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Contents: Volume 15, Number 9, 1 May 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

Zheng-Hua Xie, Yan-Nv Huang, Zhao-Xia Chen, Arthur D. Riggs, Jian-Ping Ding, Humaira Gowher, Albert Jeltsch, Hiroyuki Sasaki, Kenichiro Hata, and Guo-Liang Xu
Mutations in DNA methyltransferase DNMT3B in ICF syndrome affect its regulation by DNMT3L
Human Molecular Genetics Advance Access published on March 16, 2006
Hum. Mol. Genet. 2006 15: 1375-1385; doi:10.1093/hmg/ddl059 [Abstract] [FREE Full Text] [PDF] [Supplementary Material] [Request Permissions]  

Caroline Kappeler, Yoann Saillour, Jean-Pierre Baudoin, Françoise Phan Dinh Tuy, Chantal Alvarez, Christophe Houbron, Patricia Gaspar, Ghislaine Hamard, Jamel Chelly, Christine Métin, and Fiona Francis
Branching and nucleokinesis defects in migrating interneurons derived from doublecortin knockout mice
Human Molecular Genetics Advance Access published on March 28, 2006
Hum. Mol. Genet. 2006 15: 1387-1400; doi:10.1093/hmg/ddl062 [Abstract] [FREE Full Text] [PDF] [Supplementary Material] [Request Permissions]  

Rita Neumann and Alec J. Jeffreys
Polymorphism in the activity of human crossover hotspots independent of local DNA sequence variation
Human Molecular Genetics Advance Access published on March 16, 2006
Hum. Mol. Genet. 2006 15: 1401-1411; doi:10.1093/hmg/ddl063 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Kathleen A. Williamson, Ann M. Hever, Joe Rainger, R. Curtis Rogers, Alex Magee, Zdenek Fiedler, Wee Teik Keng, Freddie H. Sharkey, Niolette McGill, Clare J. Hill, Adele Schneider, Mario Messina, Peter D. Turnpenny, Judy A. Fantes, Veronica van Heyningen, and David R. FitzPatrick
Mutations in SOX2 cause anophthalmia-esophageal-genital (AEG) syndrome
Human Molecular Genetics Advance Access published on March 16, 2006
Hum. Mol. Genet. 2006 15: 1413-1422; doi:10.1093/hmg/ddl064 [Abstract] [FREE Full Text] [PDF] [Supplementary Material] [Request Permissions]  

Joe V. Chakkalakal, Stephanie A. Michel, Eva R. Chin, Robin N. Michel, and Bernard J. Jasmin
Targeted inhibition of Ca2+/calmodulin signaling exacerbates the dystrophic phenotype in mdx mouse muscle
Human Molecular Genetics Advance Access published on March 21, 2006
Hum. Mol. Genet. 2006 15: 1423-1435; doi:10.1093/hmg/ddl065 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Maria Manczak, Thimmappa S. Anekonda, Edward Henson, Byung S. Park, Joseph Quinn, and P. Hemachandra Reddy
Mitochondria are a direct site of Aß accumulation in Alzheimer's disease neurons: implications for free radical generation and oxidative damage in disease progression
Human Molecular Genetics Advance Access published on March 21, 2006
Hum. Mol. Genet. 2006 15: 1437-1449; doi:10.1093/hmg/ddl066 [Abstract] [FREE Full Text] [PDF] [Supplementary Material] [Request Permissions]  

Jianqing Ding, Elizabeth Allen, Wei Wang, Angela Valle, Chengbiao Wu, Timothy Nardine, Bianxiao Cui, Jing Yi, Anne Taylor, Noo Li Jeon, Steven Chu, Yuen So, Hannes Vogel, Ravi Tolwani, William Mobley, and Yanmin Yang
Gene targeting of GAN in mouse causes a toxic accumulation of microtubule-associated protein 8 and impaired retrograde axonal transport
Human Molecular Genetics Advance Access published on March 24, 2006
Hum. Mol. Genet. 2006 15: 1451-1463; doi:10.1093/hmg/ddl069 [Abstract] [FREE Full Text] [PDF] [Supplementary Material] [Request Permissions]  

Andrew J. Streets, David J. Moon, Michelle E. Kane, Tomoko Obara, and Albert C.M. Ong
Identification of an N-terminal glycogen synthase kinase 3 phosphorylation site which regulates the functional localization of polycystin-2 in vivo and in vitro
Human Molecular Genetics Advance Access published on March 21, 2006
Hum. Mol. Genet. 2006 15: 1465-1473; doi:10.1093/hmg/ddl070 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Oliver Koch, Dominic P. Kwiatkowski, and Irina A. Udalova
Context-specific functional effects of IFNGR1 promoter polymorphism
Human Molecular Genetics Advance Access published on April 6, 2006
Hum. Mol. Genet. 2006 15: 1475-1481; doi:10.1093/hmg/ddl071 [Abstract] [FREE Full Text] [PDF] [Supplementary Material] [Request Permissions]  

