Colour-changing karyotyping: an alternative to M-FISH/SKYpp263 - 264 Octavian Henegariu, Nyla A. Heerema, Patricia Bray-Ward
& David C. Ward doi:10.1038/15437 Full text|PDF
(643K)
|Supplementary Information
Mutations in SLC4A4 cause permanent isolated proximal renal tubular
acidosis with ocular abnormalitiespp264 - 266 Takashi Igarashi, Jun Inatomi, Takashi Sekine, Seok Ho Cha, Yoshikatsu Kanai, Motoei Kunimi, Kazuhisa Tsukamoto, Hiroaki Satoh, Mitsunobu Shimadzu, Fumiko Tozawa, Tetsuo Mori, Masaaki Shiobara, George Seki
& Hitoshi Endou doi:10.1038/15440 Full text|PDF
(227K)
The DNA repair gene MBD4 (MED1) is mutated in human carcinomas
with microsatellite instabilitypp266 - 268 Antonio Riccio, Lauri A. Aaltonen, Andrew K. Godwin, Anu Loukola, Antonio Percesepe, Reijo Salovaara, Valeria Masciullo, Maurizio Genuardi, Maria Paravatou-Petsotas, Daniel E. Bassi, Bruce A. Ruggeri, Andres J.P. Klein-Szanto, Joseph R. Testa, Giovanni Neri
& Alfonso Bellacosa doi:10.1038/15443 Full text|PDF
(232K)
Scd1 is expressed in sebaceous glands and is disrupted in the
asebia mousepp268 - 270 Ying Zheng, Kenneth J. Eilertsen, Lan Ge, Lin Zhang, John P. Sundberg, Stephen M. Prouty, Kurt S. Stenn
& Satish Parimoo doi:10.1038/15446 Full text|PDF
(398K)
Fine-mapping of an ancestral recombination breakpoint in DCP1pp270 - 271 Martin Farrall, Bernard Keavney, Colin McKenzie, Marc Delépine, Fumihiko Matsuda
& G. Mark Lathrop doi:10.1038/15449 Full text|PDF
(95K)
Polymorphism in intron 4 of HFE does not compromise haemochromatosis
mutation resultsp271 Alison T. Merryweather-Clarke, Jennifer J. Pointon, Jeremy D. Shearman, Kathryn J.H. Robson, Anne Marie Jouanolle, Annick Mosser, Véronique David, Jean-Yves Le Gall, David J. Halsall, Terence S. Elsey, Alison Kelly, Timothy M. Cox, Michael Clare, Adrian Bomford, Jean Luc Vandwalle, Jacques Rochette, Nicolas Borot, Hélène Coppin, Marie-Paule Roth, Eleanor Ryan, John Crowe, Angela Totaro, Paolo Gasparini, Antonella Roetto, Clara Camaschella, Chris Darke, Daniel F. Wallace, Kasra Saeb-Parsy, James S. Dooley, Mark Worwood
& Ann P. Walker doi:10.1038/15452 Full text|PDF
(81K)
|Supplementary Information
Polymorphism in intron 4 of HFE does not compromise haemochromatosis
mutation resultspp271 - 272 Walter W. Noll, Dorothy R. Belloni, Timothy T. Stenzel
& Wayne W. Grody doi:10.1038/15722 Full text|PDF
(88K)
|Supplementary Information
Polymorphism in intron 4 of HFE does not compromise haemochromatosis
mutation resultsp272 Patricia S. Gomez, Sharie Parks, Rhonda Ries, Thuan C. Tran, Paul F. Gomez
& Richard D. Press doi:10.1038/15723 Full text|PDF
(77K)
Protecting communities in research: current guidelines and limits of extrapolationpp275 - 280 Charles Weijer, Gary Goldsand
& Ezekiel J. Emanuel doi:10.1038/15455 Abstract|Full text|PDF
(98K)
A RA-dependent, tumour-growth suppressive transcription complex is the target of the PML-RAR and T18 oncoproteinspp287 - 295 Sue Zhong, Laurent Delva, Christophe Rachez, Cristina Cenciarelli, Domenica Gandini, Hui Zhang, Sundeep Kalantry, Leonard P. Freedman
& Pier Paolo Pandolfi doi:10.1038/15463 Abstract|Full text|PDF
(1,169K)
Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegiapp296 - 303 Jamilé Hazan, Nùria Fonknechten, Delphine Mavel, Caroline Paternotte, Delphine Samson, François Artiguenave, Claire-Sophie Davoine, Corinne Cruaud, Alexandra Dürr, Patrick Wincker, Philippe Brottier, Laurence Cattolico, Valérie Barbe, Jean-Marc Burgunder, Jean-François Prud'homme, Alexis Brice, Bertrand Fontaine, Roland Heilig
& Jean Weissenbach doi:10.1038/15472 Abstract|Full text|PDF
(474K)
Differential methylation of genes and retrotransposons facilitates shotgun
sequencing of the maize genomepp305 - 308 Pablo D. Rabinowicz, Kristin Schutz, Neilay Dedhia, Cristina Yordan, Laurence D. Parnell, Lincoln Stein, W. Richard McCombie
& Robert A. Martienssen doi:10.1038/15479 Abstract|Full text|PDF
(502K)
A shotgun optical map of the entire Plasmodium falciparum genomepp309 - 313 Zhongwu Lai, Junping Jing, Christopher Aston, Virginia Clarke, Jennifer Apodaca, Eileen T. Dimalanta, Daniel J. Carucci, Malcolm J. Gardner, Bud Mishra, Thomas S. Anantharaman, Salvatore Paxia, Stephen L. Hoffman, J. Craig Venter, Edward J. Huff
