Human Molecular Genetics

ARTICLES:

Laura P. O'Neill, Tamzin E. Randall, Jayne Lavender, Hugh T. Spotswood, Jeannie T. Lee, and Bryan M. Turner

X-linked genes in female embryonic stem cells carry an epigenetic mark prior to the onset of X inactivation
Hum. Mol. Genet. 2003 12: 1783-1790; doi:10.1093/hmg/ddg193 [Abstract] [FREE Full Text] [PDF] [Supplementary Material] [Request Permissions]  

Satoshi Fujii, Robert Z. Luo, Jiuhong Yuan, Mitsutaka Kadota, Mitsuo Oshimura, Sharon R. Dent, Yutaka Kondo, Jean-Pierre J. Issa, Robert C. Bast, Jr, and Yinhua Yu

Reactivation of the silenced and imprinted alleles of ARHI is associated with increased histone H3 acetylation and decreased histone H3 lysine 9 methylation
Hum. Mol. Genet. 2003 12: 1791-1800; doi:10.1093/hmg/ddg204 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Bianca L. Gebski, Chrisopher J. Mann, Susan Fletcher, and Stephen D. Wilton

Morpholino antisense oligonucleotide induced dystrophin exon 23 skipping in mdx mouse muscle
Hum. Mol. Genet. 2003 12: 1801-1811; doi:10.1093/hmg/ddg196 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

John D. Porter, Anita P. Merriam, Patrick Leahy, Bendi Gong, and Sangeeta Khanna

Dissection of temporal gene expression signatures of affected and spared muscle groups in dystrophin-deficient (mdx) mice
Hum. Mol. Genet. 2003 12: 1813-1821; doi:10.1093/hmg/ddg197 [Abstract] [FREE Full Text] [PDF] [Supplementary Material] [Request Permissions]  

Elizabeth Spiteri, Melanie Babcock, Catherine D. Kashork, Keiko Wakui, Swarna Gogineni, Debbie A. Lewis, Kisa M. Williams, Shinsei Minoshima, Takashi Sasaki, Nobuyoshi Shimizu, Lorraine Potocki, Venkat Pulijaal, Alan Shanske, Lisa G. Shaffer, and Bernice E. Morrow

Frequent translocations occur between low copy repeats on chromosome 22q11.2 (LCR22s) and telomeric bands of partner chromosomes
Hum. Mol. Genet. 2003 12: 1823-1837; doi:10.1093/hmg/ddg203 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Jan-Willem Taanman, John R. Muddle, and Ania C. Muntau

Mitochondrial DNA depletion can be prevented by dGMP and dAMP supplementation in a resting culture of deoxyguanosine kinase-deficient fibroblasts
Hum. Mol. Genet. 2003 12: 1839-1845; doi:10.1093/hmg/ddg192 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

P. Castagnet, T. Mavlyutov, Y. Cai, F. Zhong, and P. Ferreira

RPGRIP1s with distinct neuronal localization and biochemical properties associate selectively with RanBP2 in amacrine neurons
Hum. Mol. Genet. 2003 12: 1847-1863; doi:10.1093/hmg/ddg202 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Florence Demenais, Timo Kanninen, Cecilia M. Lindgren, Steven Wiltshire, Stéphane Gaget, Candice Dandrieux, Peter Almgren, Marketa Sjögren, Andrew Hattersley, Christian Dina, Tiinamaija Tuomi, Mark I. McCarthy, Philippe Froguel, and Leif C. Groop

A meta-analysis of four European genome screens (GIFT Consortium) shows evidence for a novel region on chromosome 17p11.2–q22 linked to type 2 diabetes
Hum. Mol. Genet. 2003 12: 1865-1873; doi:10.1093/hmg/ddg195 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Qi Qian, Larry W. Hunter, Ming Li, Miguel Marin-Padilla, Y.S. Prakash, Stefan Somlo, Peter C. Harris, Vicente E. Torres, and Gary C. Sieck

Pkd2 haploinsufficiency alters intracellular calcium regulation in vascular smooth muscle cells
Hum. Mol. Genet. 2003 12: 1875-1880; doi:10.1093/hmg/ddg190 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Claus Rodemer, Thanh-Phuong Thai, Britta Brugger, Thomas Kaercher, Hauke Werner, Klaus-Armin Nave, Felix Wieland, Karin Gorgas, and Wilhelm W. Just

Inactivation of ether lipid biosynthesis causes male infertility, defects in eye development and optic nerve hypoplasia in mice
Hum. Mol. Genet. 2003 12: 1881-1895; doi:10.1093/hmg/ddg191 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Christine Baldeschi, Yannick Gache, Anke Rattenholl, Pascale Bouillé, Olivier Danos, Jean-Paul Ortonne, Leena Bruckner-Tuderman, and Guerrino Meneguzzi

Genetic correction of canine dystrophic epidermolysis bullosa mediated by retroviral vectors
Hum. Mol. Genet. 2003 12: 1897-1905; doi:10.1093/hmg/ddg200 [Abstract] [FREE Full Text] [PDF] [Supplementary Material] [Request Permissions]  

Jenny M. Ekholm, Tuula Kieseppä, Tero Hiekkalinna, Timo Partonen, Tiina Paunio, Markus Perola, Jesper Ekelund, Jouko Lönnqvist, Petra Pekkarinen-Ijäs, and Leena Peltonen

Evidence of susceptibility loci on 4q32 and 16p12 for bipolar disorder
Hum. Mol. Genet. 2003 12: 1907-1915; doi:10.1093/hmg/ddg199 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Ming-Jen Lee, Dennis A. Stephenson, Michael J. Groves, Mary G. Sweeney, Mary B. Davis, Shu-Fang An, Henry Houlden, Mustafa A. M. Salih, Vincent Timmerman, Peter de Jonghe, Michaela Auer-Grumbach, Emilio Di Maria, Francesco Scaravilli, Nicholas W. Wood, and Mary M. Reilly

Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4 ) gene
Hum. Mol. Genet. 2003 12: 1917-1925; doi:10.1093/hmg/ddg198 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Minjie Du, Linda G. Beatty, Wenjing Zhou, Jocelyne Lew, Christopher Schoenherr, Rosanna Weksberg, and Paul D. Sadowski

Insulator and silencer sequences in the imprinted region of human chromosome 11p15.5
Hum. Mol. Genet. 2003 12: 1927-1939; doi:10.1093/hmg/ddg194 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

CORRIGENDUM:

M. Talat Nasim, Tatyana K. Chernova, Hasnin M. Chowdhury, Bai-Gong Yue, and Ian C. Eperon

HnRNP G and Tra2ß: opposite effects on splicing matched by antagonism in RNA binding
Hum. Mol. Genet. 2003 12: 1941; doi:10.1093/hmg/ddg201 [Extract] [FREE Full Text] [PDF] [Request Permissions]  

Liang-Ping Weng, Jessica L. Brown, Kim M. Baker, Michael C. Ostrowski, and Charis Eng

PTEN blocks insulin-mediated ETS-2 phosphorylation through MAP kinase, independently of the phosphoinositide 3-kinase pathway
Hum. Mol. Genet. 2003 12: 1943; doi:10.1093/hmg/ddg186 [Extract] [FREE Full Text] [PDF] [Request Permissions]  

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