Toward a unified genetic map of higher plants, transcending the monocot−dicot divergencepp380 - 382 Andrew H. Paterson, Tien-Hung Lan, Kim P. Reischmann, Charlene Chang, Yann-Rong Lin, Sin-Chieh Liu, Mark D. Burow, Stanley P. Kowalski, Catherine S. Katsar, Terrye A. DelMonte, Kenneth A. Feldmann, Keith F. Schertz
& Jonathan F. Wendel doi:10.1038/ng1296-380 References|PDF
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Non−canonical introns are at least 109 years oldpp383 - 384 H.-J. Wu, P. Gaubier-Comella, M. Delseny, F. Grellet, M. Van Montagu
& P. Rouzé doi:10.1038/ng1296-383 References|PDF
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Genes responsible for human hereditary deafness: symphony of a thousandpp385 - 391 Christine Petit doi:10.1038/ng1296-385 Abstract + references|PDF
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Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndromepp392 - 399 Elena V. Semina, Rebecca Reiter, Nancy J. Leysens, W. Lee M. Alward, Kent W. Small, Nicole A. Datson, Jacqueline Siegel-Bartelt, Diane Bierke-Nelson, Pierre Bitoun, Bernhard U. Zabel, John C. Carey
& Jeffrey C. Murray doi:10.1038/ng1296-392 Abstract + references|PDF
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Susceptible chiasmate configurations of chromosome 21 predispose to non−disjunction in both maternal meiosis I and meiosis IIpp400 - 405 Neil E. Lamb, Sallie B. Freeman, Amanda Savage-Austin, Dorothy Pettay, Lisa Taft, Jane Hersey, Yuanchao Gu, Joe Shen, Denise Saker, Kristen M. May, Dimitris Avramopoulos, Michael B. Petersen, Anni Hallberg, Margareta Mikkelsen, Terry J. Hassold
& Stephanie L. Sherman doi:10.1038/ng1296-400 Abstract + references|PDF
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Spontaneous X chromosome MI and MII nondisjunction events in Drosophila melanogaster oocytes have different recombinational historiespp406 - 414 Kara E. Koehler, Christina L. Boulton, Heather E. Collins, Rachael L. French, Kristin C. Herman, Soni M. Lacefield, Laurence D. Madden, Christopher D. Schuetz
& R. Scott Hawley doi:10.1038/ng1296-406 Abstract + references|PDF
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Suppression of the novel growth inhibitor p33ING1 promotes neoplastic transformationpp415 - 420 Igor Garkavtsev, Alexander Kazarov, Andrei Gudkov
& Karl Riabowol doi:10.1038/ng1296-415 Abstract + references|PDF
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A PCR−based approach for isolating pathogen resistance genes from potato with potential for wide application in plantspp421 - 429 Dario Leister, Agim Ballvora, Francesco Salamini
& Christiane Gebhardt doi:10.1038/ng1296-421 Abstract + references|PDF
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Identification of a RING protein that can interact in vivo with the BRCA1 gene productpp430 - 440 Leeju C. Wu, Zhuo Wei Wang, Julia Tsou Tsan, Monique A. Spillman, Anne Phung, Xie L. Xu, Meng-Chun W. Yang, Larn-Yuan Hwang, Anne M. Bowcock
& Richard Baer doi:10.1038/ng1296-430 Abstract + references|PDF
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Detection of heterozygous mutations in BRCA1 using high density oligonucleotide arrays and two−colour fluorescence analysispp441 - 447 Joseph G. Hacia, Lawrence C. Brody, Mark S. Chee, Stephen P.A. Fodor
& Francis S. Collins doi:10.1038/ng1296-441 Abstract + references|PDF
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Quantitative phenotypic analysis of yeast deletion mutants using a highly parallel molecular bar−coding strategypp450 - 456 Daniel D. Shoemaker, Deval A. Lashkari, Don Morris, Mike Mittmann
& Ronald W. Davis doi:10.1038/ng1296-450 Abstract + references|PDF
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Use of a cDNA microarray to analyse gene expression patterns in human cancerpp457 - 460 doi:10.1038/ng1296-457 Abstract + references|PDF
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Retinal−specific guanylate cyclase gene mutations in Leber's congenital amaurosispp461 - 464 Isabella Perrault, Jean Michel Rozet, Patrick Calvas, Sylvie Gerber, Agnès Camuzat, Hélène Dollfus, Sophie Châtelin, Eric Souied, Ihmad Ghazi, Corinne Leowski, Michel Bonnemaison, Denis Le Paslier, Jean Frézal, Jean-Louis Dufier, Steven Pittler, Arnold Munnich
& Josseline Kaplan doi:10.1038/ng1296-461 Abstract + references|PDF
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Complex interactions of new quantitative trait loci, Sluc1, Sluc2, Sluc3, and Sluc4, that influence the susceptibility to lung cancer in the mousepp465 - 467 Remond J.A. Fijneman, Sandra S. de Vries, Ritsert C. Jansen
& Peter Demant doi:10.1038/ng1296-465 Abstract + references|PDF
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Gene interaction and single gene effects in colon tumour susceptibility in micepp468 - 470 Tom van Wezel, Alphons P.M. Stassen, Corina J.A. Moen, Augustinus A.M. Hart, Martin A. van der Valk
& Peter Demant doi:10.1038/ng1296-468 Abstract + references|PDF
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A major quantitative trait locus influences hyperactivity in the WKHA ratpp471 - 473 Marie-Pierre Moisan, Hélène Courvoisier, Marie-Theérèese Bihoreau, Dominique Gauguier, Edith D. Hendley, Mark Lathrop, Michael R. James
& Pierre Mormède doi:10.1038/ng1296-471 Abstract + references|PDF
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An H−YDb epitope is encoded by a novel mouse Y chromosome genepp474 - 478 Andy Greenfield, Diane Scott, David Pennisi, Ingrid Ehrmann, Pamela Ellis, Leanne Cooper, Elizabeth Simpson
& Peter Koopman doi:10.1038/ng1296-474 Abstract + references|PDF
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Homozygosity mapping of Hallervorden−Spatz syndrome to chromosome 20p12.3−p13pp479 - 481 Todd D. Taylor, Michael Litt, Patricia Kramer, Massimo Pandolfo, Lucia Angelini, Nardo Nardocci, Suzanne Davis, M. Pineda, Haruo Hattori, Peter J. Flett, M. Roberta Cilio, Enrico Bertini
& Susan J. Hayflick doi:10.1038/ng1296-479 Abstract + references|PDF
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Identification of BTG2, an antiproliferative p53−dependent component of the DNA damage cellular response pathwaypp482 - 486 Jean-Pierre Rouault, Nicole Falette, Fabienne Guéhenneux, Céline Guillot, Ruth Rimokh, Qing Wang, Cyril Berthet, Caroline Moyret-Lalle, Pierre Savatier, Bertrand Pain, Philip Shaw, Roland Berger, Jacques Samarut, Jean-Pierre Magaud, Mehmet Ozturk, Christiane Samarut
& Alain Puisieux doi:10.1038/ng1296-482 Abstract + references|PDF
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Corrigendum: A complete set of human telomeric probes and their clinical applicationp487 doi:10.1038/ng1296-487 PDF
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Corrigendum: The insulin−like growth factor II receptor gene is a target of microsatellite instability in human gastrointestinal tumoursp488 doi:10.1038/ng1296-488a PDF
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