Genomics and future biological weapons: the need for preventive action by the biomedical communitypp253 - 256 Claire M. Fraser
& Malcolm R. Dando Published online: 22 October 2001|doi:10.1038/ng763 Abstract|Full text|PDF
(79K)
An Flp indicator mouse expressing alkaline phosphatase from the ROSA26 locuspp257 - 259 Rajeshwar Awatramani, Philippe Soriano, Jia Jia Mai
& Susan Dymecki doi:10.1038/ng1101-257 Full text|PDF
(2,957K)
|Supplementary Information
Mutations at the mitochondrial DNA polymerase (POLG) locus associated with male infertilitypp261 - 262 Anja T. Rovio, David R. Marchington, Susanne Donat, Hans-Christian Schuppe, Josef Abel, Ellen Fritsche, David J. Elliott, Pekka Laippala, Arja L. Ahola, David McNay, Robert F. Harrison, Barbara Hughes, Thomas Barrett, David M.D. Bailey, Denise Mehmet, Anne M. Jequier, Tim B. Hargreave, Shu-Huei Kao, James M. Cummins, David E. Barton, Howard J. Cooke, Yau-Huei Wei, Lars Wichmann, Joanna Poulton
& Howard T. Jacobs Published online: 22 October 2001|doi:10.1038/ng759 Abstract|Full text|PDF
(80K)
|Supplementary Information
Assembly of microarrays for genome-wide measurement of DNA copy numberpp263 - 264 Antoine M. Snijders, Norma Nowak, Richard Segraves, Stephanie Blackwood, Nils Brown, Jeffrey Conroy, Greg Hamilton, Anna Katherine Hindle, Bing Huey, Karen Kimura, Sindy Law, Ken Myambo, Joel Palmer, Bauke Ylstra, Jingzhu Pearl Yue, Joe W. Gray, Ajay N. Jain, Daniel Pinkel
& Donna G. Albertson Published online: 30 October 2001|doi:10.1038/ng754 Abstract|Full text|PDF
(208K)
|Supplementary Information
Population genetic structure of variable drug responsepp265 - 269 James F. Wilson, Michael E. Weale, Alice C. Smith, Fiona Gratrix, Benjamin Fletcher, Mark G. Thomas, Neil Bradman
& David B. Goldstein Published online: 29 October 2001|doi:10.1038/ng761 Abstract|Full text|PDF
(144K)
See also:News and Views by McLeod
Mutant protein in Huntington disease is resistant to proteolysis in affected brainpp270 - 278 Roy B. Dyer
& Cynthia T. McMurray Published online: 15 October 2001|doi:10.1038/ng745 Abstract|Full text|PDF
(5,336K)
The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile menpp279 - 286 Tomoko Kuroda-Kawaguchi, Helen Skaletsky, Laura G. Brown, Patrick J. Minx, Holland S. Cordum, Robert H. Waterston, Richard K. Wilson, Sherman Silber, Robert Oates, Steve Rozen
& David C. Page Published online: 22 October 2001|doi:10.1038/ng757 Abstract|Full text|PDF
(559K)
|Supplementary Information See also:News and Views by Yen
MID1, mutated in Opitz syndrome, encodes an ubiquitin ligase that targets phosphatase 2A for degradationpp287 - 294 Alexander Trockenbacher, Vanessa Suckow, John Foerster, Jennifer Winter, Sybille Krau, Hans-Hilger Ropers, Rainer Schneider
& Susann Schweiger Published online: 29 October 2001|doi:10.1038/ng762 Abstract|Full text|PDF
(2,487K)
Bioinformatic identification of potential autocrine signaling loops in cancers from gene expression profilespp295 - 300 Thomas G. Graeber
& David Eisenberg Published online: 29 October 2001|doi:10.1038/ng755 Abstract|Full text|PDF
(122K)
|Supplementary Information
Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle−Wells syndromepp301 - 305 Hal M. Hoffman, James L. Mueller, David H. Broide, Alan A. Wanderer
& Richard D. Kolodner Published online: 22 October 2001|doi:10.1038/ng756 Abstract|Full text|PDF
(2,329K)
|Supplementary Information See also:News and Views by Kastner & O'Shea
Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failurepp310 - 314 Ralf Birkenhäger, Edgar Otto, Maria J. Schürmann, Martin Vollmer, Eva-Maria Ruf, Irina Maier-Lutz, Frank Beekmann, Andrea Fekete, Heymut Omran, Delphine Feldmann, David V. Milford, Nicola Jeck, Martin Konrad, Daniel Landau, Nine V.A.M. Knoers, Corinne Antignac, Ralf Sudbrak, Andreas Kispert
& Friedhelm Hildebrandt Published online: 22 October 2001|doi:10.1038/ng752 Abstract|Full text|PDF
(3,318K)
|Supplementary Information
Homozygous mutations in ARIX(PHOX2A) result in congenital fibrosis of the extraocular muscles type 2pp315 - 320 Motoi Nakano, Koki Yamada, Jennifer Fain, Emin C. Sener, Carol J. Selleck, Abdulaziz H. Awad, Johan Zwaan, Paul B. Mullaney, Thomas M. Bosley
& Elizabeth C. Engle Published online: 15 October 2001|doi:10.1038/ng744 Abstract|Full text|PDF
(719K)
|Supplementary Information
A 1.5 million−base pair inversion polymorphism in families with Williams-Beuren syndromepp321 - 325 Lucy R. Osborne, Martin Li, Barbara Pober, David Chitayat, Joann Bodurtha, Ariane Mandel, Teresa Costa, Theresa Grebe, Sarah Cox, Lap-Chee Tsui
& Stephen W. Scherer Published online: 29 October 2001|doi:10.1038/ng753 Abstract|Full text|PDF
(1,717K)
Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegiapp326 - 331 Xinping Zhao, David Alvarado, Shirley Rainier, Rosemary Lemons, Peter Hedera, Christian H. Weber, Turgut Tukel, Memnune Apak, Terry Heiman-Patterson, Lei Ming, Melanie Bui
& John K. Fink Published online: 29 October 2001|doi:10.1038/ng758 Abstract|Full text|PDF
(2,432K)
|Supplementary Information
Epigenetic silencing of CD4 in T cells committed to the cytotoxic lineagepp332 - 336 Yong-Rui Zou, Mary-Jean Sunshine, Ichiro Taniuchi, Farah Hatam, Nigel Killeen
& Dan R. Littman Published online: 22 October 2001|doi:10.1038/ng750 Abstract|Full text|PDF
(900K)
|Supplementary Information
The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNApp337 - 341 Hanna Mandel, Raymonde Szargel, Valentina Labay, Orly Elpeleg, Ann Saada, Adel Shalata, Yefim Anbinder, Drora Berkowitz, Corina Hartman, Mila Barak, Staffan Eriksson
& Nadine Cohen Published online: 22 October 2001|doi:10.1038/ng746 Abstract|Full text|PDF
(1,724K)
|Supplementary Information
Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathypp342 - 344 Ann Saada, Avraham Shaag, Hanna Mandel, Yoram Nevo, Staffan Eriksson
& Orly Elpeleg Published online: 22 October 2001|doi:10.1038/ng751 Abstract|Full text|PDF
(499K)
|Supplementary Information
Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locuspp345 - 349 Elisabeth Verpy, Saber Masmoudi, Ingrid Zwaenepoel, Michel Leibovici, Tim P. Hutchin, Ignacio Del Castillo, Sylvie Nouaille, Stéphane Blanchard, Sophie Lainé, Jean-Luc Popot, Felipe Moreno, Robert F. Mueller
& Christine Petit Published online: 10 September 2001|doi:10.1038/ng726 Abstract|Full text|PDF
(2,060K)
|Supplementary Information
TGF- signaling in tumor suppression and cancer progressionp351 doi:10.1038/ng1101-351 Full text|PDF
(44K)
A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2p352 doi:10.1038/ng1101-352a Full text|PDF
(33K)
The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosisp352 doi:10.1038/ng1101-352b Full text|PDF
(33K)
A radiation hybrid transcript map of the mouse genomep352 doi:10.1038/ng1101-352c Full text|PDF
(33K)
, Hans-Hilger Ropers, Rainer Schneider
& Susann Schweiger
signaling in tumor suppression and cancer progression
