Microsatellites show mutational bias and heterozygote instabilitypp390 - 391 William Amos, Stephen J. Sawcer, Robert W. Feakes
& David C. Rubinsztein doi:10.1038/ng0896-390 References|PDF
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Directional evolution in germline microsatellite mutationspp391 - 393 Craig R. Primmer, Hans Ellegren, Nicola Saino
& Anders Pape Møller doi:10.1038/ng0896-391 References|PDF
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Non−mendelian inheritance of X chromosome markers in interspecific backcrossespp393 - 394 Yvonne Boyd doi:10.1038/ng0896-393 References|PDF
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Endothelin−3 frameshift mutation in congenital central hypoventilation syndromepp395 - 396 Stacey Bolk, Misha Angrist, Jian Xie, Masashi Yanagisawa, Jean M. Silvestri, Debra E. Weese-Mayer
& Aravinda Chakravarti doi:10.1038/ng0896-395 References|PDF
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Alternative mechanism for pathogenesis of an inherited epilepsy by a nicotinic AChR mutationpp396 - 397 Stuart A. Forman, Gary Yellen
& Elizabeth A. Thiele doi:10.1038/ng0896-396 References|PDF
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A novel MHC class I−like gene is mutated in patients with hereditary haemochromatosispp399 - 408 J.N. Feder, A. Gnirke, W. Thomas, Z. Tsuchihashi, D.A. Ruddy, A. Basava, F. Dormishian, R. Domingo Jr., M.C. Ellis, A. Fullan, L.M. Hinton, N.L. Jones, B.E. Kimmel, G.S. Kronmal, P. Lauer, V.K. Lee, D.B. Loeb, F.A. Mapa, E. McClelland, N.C. Meyer, G.A. Mintier, N. Moeller, T. Moore, E. Morikang, C.E. Prass, L. Quintana, S.M. Starnes, R.C. Schatzman, K.J. Brunke, D.T. Drayna, N.J. Risch, B.R. Bacon
& R.K. Wolff doi:10.1038/ng0896-399 Abstract + references|PDF
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X−linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane proteinpp409 - 416 Juha Kere, Anand K. Srivastava, Outi Montonen, Jonathan Zonana, Nick Thomas, Betsy Ferguson, Felix Munoz, Delyth Morgan, Angus Clarke, Primo Baybayan, Ellson Y. Chen, Sini Ezer, Ulpu Saarialho-Kere, Albert de la Chapelle
& David Schlessinger doi:10.1038/ng0895-409 Abstract + references|PDF
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A human MSX1 homeodomain missense mutation causes selective tooth agenesispp417 - 421 Heleni Vastardis, Nadeem Karimbux, Symon W. Guthua, J.G. Seidman
& Christine E. Seidman doi:10.1038/ng0896-417 Abstract + references|PDF
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A cellular mechanism governing the severity of Pelizaeus−Merzbacher diseasepp422 - 428 Alexander Gow
& Robert A. Lazzarini doi:10.1038/ng0896-422 Abstract + references|PDF
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Chromosomal mapping of quantitative trait loci contributing to stroke in a rat model of complex human diseasepp429 - 434 Speranza Rubattu, Massimo Volpe, Reinhold Kreutz, Ursula Ganten, Detlev Ganten
& Klaus Lindpaintner doi:10.1038/ng0896-429 Abstract + references|PDF
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A role for nuclear NF−B in B−cell−specific demethylation of the Ig locuspp435 - 441 Andrei Kirillov, Barbara Kistler, Raul Mostoslavsky, Howard Cedar, Thomas Wirth
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Cleavage of huntingtin by apopain, a proapoptotic cysteine protease, is modulated by the polyglutamine tractpp442 - 449 Y.P. Goldberg, D.W. Nicholson, D.M. Rasper, M.A. Kalchman, H.B. Koide, R.K. Graham, M. Bromm, P. Kazemi-Esfarjani, N.A. Thornberry, J.P. Vaillancourt
& M.R. Hayden doi:10.1038/ng0896-442 Abstract + references|PDF
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Plectin deficiency results in muscular dystrophy with epidermolysis bullosapp450 - 457 F.J.D. Smith, R.A.J. Eady, I.M. Leigh, J.R. McMillan, E.L. Rugg, D.P. Kelsell, S.P. Bryant, N.K. Spurr, J.F. Geddes, G. Kirtschig, G. Milana, A.G. de Bono, K. Owaribe, G. Wiche, L. Pulkkinen, J. Uitto, W.H.I. McLean
