DSPP mutation in dentinogenesis imperfecta Shields type IIpp151 - 152 Xiaohai Zhang, Jun Zhao, Changfu Li, Shan Gao, Changchun Qiu, Ping Liu, Guanyun Wu, Boqin Qiang, Wilson H.Y. Lo
& Yan Shen doi:10.1038/84765 Abstract|Full text|PDF
(944K)
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Epigenetic change in IGF2R is associated with fetal overgrowth after sheep embryo culturepp153 - 154 Lorraine E. Young, Kenneth Fernandes, Tom G. McEvoy, Simon C. Butterwith, Carlos G. Gutierrez, Catherine Carolan, Peter J. Broadbent, John J. Robinson, Ian Wilmut
& Kevin D. Sinclair doi:10.1038/84769 Abstract|Full text|PDF
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Great ape DNA sequences reveal a reduced diversity and an expansion in humanspp155 - 156 Henrik Kaessmann, Victor Wiebe, Gunter Weiss
& Svante Pääbo doi:10.1038/84773 Abstract|Full text|PDF
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Transgenic rescue of defective Cd36 ameliorates insulin resistance in spontaneously hypertensive ratspp156 - 158 Michal Pravenec, Vladimir Landa, Vaclav Zidek, Alena Musilova, Vladimir Kren, Ludmila Kazdova, Timothy J. Aitman, Anne M. Glazier, Azeddine Ibrahimi, Nada A. Abumrad, Nianning Qi, Jia-Ming Wang, Elizabeth M. St. Lezin
& Theodore W. Kurtz doi:10.1038/84777 Abstract|Full text|PDF
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The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndromepp159 - 166 Laura Crisponi, Manila Deiana, Angela Loi, Francesca Chiappe, Manuela Uda, Patrizia Amati, Luigi Bisceglia, Leopoldo Zelante, Ramaiah Nagaraja, Susanna Porcu, M. Serafina Ristaldi, Rosalia Marzella, Mariano Rocchi, Marc Nicolino, Anne Lienhardt-Roussie, Annie Nivelon, Alain Verloes, David Schlessinger, Paolo Gasparini, Dominique Bonneau, Antonio Cao
& Giuseppe Pilia doi:10.1038/84781 Abstract|Full text|PDF
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A candidate prostate cancer susceptibility gene at chromosome 17ppp172 - 180 Sean V. Tavtigian, Jacques Simard, David H.F. Teng, Vicki Abtin, Michelle Baumgard, Audrey Beck, Nicola J. Camp, Arlene R. Carillo, Yang Chen, Priya Dayananth, Marc Desrochers, Martine Dumont, James M. Farnham, David Frank, Cheryl Frye, Siavash Ghaffari, Jamila S. Gupte, Rong Hu, Diana Iliev, Teresa Janecki, Edward N. Kort, Kirsten E. Laity, Amber Leavitt, Gilles Leblanc, Jodi McArthur-Morrison, Amy Pederson, Brandon Penn, Kelly T. Peterson, Julia E. Reid, Sam Richards, Marianne Schroeder, Richard Smith, Sarah C. Snyder, Brad Swedlund, Jeff Swensen, Alun Thomas, Martine Tranchant, Ann-Marie Woodland, Fernand Labrie, Mark H. Skolnick, Susan Neuhausen, Johanna Rommens
& Lisa A. Cannon-Albright doi:10.1038/84808 Abstract|Full text|PDF
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Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron depositspp181 - 186 Hélène Puccio, Delphine Simon, Mireille Cossée, Paola Criqui-Filipe, Francesco Tiziano, Judith Melki, Colette Hindelang, Robert Matyas, Pierre Rustin
& Michel Koenig doi:10.1038/84818 Abstract|Full text|PDF
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Mammalian SWI/SNF complexes promote MyoD-mediated muscle differentiationpp187 - 190 Ivana L. de la Serna, Kerri A. Carlson
& Anthony N. Imbalzano doi:10.1038/84826 Abstract|Full text|PDF
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A nuclear-mitochondrial DNA interaction affecting hearing impairment in micepp191 - 194 Kenneth R. Johnson, Qing Y Zheng, Yelena Bykhovskaya, Olga Spirina
& Nathan Fischel-Ghodsian doi:10.1038/84831 Abstract|Full text|PDF
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Localized Igf-1 transgene expression sustains hypertrophy and regeneration in senescent skeletal musclepp195 - 200 Antonio Musarò, Karl McCullagh, Angelika Paul, Leslie Houghton, Gabriella Dobrowolny, Mario Molinaro, Elisabeth R. Barton, H. L Sweeney
& Nadia Rosenthal doi:10.1038/84839 Abstract|Full text|PDF
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Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPPpp201 - 204 Shangxi Xiao, Chuan Yu, Xueming Chou, Wenjuan Yuan, Ying Wang, Lei Bu, Gang Fu, Meiqian Qian, Jun Yang, Yaozhou Shi, Landian Hu, Bin Han, Zhengmin Wang, Wei Huang, Jing Liu, Zhu Chen, Guoping Zhao
& Xiangyin Kong doi:10.1038/84848 Abstract|Full text|PDF
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Regulation of glomerular basement membrane collagen expression by LMX1B contributes to renal disease in nail patella syndromepp205 - 208 Roy Morello, Guang Zhou, Sandra D. Dreyer, Scott J. Harvey, Yoshifumi Ninomiya, Paul S. Thorner, Jeffrey H. Miner, William Cole, Andreas Winterpacht, Bernhard Zabel, Kerby C. Oberg
& Brendan Lee doi:10.1038/84853 Abstract|Full text|PDF
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Targeted deletion of the gene encoding iron regulatory protein-2 causes misregulation of iron metabolism and neurodegenerative disease in micepp209 - 214 Timothy LaVaute, Sophia Smith, Sharon Cooperman, Kazuhiro Iwai, William Land, Esther Meyron-Holtz, Steven K. Drake, Georgina Miller, Mones Abu-Asab, Maria Tsokos, Robert Switzer III, Alexander Grinberg, Paul Love, Nancy Tresser
& Tracey A. Rouault doi:10.1038/84859 Abstract|Full text|PDF
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Promoter haplotype combinations of the platelet-derived growth factor -receptor gene predispose to human neural tube defectspp215 - 217 Paul H.L.J. Joosten, Mascha Toepoel, Edwin C.M. Mariman
& Everardus J.J. Van Zoelen doi:10.1038/84867 Abstract|Full text|PDF
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Linkage disequilibrium of a type 1 diabetes susceptibility locus with a regulatory IL12B allelepp218 - 221 Grant Morahan, Dexing Huang, Susie I. Ymer, Michael R. Cancilla, Katrina Stephen, Preeti Dabadghao, George Werther, Brian D. Tait, Leonard C. Harrison
& Peter G. Colman doi:10.1038/84872 Abstract|Full text|PDF
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-receptor gene predispose to human neural tube defects
