Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21pp21 - 22 Rachel V. Baxter, Kamel Ben Othmane, Julie M. Rochelle, Jason E. Stajich, Christine Hulette, Susan Dew-Knight, Faycal Hentati, Mongi Ben Hamida, S. Bel, Judy E. Stenger, John R. Gilbert, Margaret A. Pericak-Vance
& Jeffery M. Vance Published online: 17 December 2001|doi:10.1038/ng796 Abstract|Full text|PDF
(300K)
|Supplementary Information
The gene encoding ganglioside-induced differentiation-associated protein 1 is mutated in axonal Charcot-Marie-Tooth type 4A diseasepp22 - 25 Ana Cuesta, Laia Pedrola, Teresa Sevilla, Javier García-Planells, María José Chumillas, Fernando Mayordomo, Eric LeGuern, Ignacio Marín, Juan J. Vílchez
& Francesc Palau Published online: 17 December 2001|doi:10.1038/ng798 Abstract|Full text|PDF
(727K)
|Supplementary Information
Small changes in expression affect predisposition to tumorigenesispp25 - 26 Hai Yan, Zuzana Dobbie, Stephen B. Gruber, Sanford Markowitz, Kathy Romans, Francis M. Giardiello, Kenneth W. Kinzler
& Bert Vogelstein Published online: 17 December 2001|doi:10.1038/ng799 Abstract|Full text|PDF
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The penetrance of dominant erythropoietic protoporphyria is modulated by expression of wildtype FECHpp27 - 28 Laurent Gouya, Herve Puy, Anne-Marie Robreau, Monique Bourgeois, Jerôme Lamoril, Vasco Da Silva, Bernard Grandchamp
& Jean-Charles Deybach Published online: 20 December 2001|doi:10.1038/ng809 Abstract|Full text|PDF
(456K)
|Supplementary Information
Alternative splicing and genome complexitypp29 - 30 David Brett, Heike Pospisil, Juan Valcárcel, Jens Reich
& Peer Bork Published online: 17 December 2001|doi:10.1038/ng803 Abstract|Full text|PDF
(86K)
Towards genetic genome projects: genomic library screening and gene-targeting vector construction in a single steppp31 - 39 Pumin Zhang, Mamei Z. Li
& Stephen J. Elledge Published online: 20 December 2001|doi:10.1038/ng811 Abstract|Full text|PDF
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MLL translocations specify a distinct gene expression profile that distinguishes a unique leukemiapp41 - 47 Scott A. Armstrong, Jane E. Staunton, Lewis B. Silverman, Rob Pieters, Monique L. den Boer, Mark D. Minden, Stephen E. Sallan, Eric S. Lander, Todd R. Golub
& Stanley J. Korsmeyer Published online: 03 December 2001|doi:10.1038/ng765 Abstract|Full text|PDF
(1,470K)
|Supplementary Information
BCR-ABL suppresses C/EBP expression through inhibitory action of hnRNP E2pp48 - 58 Danilo Perrotti, Vincenzo Cesi, Rossana Trotta, Clara Guerzoni, Giorgia Santilli, Kenneth Campbell, Angela Iervolino, Fabrizio Condorelli, Carlo Gambacorti-Passerini, Michael A. Caligiuri
& Bruno Calabretta Published online: 20 December 2001|doi:10.1038/ng791 Abstract|Full text|PDF
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Phenotyping transgenic embryos: a rapid 3-D screening method based on episcopic fluorescence image capturingpp59 - 65 Wolfgang Johann Weninger
& Timothy Mohun Published online: 17 December 2001|doi:10.1038/ng785 Abstract|Full text|PDF
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Efficient Cre-loxP−induced mitotic recombination in mouse embryonic stem cellspp66 - 72 Pentao Liu, Nancy A. Jenkins
& Neal G. Copeland Published online: 10 December 2001|doi:10.1038/ng788 Abstract|Full text|PDF
(2,167K)
See also:News and Views by Adams & Bradley
Differentially methylated forms of histone H3 show unique association patterns with inactive human X chromosomespp73 - 76 Barbara A. Boggs, Peter Cheung, Edith Heard, David L. Spector, A. Craig Chinault
& C. David Allis Published online: 10 December 2001|doi:10.1038/ng787 Abstract|Full text|PDF
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Histone H3 lysine 9 methylation is an epigenetic imprint of facultative heterochromatinpp77 - 80 Antoine H.F.M. Peters, Jacqueline E. Mermoud, Dónal O'Carroll, Michaela Pagani, Dieter Schweizer, Neil Brockdorff
