Horizontal SINE transfer between vertebrate classespp131 - 132 D. Kordi
& F. Gubenek doi:10.1038/ng0695-131 References|PDF
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Meiotic drive and myotonic dystrophypp132 - 133 Gregory D.D. Hurst, Laurence D. Hurst
& John A. Barrett doi:10.1038/ng0695-132 References|PDF
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Reply to "Meiotic drive and myotonic dystrophy"p133 Nessa Carey, Keith Johnson, Pekka Nokelainen, Leena Peltonen, Maria-Liisa Savontaus, Vesa Juvonen, Maria Anvret, Ulla Grandell, Kokila Chotai, Elaine Robertson, Helen Middleton-Price
& Sue Malcolm doi:10.1038/ng0695-133 References|PDF
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Hyperproinsulinaemia in obese fat/fat mice associated with a carboxypeptidase E mutation which reduces enzyme activitypp135 - 142 Jürgen K. Naggert, Lloyd D. Fricker, Oleg Varlamov, Patsy M. Nishina, Yves Rouille, Donald F. Steiner, Raymond J. Carroll, Beverly J. Paigen
& Edward H. Leiter doi:10.1038/ng0695-135 Abstract + references|PDF
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Ulcerative colitis and adenocarcinoma of the colon in Gi2-deficient micepp143 - 150 Uwe Rudolph, Milton J. Finegold, Susan S. Rich, Gregory R. Harriman, Yogambal Srinivasan, Philippe Brabet, Guylain Boulay, Allan Bradley
& Lutz Birnbaumer doi:10.1038/ng0695-143 Abstract + references|PDF
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The polycystic kidney disease 1 (PKD1) gene encodes a novel protein with multiple cell recognition domainspp151 - 160 Jim Hughes, Christopher J. Ward, Belén Peral, Richard Aspinwall, Kevin Clark, José L. San Millán, Vicki Gamble
& Peter C. Harris doi:10.1038/ng0695-151 Abstract + references|PDF
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Cytokine gene expression in epidermis with biological effects following injection of naked DNApp161 - 166 Ulrich R. Hengge, Edward F. Chan, Ruth A. Foster, Patricia S. Walker
& Jonathan C. Vogel doi:10.1038/ng0695-161 Abstract + references|PDF
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A novel gene, Translin, encodes a recombination hotspot binding protein associated with chromosomal translocationspp167 - 174 Katsunori Aoki, Kenji Suzuki, Takashi Sugano, Tetsuya Tasaka, Kazuhiko Nakahara, Osamu Kuge, Akira Omori
& Masataka Kasai doi:10.1038/ng0695-167 Abstract + references|PDF
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A subset of p53-deficient embryos exhibit exencephalypp175 - 180 Valerie P. Sah, Laura D. Attardi, George J. Mulligan, Bart O. Williams, Roderick T. Bronson
& Tyler Jacks doi:10.1038/ng0695-175 Abstract + references|PDF
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A teratologic suppressor role for p53 in benzo(a)pyrene−treated transgenic p53-deficient micepp181 - 187 Christopher J. Nicol, Maureen L. Harrison, Rebecca R. Laposa, Inga L. Gimelshtein
& Peter G. Wells doi:10.1038/ng0695-181 Abstract + references|PDF
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p53 modulation of TFIIH−associated nucleotide excision repair activitypp188 - 195 X.W. Wang, H. Yeh, L. Schaeffer, R. Roy, V. Moncollin, J.-M. Egly, Z. Wang, E.C. Friedberg, M.K. Evans, B.G. Taffe, V.A. Bohr, G. Weeda, J.H.J. Hoeijmakers, K. Forrester
& C.C. Harris doi:10.1038/ng0695-188 Abstract + references|PDF
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Deregulation of both imprinted and expressed alleles of the insulin−like growth factor 2 gene during −cell tumorigenesispp196 - 201 Gerhard Christofori, Paul Naik
& Douglas Hanahan doi:10.1038/ng0695-196 Abstract + references|PDF
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Mapping of the congenital generalized hypertrichosis locus to chromosome Xq24−q27.1pp202 - 207 Luis E. Figuera, Massimo Pandolfo, Patrick W. Dunne, Jose M. Cantú
& Pragna I. Patel doi:10.1038/ng0695-202 Abstract + references|PDF
(630K)
