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Previous Next 		Contents: Volume 15, Number 1, 1 January 2006   [Index by Author] 

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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.

ARTICLES Back

Ali Al-Zahrani, Manjinder S. Sandhu, Robert N. Luben, Deborah Thompson, Caroline Baynes, Karen A. Pooley, Craig Luccarini, Hannah Munday, Barbara Perkins, Paula Smith, Paul D.P. Pharoah, Nicholas J. Wareham, Douglas F. Easton, Bruce A.J. Ponder, and Alison M. Dunning
IGF1 and IGFBP3 tagging polymorphisms are associated with circulating levels of IGF1, IGFBP3 and risk of breast cancer
Human Molecular Genetics Advance Access published on November 23, 2005
Hum. Mol. Genet. 2006 15: 1-10; doi:10.1093/hmg/ddi398 [Abstract] [FREE Full Text] [PDF] [Supplementary Material] [Request Permissions]  

Erica Allen, Klaus B. Piontek, Elizabeth Garrett-Mayer, Miguel Garcia-Gonzalez, Kerry Lee Gorelick, and Gregory G. Germino
Loss of polycystin-1 or polycystin-2 results in dysregulated apolipoprotein expression in murine tissues via alterations in nuclear hormone receptors
Human Molecular Genetics Advance Access published on November 21, 2005
Hum. Mol. Genet. 2006 15: 11-21; doi:10.1093/hmg/ddi421 [Abstract] [FREE Full Text] [PDF] [Supplementary Material] [Request Permissions]  

Janet E. Davies, Sovan Sarkar, and David C. Rubinsztein
Trehalose reduces aggregate formation and delays pathology in a transgenic mouse model of oculopharyngeal muscular dystrophy
Human Molecular Genetics Advance Access published on November 25, 2005
Hum. Mol. Genet. 2006 15: 23-31; doi:10.1093/hmg/ddi422 [Abstract] [FREE Full Text] [PDF] [Supplementary Material] [Request Permissions]  

John S. Bett, Geoffrey M. Goellner, Ben Woodman, Gregory Pratt, Martin Rechsteiner, and Gillian P. Bates
Proteasome impairment does not contribute to pathogenesis in R6/2 Huntington's disease mice: exclusion of proteasome activator REG{gamma} as a therapeutic target
Human Molecular Genetics Advance Access published on November 25, 2005
Hum. Mol. Genet. 2006 15: 33-44; doi:10.1093/hmg/ddi423 [Abstract] [FREE Full Text] [PDF]   OPEN ACCESS ARTICLE  

Duncan M. Baird, Bethan Britt-Compton, Jan Rowson, Nazar N. Amso, Linda Gregory, and David Kipling
Telomere instability in the male germline
Human Molecular Genetics Advance Access published on November 25, 2005
Hum. Mol. Genet. 2006 15: 45-51; doi:10.1093/hmg/ddi424 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Caroline Sevin, Abdellatif Benraiss, Debby Van Dam, Delphine Bonnin, Guy Nagels, Lucie Verot, Ingrid Laurendeau, Michel Vidaud, Volkmar Gieselmann, Marie Vanier, Peter Paul De Deyn, Patrick Aubourg, and Nathalie Cartier
Intracerebral adeno-associated virus-mediated gene transfer in rapidly progressive forms of metachromatic leukodystrophy
Human Molecular Genetics Advance Access published on November 25, 2005
Hum. Mol. Genet. 2006 15: 53-64; doi:10.1093/hmg/ddi425 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Bo Wen Sun, A. Cong Yang, Yun Feng, Yi Juan Sun, Yu fei Zhu, Yi Zhang, Hua Jiang, Chun Liang Li, Fu Rong Gao, Zhi Hong Zhang, Wei Cheng Wang, Xiang Yin Kong, Gang Jin, Shi Jun Fu, and Ying Jin
Temporal and parental-specific expression of imprinted genes in a newly derived Chinese human embryonic stem cell line and embryoid bodies
Human Molecular Genetics Advance Access published on November 30, 2005
Hum. Mol. Genet. 2006 15: 65-75; doi:10.1093/hmg/ddi427 [Abstract] [FREE Full Text] [PDF] [Supplementary Material] [Request Permissions]  

