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Previous Next 		Contents: Volume 15, Number 10, 15 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

Katherine E. Burdick, Todd Lencz, Birgit Funke, Christine T. Finn, Philip R. Szeszko, John M. Kane, Raju Kucherlapati, and Anil K. Malhotra
Genetic variation in DTNBP1 influences general cognitive ability
Human Molecular Genetics Advance Access published on January 13, 2006
Hum. Mol. Genet. 2006 15: 1563-1568; doi:10.1093/hmg/ddi481 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Rector Arya, Ellen Demerath, Christopher P. Jenkinson, Harald H.H. Göring, Sobha Puppala, Vidya Farook, Sharon Fowler, Jennifer Schneider, Richard Granato, Roy G. Resendez, Thomas D. Dyer, Shelley A. Cole, Laura Almasy, Anthony G. Comuzzie, Roger M. Siervogel, Benjamin Bradshaw, Ralph A. DeFronzo, Jean MacCluer, Michael P. Stern, Bradford Towne, John Blangero, and Ravindranath Duggirala
A quantitative trait locus (QTL) on chromosome 6q influences birth weight in two independent family studies
Human Molecular Genetics Advance Access published on April 12, 2006
Hum. Mol. Genet. 2006 15: 1569-1579; doi:10.1093/hmg/ddl076 [Abstract] [FREE Full Text] [PDF]   OPEN ACCESS ARTICLE  

Sung-Jo Kim, Zhongjian Zhang, Yi-Ching Lee, and Anil B. Mukherjee
Palmitoyl-protein thioesterase-1 deficiency leads to the activation of caspase-9 and contributes to rapid neurodegeneration in INCL
Human Molecular Genetics Advance Access published on March 28, 2006
Hum. Mol. Genet. 2006 15: 1580-1586; doi:10.1093/hmg/ddl078 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Holly B. Kordasiewicz, Randall M. Thompson, H. Brent Clark, and Christopher M. Gomez
C-termini of P/Q-type Ca2+ channel {alpha}1A subunits translocate to nuclei and promote polyglutamine-mediated toxicity
Human Molecular Genetics Advance Access published on April 4, 2006
Hum. Mol. Genet. 2006 15: 1587-1599; doi:10.1093/hmg/ddl080 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Takahiro Yamada, Hisamitsu Ishihara, Akira Tamura, Rui Takahashi, Suguru Yamaguchi, Daisuke Takei, Ai Tokita, Chihiro Satake, Fumi Tashiro, Hideki Katagiri, Hiroyuki Aburatani, Jun-ichi Miyazaki, and Yoshitomo Oka
WFS1-deficiency increases endoplasmic reticulum stress, impairs cell cycle progression and triggers the apoptotic pathway specifically in pancreatic ß-cells
Human Molecular Genetics Advance Access published on March 28, 2006
Hum. Mol. Genet. 2006 15: 1600-1609; doi:10.1093/hmg/ddl081 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Sheng Li, En Kimura, Rainer Ng, Brent M. Fall, Leonard Meuse, Morayma Reyes, John A. Faulkner, and Jeffrey S. Chamberlain
A highly functional mini-dystrophin/GFP fusion gene for cell and gene therapy studies of Duchenne muscular dystrophy
Human Molecular Genetics Advance Access published on April 4, 2006
Hum. Mol. Genet. 2006 15: 1610-1622; doi:10.1093/hmg/ddl082 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Kleopas A. Kleopa, Anthi Drousiotou, Eleni Mavrikiou, Annita Ormiston, and Theodoros Kyriakides
Naturally occurring utrophin correlates with disease severity in Duchenne muscular dystrophy
Human Molecular Genetics Advance Access published on April 4, 2006
Hum. Mol. Genet. 2006 15: 1623-1628; doi:10.1093/hmg/ddl083 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Jelena S. Arnold, Evan M. Braunstein, Takahiro Ohyama, Andrew K. Groves, Joe C. Adams, M. Christian Brown, and Bernice E. Morrow
Tissue-specific roles of Tbx1 in the development of the outer, middle and inner ear, defective in 22q11DS patients
Human Molecular Genetics Advance Access published on April 6, 2006
Hum. Mol. Genet. 2006 15: 1629-1639; doi:10.1093/hmg/ddl084 [Abstract] [FREE Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Craig R. Lee, Kari E. North, Molly S. Bray, Myriam Fornage, John M. Seubert, John W. Newman, Bruce D. Hammock, David J. Couper, Gerardo Heiss, and Darryl C. Zeldin
Genetic variation in soluble epoxide hydrolase (EPHX2) and risk of coronary heart disease: The Atherosclerosis Risk in Communities (ARIC) study
Human Molecular Genetics Advance Access published on April 4, 2006
Hum. Mol. Genet. 2006 15: 1640-1649; doi:10.1093/hmg/ddl085 [Abstract] [FREE Full Text] [PDF] [Supplementary Material] [Request Permissions]  

