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| Editorials |  Top |
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Human genetics at the Whitehead pp205 - 206
doi:10.1038/ng1193-205
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(243K)
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Money matters p206
doi:10.1038/ng1193-206
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(108K)
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| News and Views | Top |
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Experimental models of human carcinogenesis pp207 - 208
Michael B. Kastan
doi:10.1038/ng1193-207
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(196K)
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Flipping the tip of the X p209
Edward G. D. Tuddenham
doi:10.1038/ng1193-209
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(122K)
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The case for matching MHC genes in human organ transplantation pp210 - 213
Susan Martin
& Philip A. Dyer
doi:10.1038/ng1193-210a
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(517K)
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Is MHC matching as a primary criterion in kidney allocation justified? pp210 - 213
Arthur J. Matas
doi:10.1038/ng1193-210b
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(517K)
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Allocating organs p211
doi:10.1038/ng1193-211
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(198K)
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| Correspondence | Top |
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Site of (CCG) polymorphism in the HD gene pp214 - 215
David C. Rubinsztein, Jayne Leggo, David E. Barton
& Malcolm A. Ferguson-Smith
doi:10.1038/ng1193-214
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(193K)
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Mitotic errors in trisomy 21 p215
Alberto Sensi
& Nicola Ricci
doi:10.1038/ng1193-215a
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(82K)
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Discrepancy resolved p215
Richard H. Myers, Marcy E. MacDonald
& James F. Gusella
doi:10.1038/ng1193-215b
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(82K)
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| Articles | Top |
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Mice with DNA repair gene (ERCC-1) deficiency have elevated levels of p53, liver nuclear abnormalities and die before weaning pp217 - 224
Jim McWhir, Jim Selfridge, David J. Harrison, Shoshana Squires
& David W. Melton
doi:10.1038/ng1193-217
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(924K)
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Spontaneous and carcinogen−induced tumorigenesis in p53−deficient mice pp225 - 229
Michele Harvey, Mark J. McArthur, Charles A. Montgomery Jr., Janet S. Butel, Allan Bradley
& Lawrence A. Donehower
doi:10.1038/ng1193-225
Abstract + references | PDF
(560K)
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Fusion of a fork head domain gene to PAX3 in the solid tumour alveolar rhabdomyosarcoma pp230 - 235
Naomi Galili, Richard J. Davis, William J. Fredericks, Sunil Mukhopadhyay, Frank J. Rauscher III, Beverly S. Emanuel, Giovanni Rovera
& Frederic G. Barr
doi:10.1038/ng1193-230
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(678K)
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Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A pp236 - 241
Delia Lakich, Haig H. Kazazian Jr., Stylianos E. Antonarakis
& Jane Gitschier
doi:10.1038/ng1193-236
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(732K)
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Nonsense mutations in the C−terminal SH2 region of the GTPase activating protein (GAP) gene in human tumours pp242 - 247
Eitan Friedman, Pablo V. Gejman, George A. Martin
& Frank McCormick
doi:10.1038/ng1193-242
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(887K)
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A complex mutable polymorphism located within the fragile X gene pp248 - 253
Nan Zhong, Carl Dobkin
& W. Ted Brown
doi:10.1038/ng1193-248
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(629K)
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Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I pp254 - 258
Ming-yi Chung, Laura P.W. Ranum, Lisa A. Duvick, Antonio Servadio, Huda Y. Zoghbi
& Harry T. Orr
doi:10.1038/ng1193-254
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(698K)
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Widespread expression of the human and rat Huntington's disease gene in brain and nonneural tissues pp259 - 265