Brian C. Kraemer, Jack K. Burgess, Jin H. Chen, James H. Thomas, and Gerard D. Schellenberg
Molecular pathways that influence human tau-induced pathology in Caenorhabditis elegans
Human Molecular Genetics Advance Access published on April 6, 2006
Hum. Mol. Genet. 2006 15: 1483-1496; doi:10.1093/hmg/ddl067 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Xiaoli Zhong, Jinrong R. Liu, John W. Kyle, Dorothy A. Hanck, and William S. Agnew
A profile of alternative RNA splicing and transcript variation of CACNA1H, a human T-channel gene candidate for idiopathic generalized epilepsies
Human Molecular Genetics Advance Access published on March 24, 2006
Hum. Mol. Genet. 2006 15: 1497-1512; doi:10.1093/hmg/ddl068 [Abstract] [FREE Full Text] [PDF] [Supplementary Material]   OPEN ACCESS ARTICLE  

Jeremy M. Van Raamsdonk, William T. Gibson, Jacqueline Pearson, Zoe Murphy, Ge Lu, Blair R. Leavitt, and Michael R. Hayden
Body weight is modulated by levels of full-length Huntingtin
Human Molecular Genetics Advance Access published on March 28, 2006
Hum. Mol. Genet. 2006 15: 1513-1523; doi:10.1093/hmg/ddl072 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Laetitia Davidovic, Elias Bechara, Maud Gravel, Xavier H. Jaglin, Sandra Tremblay, Attila Sik, Barbara Bardoni, and Edouard W. Khandjian
The nuclear MicroSpherule protein 58 is a novel RNA-binding protein that interacts with fragile X mental retardation protein in polyribosomal mRNPs from neurons
Human Molecular Genetics Advance Access published on March 28, 2006
Hum. Mol. Genet. 2006 15: 1525-1538; doi:10.1093/hmg/ddl074 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Howard J. Edenberg, Xiaoling Xuei, Hui-Ju Chen, Huijun Tian, Leah Flury Wetherill, Danielle M. Dick, Laura Almasy, Laura Bierut, Kathleen K. Bucholz, Alison Goate, Victor Hesselbrock, Samuel Kuperman, John Nurnberger, Bernice Porjesz, John Rice, Marc Schuckit, Jay Tischfield, Henri Begleiter, and Tatiana Foroud
Association of alcohol dehydrogenase genes with alcohol dependence: a comprehensive analysis
Human Molecular Genetics Advance Access published on March 28, 2006
Hum. Mol. Genet. 2006 15: 1539-1549; doi:10.1093/hmg/ddl073 [Abstract] [FREE Full Text] [PDF]   OPEN ACCESS ARTICLE  

Jamie Cameron, Øystein L. Holla, Trine Ranheim, Mari Ann Kulseth, Knut Erik Berge, and Trond P. Leren
Effect of mutations in the PCSK9 gene on the cell surface LDL receptors
Human Molecular Genetics Advance Access published on March 28, 2006
Hum. Mol. Genet. 2006 15: 1551-1558; doi:10.1093/hmg/ddl077 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

CORRIGENDA Back

Debra A. Thompson, Andreas R. Janecke, Jessica Lange, Kecia L. Feathers, Christian A. Hübner, Christina L. McHenry, David W. Stockton, Gabriele Rammesmayer, James R. Lupski, Guillermo Antinolo, Carmen Ayuso, Montserrat Baiget, Peter Gouras, John R. Heckenlively, Anneke den Hollander, Samuel G. Jacobson, Richard A. Lewis, Paul A. Sieving, Bernd Wissinger, Suzanne Yzer, Eberhart Zrenner, Gerd Utermann, and Andreas Gal
Retinal degeneration associated with RDH12 mutations results from decreased 11-cis retinal synthesis due to disruption of the visual cycle
Hum. Mol. Genet. 2006 15: 1559; doi:10.1093/hmg/ddl079 [Extract] [FREE Full Text] [PDF] [Request Permissions]  

Youssef A. Elhaji, Ileana Stoica, Sheldon Dennis, Enrico O. Purisima, Rose Lumbroso, Lenore K. Beitel, and Mark A. Trifiro
Impaired helix 12 dynamics due to proline 892 substitutions in the androgen receptor are associated with complete androgen insensitivity
Hum. Mol. Genet. 2006 15: 1561; doi:10.1093/hmg/ddl075 [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.