& Thomas Jenuwein Published online: 10 December 2001|doi:10.1038/ng789 Abstract|Full text|PDF
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Mutations in genes encoding melanosomal proteins cause pigmentary glaucoma in DBA/2J micepp81 - 85 Michael G. Anderson, Richard S. Smith, Norman L. Hawes, Adriana Zabaleta, Bo Chang, Janey L. Wiggs
& Simon W.M. John Published online: 17 December 2001|doi:10.1038/ng794 Abstract|Full text|PDF
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Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexiapp86 - 91 Simon E. Fisher, Clyde Francks, Angela J. Marlow, I. Laurence MacPhie, Dianne F. Newbury, Lon R. Cardon, Yumiko Ishikawa-Brush, Alex J. Richardson, Joel B. Talcott, Javier Gayán, Richard K. Olson, Bruce F. Pennington, Shelley D. Smith, John C. DeFries, John F. Stein
& Anthony P. Monaco Published online: 17 December 2001|doi:10.1038/ng792 Abstract|Full text|PDF
(133K)
|Supplementary Information
Regulation of DNA methylation of Rasgrf1pp92 - 96 Bong June Yoon, Herry Herman, Aimee Sikora, Laura T. Smith, Christoph Plass
& Paul D. Soloway Published online: 20 December 2001|doi:10.1038/ng795 Abstract|Full text|PDF
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Merlin—rapid analysis of dense genetic maps using sparse gene flow treespp97 - 101 Gonçalo R. Abecasis, Stacey S. Cherny, William O. Cookson
& Lon R. Cardon Published online: 03 December 2001|doi:10.1038/ng786 Abstract|Full text|PDF
(208K)
See also:News and Views by Nicolae & Cox
Linkage of high-density lipoprotein−cholesterol concentrations to a locus on chromosome 9p in Mexican Americanspp102 - 105 Rector Arya, Ravindranath Duggirala, Laura Almasy, David L. Rainwater, Michael C. Mahaney, Shelley Cole, Thomas D. Dyer, Ken Williams, Robin J. Leach, James E. Hixson, Jean W. MacCluer, Peter O'Connell, Michael P. Stern
& John Blangero Published online: 17 December 2001|doi:10.1038/ng810 Abstract|Full text|PDF
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Loss of the SKI proto-oncogene in individuals affected with 1p36 deletion syndrome is predicted by strain-dependent defects in Ski-/- micepp106 - 109 Clemencia Colmenares, Heidi A. Heilstedt, Lisa G. Shaffer, Stuart Schwartz, Michael Berk, Jeffrey C. Murray
& Ed Stavnezer Published online: 03 December 2001|doi:10.1038/ng770 Abstract|Full text|PDF
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Positional cloning of the combined hyperlipidemia gene Hyplip1pp110 - 116 Jackie S. Bodnar, Aurobindo Chatterjee, Lawrence W. Castellani, David A. Ross, Jeffrey Ohmen, James Cavalcoli, Chenyan Wu, Katherine M. Dains, Joe Catanese, Michael Chu, Sonal S. Sheth, Kanti Charugundla, Peter Demant, David B. West, Pieter de Jong
& Aldons J. Lusis Published online: 20 December 2001|doi:10.1038/ng811 Abstract|Full text|PDF
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Otx5 regulates genes that show circadian expression in the zebrafish pineal complexpp117 - 121 Joshua T. Gamse, Yu-Chi Shen, Christine Thisse, Bernard Thisse, Pamela A. Raymond, Marnie E. Halpern
& Jennifer O. Liang Published online: 20 December 2001|doi:10.1038/ng793 Abstract|Full text|PDF
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A CTG trinucleotide repeat expansion in the gene encoding junctophilin-3 is associated with Huntington disease−like 2p123 doi:10.1038/ng0102-123a Full text|PDF
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MID1, mutated in Opitz syndrome, encodes a ubiquitin ligase that targets phosphatase 2A for degradationp123 doi:10.1038/ng0102-123b Full text|PDF
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A QTL for flowering time in Arabidopsis reveals a novel allele of CRY2p123 doi:10.1038/ng0102-123c Full text|PDF
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Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndromep123 doi:10.1038/ng0102-123d Full text|PDF
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expression through inhibitory action of hnRNP E2