Porat M. Erlich, Kathryn L. Lunetta, L. Adrienne Cupples, Matthew Huyck, Robert C. Green, Clinton T. Baldwin, and Lindsay A. Farrer for the MIRAGE Study Group
Polymorphisms in the PON gene cluster are associated with Alzheimer disease
Human Molecular Genetics Advance Access published on November 30, 2005
Hum. Mol. Genet. 2006 15: 77-85; doi:10.1093/hmg/ddi428 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

April Stetler, Claudia Winograd, Joyce Sayegh, Anne Cheever, Erin Patton, Xing Zhang, Steven Clarke, and Stephanie Ceman
Identification and characterization of the methyl arginines in the fragile X mental retardation protein Fmrp
Human Molecular Genetics Advance Access published on November 30, 2005
Hum. Mol. Genet. 2006 15: 87-96; doi:10.1093/hmg/ddi429 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Sakari Vanharanta, Patrick J. Pollard, Heli J. Lehtonen, Päivi Laiho, Jari Sjöberg, Arto Leminen, Kristiina Aittomäki, Johanna Arola, Mogens Kruhoffer, Torben F. Ørntoft, Ian P. Tomlinson, Maija Kiuru, Diego Arango, and Lauri A. Aaltonen
Distinct expression profile in fumarate-hydratase-deficient uterine fibroids
Human Molecular Genetics Advance Access published on November 30, 2005
Hum. Mol. Genet. 2006 15: 97-103; doi:10.1093/hmg/ddi431 [Abstract] [FREE Full Text] [PDF] [Supplementary Material] [Request Permissions]  

Peter Verheesen, Anna de Kluijver, Silvana van Koningsbruggen, Marjolein de Brij, Hans J. de Haard, Gert-Jan B. van Ommen, Silvère M. van der Maarel, and C. Theo Verrips
Prevention of oculopharyngeal muscular dystrophy-associated aggregation of nuclear poly(A)-binding protein with a single-domain intracellular antibody
Human Molecular Genetics Advance Access published on November 30, 2005
Hum. Mol. Genet. 2006 15: 105-111; doi:10.1093/hmg/ddi432 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Katsuhiko Togawa, Maki Moritani, Hiroshi Yaguchi, and Mitsuo Itakura
Multidimensional genome scans identify the combinations of genetic loci linked to diabetes-related phenotypes in mice
Human Molecular Genetics Advance Access published on December 1, 2005
Hum. Mol. Genet. 2006 15: 113-128; doi:10.1093/hmg/ddi433 [Abstract] [FREE Full Text] [PDF] [Supplementary Material]   OPEN ACCESS ARTICLE  

Delia J. Hernández-Deviez, Sally Martin, Steven H. Laval, Harriet P. Lo, Sandra T. Cooper, Kathryn N. North, Kate Bushby, and Robert G. Parton
Aberrant dysferlin trafficking in cells lacking caveolin or expressing dystrophy mutants of caveolin-3
Human Molecular Genetics Advance Access published on November 30, 2005
Hum. Mol. Genet. 2006 15: 129-142; doi:10.1093/hmg/ddi434 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Milana Koulintchenko, Richard J. Temperley, Penelope A. Mason, André Dietrich, and Robert N. Lightowlers
Natural competence of mammalian mitochondria allows the molecular investigation of mitochondrial gene expression
Human Molecular Genetics Advance Access published on December 1, 2005
Hum. Mol. Genet. 2006 15: 143-154; doi:10.1093/hmg/ddi435 [Abstract] [FREE Full Text] [PDF]   OPEN ACCESS ARTICLE  

James A. Traherne, Lisa F. Barcellos, Stephen J. Sawcer, Alastair Compston, Patricia P. Ramsay, Stephen L. Hauser, Jorge R. Oksenberg, and John Trowsdale
Association of the truncating splice site mutation in BTNL2 with multiple sclerosis is secondary to HLA-DRB1*15
Human Molecular Genetics Advance Access published on December 1, 2005
Hum. Mol. Genet. 2006 15: 155-161; doi:10.1093/hmg/ddi436 [Abstract] [FREE Full Text] [PDF]   OPEN ACCESS ARTICLE  

CORRIGENDUM Back

T. Hummelshoj, L. Munthe-Fog, H.O. Madsen, T. Fujita, M. Matsushita, and P. Garred
Polymorphisms in the FCN2 gene determine serum variation and function of Ficolin-2
Hum. Mol. Genet. 2006 15: 163-165; doi:10.1093/hmg/ddi437 [Extract] [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.