'Polynesian' mtDNA in the Malagasypp377 - 378 Himla Soodyall, Trefor Jenkins
& Mark Stoneking doi:10.1038/ng0895-377 References|PDF
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Insulin expression: is VNTR allele 698 really anomalous?pp378 - 379 Ralph E. McGinnis
& Richard S. Spielman doi:10.1038/ng0895-378 References|PDF
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Reply to "Insulin expression: is VNTR allele 698 really anomalous?"pp379 - 380 Simon T. Bennett, Anneke M. Lucassen, Stephen C.L. Gough, Elizabeth E. Powell, Lynn E. Pritchard, Marilyn E. Merriman, Yoshihiko Kawaguchi, John A. Todd, Dag E. Undlien, Kjersti S. Rønningen, Flemming Pociot, Jørn Nerup, Nourdine Bouzekri, Anne Cambon-Thomsen, Mark J. Dronsfield, Anthony H. Barnett
& Stephen C. Bain doi:10.1038/ng0895-379 References|PDF
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Expanded CAG repeats in schizophrenia and bipolar disorderpp380 - 381 M.C. O'Donovan, C. Guy, N. Craddock, K.C. Murphy, A.G. Cardno, L.A. Jones, M.J. Owen
& P. McGuffin doi:10.1038/ng0895-380 References|PDF
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Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA−binding protein genepp383 - 393 Renee Reijo, Tien-Yi Lee, Pia Salo, Raaji Alagappan, Laura G. Brown, Michael Rosenberg, Steve Rozen, Tom Jaffe, Donald Straus, Outi Hovatta, Albert de la Chapelle, Sherman Silber
& David C. Page doi:10.1038/ng0895-383 Abstract + references|PDF
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Human hypertension caused by mutations in the kidney isozyme of 11−hydroxysteroid dehydrogenasepp394 - 399 Tomoatsu Mune, Fraser M. Rogerson, Heli Nikkilä, Anil K. Agarwal
& Perrin C. White doi:10.1038/ng0895-394 Abstract + references|PDF
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The renal glomerulus of mice lacking s−laminin/laminin 2: nephrosis despite molecular compensation by laminin 1pp400 - 406 Peter G. Noakes, Jeffrey H. Miner, Medha Gautam, Jeanette M. Cunningham, Joshua R. Sanes
& John P. Merlie doi:10.1038/ng0895-400 Abstract + references|PDF
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New HLA−DPB1 alleles generated by interallelic gene conversion detected by analysis of spermpp407 - 414 Gabriele Zangenberg, Mei-Mei Huang, Norman Arnheim
& Henry Erlich doi:10.1038/ng0895-407 Abstract + references|PDF
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Gene−based sequence−tagged−sites (STSs) as the basis for a human gene mappp415 - 423 Rebecca Berry, T.J. Stevens, Nicole A.R. Walter, Andrea S. Wilcox, Todd Rubano, Janet A. Hopkins, James Weber, Richard Goold, Marcelo Bento Soares
& James M. Sikela doi:10.1038/ng0895-415 Abstract + references|PDF
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Distinct genetic loci control development of benign and malignant skin tumours in micepp424 - 429 Hiroki Nagase, Sheila Bryson, Heather Cordell, Christopher J. Kemp, Frances Fee
& Allan Balmain doi:10.1038/ng0895-424 Abstract + references|PDF
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Gene therapy of metastatic cancer by in vivo retroviral gene targetingpp430 - 435 Robert K. Hurford Jr., Glenn Dranoff, Richard C. Mulligan
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Recurrent rearrangements in the high mobility group protein gene, HMGI-C, in benign mesenchymal tumourspp436 - 444 Eric F.P.M. Schoenmakers, Sylke Wanschura, Raf Mols, Jörn Bullerdiek, Herman Van den Berghe
& Wim J.M. Van de Ven doi:10.1038/ng0895-436 Abstract + references|PDF
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Generation and characterization of a F508 cystic fibrosis mouse modelpp445 - 452 William H. Colledge, Benjamin S. Abella, Kevin W. Southern, Rosemary Ratcliff, Canwen Jiang, Seng H. Cheng, Lesley J. MacVinish, Janice R. Anderson, Alan W. Cuthbert
& Martin J. Evans doi:10.1038/ng0895-445 Abstract + references|PDF
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Pharmacological correction of neonatal lethal hepatic dysfunction in a murine model of hereditary tyrosinaemia type Ipp453 - 460 Markus Grompe, Sven Lindstedt, Muhsen Al-Dhalimy, Nancy G. Kennaway, John Papaconstantinou, Carlos A. Torres-Ramos, Ching-Nau Ou
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Mutation of a new sodium channel gene, Scn8a, in the mouse mutant 'motor endplate disease'pp461 - 465 Daniel L. Burgess, David C. Kohrman, James Galt, Nicholas W. Plummer, Julie M. Jones, Brett Spear
& Miriam H. Meisler doi:10.1038/ng0895-461 Abstract + references|PDF
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Different chromosomal localization of the Clcn4 gene in Mus spretus and C57BL/6J micepp466 - 471 Elena I. Rugarli, David A. Adler, Giuseppe Borsani, Karen Tsuchiya, Brunella Franco, Xueya Hauge, Christine Disteche, Verne Chapman
& Andrea Ballabio doi:10.1038/ng0895-466 Abstract + references|PDF
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A contravention of Ohno's law in micepp472 - 476 Steve Palmer, Jo Perry
& Alan Ashworth doi:10.1038/ng0895-472 Abstract + references|PDF
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High resolution DNA Fiber−fish on yeast artificial chromosomes: direct visualization of DNA replicationpp477 - 479 Carla Rosenberg, Ralph J. Florijn, Frans M. Van De Rijke, Lau A.J. Blonden, Ton K. Raap, Gert-Jan B. Van Ommen
& Johan T. Den Dunnen doi:10.1038/ng0895-477 Abstract + references|PDF
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Expression of a linear Sry transcript in the mouse genital ridgepp480 - 482 Yvette W.A. Jeske, Josephine Bowles, Andy Greenfield
& Peter Koopman doi:10.1038/ng0895-480 Abstract + references|PDF
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Intragenic loss of function mutations demonstrate the primary role of FMR1 in fragile X syndromepp483 - 485 Kellie A. Lugenbeel, Andrea M. Peier, Nancy L. Carson, Albert E. Chudley
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A4POE*4-associated Alzheimer's disease risk is modified by 1−antichymotrypsin polymorphismpp486 - 488 M. Ilyas Kamboh, Dharambir K. Sanghera, Robert E. Ferrell
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−hydroxysteroid dehydrogenase
F508 cystic fibrosis mouse model
1−antichymotrypsin polymorphism
