Artificial chromosome transgenesis reveals long-distance negative regulation
of rag1 in zebrafishpp15 - 16 Jason R. Jessen, Catherine E. Willett
& Shuo Lin doi:10.1038/12609 Full text|PDF
(337K)
Mutations in GJB6 cause nonsyndromic autosomal dominant deafness
at DFNA3 locuspp16 - 18 Anna Grifa, Carsten A. Wagner, Lucrezia D'Ambrosio, Salvatore Melchionda, Francesco Bernardi, Nuria Lopez-Bigas, Raquel Rabionet, Mariona Arbones, Matteo Della Monica, Xavier Estivill, Leopoldo Zelante, Florian Lang
& Paolo Gasparini doi:10.1038/12612 Full text|PDF
(246K)
Frequent activating mutations of FGFR3 in human bladder and cervix carcinomas
pp18 - 20 David Cappellen, Catherine De Oliveira, David Ricol, Sixtina de Medina, Jérôme Bourdin, Xavier Sastre-Garau, Dominique Chopin, Jean Paul Thiery
& François Radvanyi doi:10.1038/12615 Full text|PDF
(260K)
Cardiac conduction defects associate with mutations in SCN5App20 - 21 Jean-Jacques Schott, Connie Alshinawi, Florence Kyndt, Vincent Probst, Theo M. Hoorntje, Miriam Hulsbeek, Arthur A.M. Wilde, Denis Escande, Marcel M.A.M. Mannens
& Hervé Le Marec doi:10.1038/12618 Full text|PDF
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A new member of the IL-1 receptor family highly expressed in hippocampus
and involved in X-linked mental retardationpp25 - 31 Alain Carrié, Lin Jun, Thierry Bienvenu, Marie-Claude Vinet, Nathalie McDonell, Philippe Couvert, Ramzi Zemni, Ana Cardona, Griet Van Buggenhout, Suzanna Frints, Ben Hamel, Claude Moraine, Hans H. Ropers, Tim Strom, Gareth R. Howell, Adam Whittaker, Mark T. Ross, Axel Kahn, Jean-Pierre Fryns, Cherif Beldjord, Peter Marynen
& Jamel Chelly doi:10.1038/12623 Abstract|Full text|PDF
(1,009K)
Irs-2 coordinates Igf-1 receptor-mediated -cell development and
peripheral insulin signallingpp32 - 40 Dominic J. Withers, Deborah J. Burks, Heather H. Towery, Shari L. Altamuro, Carrie L. Flint
& Morris F. White doi:10.1038/12631 Abstract|Full text|PDF
(1,253K)
Genome-wide analysis of DNA copy-number changes using cDNA microarrayspp41 - 46 Jonathan R. Pollack, Charles M. Perou, Ash A. Alizadeh, Michael B. Eisen, Alexander Pergamenschikov, Cheryl F. Williams, Stefanie S. Jeffrey, David Botstein
& Patrick O. Brown doi:10.1038/12640 Abstract|Full text|PDF
(1,244K)
Intragenic deletion in the gene encoding ubiquitin carboxy-terminal hydrolase
in gad micepp47 - 51 Kazumasa Saigoh, Yu-Lai Wang, Jun-Gyo Suh, Toshiyuki Yamanishi, Yoshihisa Sakai, Hidenori Kiyosawa, Takayuki Harada, Nobutsune Ichihara, Shigeharu Wakana, Tateki Kikuchi
& Keiji Wada doi:10.1038/12647 Abstract|Full text|PDF
(592K)
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Non-type I cystinuria caused by mutations in SLC7A9, encoding
a subunit (bo,+AT) of rBATpp52 - 57 Lídia Feliubadaló, Mariona Font, Jesús Purroy, Ferran Rousaud, Xavier Estivill, Virginia Nunes, Eliahu Golomb, Michael Centola, Ivona Aksentijevich, Yitshak Kreiss, Boleslaw Goldman, Mordechai Pras, Daniel L. Kastner, Elon Pras, Paolo Gasparini, Luigi Bisceglia, Ercole Beccia, Michele Gallucci, Luisa de Sanctis, Alberto Ponzone, Gian Franco Rizzoni, Leopoldo Zelante, Maria Teresa Bassi, Alfred L. George Jr, Marta Manzoni, Alessandro De Grandi, Mirko Riboni, John K. Endsley, Andrea Ballabio, Giuseppe Borsani, Núria Reig, Esperanza Fernández, Raúl Estévez, Marta Pineda, David Torrents, Marta Camps, Jorge Lloberas, Antonio Zorzano
& Manuel Palacín doi:10.1038/12652 Abstract|Full text|PDF
(361K)
MBD2 is a transcriptional repressor belonging to the MeCP1 histone deacetylase
complexpp58 - 61 Huck-Hui Ng, Yi Zhang, Brian Hendrich, Colin A. Johnson, Bryan M. Turner, Hediye Erdjument-Bromage, Paul Tempst, Danny Reinberg
& Adrian Bird doi:10.1038/12659 Abstract|Full text|PDF
(282K)
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Mi-2 complex couples DNA methylation to chromatin remodelling and histone
deacetylationpp62 - 66 Paul A. Wade, Anne Gegonne, Peter L. Jones, Esteban Ballestar, Florence Aubry
