Human Molecular Genetics

ARTICLES:

Katherine Kaempchen, Kirsten Mielke, Tamara Utermark, Sonja Langmesser, and C. Oliver Hanemann

Upregulation of the Rac1/JNK signaling pathway in primary human schwannoma cells
Hum. Mol. Genet. 2003 12: 1211-1221; doi:10.1093/hmg/ddg146 [Abstract] [FREE Full Text] [PDF] [Supplementary Material] [Request Permissions]  

Frank P. Marx, Carsten Holzmann, Karsten M. Strauss, Lei Li, Olaf Eberhardt, Ellen Gerhardt, Mark R. Cookson, Dena Hernandez, Matt J. Farrer, Jennifer Kachergus, Simone Engelender, Christopher A. Ross, Klaus Berger, Ludger Schöls, Jörg B. Schulz, Olaf Riess, and Rejko Krüger

Identification and functional characterization of a novel R621C mutation in the synphilin-1 gene in Parkinson's disease
Hum. Mol. Genet. 2003 12: 1223-1231; doi:10.1093/hmg/ddg134 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Jeanne-Claire Lesbordes, Carmen Cifuentes-Diaz, Audrey Miroglio, Vandana Joshi, Thierry Bordet, Axel Kahn, and Judith Melki

Therapeutic benefits of cardiotrophin-1 gene transfer in a mouse model of spinal muscular atrophy
Hum. Mol. Genet. 2003 12: 1233-1239; doi:10.1093/hmg/ddg143 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

N.A. Alam, A.J. Rowan, N.C. Wortham, P.J. Pollard, M. Mitchell, J.P. Tyrer, E. Barclay, E. Calonje, S. Manek, S.J. Adams, P.W. Bowers, N.P. Burrows, R. Charles-Holmes, L.J. Cook, B.M. Daly, G.P. Ford, L.C. Fuller, S.E. Hadfield-Jones, N. Hardwick, A.S. Highet, M. Keefe, S.P. MacDonald-Hull, E.D.A. Potts, M. Crone, S. Wilkinson, F. Camacho-Martinez, S. Jablonska, R. Ratnavel, A. MacDonald, R.J. Mann, K. Grice, G. Guillet, M.S. Lewis-Jones, H. McGrath, D.C. Seukeran, P.J. Morrison, S. Fleming, S. Rahman, D. Kelsell, I. Leigh, S. Olpin, and I.P.M. Tomlinson

Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiency
Hum. Mol. Genet. 2003 12: 1241-1252; doi:10.1093/hmg/ddg148 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Yoshitaka Nagai, Nobuhiro Fujikake, Katsuhito Ohno, Hiroyuki Higashiyama, Helena A. Popiel, Julia Rahadian, Masamitsu Yamaguchi, Warren J. Strittmatter, James R. Burke, and Tatsushi Toda

Prevention of polyglutamine oligomerization and neurodegeneration by the peptide inhibitor QBP1 in Drosophila
Hum. Mol. Genet. 2003 12: 1253-1259; doi:10.1093/hmg/ddg144 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

R. David Hawkins, Stavros Bashiardes, Cynthia A. Helms, Lydia Hu, Nancy Lim Saccone, Mark E. Warchol, and Michael Lovett

Gene expression differences in quiescent versus regenerating hair cells of avian sensory epithelia: implications for human hearing and balance disorders
Hum. Mol. Genet. 2003 12: 1261-1272; doi:10.1093/hmg/ddg150 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Maolian Gong, Hongye Zhang, Herbert Schulz, Young-Ae Lee, Kai Sun, Sylvia Bähring, Friedrich C. Luft, Peter Nürnberg, André Reis, Klaus Rohde, Detlev Ganten, Rutai Hui, and Norbert Hübner

Genome-wide linkage reveals a locus for human essential (primary) hypertension on chromosome 12p
Hum. Mol. Genet. 2003 12: 1273-1277; doi:10.1093/hmg/ddg135 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Hyoung Doo Shin, Lyoung Hyo Kim, Byung Lae Park, Ji Hyun Jung, Jun Yeon Kim, Il-Yup Chung, Jung Sun Kim, June Hyuk Lee, Sun Hee Chung, Yong Hoon Kim, Hae-Sim Park, Jeong Hee Choi, Young Mok Lee, Sung Woo Park, Byoung Whui Choi, Soo-Jong Hong, and Choon-Sik Park

Association of Eotaxin gene family with asthma and serum total IgE
Hum. Mol. Genet. 2003 12: 1279-1285; doi:10.1093/hmg/ddg142 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Rénald Gilbert, Roy W. R. Dudley, An-Bang Liu, Basil J. Petrof, Josephine Nalbantoglu, and George Karpati

Prolonged dystrophin expression and functional correction of mdx mouse muscle following gene transfer with a helper-dependent (gutted) adenovirus-encoding murine dystrophin
Hum. Mol. Genet. 2003 12: 1287-1299; doi:10.1093/hmg/ddg141 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Ekaterina Semenova, XiaoFei Wang, Monica M. Jablonski, John Levorse, and Shirley M. Tilghman

An engineered 800 kilobase deletion of Uchl3 and Lmo7 on mouse chromosome 14 causes defects in viability, postnatal growth and degeneration of muscle and retina
Hum. Mol. Genet. 2003 12: 1301-1312; doi:10.1093/hmg/ddg140 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Ramil N. Nurtdinov, Irena I. Artamonova, Andrei A. Mironov, and Mikhail S. Gelfand

Low conservation of alternative splicing patterns in the human and mouse genomes
Hum. Mol. Genet. 2003 12: 1313-1320; doi:10.1093/hmg/ddg137 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Yosuke Ejima and Lichun Yang

Trans mobilization of genomic DNA as a mechanism for retrotransposon-mediated exon shuffling
Hum. Mol. Genet. 2003 12: 1321-1328; doi:10.1093/hmg/ddg138 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Yi Ning, Jing-fan Xu, Yu Li, Liz Chavez, Harold C. Riethman, Peter M. Lansdorp, and Nan-ping Weng

Telomere length and the expression of natural telomeric genes in human fibroblasts
Hum. Mol. Genet. 2003 12: 1329-1336; doi:10.1093/hmg/ddg139 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

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: 1337-1348; doi:10.1093/hmg/ddg136 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Frank J. Kaiser, Kamiab Tavassoli, Gert-Jan Van den Bemd, Glenn T.G. Chang, Bernhard Horsthemke, Tarik Möröy, and Hermann-Josef Lüdecke

Nuclear interaction of the dynein light chain LC8a with the TRPS1 transcription factor suppresses the transcriptional repression activity of TRPS1
Hum. Mol. Genet. 2003 12: 1349-1358; doi:10.1093/hmg/ddg145 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

CORRIGENDUM:

Sakae Ikeda, Leslie A. Cunningham, Dawnalyn Boggess, Craig D. Hobson, John P. Sundberg, Jürgen K. Naggert, Richard S. Smith, and Patsy M. Nishina

Aberrant actin cytoskeleton leads to accelerated proliferation of corneal epithelial cells in mice deficient for destrin (actin depolymerizing factor)
Hum. Mol. Genet. 2003 12: 1359; doi:10.1093/hmg/ddg154 [Extract] [FREE Full Text] [PDF] [Request Permissions]  

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