The APC I1307K allele and breast cancer riskpp13 - 14 Mark Redston, Katherine L. Nathanson, Zhi Qiang Yuan, Susan L. Neuhausen, Jaya Satagopan, Nora Wong, Diana Yang, Doudja Nafa, John Abrahamson, Hilmi Ozcelik, Danielle Antin-Ozerkis, Irene Andrulis, Mary Daly, Leonard Pinsky, Deborah Schrag, Steven Gallinger, Michael Kaback, Mary-Claire King, Trevor Woodage, Lawrence C. Brody, Andrew Godwin, Ellen Warner, Barbara Weber, William Foulkes
& Kenneth Offit doi:10.1038/1666 Full text|PDF
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Data management and analysis for gene expression arrayspp19 - 23 Olga Ermolaeva, Mohit Rastogi, Kim D. Pruitt, Gregory D. Schuler, Michael L. Bittner, Yidong Chen, Richard Simon, Paul Meltzer, Jeffrey M. Trent
& Mark S. Boguski doi:10.1038/1670 Abstract|Full text|PDF
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PAK3 mutation in nonsyndromic X-linked mental retardationpp25 - 30 Kristina M. Allen, Joseph G. Gleeson, Shubha Bagrodia, Michael W. Partington, John C. MacMillan, Richard A. Cerione, John C. Mulley
& Christopher A. Walsh doi:10.1038/1675 Abstract|Full text|PDF
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Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy
and limb girdle muscular dystrophypp31 - 36 Jing Liu, Masashi Aoki, Isabel Illa, Chenyan Wu, Michel Fardeau, Corrado Angelini, Carmen Serrano, J. Andoni Urtizberea, Faycal Hentati, Mongi Ben Hamida, Saeed Bohlega, Edward J. Culper, Anthony A. Amato, Karen Bossie, Joshua Oeltjen, Khemissa Bejaoui, Diane McKenna-Yasek, Betsy A. Hosler, Erwin Schurr, Kiichi Arahata, Pieter J. de Jong
& Robert H. Brown Jr doi:10.1038/1682 Abstract|Full text|PDF
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A gene related to Caenorhabditis elegans spermatogenesis factor
fer-1 is mutated in limb-girdle muscular dystrophy type 2Bpp37 - 42 Rumaisa Bashir, Stephen Britton, Tom Strachan, Sharon Keers, Elizabeth Vafiadaki, Majlinda Lako, Isabelle Richard, Sylvie Marchand, Nathalie Bourg, Zohar Argov, Menachem Sadeh, Ibrahim Mahjneh, Giampiero Marconi, Maria Rita Passos-Bueno, Eloisa de S Moreira, Mayana Zatz, Jacques S. Beckmann
& Kate Bushby doi:10.1038/1689 Abstract|Full text|PDF
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The paleontology of intergene retrotransposons of maizepp43 - 45 Phillip SanMiguel, Brandon S. Gaut, Alexander Tikhonov, Yuko Nakajima
& Jeffrey L. Bennetzen doi:10.1038/1695 Abstract|Full text|PDF
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Mass spectrometry and EST-database searching allows characterization
of the multi-protein spliceosome complexpp46 - 50 Gitte Neubauer, Angus King, Juri Rappsilber, Cinzia Calvio, Mark Watson, Paul Ajuh, Judith Sleeman, Angus Lamond
& Matthias Mann doi:10.1038/1700 Abstract|Full text|PDF
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Mutations in a polycistronic nuclear gene associated with molybdenum
cofactor deficiencypp51 - 53 Jochen Reiss, Nadine Cohen, Claude Dorche, Hanna Mandel, Ralf R. Mendel, Birgit Stallmeyer, Marie-Therese Zabot
& Thomas Dierks doi:10.1038/1706 Abstract|Full text|PDF
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Essential function of Gli2 and Gli3 in the formation of
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& Chi-chung Hui doi:10.1038/1711 Abstract|Full text|PDF
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The APC I1307K allele and cancer risk in a community-based study