& Alan P. Wolffe doi:10.1038/12664 Abstract|Full text|PDF
(716K)
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Selective agenesis of the dorsal pancreas in mice lacking homeobox gene
Hlxb9pp67 - 70 Hao Li, Silvia Arber, Thomas M. Jessell
& Helena Edlund doi:10.1038/12669 Abstract|Full text|PDF
(1,972K)
Pancreas dorsal lobe agenesis and abnormal islets of Langerhans in Hlxb9-deficient micepp71 - 75 Kathleen A. Harrison, Joshua Thaler, Samuel L. Pfaff, Hua Gu
& John H. Kehrl doi:10.1038/12674 Abstract|Full text|PDF
(1,807K)
Functions of poly(ADP-ribose) polymerase in controlling telomere length and chromosomal stabilitypp76 - 80 Fabrizio d'Adda di Fagagna, M. Prakash Hande, Wei-Min Tong, Peter M. Lansdorp, Zhao-Qi Wang
& Stephen P. Jackson doi:10.1038/12680 Abstract|Full text|PDF
(388K)
Gross chromosomal rearrangements in Saccharomyces cerevisiae replication
and recombination defective mutantspp81 - 85 Clark Chen
& Richard D. Kolodner doi:10.1038/12687 Abstract|Full text|PDF
(122K)
A radiation hybrid map of the zebrafish genomepp86 - 89 Robert Geisler, Gerd-Jörg Rauch, Herwig Baier, Frauke van Bebber, Linda Bro, Marcus P.S. Dekens, Karin Finger, Cornelia Fricke, Michael A. Gates, Horst Geiger, Silke Geiger-Rudolph, Darren Gilmour, Stefanie Glaser, Lara Gnügge, Hinrich Habeck, Katy Hingst, Scott Holley, Jeremy Keenan, Anette Kirn, Holger Knaut, Deval Lashkari, Florian Maderspacher, Ulrike Martyn, Stephan Neuhauss, Carl Neumann, Teresa Nicolson, Francisco Pelegri, Russell Ray, Jens M. Rick, Henry Roehl, Tobias Roeser, Heike E. Schauerte, Alexander F. Schier, Ulrike Schönberger, Helia-Berrit Schönthaler, Stefan Schulte-Merker, Catrin Seydler, William S. Talbot, Christian Weiler, Christiane Nüsslein-Volhard
& Pascal Haffter doi:10.1038/12692 Abstract|Full text|PDF
(98K)
|Supplementary Information
Mitochondrial DNA genotypes in nuclear transfer-derived cloned sheeppp90 - 93 Matthew J. Evans, Cagan Gurer, John D. Loike, Ian Wilmut, Angelika E. Schnieke
& Eric A. Schon doi:10.1038/12696 Abstract|Full text|PDF
(300K)
Mutations in the CCN gene family member WISP3 cause progressive
pseudorheumatoid dysplasiapp94 - 98 Jennifer R. Hurvitz, Wafaa M. Suwairi, Wim Van Hul, Hatem El-Shanti, Andrea Superti-Furga, Jean Roudier, Daniel Holderbaum, Richard M. Pauli, J. Kenneth Herd, Els Van Hul, Hossien Rezai-Delui, Eric Legius, Martine Le Merrer, Jamil Al-Alami, Sultan A. Bahabri
& Matthew L. Warman doi:10.1038/12699 Abstract|Full text|PDF
(318K)
|Supplementary Information
Disruption of the glucocorticoid receptor gene in the nervous system
results in reduced anxietypp99 - 103 François Tronche, Christoph Kellendonk, Oliver Kretz, Peter Gass, Katrin Anlag, Paul C. Orban, Rudolf Bock, Rüdiger Klein
& Günther Schütz doi:10.1038/12703 Abstract|Full text|PDF
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A novel member of the F-box/WD40 gene family, encoding dactylin, is disrupted
in the mouse dactylaplasia mutantpp104 - 107 Arend Sidow, Monique S. Bulotsky, Anne W. Kerrebrock, Bruce W. Birren, David Altshuler, Rudolf Jaenisch, Kenneth R. Johnson
& Eric S. Lander doi:10.1038/12709 Abstract|Full text|PDF
(574K)
Ocular albinism: evidence for a defect in an intracellular signal transduction
systempp108 - 112 M. Vittoria Schiaffino, Marilena d'Addio, Anna Alloni, Cinzia Baschirotto, Caterina Valetti, Katia Cortese, Claudia Puri, M. Teresa Bassi, Cristina Colla, Michele De Luca, Carlo Tacchetti
& Andrea Ballabio doi:10.1038/12715 Abstract|Full text|PDF
(721K)
Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordiapp113 - 117 Pin-Xian Xu, Joe Adams, Heiko Peters, M. Christian Brown, Shaun Heaney
& Richard Maas doi:10.1038/12722 Abstract|Full text|PDF
(1,541K)
Globozoospermia in mice lacking the casein kinase II ' catalytic subunitpp118 - 121 Xin Xu, Paul A. Toselli, Lonnie D. Russell
& David C. Seldin doi:10.1038/12729 Abstract|Full text|PDF
(984K)
-cell development and
peripheral insulin signalling
' catalytic subunit