& David C. Schwartz doi:10.1038/15484 Abstract|Full text|PDF
(1,417K)
CACP, encoding a secreted proteoglycan, is mutated in camptodactyly-arthropathy-coxa
vara-pericarditis syndromepp319 - 322 Jose Marcelino, John D. Carpten, Wafaa M. Suwairi, Orlando M. Gutierrez, Stuart Schwartz, Christiane Robbins, Raman Sood, Izabela Makalowska, Andy Baxevanis, Brian Johnstone, Ronald M. Laxer, Lawrence Zemel, Chong Ae Kim, J. Kenneth Herd, Johannes Ihle, Cal Williams, Mark Johnson, Vidya Raman, Luís Garcia Alonso, Decio Brunoni, Amy Gerstein, Nickolas Papadopoulos, Sultan A. Bahabri, Jeffrey M. Trent
& Matthew L. Warman doi:10.1038/15496 Abstract|Full text|PDF
(710K)
|Supplementary Information
Mutations in NEUROD1 are associated with the development of type
2 diabetes mellituspp323 - 328 Maciej T. Malecki, Ulupi S. Jhala, Anthony Antonellis, Liz Fields, Alessandro Doria, Tihamer Orban, Mohammed Saad, James H. Warram, Marc Montminy
& Andrzej S. Krolewski doi:10.1038/15500 Abstract|Full text|PDF
(247K)
The pallid gene encodes a novel, syntaxin 13-interacting protein involved in platelet storage pool deficiencypp329 - 332 Liping Huang, Yien-Ming Kuo
& Jane Gitschier doi:10.1038/15507 Abstract|Full text|PDF
(433K)
Fatal infantile cardioencephalomyopathy with COX deficiency and mutations
in SCO2, a COX assembly genepp333 - 337 Lefkothea C. Papadopoulou, Carolyn M. Sue, Mercy M. Davidson, Kurenai Tanji, Ichizo Nishino, James E. Sadlock, Sindu Krishna, Winsome Walker, Jeanette Selby, D. Moira Glerum, Rudy Van Coster, Gilles Lyon, Emmanuel Scalais, Roger Lebel, Paige Kaplan, Sara Shanske, Darryl C. De Vivo, Eduardo Bonilla, Michio Hirano, Salvatore DiMauro
& Eric A. Schon doi:10.1038/15513 Abstract|Full text|PDF
(1,264K)
Chimaeric mice deficient in dystroglycans develop muscular dystrophy
and have disrupted myoneural synapsespp338 - 342 Patrice D. Côté, Hakima Moukhles, Michael Lindenbaum
& Salvatore Carbonetto doi:10.1038/15519 Abstract|Full text|PDF
(1,205K)
See also:News and Views by Chamberlain
A humanized model for multiple sclerosis using HLA-DR2 and a human T-cell
receptorpp343 - 347 Lars S. Madsen, Ellen Christina Andersson, Liselotte Jansson, Michelle Krogsgaard, Claus B. Andersen, Jan Engberg, Jack L. Strominger, Arne Svejgaard, Jens Peter Hjorth, Rikard Holmdahl, Kai W. Wucherpfennig
& Lars Fugger doi:10.1038/15525 Abstract|Full text|PDF
(1,090K)
See also:News and Views by Ebers
Leukaemia disease genes: large-scale cloning and pathway predictionspp348 - 353 Jiayin Li, Haifa Shen, Karen L. Himmel, Adam J. Dupuy, David A. Largaespada, Takuro Nakamura, John D. Shaughnessy Jr, Nancy A. Jenkins
& Neal G. Copeland doi:10.1038/15531 Abstract|Full text|PDF
(135K)
Perlecan is essential for cartilage and cephalic developmentpp354 - 358 Eri Arikawa-Hirasawa, Hideto Watanabe, Hiroya Takami, John R. Hassell
& Yoshihiko Yamada doi:10.1038/15537 Abstract|Full text|PDF
(1,344K)
HNPCC-like cancer predisposition in mice through simultaneous loss of
Msh3 and Msh6 mismatch-repair protein functionspp359 - 362 Niels de Wind, Marleen Dekker, Nanna Claij, Léon Jansen, Yvonne van Klink, Miroslav Radman, Greg Riggins, Martin van der Valk, Karin van 't Wout
& Hein te Riele doi:10.1038/15544 Abstract|Full text|PDF
(396K)
Mammalian (cytosine-5) methyltransferases cause genomic DNA methylation
and lethality in Drosophilapp363 - 366 Frank Lyko, Bernard H. Ramsahoye, Helena Kashevsky, Matthew Tudor, Mary-Ann Mastrangelo, Terry L. Orr-Weaver
& Rudolf Jaenisch doi:10.1038/15551 Abstract|Full text|PDF
(418K)
Meiotic instability of human minisatellite CEB1 in yeast requires
DNA double-strand breakspp367 - 371 Hélène Debrauwère, Jérôme Buard, Jacques Tessier, Dominique Aubert, Gilles Vergnaud
& Alain Nicolas doi:10.1038/15557 Abstract|Full text|PDF
(272K)
|Supplementary Information
Characterization of single-nucleotide polymorphisms in coding regions of human genesp373 Michele Cargill doi:10.1038/15564 Full text|PDF
(68K)
Griscelli disease maps to chromocome 15q and is associated with mutations in the Myosin-Va genep373 Elodie Pastural doi:10.1038/15565 Full text|PDF
(68K)
Suppression of the novel growth inhibitor p33ING1 promotes
neoplastic transformationp373 Igor Garkavtsev doi:10.1038/15566 Full text|PDF
(68K)
and T18 oncoproteins