Theresa V. Strong, Danilo A. Tagle, John M. Valdes, Lawrence W. Elmer, Karina Boehm, Manju Swaroop, Kevin W. Kaatz, Francis S. Collins
& Roger L. Albin
doi:10.1038/ng1193-259
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(1,250K)
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De novo mutation of the myelin Po gene in Dejerine−Sottas disease (hereditary motor and sensory neuropathy type III) pp266 - 268
Kiyoshi Hayasaka, Masato Himoro, Yukio Sawaishi, Kenji Nanao, Tsutomu Takahashi, Goro Takada, Garth A. Nicholson, Robert A. Ouvrier
& Nobutada Tachi
doi:10.1038/ng1193-266
Abstract + references | PDF
(327K)
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Dejerine−Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) gene pp269 - 273
Benjamin B. Roa, Peter J. Dyck, Harold G. Marks, Phillip F. Chance
& James R. Lupski
doi:10.1038/ng1193-269
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(577K)
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A mutation in CFTR produces different phenotypes depending on chromosomal background pp274 - 278
S. Kiesewetter, M. Macek Jr., C. Davis, S. M. Curristin, C.-S. Chu, C. Graham, A. E. Shrimpton, S. M. Cashman, L.-C. Tsui, J. Mickle, J. Amos, W. E. Highsmith, A. Shuber, D. R. Witt, R. G. Crystal
& G. R. Cutting
doi:10.1038/ng1193-274
Abstract + references | PDF
(490K)
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Genetic mapping of a second locus predisposing to hereditary non−polyposis colon cancer pp279 - 282
Annika Lindblom, Pia Tannergård, Barbro Werelius
& Magnus Nordenskjöld
doi:10.1038/ng1193-279
Abstract + references | PDF
(447K)
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Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31−33 pp283 - 286
T. Toda, M. Segawa, Y. Nomura, I. Nonaka, K. Masuda, T. Ishihara, M. Suzuki, I. Tomita, Y. Origuchi, K. Ohno, N. Misugi, Y. Sasaki, K. Takada, M. Kawai, K. Otani, T. Murakami, K. Saito, Y. Fukuyama, T. Shimizu, I. Kanazawa
& Y. Nakamura
doi:10.1038/ng1193-283
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(697K)
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A homozygous insertion−deletion in the type VII collagen gene (COL7A1) in Hallopeau−Siemens dystrophic epidermolysis bullosa pp287 - 293
Latifa Hilal, Ariane Rochat, Philippe Duquesnoy, Claudine Blanchet-Bardon, Janine Wechsler, Nadine Martin, Angela M. Christiano, Yann Barrandon, Jouni Uitto, Michel Goossens
& Alain Hovnanian
doi:10.1038/ng1193-287
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(880K)
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Missing links: Weber−Cockayne keratin mutations implicate the L12 linker domain in effective cytoskeleton function pp294 - 300
E.L. Rugg, S.M. Morley, F.J.D. Smith, M. Boxer, M.J. Tidman, H. Navsaria, I.M. Leigh
& E.B. Lane
doi:10.1038/ng1193-294
Abstract + references | PDF
(846K)
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Deletion of Y chromosome sequences located outside the testis determining region can cause XY female sex reversal pp301 - 307
Blanche Capel, Carol Rasberry, Julian Dyson, Colin E. Bishop, Elizabeth Simpson, Nigel Vivian, Robin Lovell-Badge, Sohaila Rastan
& Bruce M. Cattanach
doi:10.1038/ng1193-301
Abstract + references | PDF
(707K)
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A gene for Stargardt's disease (fundus flavimaculatus) maps to the short arm of chromosome 1 pp308 - 311
Josseline Kaplan, Sylvie Gerber, Dominique Larget-Piet, Jean-Michel Rozet, Hélène Dollfus, Jean-Louis Dufier, Sylvie Odent, Anne Postel-Vinay, Nicolas Janin, Marie-Louise Briard, Jean Frézal
& Arnold Munnich
doi:10.1038/ng1193-308
Abstract + references | PDF
(477K)
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| Corrections | Top |
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Corrigendum: Non−invasive liposome−mediated gene delivery can correct the ion transport defect in cystic fibrosis mutant mice p312
doi:10.1038/ng1193-312a
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(156K)
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Corrigendum: Tissue specific expression of FMR−1 provides evidence for a functional role in fragile X syndrome p312
doi:10.1038/ng1193-312b
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(156K)
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Corrigendum: Cloning of human, mouse and fission yeast recombination genes homologous to RAD51 and recA p312
doi:10.1038/ng1193-312c
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(156K)
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Corrigendum: Introduction and expression of the 400 kilobase amyloid precursor protein gene in transgenic mice p312
doi:10.1038/ng1193-312d
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(156K)
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