Human Molecular Genetics

ARTICLES:

Sophia Millington-Ward, Carolina Allers, Gearóid Tuohy, Paulette Conget, Danny Allen, Helena P. McMahon, Paul F. Kenna, Peter Humphries, and G. Jane Farrar

Validation in mesenchymal progenitor cells of a mutation-independent ex vivo approach to gene therapy for osteogenesis imperfecta
Hum. Mol. Genet. 2002 11: 2201-2206; doi:10.1093/hmg/11.19.2201 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Andrew D. Strand, James M. Olson, and Charles Kooperberg

Estimating the statistical significance of gene expression changes observed with oligonucleotide arrays
Hum. Mol. Genet. 2002 11: 2207-2221; doi:10.1093/hmg/11.19.2207 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Charles Kooperberg, Simonetta Sipione, Michael LeBlanc, Andrew D. Strand, Elena Cattaneo, and James M. Olson

Evaluating test statistics to select interesting genes in microarray experiments
Hum. Mol. Genet. 2002 11: 2223-2232; doi:10.1093/hmg/11.19.2223 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Elisa Fossale, Vanessa C. Wheeler, Vladimir Vrbanac, Lori-Anne Lebel, Allison Teed, Jayalakshmi S. Mysore, James F. Gusella, Marcy E. MacDonald, and Francesca Persichetti

Identification of a presymptomatic molecular phenotype in Hdh CAG knock-in mice
Hum. Mol. Genet. 2002 11: 2233-2241; doi:10.1093/hmg/11.19.2233 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Hélène Jacquet, Grégory Raux, Florence Thibaut, Bernadette Hecketsweiler, Emmanuelle Houy, Caroline Demilly, Sadeq Haouzir, Gabrielle Allio, Gael Fouldrin, Valérie Drouin, Jacqueline Bou, Michel Petit, Dominique Campion, and Thierry Frébourg

PRODH mutations and hyperprolinemia in a subset of schizophrenic patients
Hum. Mol. Genet. 2002 11: 2243-2249; doi:10.1093/hmg/11.19.2243 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

The Multiple Sclerosis Genetics Group, Jonathan L. Haines, Yuki Bradford, Melissa E. Garcia, Allison D. Reed, Elizabeth Neumeister, Margaret A. Pericak-Vance, Jacqueline B. Rimmler, Marissa M. Menold, Eden R. Martin, Jorge R. Oksenberg, Lisa F. Barcellos, Robin Lincoln, and Stephen L. Hauser

Multiple susceptibility loci for multiple sclerosis
Hum. Mol. Genet. 2002 11: 2251-2256; doi:10.1093/hmg/11.19.2251 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Janna Saarela, Marlena Schoenberg Fejzo, Daniel Chen, Saara Finnilä, Maikki Parkkonen, Satu Kuokkanen, Eric Sobel, Pentti J. Tienari, Marja-Liisa Sumelahti, Juhani Wikström, Irina Elovaara, Keijo Koivisto, Tuula Pirttilä, Mauri Reunanen, Aarno Palotie, and Leena Peltonen

Fine mapping of a multiple sclerosis locus to 2.5 Mb on chromosome 17q22–q24
Hum. Mol. Genet. 2002 11: 2257-2267; doi:10.1093/hmg/11.19.2257 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Michael Kressel and Beatrice Schmucker

Nucleocytoplasmic transfer of the NF2 tumor suppressor protein merlin is regulated by exon 2 and a CRM1-dependent nuclear export signal in exon 15
Hum. Mol. Genet. 2002 11: 2269-2278; doi:10.1093/hmg/11.19.2269 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Hiroko Kita, Jenny Carmichael, Jina Swartz, Shizuko Muro, Andreas Wyttenbach, Kenichi Matsubara, David C. Rubinsztein, and Kikuya Kato

Modulation of polyglutamine-induced cell death by genes identified by expression profiling
Hum. Mol. Genet. 2002 11: 2279-2287; doi:10.1093/hmg/11.19.2279 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Omar M.E. Albagha, Paul N. Tasker, Fiona E.A. McGuigan, David M. Reid, and Stuart H Ralston

Linkage disequilibrium between polymorphisms in the human TNFRSF1B gene and their association with bone mass in perimenopausal women
Hum. Mol. Genet. 2002 11: 2289-2295; doi:10.1093/hmg/11.19.2289 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Anna Buj-Bello, Denis Furling, Hélène Tronchère, Jocelyn Laporte, Thierry Lerouge, Gillian S. Butler-Browne, and Jean-Louis Mandel

Muscle-specific alternative splicing of myotubularin-related 1 gene is impaired in DM1 muscle cells
Hum. Mol. Genet. 2002 11: 2297-2307; doi:10.1093/hmg/11.19.2297 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Ivan P. Gorlov, Aparna Kamat, Natalia V. Bogatcheva, Eric Jones, Dolores J. Lamb, Anne Truong, Colin E. Bishop, Ken McElreavey, and Alexander I. Agoulnik

Mutations of the GREAT gene cause cryptorchidism
Hum. Mol. Genet. 2002 11: 2309-2318; doi:10.1093/hmg/11.19.2309 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Alka Saxena, Lee H. Wong, Paul Kalitsis, Elizabeth Earle, Lisa G. Shaffer, and K.H. Andy Choo

Poly(ADP-ribose) polymerase 2 localizes to mammalian active centromeres and interacts with PARP-1, Cenpa, Cenpb and Bub3, but not Cenpc
Hum. Mol. Genet. 2002 11: 2319-2329; doi:10.1093/hmg/11.19.2319 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Claudia E. Grubenmann, Christian G. Frank, Susanne Kjaergaard, Eric G. Berger, Markus Aebi, and Thierry Hennet

ALG12 mannosyltransferase defect in congenital disorder of glycosylation type lg
Hum. Mol. Genet. 2002 11: 2331-2339; doi:10.1093/hmg/11.19.2331 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

P. Jeremy Wang and David C. Page

Functional substitution for TAF_II250 by a retroposed homolog that is expressed in human spermatogenesis
Hum. Mol. Genet. 2002 11: 2341-2346; doi:10.1093/hmg/11.19.2341 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

To see an article, click its [Full Text] or [PDF] link. To review many abstracts, check the boxes to the left of the titles you want, and click the 'Get All Checked Abstract(s)' button. To see one abstract at a time, click its [Abstract] link.