Rapid detection of BRCA1 mutations by the protein truncation testpp208 - 212 Frans B.L. Hogervorst, Renée S. Cornelis, Mattie Bout, Margreethe van Vliet, Jan C. Oosterwijk, Renske Olmer, Bert Bakker, Jan G.M. Klijn, Hans F.A. Vasen, Hanna Meijers-Heijboer, Fred H. Menko, Cees J. Cornelisse, Johan T. den Dunnen, Peter Devilee
& Gert-Jan B. van Ommen doi:10.1038/ng0695-208 Abstract + references|PDF
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Expansion and deletion of CTG repeats from human disease genes are determined by the direction of replication in E. colipp213 - 218 Seongman Kang, Adam Jaworski, Keiichi Ohshima
& Robert D. Wells doi:10.1038/ng0695-213 Abstract + references|PDF
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Rapid evolution of a unique family of primate ribonuclease genespp219 - 223 Helene F. Rosenberg, Kimberly D. Dyer, H. Lee Tiffany
& Monica Gonzalez doi:10.1038/ng0695-219 Abstract + references|PDF
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Disruption of a GATA motif in the Duffy gene promoter abolishes erythroid gene expression in Duffy−negative individualspp224 - 228 Christophe Tournamille, Yves Colin, Jean Pierre Cartron
& Caroline Le Van Kim doi:10.1038/ng0695-224 Abstract + references|PDF
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Integrin 4 mutations associated with junctional epidermolysis bullosa with pyloric atresiapp229 - 234 Frédérique Vidal, Daniel Aberdam, Corinne Miquel, Angela M. Christiano, Leena Pulkkinen, Jouni Uitto, Jean-Paul Ortonne
& Guerrino Meneguzzi doi:10.1038/ng0695-229 Abstract + references|PDF
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Linkage of pycnodysostosis to chromosome 1q21 by homozygosity mappingpp235 - 237 Bruce D. Gelb, Jacob G. Edelson
& Robert J. Desnick doi:10.1038/ng0695-235 Abstract + references|PDF
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The gene for pycnodysostosis maps to human chromosome 1cen−q21pp238 - 239 Mihael H. Polymeropoulos, Rosa Isela Ortiz De Luna, Susan E. Ide, Rosarelis Torres, Jeffrey Rubenstein
& Clair A. Francomano doi:10.1038/ng0695-238 Abstract + references|PDF
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Linkage and association between insulin−dependent diabetes mellitus (IDDM) susceptibility and markers near the glucokinase gene on chromosome 7pp240 - 242 Rachel E. Rowe, Beth Wapelhorst, Graeme I. Bell, Neil Risch, Richard S. Spielman
& Patrick Concannon doi:10.1038/ng0695-240 Abstract + references|PDF
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Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severitypp243 - 245 F. Piccolo, S.L. Roberds, M. Jeanpierre, F. Leturcq, K. Azibi, C. Beldjord, A. Carrié, D. Récan, M. Chaouch, A. Reghis, F. El Kerch, A. Sefiani, T. Voit, L. Merlini, H. Collin, B. Eymard, J.S. Beckmann, N.B. Romero, F.M.S. Tomé, M. Fardeau, K.P. Campbell
& J-C. Kaplan doi:10.1038/ng0695-243 Abstract + references|PDF
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Linkage of the gene for cystinosis to markers on the short arm of chromosome 17pp246 - 248 Geraldine A. McDowell, William A. Gahl, Leah A. Stephenson, Jerry A. Schneider, Jean Weissenbach, Mihael H. Polymeropoulos, Margaret M. Town, William van't Hoff, Martin Farrall
& Christopher G. Mathew doi:10.1038/ng0695-246 Abstract + references|PDF
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Corrigendum: A mutation in the tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy NEM1p249 doi:10.1038/ng0695-249a PDF
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Corrigendum: Stability of an expanded trinucleotide repeat in the androgen receptor gene in transgenic micep249 doi:10.1038/ng0695-249b PDF
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Corrigendum: Inherited microdeletions in the Angelman and Prader−Willi syndromes define an imprinting centre on human chromosome 15p249 doi:10.1038/ng0695-249c PDF
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& F. Guben
i2-deficient mice
−cell tumorigenesis