& E.B. Lane doi:10.1038/ng0896-450 Abstract + references|PDF
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A common region of 10p deleted in DiGeorge and velocardiofacial syndromespp458 - 460 Sara C.M. Daw, Catherine Taylor, Matthew Kraman, Kathy Call, Jen-i Mao, Simone Schuffenhauer, Thomas Meitinger, Tony Lipson, Judith Goodship
& Peter Scambler doi:10.1038/ng0896-458 Abstract + references|PDF
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Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12−q21pp461 - 463 Nazneen Rahman, Laura Arbour, Patricia Tonin, Jane Renshaw, Jerry Pelletier, Sylvain Baruchel, Kathryn Pritchard-Jones, Michael R. Stratton
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A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22pp464 - 468 Stephen Sawcer, Hywel B. Jones, Robert Feakes, Julia Gray, Niki Smaldon, Jeremy Chataway, Neil Robertson, David Clayton, Peter N. Goodfellow
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A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complexpp469 - 471 J.L. Haines, M. Ter-Minassian, A. Bazyk, J.F. Gusella, D.J. Kim, H. Terwedow, M.A. PericakVance, J.B. Rimmler, C.S. Haynes, A.D. Roses, A. Lee, B. Shaner, M. Menold, E. Seboun, R-P. Fitoussi, C. Gartioux, C. Reyes, F. Ribierre, G. Gyapay, J. Weissenbach, S.L. Hauser, D.E. Goodkin, R. Lincoln, K. Usuku, A. Garcia-Merino, N. Gatto, S. Young
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A full genome search in multiple sclerosispp472 - 476 George C. Ebers, Kim Kukay, Dennis E. Bulman, Adele D. Sadovnick, George Rice, Carol Anderson, Holly Armstrong, Keith Cousin, Robert B. Bell, Walter Hader, Donald W. Paty, Stanley Hashimoto, Joel Oger, Pierre Duquette, Sharon Warren, Trevor Gray, Paul O'Connor, Avindra Nath, Anthony Auty, Luanne Metz, Gordon Francis, John E. Paulseth, T. John Murray, William Pryse-Phillips, Robert Nelson, Mark Freedman, Donald Brunet, Jean-Pierre Bouchard, David Hinds
& Neil Risch doi:10.1038/ng0896-472 Abstract + references|PDF
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A putative vulnerability locus to multiple sclerosis maps to 5p14−p12 in a region syntenic to the murine locus Eae2pp477 - 480 Satu Kuokkanen, Mats Sundvall, Joseph D. Terwilliger, Pentti J. Tienari, Juhani Wikström, Rikard Holmdahl, Ulf Pettersson
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Double−strand breaks on YACs during yeast meiosis may reflect meiotic recombination in the human genomepp481 - 484 Shoshana Klein, Drora Zenvirth, Amir Sherman, Karin Ried, Gudrun Rappold
& Giora Simchen doi:10.1038/ng0896-481 Abstract + references|PDF
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Mutations in the TRKA/NGF receptor gene in patients with congenital insensitivity to pain with anhidrosispp485 - 488 Yasuhiro Indo, Motoko Tsuruta, Yumi Hayashida, Mohammad Azharul Karim, Kohji Ohta, Tomoyasu Kawano, Hiroshi Mitsubuchi, Hidefumi Tonoki, Yutaka Awaya
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DNA ligase I is required for fetal liver erythropoiesis but is not essential for mammalian cell viabilitypp489 - 491 Darren J. Bentley, Jim Selfridge, J. Kirsty Millar, Kay Samuel, Nicholas Hole, John D. Ansell
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Fibroblast growth factor receptor 2 mutations in Beare−Stevenson cutis gyrata syndromepp492 - 494 Kelly A. Przylepa, William Paznekas, Minghuang Zhang, Mahin Golabi, Wilma Bias, Michael J. Bamshad, John C. Carey, Bryan D. Hall, Roger Stevenson, Seth J. Orlow, M. Michael Cohen Jr.
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B in B−cell−specific demethylation of the Ig