of Ashkenazi Jewspp62 - 65 Trevor Woodage, Sonya M. King, Sholom Wacholder, Patricia Hartge, Jeffery P. Struewing, Mary McAdams, Steven J. Laken, Margaret A. Tucker
& Lawrence C. Brody doi:10.1038/1722 Abstract|Full text|PDF
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Trisomy 7-harbouring non-random duplication of the mutant MET
allele in hereditary papillary renal carcinomaspp66 - 69 Zhengping Zhuang, Won-Sang Park, Svetlana Pack, Laura Schmidt, Alexander O. Vortmeyer, Evgenia Pak, Thu Pham, Robert J. Weil, Sonja Candidus, Irina A. Lubensky, W. Marston Linehan, Berton Zbar
& Gregor Weirich doi:10.1038/1727 Abstract|Full text|PDF
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Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21pp70 - 73 Jean-Louis Blouin, Beth A. Dombroski, Swapan K. Nath, Virginia K. Lasseter, Paula S. Wolyniec, Gerald Nestadt, Mary Thornquist, Gail Ullrich, John McGrath, Laura Kasch, Malgorzata Lamacz, Marion G. Thomas, Corinne Gehrig, Uppala Radhakrishna, Sarah E. Snyder, Katherine G. Balk, Karin Neufeld, Karen L. Swartz, Nicola DeMarchi, George N. Papadimitriou, Dimitris G. Dikeos, Costas N. Stefanis, Aravinda Chakravarti, Barton Childs, David E. Housman, Haig H. Kazazian, Stylianos E. Antonarakis
& Ann E. Pulver doi:10.1038/1734 Abstract|Full text|PDF
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HIRA, a mammalian homologue of Saccharomyces cerevisiae transcriptional
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& Peter J. Scambler doi:10.1038/1739 Abstract|Full text|PDF
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Targeted disruption of the biglycan gene leads to an osteoporosis-like phenotype in micepp78 - 82 Tianshun Xu, Paolo Bianco, Larry W. Fisher, Glenn Longenecker, Erica Smith, Steven Goldstein, Jeffrey Bonadio, Adele Boskey, Anne-Marie Heegaard, Beatrice Sommer, Kazuhito Satomura, Pedro Dominguez, Chengyan Zhao, Ashok B. Kulkarni, Pamela Gehron Robey
& Marian F. Young doi:10.1038/1746 Abstract|Full text|PDF
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Identification of a candidate modifying gene for spinal muscular atrophy by comparative genomicspp83 - 86 Jeremiah M. Scharf, Matthew G. Endrizzi, Axel Wetter, Sidong Huang, Terri G. Thompson, Klaus Zerres, William F. Dietrich, Brunhilde Wirth
& Louis M. Kunkel doi:10.1038/1753 Abstract|Full text|PDF
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Sensory ataxia and muscle spindle agenesis in mice lacking the transcription factor Egr3pp87 - 91 Warren G. Tourtellotte
& Jeffrey Milbrandt doi:10.1038/1757 Abstract|Full text|PDF
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A missense mutation in the B-crystallin chaperone gene causes a desmin-related myopathypp92 - 95 Patrick Vicart, Anne Caron, Pascale Guicheney, Zhenlin Li, Marie-Christine Prévost, Armelle Faure, Danielle Chateau, Françoise Chapon, Fernando Tomé, Jean-Marie Dupret, Denise Paulin
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Assignment of Tangier disease to chromosome 9q31 by a graphical linkage exclusion strategypp96 - 98 Stephan Rust, Michael Walter, Harald Funke, Arnold von Eckardstein, Paul Cullen, Hester Y. Kroes, Roel Hordijk, Jürgen Geisel, John Kastelein, Henri O.F. Molhuizen, Michaela Schreiner, Anja Mischke, Harry W. Hahmann
& Gerd Assmann doi:10.1038/1770 Abstract|Full text|PDF
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B-crystallin chaperone gene causes a desmin-related myopathy
