linette R. Eagle, Xiaoying Yin, Arthur R. Brothman, Briana J. Williams, N.B. Atkin
& Edward V. Prochownik doi:10.1038/ng0395-249 Abstract + references|PDF
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Transplantation to the rat brain of human neural progenitors that were genetically modified using adenovirusespp256 - 260 Olivier Sabaté, Philippe Horellou, Emmanuelle Vigne, Philippe Colin, Michel Perricaudet, Marie-Hélène Buc-Caron
& Jacques Mallet doi:10.1038/ng0395-256 Abstract + references|PDF
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A 2D crossover−based map of the human X chromosome as a model for map integrationpp261 - 266 Pamela R. Fain, Edward N. Kort, Phillip F. Chance, Kim Nguyen, Douglas F. Redd, Michael J. Econs
& David F. Barker doi:10.1038/ng0395-261 Abstract + references|PDF
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A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humanspp267 - 272 Kunihiro Yoshida, Kenichi Furihata, Shin'ichi Takeda, Akinori Nakamura, Kanji Yamamoto, Hiroshi Morita, Shuichi Hiyamuta, Shu-ichi Ikeda, Norikazu Shimizu
& Nobuo Yanagisawa doi:10.1038/ng0395-267 Abstract + references|PDF
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Keratin 16 and keratin 17 mutations cause pachyonychia congenitapp273 - 278 W.H.I. McLean, E.L. Rugg, D.P. Lunny, S.M. Morley, E.B. Lane, O. Swensson, P.J.C. Dopping-Hepenstal, W.A.D. Griffiths, R.A.J. Eady, C. Higgins, H.A. Navsaria, I.M. Leigh, T. Strachan, L. Kunkeler
& C.S. Munro doi:10.1038/ng0395-273 Abstract + references|PDF
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Mutations in the gene for transglutaminase 1 in autosomal recessive lamellar ichthyosispp279 - 283 Laura J. Russell, John J. DiGiovanna, Geraldine R. Rogers, Peter M. Steinert, Nemat Hashem, John G. Compton
& Sherri J. Bale doi:10.1038/ng0395-279 Abstract + references|PDF
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Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locuspp284 - 292 S.T. Bennett, A.M. Lucassen, S.C.L. Gough, E.E. Powell, D.E. Undlien, L.E. Pritchard, M.E. Merriman, Y. Kawaguchi, M.J. Dronsfield, F. Pociot, J. Nerup, N. Bouzekri, A. Cambon-Thomsen, K.S. Rønningen, A.H. Barnett, S.C. Bain
& J.A. Todd doi:10.1038/ng0395-284 Abstract + references|PDF
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The minisatellite in the diabetes susceptibility locus IDDM2 regulates insulin transcriptionpp293 - 298 Giulia Catignani Kennedy, Michael S. German
& William J. Rutter doi:10.1038/ng0395-293 Abstract + references|PDF
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A missense mutation in the glucagon receptor gene is associated with non−insulin−dependent diabetes mellituspp299 - 304 J. Hager, L. Hansen, C. Vaisse, N. Vionnet, A. Philippi, W. Poller, G. Velho, C. Carcassi, L. Contu, C. Julier, F. Cambien, P. Passa, M. Lathrop, W. Kindsvogel, F. Demenais, E. Nishimura
& P. Froguel doi:10.1038/ng0395-299 Abstract + references|PDF
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A mutant p53 transgene accelerates tumour development in heterozygous but not nullizygous p53−deficient micepp305 - 311 Michele Harvey, Hannes Vogel, Danna Morris, Allan Bradley, Alan Bernstein
& Lawrence A. Donehower doi:10.1038/ng0395-305 Abstract + references|PDF
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Gamete−specific methylation correlates with imprinting of the murine Xist genepp312 - 315 Mira Ariel, Edward Robinson, John R. McCarrey
& Howard Cedar doi:10.1038/ng0395-312 Abstract + references|PDF
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Methylation of the mouse Xist gene in sperm and eggs correlates with imprinted Xist expression and paternal X−inactivationpp316 - 320 Maurizio Zuccotti
& Marilyn Monk doi:10.1038/ng0395-316 Abstract + references|PDF
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Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3pp321 - 328 Patricia L. Tavormina, Rita Shiang, Leslie M. Thompson, Ya-Zhen Zhu, Douglas J. Wilkin, Ralph S. Lachman, William R. Wilcox, David L. Rimoin, Daniel H. Cohn
& John J. Wasmuth doi:10.1038/ng0395-321 Abstract + references|PDF
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