Estimating rates of alternative splicing in mammals and invertebratespp915 - 916 Heebal Kim, Robert Klein, Jacek Majewski
& Jurg Ott doi:10.1038/ng0904-915 Full text|PDF
(149K)
|Supplementary Information
Estimating rates of alternative splicing in mammals and invertebratespp916 - 917 E D Harrington, S Boue, Juan Valcarcel, Jens G Reich
& Peer Bork doi:10.1038/ng0904-916 Full text|PDF
(149K)
|Supplementary Information
The Knockout Mouse Projectpp921 - 924 The Comprehensive Knockout Mouse Project Consortium: Christopher P Austin, James F Battey, Allan Bradley, Maja Bucan, Mario Capecchi, Francis S Collins, William F Dove, Geoffrey Duyk, Susan Dymecki, Janan T Eppig, Franziska B Grieder, Nathaniel Heintz, Geoff Hicks, Thomas R Insel, Alexandra Joyner, Beverly H Koller, K C Kent Lloyd, Terry Magnuson, Mark W Moore, Andras Nagy, Jonathan D Pollock, Allen D Roses, Arthur T Sands, Brian Seed, William C Skarnes, Jay Snoddy, Philippe Soriano, David J Stewart, Francis Stewart, Bruce Stillman, Harold Varmus, Lyuba Varticovski, Inder M Verma, Thomas F Vogt, Harald von Melchner, Jan Witkowski, Richard P Woychik, Wolfgang Wurst, George D Yancopoulos, Stephen G Young
& Brian Zambrowicz doi:10.1038/ng0904-921 Abstract|Full text|PDF
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The European dimension for the mouse genome mutagenesis programpp925 - 927 The European Mouse Mutagenesis Consortium: Johan Auwerx, Phil Avner, Richard Baldock, Andrea Ballabio, Rudi Balling, Mariano Barbacid, Anton Berns, Allan Bradley, Steve Brown, Peter Carmeliet, Pierre Chambon, Roger Cox, Duncan Davidson, Kay Davies, Denis Duboule, Jiri Forejt, Francesca Granucci, Nick Hastie, Martin Hrabé de Angelis, Ian Jackson, Dimitris Kioussis, George Kollias, Mark Lathrop, Urban Lendahl, Marcos Malumbres, Harald von Melchner, Werner Müller, Juha Partanen, Paola Ricciardi-Castagnoli, Peter Rigby, Barry Rosen, Nadia Rosenthal, Bill Skarnes, A Francis Stewart, Janet Thornton, Glauco Tocchini-Valentini, Erwin Wagner, Walter Wahli
& Wolfgang Wurst doi:10.1038/ng0904-925 Abstract|Full text|PDF
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Towards sound epistemological foundations of statistical methods for high-dimensional biologypp943 - 947 Tapan Mehta, Murat Tanik
& David B Allison Published online: 30 August 2004|doi:10.1038/ng1422 Abstract|Full text|PDF
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Detection of large-scale variation in the human genomepp949 - 951 A John Iafrate, Lars Feuk, Miguel N Rivera, Marc L Listewnik, Patricia K Donahoe, Ying Qi, Stephen W Scherer
& Charles Lee Published online: 01 August 2004|doi:10.1038/ng1416 Abstract|Full text|PDF
(352K)
|Supplementary Information See also:News and Views by Carter
Genomic segmental polymorphisms in inbred mouse strainspp952 - 954 Jiangzhen Li, Tao Jiang, Jian-Hua Mao, Allan Balmain, Leif Peterson, Charles Harris, Pulivarthi H Rao, Paul Havlak, Richard Gibbs
& Wei-Wen Cai Published online: 22 August 2004|doi:10.1038/ng1417 Abstract|Full text|PDF
(1,103K)
|Supplementary Information
