The candidate spermatogenesis gene RBMY has a homologue on the human X chromosomepp223 - 224 Margaret L. Delbridge, Patricia A. Lingenfelter, Christine M. Disteche
& Jennifer A. Marshall Graves doi:10.1038/10279 Full text|PDF
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RBMY evolved on the Y chromosome from a ubiquitously transcribed X-Y identical genepp224 - 226 Sophie Mazeyrat, Noëmie Saut, Marie-Geneviève Mattei
& Michael J. Mitchell doi:10.1038/10282 Full text|PDF
(319K)
Absence of Cd36 mutation in the original spontaneously hypertensive rats with insulin resistancepp226 - 228 Takanari Gotoda, Yoko Iizuka, Norihiro Kato, Jun-ichi Osuga, Marie-Therese Bihoreau, Toru Murakami, Yukio Yamori, Hitoshi Shimano, Shun Ishibashi
& Nobuhiro Yamada doi:10.1038/10285 Full text|PDF
(128K)
Characterization of single-nucleotide polymorphisms in coding regions
of human genespp231 - 238 Michele Cargill, David Altshuler, James Ireland, Pamela Sklar, Kristin Ardlie, Nila Patil, Charles R. Lane, Esther P. Lim, Nilesh Kalyanaraman, James Nemesh, Liuda Ziaugra, Lisa Friedland, Alex Rolfe, Janet Warrington, Robert Lipshutz, George Q. Daley
& Eric S. Lander doi:10.1038/10290 Abstract|Full text|PDF
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Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure
homeostasispp239 - 247 Marc K. Halushka, Jian-Bing Fan, Kimberly Bentley, Linda Hsie, Naiping Shen, Alan Weder, Richard Cooper, Robert Lipshutz
& Aravinda Chakravarti doi:10.1038/10297 Abstract|Full text|PDF
(95K)
Mutations in a gene encoding a new oxygen-regulated photoreceptor protein
cause dominant retinitis pigmentosapp248 - 254 Eric A. Pierce, Tracey Quinn, Terrence Meehan, Terri L. McGee, Eliot L. Berson
& Thaddeus P. Dryja doi:10.1038/10305 Abstract|Full text|PDF
(632K)
Mutations in a novel retina-specific gene cause autosomal dominant retinitis
pigmentosapp255 - 259 Lori S. Sullivan, John R. Heckenlively, Sara J. Bowne, Jian Zuo, Winston A. Hide, Andreas Gal, Michael Denton, Chris F. Inglehearn, Susan H. Blanton
& Stephen P. Daiger doi:10.1038/10314 Abstract|Full text|PDF
(581K)
Regulation of anterior/posterior patterning of the axial skeleton by
growth/differentiation factor 11pp260 - 264 Alexandra C. McPherron, Ann M. Lawler
& Se-Jin Lee doi:10.1038/10320 Abstract|Full text|PDF
(2,346K)
A map for sequence analysis of the Arabidopsis thaliana genome
pp265 - 270 Marco Marra, Tamara Kucaba, Mandeep Sekhon, LaDeana Hillier, Robert Martienssen, Asif Chinwalla, Jye'mon Crockett, Jacqueline Fedele, Heather Grover, Christopher Gund, W. Richard McCombie, Ken McDonald, John McPherson, Nancy Mudd, Larry Parnell, Jacqueline Schein, Ryan Seim, Proteon Shelby, Robert Waterston
& Richard Wilson doi:10.1038/10327 Abstract|Full text|PDF
(317K)
See also:News and Views by Gibbs
A complete BAC-based physical map of the Arabidopsis thaliana genome
pp271 - 275 Teresa Mozo, Ken Dewar, Pat Dunn, Joseph R. Ecker, Sabine Fischer, Sebastian Kloska, Hans Lehrach, Marco Marra, Robert Martienssen, Sebastian Meier-Ewert
& Thomas Altmann doi:10.1038/10334 Abstract|Full text|PDF
(319K)
See also:News and Views by Gibbs
The lack of chromosomal protein Hmg1 does not disrupt cell growth but
causes lethal hypoglycaemia in newborn micepp276 - 280 Sabina Calogero, Fabio Grassi, Adriano Aguzzi, Till Voigtländer, Pierre Ferrier, Simona Ferrari
& Marco E. Bianchi doi:10.1038/10338 Abstract|Full text|PDF
(398K)
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Systematic determination of genetic network architecturepp281 - 285 Saeed Tavazoie, Jason D. Hughes, Michael J. Campbell, Raymond J. Cho
& George M. Church doi:10.1038/10343 Abstract|Full text|PDF
(836K)
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Mutations in a 8-7 sterol
isomerase in the tattered mouse and X-linked dominant chondrodysplasia punctata
pp286 - 290 Jonathan M.J. Derry, Emmanuelle Gormally, Gary D. Means, Wei Zhao, Alfons Meindl, Richard I. Kelley, Yvonne Boyd
& Gail E. Herman doi:10.1038/10350 Abstract|Full text|PDF
(410K)
Mutations in the gene encoding 3- hydroxysteroid-
8,7- isomerase cause X-linked
dominant Conradi-Hünermann syndromepp291 - 294 Nancy Braverman, Paul Lin, Fabian F. Moebius, Cassandra Obie, Ann Moser, Hartmut Glossmann, William R. Wilcox, David L. Rimoin, Moyra Smith, Lisa Kratz, Richard I. Kelley
& David Valle doi:10.1038/10357 Abstract|Full text|PDF
(237K)
Cryptorchidism in mice mutant for Insl3pp295 - 299 Serge Nef
& Luis F. Parada doi:10.1038/10364 Abstract|Full text|PDF
(1,830K)
Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia
associated with diabetes mellitus and deafnesspp300 - 304 Valentina Labay, Tal Raz, Dana Baron, Hanna Mandel, Hawys Williams, Timothy Barrett, Raymonde Szargel, Louise McDonald, Adel Shalata, Kazuto Nosaka, Simon Gregory
& Nadine Cohen doi:10.1038/10372 Abstract|Full text|PDF
(384K)
The gene mutated in thiamine-responsive anaemia with diabetes and deafness
(TRMA) encodes a functional thiamine transporterpp305 - 308 Judith C. Fleming, Elena Tartaglini, Mara P. Steinkamp, Daniel F. Schorderet, Nadine Cohen
& Ellis J. Neufeld doi:10.1038/10379 Abstract|Full text|PDF
(536K)
Mutations in a new gene encoding a thiamine transporter cause thiamine-responsive
megaloblastic anaemia syndromepp309 - 312 George A. Diaz, Maryam Banikazemi, Kimihiko Oishi, Robert J. Desnick
& Bruce D. Gelb doi:10.1038/10385 Abstract|Full text|PDF
(219K)
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