Conditional deletion of Xist disrupts histone macroH2A localization
but not maintenance of X inactivationpp323 - 324 Györgyi Csankovszki, Barbara Panning, Brian Bates, John R. Pehrson
& Rudolf Jaenisch doi:10.1038/11887 Full text|PDF
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Transmission ratio distortion at the INS-IGF2 VNTRpp324 - 325 Iain A. Eaves, Simon T. Bennett, Peter Forster, Karin M. Ferber, David Ehrmann, Amanda J. Wilson, Sumit Bhattacharyya, Anette-G. Ziegler, Bernd Brinkmann
& John A. Todd doi:10.1038/11890 Full text|PDF
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Polymorphism in intron 4 of HFE may cause overestimation of C282Y homozygote prevalence in haemochromatosispp325 - 326 Gary P. Jeffrey, Subrata Chakrabarti, Robert A. Hegele
& Paul C. Adams doi:10.1038/11892 Full text|PDF
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FDA comments on phase I clinical trials without vector biodistribution datap326 Suzanne Epstein, Steven Bauer, Andra Miller, Anne Pilaro
& Philip Noguchi doi:10.1038/11895 Full text|PDF
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BAC-mediated gene-dosage analysis reveals a role for Zipro1 (Ru49/Zfp38) in progenitor cell proliferation in cerebellum and
skinpp327 - 335 Xiangdong W. Yang, Christopher Wynder, Martin L. Doughty
& Nathaniel Heintz doi:10.1038/11896 Abstract|Full text|PDF
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Mutations in ABC1 in Tangier disease and familial high-density
lipoprotein deficiencypp336 - 345 Angela Brooks-Wilson, Michel Marcil, Susanne M. Clee, Lin-Hua Zhang, Kirsten Roomp, Marjel van Dam, Lu Yu, Carl Brewer, Jennifer A. Collins, Henri O.F. Molhuizen, Odell Loubser, B.F. Francis Ouelette, Keith Fichter, Katherine J.D. Ashbourne-Excoffon, Christoph W. Sensen, Stephen Scherer, Stephanie Mott, Maxime Denis, Duane Martindale, Jiri Frohlich, Kenneth Morgan, Ben Koop, Simon Pimstone, John J.P. Kastelein, Jacques Genest Jr
& Michael R. Hayden doi:10.1038/11905 Abstract|Full text|PDF
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The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier
diseasepp347 - 351 Marek Bodzioch, Evelyn Orsó, Jochen Klucken, Thomas Langmann, Alfred Böttcher, Wendy Diederich, Wolfgang Drobnik, Stefan Barlage, Christa Büchler, Mustafa Porsch-Özcürümez, Wolfgang E. Kaminski, Harry W. Hahmann, Kurt Oette, Gregor Rothe, Charalampos Aslanidis, Karl J. Lackner
& Gerd Schmitz doi:10.1038/11914 Abstract|Full text|PDF
(507K)
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Tangier disease is caused by mutations in the gene encoding ATP-binding
cassette transporter 1pp352 - 355 Stephan Rust, Marie Rosier, Harald Funke, José Real, Zahir Amoura, Jean-Charles Piette, Jean-Francois Deleuze, H. Bryan Brewer, Nicolas Duverger, Patrice Denèfle
& Gerd Assmann doi:10.1038/11921 Abstract|Full text|PDF
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Klf4 is a transcription factor required for establishing the barrier function of the skinpp356 - 360 Julia A. Segre, Christoph Bauer
& Elaine Fuchs doi:10.1038/11926 Abstract|Full text|PDF
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Requirement for Wnt3 in vertebrate axis formationpp361 - 365 Pentao Liu, Maki Wakamiya, Martin J. Shea, Urs Albrecht, Richard R. Behringer
& Allan Bradley doi:10.1038/11932 Abstract|Full text|PDF
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Mutations in the human homologue of mouse dl cause autosomal recessive
and dominant hypohidrotic ectodermal dysplasiapp366 - 369 Alex W. Monreal, Betsy M. Ferguson, Denis J. Headon, Summer L. Street, Paul A. Overbeek
& Jonathan Zonana doi:10.1038/11937 Abstract|Full text|PDF
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Engineering a mouse balancer chromosomepp375 - 378 Binhai Zheng, Marijke Sage, Wei-Wen Cai, Debrah M. Thompson, Beril C. Tavsanli, Yin-Chai Cheah
& Allan Bradley doi:10.1038/11949 Abstract|Full text|PDF
(406K)
Spontaneous functional correction of homozygous Fanconi anaemia alleles reveals novel mechanistic basis for reverse mosaicismpp379 - 383 Quinten Waisfisz, Neil V. Morgan, Maria Savino, Johan P. de Winter, Carola G.M. van Berkel, Maureen E. Hoatlin, Leonarda Ianzano, Rachel A. Gibson, Fre Arwert, Anna Savoia, Christopher G. Mathew, Jan C. Pronk
& Hans Joenje doi:10.1038/11956 Abstract|Full text|PDF
(219K)
Radiation hybrid map of the mouse genomepp384 - 387 William J. Van Etten, Robert G. Steen, Huy Nguyen, Andrew B. Castle, Donna K. Slonim, Bing Ge, Chad Nusbaum, Greg D. Schuler, Eric S. Lander
& Thomas J. Hudson doi:10.1038/11962 Abstract|Full text|PDF
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A YAC-based physical map of the mouse genomepp388 - 393 Chad Nusbaum, Donna K. Slonim, Katrina L. Harris, Bruce W. Birren, Robert G. Steen, Lincoln D. Stein, Joyce Miller, William F. Dietrich, Robert Nahf, Victoria Wang, Olga Merport, Andrew B. Castle, Zeeshan Husain, Gail Farino, Delphine Gray, Mechele O. Anderson, Richard Devine, Lloyd T. Horton Jr, Wenjuan Ye, Xiaoyun Wu, Vardouhie Kouyoumjian, Irina S. Zemsteva, Yi Wu, Alville J. Collymore, Dorothy F. Courtney, James Tam, Matthew Cadman, Andrew R. Haynes, Christine Heuston, Tracy Marsland, Anne Southwell, Pamela Trickett, Mark A. Strivens, Mark T. Ross, Wojciech Makalowski, Yixun Xu, Mark S. Boguski, Nigel P. Carter, Paul Denny, Steve D.M. Brown, Thomas J. Hudson
& Eric S. Lander doi:10.1038/11967 Abstract|Full text|PDF
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RLIM inhibits functional activity of LIM homeodomain transcription factors
via recruitment of the histone deacetylase complexpp394 - 399 Ingolf Bach, Concepción Rodriguez-Esteban, Catherine Carrière, Anil Bhushan, Anna Krones, David W. Rose, Christopher K. Glass, Bogi Andersen, Juan Carlos Izpisúa Belmonte
& Michael G. Rosenfeld doi:10.1038/11970 Abstract|Full text|PDF
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Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tardapp400 - 404 Ági K. Gedeon, Alison Colley, Robyn Jamieson, Elizabeth M. Thompson, John Rogers, David Sillence, George E. Tiller, John C. Mulley
& Jozef Gécz doi:10.1038/11976 Abstract|Full text|PDF
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Sry requires a CAG repeat domain for male sex determination in Mus musculuspp405 - 408 Josephine Bowles, Leanne Cooper, Jennifer Berkman
& Peter Koopman doi:10.1038/11981 Abstract|Full text|PDF
(433K)
