Human Molecular Genetics

ARTICLES:

Gabriele Duetsch, Thomas Illig, Sabine Loesgen, Klaus Rohde, Norman Klopp, Nicole Herbon, Henning Gohlke, Janine Altmueller, and Matthias Wjst

STAT6 as an asthma candidate gene: polymorphism-screening, association and haplotype analysis in a Caucasian sib-pair study
Hum. Mol. Genet. 2002 11: 613-621; doi:10.1093/hmg/11.6.613 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Edwin K. Silverman, Jonathan D. Mosley, Lyle J. Palmer, Matthew Barth, Jody M. Senter, Alison Brown, Jeffrey M. Drazen, David J. Kwiatkowski, Harold A. Chapman, Edward J. Campbell, Michael A. Province, D. C. Rao, John J. Reilly, Leo C. Ginns, Frank E. Speizer, and Scott T. Weiss

Genome-wide linkage analysis of severe, early-onset chronic obstructive pulmonary disease: airflow obstruction and chronic bronchitis phenotypes
Hum. Mol. Genet. 2002 11: 623-632; doi:10.1093/hmg/11.6.623 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Vanessa C. Wheeler, Claire-Anne Gutekunst, Vladimir Vrbanac, Lori-Anne Lebel, Gabriele Schilling, Steven Hersch, Robert M. Friedlander, James F. Gusella, Jean-Paul Vonsattel, David R. Borchelt, and Marcy E. MacDonald

Early phenotypes that presage late-onset neurodegenerative disease allow testing of modifiers in Hdh CAG knock-in mice
Hum. Mol. Genet. 2002 11: 633-640; doi:10.1093/hmg/11.6.633 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Daniëlle Bodmer, Marc Eleveld, Ellen Kater-Baats, Irene Janssen, Bert Janssen, Marian Weterman, Eric Schoenmakers, Michael Nickerson, Marston Linehan, Berton Zbar, and Ad Geurts van Kessel

Disruption of a novel MFS transporter gene, DIRC2, by a familial renal cell carcinoma-associated t(2;3)(q35;q21)
Hum. Mol. Genet. 2002 11: 641-649; doi:10.1093/hmg/11.6.641 [Abstract] [FREE Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Jian-Kan Guo, Aswin L. Menke, Marie-Claire Gubler, Alan R. Clarke, David Harrison, Annette Hammes, Nicholas D. Hastie, and Andreas Schedl

WT1 is a key regulator of podocyte function: reduced expression levels cause crescentic glomerulonephritis and mesangial sclerosis
Hum. Mol. Genet. 2002 11: 651-659; doi:10.1093/hmg/11.6.651 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Asem Alkhateeb, Gary L. Stetler, William Old, Janet Talbert, Cynthia Uhlhorn, Melanie Taylor, Angela Fox, Cynthia Miller, Diana G. Dills, E. Chester Ridgway, Dorothy C. Bennett, Pamela R. Fain, and Richard A. Spritz

Mapping of an autoimmunity susceptibility locus (AIS1) to chromosome 1p31.3–p32.2
Hum. Mol. Genet. 2002 11: 661-667; doi:10.1093/hmg/11.6.661 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Alexey S. Kondrashov and Svetlana A. Shabalina

Classification of common conserved sequences in mammalian intergenic regions
Hum. Mol. Genet. 2002 11: 669-674; doi:10.1093/hmg/11.6.669 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Pierre-François Cartron, Lisa Oliver, Stéphane Martin, Carole Moreau, Marie-Thérèse LeCabellec, Pascal Jezequel, Khaled Meflah, and François M. Vallette

The expression of a new variant of the pro-apoptotic molecule Bax, Bax, is correlated with an increased survival of glioblastoma multiforme patients
Hum. Mol. Genet. 2002 11: 675-687; doi:10.1093/hmg/11.6.675 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Bernie Devlin, Silviu-Alin Bacanu, Kelly L. Klump, Cynthia M. Bulik, Manfred M. Fichter, Katherine A. Halmi, Allan S. Kaplan, Michael Strober, Janet Treasure, D. Blake Woodside, Wade H. Berrettini, and Walter H. Kaye

Linkage analysis of anorexia nervosa incorporating behavioral covariates
Hum. Mol. Genet. 2002 11: 689-696; doi:10.1093/hmg/11.6.689 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Qing Zhang, Wei Li, Edward K. Novak, Amna Karim, Vishnu S. Mishra, Stephen F. Kingsmore, Bruce A. Roe, Tamio Suzuki, and Richard T. Swank

The gene for the muted (mu) mouse, a model for Hermansky–Pudlak syndrome, defines a novel protein which regulates vesicle trafficking
Hum. Mol. Genet. 2002 11: 697-706; doi:10.1093/hmg/11.6.697 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Jayne C. Boyer, Nazumi A. Yamada, C. Natalia Roques, Stephanie B. Hatch, Kevin Riess, and Rosann A. Farber

Sequence dependent instability of mononucleotide microsatellites in cultured mismatch repair proficient and deficient mammalian cells
Hum. Mol. Genet. 2002 11: 707-713; doi:10.1093/hmg/11.6.707 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Inés Ibañez-Tallon, Svetlana Gorokhova, and Nathaniel Heintz

Loss of function of axonemal dynein Mdnah5 causes primary ciliary dyskinesia and hydrocephalus
Hum. Mol. Genet. 2002 11: 715-721; doi:10.1093/hmg/11.6.715 [Abstract] [FREE Full Text] [PDF] [Supplementary Data] [Request Permissions]  

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