Mutations in a new member of the chromodomain gene family cause CHARGE syndromepp955 - 957 Lisenka E L M Vissers, Conny M A van Ravenswaaij, Ronald Admiraal, Jane A Hurst, Bert B A de Vries, Irene M Janssen, Walter A van der Vliet, Erik H L P G Huys, Pieter J de Jong, Ben C J Hamel, Eric F P M Schoenmakers, Han G Brunner, Joris A Veltman
& Ad Geurts van Kessel Published online: 08 August 2004|doi:10.1038/ng1407 Abstract|Full text|PDF
(256K)
|Supplementary Information
Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndromepp958 - 960 Angela Sparago, Flavia Cerrato, Maria Vernucci, Giovanni Battista Ferrero, Margherita Cirillo Silengo
& Andrea Riccio Published online: 15 August 2004|doi:10.1038/ng1410 Abstract|Full text|PDF
(376K)
|Supplementary Information
Effects of G-protein mutations on skin colorpp961 - 968 Catherine D Van Raamsdonk, Karen R Fitch, Helmut Fuchs, Martin Hrabé de Angelis
& Gregory S Barsh Published online: 22 August 2004|doi:10.1038/ng1412 Abstract|Full text|PDF
(805K)
See also:News and Views by Jackson
Abnormal TNF activity in Timp3-/- mice leads to chronic hepatic inflammation and failure of liver regenerationpp969 - 977 Fazilat F Mohammed, David S Smookler, Suzanne E M Taylor, Barbara Fingleton, Zamaneh Kassiri, Otto H Sanchez, Jane L English, Lynn M Matrisian, Billie Au, Wen-Chen Yeh
& Rama Khokha Published online: 22 August 2004|doi:10.1038/ng1413 Abstract|Full text|PDF
(1,947K)
See also:News and Views by Black
Nonsense-mediated decay microarray analysis identifies mutations of EPHB2 in human prostate cancerpp979 - 983 Pia Huusko, Damaris Ponciano-Jackson, Maija Wolf, Jeff A Kiefer, David O Azorsa, Sukru Tuzmen, Don Weaver, Christiane Robbins, Tracy Moses, Minna Allinen, Sampsa Hautaniemi, Yidong Chen, Abdel Elkahloun, Mark Basik, G Steven Bova, Lukas Bubendorf, Alessandro Lugli, Guido Sauter, Johanna Schleutker, Hilmi Ozcelik, Sabine Elowe, Tony Pawson, Jeffrey M Trent, John D Carpten, Olli-P Kallioniemi
& Spyro Mousses Published online: 08 August 2004|doi:10.1038/ng1408 Abstract|Full text|PDF
(308K)
|Supplementary Information
In situ analyses of genome instability in breast cancerpp984 - 988 Koei Chin, Carlos Ortiz de Solorzano, David Knowles, Arthur Jones, William Chou, Enrique Garcia Rodriguez, Wen-Lin Kuo, Britt-Marie Ljung, Karen Chew, Kenneth Myambo, Monica Miranda, Sheryl Krig, James Garbe, Martha Stampfer, Paul Yaswen, Joe W Gray
& Stephen J Lockett Published online: 08 August 2004|doi:10.1038/ng1409 Abstract|Full text|PDF
(616K)
|Supplementary Information See also:News and Views by DePinho & Polyak
Mutations in a member of the Ras superfamily of small GTP-binding proteins causes Bardet-Biedl syndromepp989 - 993 Yanli Fan, Muneer A Esmail, Stephen J Ansley, Oliver E Blacque, Keith Boroevich, Alison J Ross, Susan J Moore, Jose L Badano, Helen May-Simera, Deanna S Compton, Jane S Green, Richard Alan Lewis, Mieke M van Haelst, Patrick S Parfrey, David L Baillie, Philip L Beales, Nicholas Katsanis, William S Davidson
& Michel R Leroux Published online: 15 August 2004|doi:10.1038/ng1414 Abstract|Full text|PDF
(319K)
|Supplementary Information
Loss of BBS proteins causes anosmia in humans and defects in olfactory cilia structure and function in the mousepp994 - 998 Heather M Kulaga, Carmen C Leitch, Erica R Eichers, Jose L Badano, Alysa Lesemann, Bethan E Hoskins, James R Lupski, Philip L Beales, Randall R Reed
