Lack of apolipoprotein E dramatically reduces amyloid -peptide depositionpp263 - 264 Kelly R. Bales, Tatyana Verina, Richard C. Dodel, Yansheng Du, Larry Altstiel, Mark Bender, Paul Hyslop, Edward M. Johnstone, Sheila P. Little, David J. Cummins, Pedro Piccardo, Bernardino Ghetti
& Steven M. Paul doi:10.1038/ng1197-263 References|PDF
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PEX12 encodes an integral membrane protein of peroxisomespp265 - 266 Kanji Okumoto
& Yukio Fujiki doi:10.1038/ng1197-265 References|PDF
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KCNE1 mutations cause Jervell and Lange-Nielsen syndromepp267 - 268 Eric Schulze-Bahr, Qing Wang, Horst Wedekind, Wilhelm Haverkamp, Qiuyun Chen, Yaling Sun, Claudia Ruble, Marco Hördt, Jeffrey A. Towbin, Martin Borggrefe, Gerd Assmann, Xiangdong Qu, John C. Somberg, Günter Breithardt, Carlos Oberti
& Harald Funke doi:10.1038/ng1197-267 References|PDF
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Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA genepp268 - 269 Xue-Zhong Liu, James Walsh, Yuya Tamagawa, Ken Kitamura, Masatoyo Nishizawa, Karen P. Steel
& Steve D.M. Brown doi:10.1038/ng1197-268 References|PDF
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Mutation in GLI3 in postaxial polydactyly type App269 - 271 Uppala Radhakrishna, Anja Wild, Karl-Heinz Grzeschik
& Stylianos E. Antonarakis doi:10.1038/ng1197-269 References|PDF
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Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancerpp271 - 272 Michiko Miyaki, Motoko Konishi, Kiyoko Tanaka, Rei Kikuchi-Yanoshita, Masatoshi Muraoka, Masamichi Yasuno, Tohru Igari, Morio Koike, Mitsuro Chiba
& Takeo Mori doi:10.1038/ng1197-271 References|PDF
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Overexpression of Agrt leads to obesity in transgenic micepp273 - 274 Melissa Graham, John R. Shutter, Ulla Sarmiento, lldiko Sarosi
& Kevin L Stark doi:10.1038/ng1197-273 References|PDF
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The pre-implantation ontogeny of the H19 methylation imprintpp275 - 276 Alexander Olek
& Jörn Walter doi:10.1038/ng1197-275 References|PDF
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Communal discourse as a supplement to informed consent for genetic researchpp277 - 279 Morris W. Foster, Ann J. Eisenbraun
& Thomas H. Carter doi:10.1038/ng1197-277 Abstract + references|PDF
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Theoretical and empirical issues for marker-assisted breeding of congenic mouse strainspp280 - 284 Paul Markel, Pei Shu, Chris Ebeling, George A. Carlson, Deborah L. Nagle, John S. Smutko
& Karen J. Moore doi:10.1038/ng1197-280 Abstract + references|PDF
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Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22pp285 - 291 Nandita A. Quaderi, Susann Schweiger, Karin Gaudenz, Brunella Franco, Elena I. Rugarli, Wolfgang Berger, George J. Feldman, Manuela Volta, Grazia Andolfi, S. Gilgenkrantz, Robert W. Marion, Raoul C.M. Hennekam, John M. Opitz, Maximilian Muenke, Hilger H. Ropers
& Andrea Ballabio doi:10.1038/ng1197-285 Abstract + references|PDF
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A novel gene involved in zinc transport is deficient in the lethal milk mousepp292 - 297 Liping Huang
& Jane Gitschier doi:10.1038/ng1197-292 Abstract + references|PDF
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Trinucleotide repeats affect DNA replication in vivopp298 - 304 George M. Samadashwily, Gordana Raca
& Sergei M. Mirkin doi:10.1038/ng1197-298 Abstract + references|PDF
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X-linked situs abnormalities result from mutations in ZIC3pp305 - 308 Marinella Gebbia, Giovanni B. Ferrero, Giuseppe Pilia, Maria T. Bassi, Arthur S. Aylsworth, Miranda Penman-Splitt, Lynne M. Bird, John S. Bamforth, John Burn, David Schlessinger, David L. Nelson
& Brett Casey doi:10.1038/ng1197-305 Abstract + references|PDF
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The EWS-WT1 translocation product induces PDGFA in desmoplastic small round-cell tumourpp309 - 313 Sean Bong Lee, Kathryn Ann Kolquist, Kim Nichols, Christoph Englert, Shyamala Maheswaran, Marc Ladanyi, William L. Gerald
& Daniel A. Haber doi:10.1038/ng1197-309 Abstract + references|PDF
