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Nature Genetics
ISSUE
November 1998, Volume 20 No 3
Editorial
News and Views
Correspondence
Articles
Letters
Errata
About the cover
Editorial Top
SNP attack on complex traits pp217 - 218
doi:10.1038/3011
Full text | PDF (43K)
News and Views Top
Women on the move pp219 - 220
Mark Stoneking
doi:10.1038/3012
Full text | PDF (89K)
See also: Letter by Seielstad et al.
Life, death and nuclear spots pp220 - 222
Jay L Hess & Stanley J Korsmeyer
doi:10.1038/3014
Full text | PDF (110K)
See also: Article by Quignon et al.  | Article by Wang et al.
The zebrafish and haematopoietic justice pp222 - 223
Chris T Amemiya
doi:10.1038/3016
Full text | PDF (53K)
See also: Article by Brownlie et al.
Type 2 diabetes — who is conducting the orchestra? pp223 - 225
Barbara B Kahn & Luciano Rossetti
doi:10.1038/3018
Full text | PDF (183K)
See also: Letter by Lauro et al.
Touching base p226
doi:10.1038/3021
Full text | PDF (74K)
Correspondence Top
Stable dicentric X chromosomes with two functional centromeres pp227 - 228
Beth A. Sullivan & Huntington F. Willard
doi:10.1038/3024
Full text | PDF (63K)
Fetal exposure to DES results in de-regulation of Wnt7a during uterine morphogenesis pp228 - 230
Cary Miller, Karl Degenhardt & David A. Sassoon
doi:10.1038/3027
Full text | PDF (241K)
Differential SMN2 expression associated with SMA severity pp230 - 231
Dimitar K. Gavrilov, Xiangyang Shi, Kamna Das, T. Conrad Gilliam & Ching H. Wang
doi:10.1038/3030
Full text | PDF (55K)
DRPLA aggregation and transglutaminase, revisited p231
Laszlo Lorand
doi:10.1038/3033
Full text | PDF (31K)
Articles Top
A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis pp233 - 238
Sandra S. Strautnieks, Laura N. Bull, Alexander S. Knisely, Samuel A. Kocoshis, Niklas Dahl, Henrik Arnell, Etienne Sokal, Karine Dahan, Sarah Childs, Victor Ling, M. Stuart Tanner, Amir F. Kagalwalla, Antal Németh, Joanna Pawlowska, Alastair Baker, Giorgina Mieli-Vergani, Nelson B. Freimer, R. Mark Gardiner & Richard J. Thompson
doi:10.1038/3034
Abstract | Full text | PDF (163K)
A zebrafish model for hepatoerythropoietic porphyria pp239 - 243
Han Wang, Qiaoming Long, Scott D. Marty, Shigeru Sassa & Shuo Lin
doi:10.1038/3041
Abstract | Full text | PDF (240K)
See also: News and Views by Hess & Korsmeyer
Positional cloning of the zebrafish sauternes gene: a model for congenital sideroblastic anaemia pp244 - 250
Alison Brownlie, Adriana Donovan, Stephen J. Pratt, Barry H. Paw, Andrew C. Oates, Carlo Brugnara, H. Ewa Witkowska, Shigeru Sassa & Leonard I. Zon
doi:10.1038/3049
Abstract | Full text | PDF (790K)
See also: News and Views by Hess & Korsmeyer
Progressive ataxia, myoclonic epilepsy and cerebellar apoptosis in cystatin B-deficient mice pp251 - 258
Len A. Pennacchio, Donna M. Bouley, Kay M. Higgins, Matthew P. Scott, Jeffrey L. Noebels & Richard M. Myers
doi:10.1038/3059
Abstract | Full text | PDF (340K)
PML induces a novel caspase-independent death process pp259 - 265
Frédérique Quignon, Frédéric De Bels, Marcel Koken, Jean Feunteun, Jean-Claude Ameisen & Hugues de Thé
doi:10.1038/3068
Abstract | Full text | PDF (227K)
See also: News and Views by Amemiya
Pml is essential for multiple apoptotic pathways pp266 - 272
Zhu-Gang Wang, Davide Ruggero, Simona Ronchetti, Sue Zhong, Mirella Gaboli, Roberta Rivi & Pier Paolo Pandolfi
doi:10.1038/3073
Abstract | Full text | PDF (324K)
See also: News and Views by Amemiya
Letters Top
