The molecular basis of alkaptonuriapp19 - 24 José M. Fernández-Cañón, Begoña Granadino, Daniel Beltrán−Valero De Bernabé, Mónica Renedo, Elena Fernández-Ruiz, Miguel A. Peñalva
& Santiago Rodríguez De Córdoba doi:10.1038/ng0996-19 Abstract + references|PDF
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The EXT2 multiple exostoses gene defines a family of putative tumour suppressor genespp25 - 32 Dominique Stickens, Gregory Clines, David Burbee, Purita Ramos, Sylvia Thomas, Deborah Hogue, Jacqueline T. Hecht, Michael Lovett
& Glen A. Evans doi:10.1038/ng0996-25 Abstract + references|PDF
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The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB−binding proteinpp33 - 41 Julian Borrow, Vincent P. Stanton Jr, J. Michael Andresen, Reinhard Becher, Frederick G. Behm, Raju S. K. Chaganti, Curt I. Civin, Christine Disteche, Ian Dubé, Anna Marie Frischauf, Doug Horsman, Felix Mitelman, Stefano Volinia, Ann E. Watmore
& David E. Housman doi:10.1038/ng0996-33 Abstract + references|PDF
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Yeast SAS silencing genes and human genes associated with AML and HIV−1 Tat interactions are homologous with acetyltransferasespp42 - 49 Cheryl Reifsnyder, Joanna Lowell, Astrid Clarke
& Lorraine Pillus doi:10.1038/ng0996-42 Abstract + references|PDF
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Ectopic expression of MITF, a gene for Waardenburg syndrome type 2, converts fibroblasts to cells with melanocyte characteristicspp50 - 54 Masayoshi Tachibana, Kazuhisa Takeda, Yoshitaka Nobukuni, Kazunori Urabe, Jason E. Long, Kimberly A. Meyers, Stuart A. Aaronson
& Toru Miki doi:10.1038/ng0996-50 Abstract + references|PDF
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Apolipoprotein E allele−specific antioxidant activity and effects on cytotoxicity by oxidative insults and −amyloid peptidespp55 - 61 Masaaki Miyata
& Jonathan D. Smith doi:10.1038/ng0996-55 Abstract + references|PDF
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Sox9 expression during gonadal development implies a conserved role for the gene in testis differentiation in mammals and birdspp62 - 68 Sara Morais da Silva, Adam Hacker, Vince Harley, Peter Goodfellow, Amanda Swain
& Robin Lovell-Badge doi:10.1038/ng0996-62 Abstract + references|PDF
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BIN1 is a novel MYC−interacting protein with features of a tumour suppressorpp69 - 77 Daitoku Sakamuro, Katharine J. Elliott, Robert Wechsler-Reya
& George C. Prendergast doi:10.1038/ng0996-69 Abstract + references|PDF
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The role of the human homologue of Drosophila patched in sporadic basal cell carcinomaspp78 - 81 Mae R. Gailani, Mona Ståhle-Bäckdahl, David J. Leffell, Michael Glyn, Peter G. Zaphiropoulos, Anne Birgitte Undén, Michael Dean, Douglas E. Brash, Allen E. Bale
& Rune Toftgård doi:10.1038/ng0996-78 Abstract + references|PDF
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A genome scan localizes five non−MHC loci controlling collagen−induced arthritis in ratspp82 - 85 Elaine F. Remmers, Ryan E. Longman, Ying Du, Ann O'Hare, Grant W. Cannon, Marie M. Griffiths
& Ronald L. Wilder doi:10.1038/ng0996-82 Abstract + references|PDF
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A complete set of human telomeric probes and their clinical applicationpp86 - 89 Yi Ning, Anna Roschke, Ann C.M. Smith, Michelle Macha, Kathrin Precht, Harold Riethman, David H. Ledbetter, Jonathan Flint, Sharon Horsley, Regina Regan, Lyndal Kearney, Samantha Knight, Kirsti Kvaloy
& William R.A. Brown doi:10.1038/ng0996-86 Abstract + references|PDF
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Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish familiespp90 - 94 Melanie M. Mahtani, Elisabeth Widén, Markku Lehto, Jeffrey Thomas, Mark McCarthy, James Brayer, Barbara Bryant, Gayun Chan, Mark Daly, Carol Forsblom, Timo Kanninen, Andrew Kirby, Leonid Kruglyak, Kevin Munnelly, Maikki Parkkonen, Mary Pat Reeve-Daly, Alix Weaver, Thomas Brettin, Geoffrey Duyk, Eric S. Lander
& Leif C. Groop doi:10.1038/ng0996-90 Abstract + references|PDF
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Leptin activation of Stat3 in the hypothalamus of wild−type and ob/ob mice but not db/db micepp95 - 97 Christian Vaisse, Jeffrey L Halaas, Curt M. Horvath, James E. Darnell Jr, Markus Stoffel
& Jeffrey M. Friedman doi:10.1038/ng0996-95 Abstract + references|PDF
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Elevated alcohol consumption in null mutant mice lacking 5−HT1B serotonin receptorspp98 - 101 John C. Crabbe, Tamara J. Phillips, Daniel J. Feller, René Hen, Charlotte D. Wenger, Christina N. Lessov
& Gwen L. Schafer doi:10.1038/ng0996-98 Abstract + references|PDF
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Mutation of MSH3 in endometrial cancer and evidence for its functional role in heteroduplex repairpp102 - 105 John I. Risinger, Asad Umar, Jeff Boyd, Andrew Berchuck, Thomas A. Kunkel
& J. Carl Barrett doi:10.1038/ng0996-102 Abstract + references|PDF
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Identification of Grf1 on mouse chromosome 9 as an imprinted gene by RLGS−Mpp106 - 109 Christoph Plass, Hideo Shibata, Iveta Kalcheva, Linda Mullins, Nina Kotelevtseva, John Mullins, Reiko Kato, Hiroyuki Sasaki, Shinji Hirotsune, Yasushi Okazaki, William A. Held, Yoshihide Hayashizaki
& Verne M. Chapman doi:10.1038/ng0996-106 Abstract + references|PDF
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Identification of NF1 mutations in both alleles of a dermal neurofibromapp110 - 112 Shun'ichi Sawada, Scott Florell, Smita M. Purandare, Mayumi Ota, Karen Stephens
& David Viskochil doi:10.1038/ng0996-110 Abstract + references|PDF
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Type VI collagen mutations in Bethlem myopathy, an autosomal dominant myopathy with contracturespp113 - 115 G. Joost Jöbsis, H. Keizers, Jeroen P. Vreijling, Marianne de Visser, Marcy C. Speer, Ruud A. Wolterman, Frank Baas
& Pieter A. Bolhuis doi:10.1038/ng0996-113 Abstract + references|PDF
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−amyloid peptides