& Nicholas Katsanis Published online: 22 August 2004|doi:10.1038/ng1418 Abstract|Full text|PDF
(566K)
|Supplementary Information
Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorderpp999 - 1002 Robert Kleta, Elisa Romeo, Zorica Ristic, Toshihiro Ohura, Caroline Stuart, Mauricio Arcos-Burgos, Mital H Dave, Carsten A Wagner, Simone R M Camargo, Sumiko Inoue, Norio Matsuura, Amanda Helip-Wooley, Detlef Bockenhauer, Richard Warth, Isa Bernardini, Gepke Visser, Thomas Eggermann, Philip Lee, Arthit Chairoungdua, Promsuk Jutabha, Ellappan Babu, Sirinun Nilwarangkoon, Naohiko Anzai, Yoshikatsu Kanai, Francois Verrey, William A Gahl
& Akio Koizumi Published online: 01 August 2004|doi:10.1038/ng1405 Abstract|Full text|PDF
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Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19pp1003 - 1007 Heng F Seow, Stefan Bröer, Angelika Bröer, Charles G Bailey, Simon J Potter, Juleen A Cavanaugh
& John E J Rasko Published online: 01 August 2004|doi:10.1038/ng1406 Abstract|Full text|PDF
(265K)
|Supplementary Information
Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndromepp1008 - 1013 Russell J Ferland, Wafaa Eyaid, Randall V Collura, Laura D Tully, R Sean Hill, Doha Al-Nouri, Ahmed Al-Rumayyan, Meral Topcu, Generoso Gascon, Adria Bodell, Yin Yao Shugart, Maryellen Ruvolo
& Christopher A Walsh Published online: 22 August 2004|doi:10.1038/ng1419 Abstract|Full text|PDF
(650K)
|Supplementary Information See also:News and Views by Mercola & Welsh
Gene loops juxtapose promoters and terminators in yeastpp1014 - 1018 Justin M O'Sullivan, Sue Mei Tan-Wong, Antonin Morillon, Barbara Lee, Joel Coles, Jane Mellor
& Nick J Proudfoot Published online: 15 August 2004|doi:10.1038/ng1411 Abstract|Full text|PDF
(289K)
|Supplementary Information
Evidence for a fruit fly hemangioblast and similarities between lymph-gland hematopoiesis in fruit fly and mammal aorta-gonadal-mesonephros mesodermpp1019 - 1023 Lolitika Mandal, Utpal Banerjee
& Volker Hartenstein Published online: 01 August 2004|doi:10.1038/ng1404 Abstract|Full text|PDF
(717K)
Corrigendum: TGF signaling in health and diseasep1024 R J Akhurst doi:10.1038/ng0904-1024a Full text|PDF
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Corrigendum: A functional variant of SUMO4, a new IB modifier, is associated with type 1 diabetesp1024 D Guo, M Li, Y Zhang, P Yang, S Eckenrode, D Hopkins, W Zheng, S Purohit, R H Podolsky, A Muir, J Wang, Z Dong, T Brusko, M Atkinson, P Pozzilli, A Zeidler, L J Raffel, C O Jacob, Y Park, M Serrano-Rios, M T Martinez Larrad, Z Zhang, H-J Garchon, J-F Bach, J I Rotter, J-X She
& C-Y Wang doi:10.1038/ng0904-1024b Full text|PDF
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Corrigendum: Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause severe childhood-onset retinal dystrophyp1024 A R Janecke, D A Thompson, G Utermann, C Becker, C A Hübner, E Schmid, C L McHenry, A R Nair, F Rüschendorf, J Heckenlively, B Wissinger, P Nürnberg
& A Gal doi:10.1038/ng0904-1024c Full text|PDF
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signaling in health and disease
B
modifier, is associated with type 1 diabetes
