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Contents: Volume 17, Number 17, 1 September 2008   [Index by Author] 

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ARTICLES Back

Jie Lian, Yimeng Yin, Maria Oliver-Bonet, Thomas Liehr, Evelyn Ko, Paul Turek, Fei Sun, and Renée H. Martin
Variation in crossover interference levels on individual chromosomes from human males
Human Molecular Genetics Advance Access published on May 23, 2008
Hum. Mol. Genet. 2008 17: 2583-2594; doi:10.1093/hmg/ddn158 [Abstract] [Full Text] [PDF] [Request Permissions]  

Felix J. Bode, Michael Stephan, Hendrik Suhling, Reinhard Pabst, Rainer H. Straub, Kerstin A. Raber, Michael Bonin, Huu Phuc Nguyen, Olaf Riess, Andreas Bauer, Charlotte Sjoberg, Åsa Petersén, and Stephan von Hörsten
Sex differences in a transgenic rat model of Huntington's disease: decreased 17β-estradiol levels correlate with reduced numbers of DARPP32+ neurons in males
Human Molecular Genetics Advance Access published on May 23, 2008
Hum. Mol. Genet. 2008 17: 2595-2609; doi:10.1093/hmg/ddn159 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Alessandro Fraldi, Ester Zito, Fabio Annunziata, Alessia Lombardi, Marianna Cozzolino, Maria Monti, Carmine Spampanato, Andrea Ballabio, Piero Pucci, Roberto Sitia, and Maria Pia Cosma
Multistep, sequential control of the trafficking and function of the multiple sulfatase deficiency gene product, SUMF1 by PDI, ERGIC-53 and ERp44
Human Molecular Genetics Advance Access published on May 28, 2008
Hum. Mol. Genet. 2008 17: 2610-2621; doi:10.1093/hmg/ddn161 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Mohammad M. Ghahramani Seno, Ian R. Graham, Takis Athanasopoulos, Capucine Trollet, Marita Pohlschmidt, Mark R. Crompton, and George Dickson
RNAi-mediated knockdown of dystrophin expression in adult mice does not lead to overt muscular dystrophy pathology
Human Molecular Genetics Advance Access published on May 28, 2008
Hum. Mol. Genet. 2008 17: 2622-2632; doi:10.1093/hmg/ddn162 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Yoko Ito, Thibaud Koessler, Ashraf E.K. Ibrahim, Sushma Rai, Sarah L. Vowler, Sayeda Abu-Amero, Ana-Luisa Silva, Ana-Teresa Maia, Joanna E. Huddleston, Santiago Uribe-Lewis, Kathryn Woodfine, Maja Jagodic, Raffaella Nativio, Alison Dunning, Gudrun Moore, Elena Klenova, Sheila Bingham, Paul D.P. Pharoah, James D. Brenton, Stephan Beck, Manjinder S. Sandhu, and Adele Murrell
Somatically acquired hypomethylation of IGF2 in breast and colorectal cancer
Human Molecular Genetics Advance Access published on June 9, 2008
Hum. Mol. Genet. 2008 17: 2633-2643; doi:10.1093/hmg/ddn163 [Abstract] [FREE Full Text] [PDF] [Supplementary Data]   OPEN ACCESS ARTICLE  

Sibel Aylin Ugur and Aslihan Tolun
Homozygous WNT10b mutation and complex inheritance in Split-Hand/Foot Malformation
Human Molecular Genetics Advance Access published on May 30, 2008
Hum. Mol. Genet. 2008 17: 2644-2653; doi:10.1093/hmg/ddn164 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Ye-Guang Hu, Ryutaro Hirasawa, Jia-Lei Hu, Kenichiro Hata, Chun-Liang Li, Ying Jin, Taiping Chen, En Li, Muriel Rigolet, Evani Viegas-Péquignot, Hiroyuki Sasaki, and Guo-Liang Xu
Regulation of DNA methylation activity through Dnmt3L promoter methylation by Dnmt3 enzymes in embryonic development
Human Molecular Genetics Advance Access published on June 10, 2008
Hum. Mol. Genet. 2008 17: 2654-2664; doi:10.1093/hmg/ddn165 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Sonja I. Berndt, John D. Potter, Aditi Hazra, Meredith Yeager, Gilles Thomas, Karen W. Makar, Robert Welch, Amanda J. Cross, Wen-Yi Huang, Robert E. Schoen, Edward Giovannucci, Andrew T. Chan, Stephen J. Chanock, Ulrike Peters, David J. Hunter, and Richard B. Hayes
Pooled analysis of genetic variation at chromosome 8q24 and colorectal neoplasia risk
Human Molecular Genetics Advance Access published on June 4, 2008
Hum. Mol. Genet. 2008 17: 2665-2672; doi:10.1093/hmg/ddn166 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Peter J. Francis, Binoy Appukuttan, Emily Simmons, Noelle Landauer, Jonathan Stoddard, Sara Hamon, Jurg Ott, Betsy Ferguson, Michael Klein, J. Timothy Stout, and Martha Neuringer
Rhesus monkeys and humans share common susceptibility genes for age-related macular disease
Human Molecular Genetics Advance Access published on June 4, 2008
Hum. Mol. Genet. 2008 17: 2673-2680; doi:10.1093/hmg/ddn167 [Abstract] [Full Text] [PDF] [Request Permissions]  