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Sustained expression of genes delivered directly into liver and muscle by lentiviral vectorspp314 - 317 Tal Kafri, Ulrike Blömer, Daniel A. Peterson, Fred H. Gage
& Inder M. Verma doi:10.1038/ng1197-314 Abstract + references|PDF
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Absence of integrin 7 causes a novel form of muscular dystrophypp318 - 323 Ulrike Mayer, Gesine Saher, Reinhard Fässler, Antje Bornemann, Frank Echtermeyer, Helga von der Mark, Nicolai Miosge, Ernst Pösch
& Klaus von der Mark doi:10.1038/ng1197-318 Abstract + references|PDF
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Mutations in GLUT2, the gene for the liver-type glucose transporter, in patients with Fanconi-Bickel syndromepp324 - 326 René Santer, Reinhard Schneppenheim, Anja Dombrowski, Hermann Götze, Beat Steinmann
& Jürgen Schaub doi:10.1038/ng1197-324 Abstract + references|PDF
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Early diabetes and abnormal postnatal pancreatic islet development in mice lacking Glut-2pp327 - 330 Marie-Thérèse Guillam, Edith Hümmler, Elisabeth Schaerer, J.-Y Wu, Morris J. Birnbaum, Friedrich Beermann, Andrea Schmidt, Nathalie Dériaz
& Bernard Thorens doi:10.1038/ng1197-327 Abstract + references|PDF
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Quantitative trait locus analysis of contextual fear conditioning in micepp331 - 334 Jeanne M. Wehner, Richard A. Radcliffe, Shelby T. Rosmann, Steven C. Christensen, Duffy L. Rasmussen, David W. Fulker
& Michelle Wiles doi:10.1038/ng1197-331 Abstract + references|PDF
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Quantitative trait loci analysis affecting contextual conditioning in micepp335 - 337 Barbara Caldarone, Carlos Saavedra, Kathleen Tartaglia, Jeanne M Wehner, Bruce C Dudek
& Lorraine Flaherty doi:10.1038/ng1197-335 Abstract + references|PDF
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Mutations in the hminK gene cause long QT syndrome and suppress lKs functionpp338 - 340 Igor Splawski, Martin Tristani-Firouzi, Michael H. Lehmann, Michael C. Sanguinetti
& Mark T. Keating doi:10.1038/ng1197-338 Abstract + references|PDF
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BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patientspp341 - 345 Anne Petrij-Bosch, Tamara Peelen, Margreethe van Vliet, Ronald van Eijk, Renske Olmer, Marion Drüsedau, Frans B.L. Hogervorst, Sandra Hageman, Petronella J.W. Arts, Marjolijn J.L. Ligtenberg, Hanne Meijers-Heijboer, Jan G.M. Klijn, Hans R.A. Vasen, Cees J. Cornelisse, Laura J. van't Veer, Egbert Bakker, Gert-Jan B. van Ommen
& Peter Devilee doi:10.1038/ng1197-341 Abstract + references|PDF
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Disruption of the mouse L1 gene leads to malformations of the nervous systempp346 - 349 Miriam Dahme, Udo Bartsch, Rudolf Martini, Brigitte Anliker, Melitta Schachner
& Ned Mantei doi:10.1038/ng1197-346 Abstract + references|PDF
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Insulin VNTR allele-specific effect in type 1 diabetes depends on identity of untransmitted paternal allelepp350 - 352 Simon T. Bennett, Amanda J. Wilson, Laura Esposito, Nourdine Bouzekri, Dag E. Undlien, Francesco Cucca, Lorenza Nisticò, Raffaella Buzzetti, , the IMDIAB Group, Emanuele Bosi, Flemming Pociot, Jørn Nerup, Anne Cambon-Thomsen, Alberto Pugliese, Julian P.H. Shield, Patricia A. McKinney, Stephen C. Bain, Constantin Polychronakos
& John A. Todd doi:10.1038/ng1197-350 Abstract + references|PDF
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A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivationpp353 - 356 Robert M. Plenge, Brian D. Hendrich, Charles Schwartz, J. Fernando Arena, Anna Naumova, Carmen Sapienza, Robin M. Winter
& Huntington F. Willard doi:10.1038/ng1197-353 Abstract + references|PDF
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The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal regionpp357 - 361 Philippe Jay, Claire Rougeulle, Annick Massacrier, Anne Moncla, Marie-Geneviève Mattel, Perrine Malzac, Nathalie Roëckel, Sylvie Taviaux, Jean-Louis Bergé Lefranc, Pierre Cau, Philippe Berta, Marc Lalande
& Françoise Muscatelli doi:10.1038/ng1197-357 Abstract + references|PDF
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-peptide deposition
7 causes a novel form of muscular dystrophy