A gene encoding a novel RFX-associated transactivator is mutated in the majority of MHC class II deficiency patients pp273 - 277
Krzysztof Masternak, Emmanuèle Barras, Madeleine Zufferey, Bernard Conrad, Garry Corthals, Ruedi Aebersold, Jean-Charles Sanchez, Denis F. Hochstrasser, Bernard Mach & Walter Reith
doi:10.1038/3081
Abstract | Full text | PDF (208K)
Genetic evidence for a higher female migration rate in humans pp278 - 280
Mark T. Seielstad, Eric Minch & L. Luca Cavalli-Sforza
doi:10.1038/3088
Abstract | Full text | PDF (55K)
See also: News and Views by Stoneking
The Fanconi anaemia group G gene FANCG is identical with XRCC9 pp281 - 283
Johan P. de Winter, Quinten Waisfisz, Martin A. Rooimans, Carola G.M. van Berkel, Lucine Bosnoyan-Collins, Noa Alon, Madeleine Carreau, Olaf Bender, Ilja Demuth, Detlev Schindler, Jan C. Pronk, Fré Arwert, Holger Hoehn, Martin Digweed, Manuel Buchwald & Hans Joenje
doi:10.1038/3093
Abstract | Full text | PDF (123K)
A Pro12Ala substitution in PPARgamma2 associated with decreased receptor activity, lower body mass index and improved insulin sensitivity pp284 - 287
Samir S. Deeb, Lluis Fajas, Masami Nemoto, Jussi Pihlajamäki, Leena Mykkänen, Johanna Kuusisto, Markku Laakso, Wilfred Fujimoto & Johan Auwerx
doi:10.1038/3099
Abstract | Full text | PDF (81K)
Rapid amplification of a retrotransposon subfamily is evolving the mouse genome pp288 - 290
Ralph J. DeBerardinis, John L. Goodier, Eric M. Ostertag & Haig H. Kazazian Jr
doi:10.1038/3104
Abstract | Full text | PDF (100K)
Somatic mutations of the mitochondrial genome in human colorectal tumours pp291 - 293
Kornelia Polyak, Yunbo Li, Hong Zhu, Christoph Lengauer, James K.V. Willson, Sanford D. Markowitz, Michael A. Trush, Kenneth W. Kinzler & Bert Vogelstein
doi:10.1038/3108
Abstract | Full text | PDF (132K)
Impaired glucose tolerance in mice with a targeted impairment of insulin action in muscle and adipose tissue pp294 - 298
Davide Lauro, Yoshiaki Kido, Arthur L. Castle, Mary-Jane Zarnowski, Hideki Hayashi, Yousuke Ebina & Domenico Accili
doi:10.1038/3112
Abstract | Full text | PDF (339K)
See also: News and Views by Kahn & Rossetti
Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction pp299 - 303
Nahid G. Robertson, Leonard Lu, Stefan Heller, Saumil N. Merchant, Roland D. Eavey, Michael McKenna, Joseph B. Nadol Jr, Richard T. Miyamoto, Frederick H. Linthicum Jr, José F. Lubianca Neto, A.J. Hudspeth, Christine E. Seidman, Cynthia C. Morton & J.G. Seidman
doi:10.1038/3118
Abstract | Full text | PDF (232K)
A genome-wide scan for human obesity genes reveals a major susceptibility locus on chromosome 10 pp304 - 308
Jörg Hager, Christian Dina, Stephan Francke, Severine Dubois, Mouna Houari, Vincent Vatin, Emmanuel Vaillant, Nathalie Lorentz, Arnaud Basdevant, Karine Clement, Bernard Guy-Grand & Philippe Froguel
doi:10.1038/3123
Abstract | Full text | PDF (886K)
Esx1 is an X-chromosome-imprinted regulator of placental development and fetal growth pp309 - 311
Yuanhao Li & Richard R. Behringer
doi:10.1038/3129
Abstract | Full text | PDF (263K)
Errata Top
Assignment of Tangier disease to chromosome 9q31 by a graphical linkage exclusion strategy p312
Stephan Rust et al.
doi:10.1038/3134
Full text | PDF (273K)
Inversin, a novel gene in the vertebrate left-right axis pathway, is partially deleted in the inv mouse p312
David Morgan et al.
doi:10.1038/3136
Full text | PDF (273K)
  Top
 
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Nature Genetics
ISSN: 1061-4036
EISSN: 1546-1718
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