Max A. Seibold, Bin Wang, Celeste Eng, Gunjan Kumar, Kenneth B. Beckman, Saunak Sen, Shweta Choudhry, Kelley Meade, Michael Lenoir, H. Geoffrey Watson, Shannon Thyne, L. Keoki Williams, Rajesh Kumar, Kevin B. Weiss, Leslie C. Grammer, Pedro C. Avila, Robert P. Schleimer, Esteban González Burchard, and Robert Brenner
An african-specific functional polymorphism in KCNMB1 shows sex-specific association with asthma severity
Human Molecular Genetics Advance Access published on June 4, 2008
Hum. Mol. Genet. 2008 17: 2681-2690; doi:10.1093/hmg/ddn168 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Francois Gros-Louis, Jasna Kriz, Edor Kabashi, Jonathan McDearmid, Stéphanie Millecamps, Makoto Urushitani, Li Lin, Patrick Dion, Qinzhang Zhu, Pierre Drapeau, Jean-Pierre Julien, and Guy A. Rouleau
Als2 mRNA splicing variants detected in KO mice rescue severe motor dysfunction phenotype in Als2 knock-down zebrafish
Human Molecular Genetics Advance Access published on June 16, 2008
Hum. Mol. Genet. 2008 17: 2691-2702; doi:10.1093/hmg/ddn171 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Adèle Salin-Cantegrel, Masoud Shekarabi, Sébastien Holbert, Patrick Dion, Daniel Rochefort, Janet Laganière, Sandra Dacal, Pascale Hince, Liliane Karemera, Claudia Gaspar, Jean-Yves Lapointe, and Guy A. Rouleau
HMSN/ACC truncation mutations disrupt brain-type creatine kinase-dependant activation of K+/Cl co-transporter 3
Human Molecular Genetics Advance Access published on June 19, 2008
Hum. Mol. Genet. 2008 17: 2703-2711; doi:10.1093/hmg/ddn172 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Lisa M. Giles, Jue Chen, Lian Li, and Lih-Shen Chin
Dystonia-associated mutations cause premature degradation of torsinA protein and cell-type-specific mislocalization to the nuclear envelope
Human Molecular Genetics Advance Access published on June 14, 2008
Hum. Mol. Genet. 2008 17: 2712-2722; doi:10.1093/hmg/ddn173 [Abstract] [Full Text] [PDF] [Request Permissions]  

Silvia Vergarajauregui, Patricia S. Connelly, Mathew P. Daniels, and Rosa Puertollano
Autophagic dysfunction in mucolipidosis type IV patients
Human Molecular Genetics Advance Access published on June 11, 2008
Hum. Mol. Genet. 2008 17: 2723-2737; doi:10.1093/hmg/ddn174 [Abstract] [FREE Full Text] [PDF] [Supplementary Data]   OPEN ACCESS ARTICLE  

Chuan-En Wang, Suzanne Tydlacka, Adam L. Orr, Shang-Hsun Yang, Rona K. Graham, Michael R. Hayden, Shihua Li, Anthony W.S. Chan, and Xiao-Jiang Li
Accumulation of N-terminal mutant huntingtin in mouse and monkey models implicated as a pathogenic mechanism in Huntington's disease
Human Molecular Genetics Advance Access published on June 16, 2008
Hum. Mol. Genet. 2008 17: 2738-2751; doi:10.1093/hmg/ddn175 [Abstract] [Full Text] [PDF] [Supplementary Data] [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.