Zhiguang Su, Yuhua Li, Jessica C. James, Alan H. Matsumoto, Gregory A. Helm, Aldons J. Lusis, and Weibin Shi
Genetic linkage of hyperglycemia, body weight and serum amyloid-P in an intercross between C57BL/6 and C3H apolipoprotein E-deficient mice
Human Molecular Genetics Advance Access published on April 4, 2006
Hum. Mol. Genet. 2006 15: 1650-1658; doi:10.1093/hmg/ddl088 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Silvia Paracchini, Ankur Thomas, Sandra Castro, Cecilia Lai, Murugan Paramasivam, Yu Wang, Brendan J. Keating, Jennifer M. Taylor, Douglas F. Hacking, Thomas Scerri, Clyde Francks, Alex J. Richardson, Richard Wade-Martins, John F. Stein, Julian C. Knight, Andrew J. Copp, Joseph LoTurco, and Anthony P. Monaco
The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration
Human Molecular Genetics Advance Access published on April 6, 2006
Hum. Mol. Genet. 2006 15: 1659-1666; doi:10.1093/hmg/ddl089 [Abstract] [FREE Full Text] [PDF] [Supplementary Material]   OPEN ACCESS ARTICLE  

Ville Pulkkinen, Marja-Leena Majuri, Guoying Wang, Päivi Holopainen, Yasushi Obase, Johanna Vendelin, Henrik Wolff, Paula Rytilä, Lauri A. Laitinen, Tari Haahtela, Tarja Laitinen, Harri Alenius, Juha Kere, and Marko Rehn
Neuropeptide S and G protein-coupled receptor 154 modulate macrophage immune responses
Human Molecular Genetics Advance Access published on April 6, 2006
Hum. Mol. Genet. 2006 15: 1667-1679; doi:10.1093/hmg/ddl090 [Abstract] [FREE Full Text] [PDF] [Supplementary Material] [Request Permissions]  

Xinhua Shu, Brian Tulloch, Alan Lennon, Dafni Vlachantoni, Xinzhi Zhou, Caroline Hayward, and Alan F. Wright
Disease mechanisms in late-onset retinal macular degeneration associated with mutation in C1QTNF5
Human Molecular Genetics Advance Access published on April 6, 2006
Hum. Mol. Genet. 2006 15: 1680-1689; doi:10.1093/hmg/ddl091 [Abstract] [FREE Full Text] [PDF] [Supplementary Material] [Request Permissions]  

Austen J. Milnerwood, Damian M. Cummings, Glenn M. Dallérac, Jacki Y. Brown, Sarat C. Vatsavayai, Mark C. Hirst, Payam Rezaie, and Kerry P.S.J. Murphy
Early development of aberrant synaptic plasticity in a mouse model of Huntington's disease
Human Molecular Genetics Advance Access published on April 6, 2006
Hum. Mol. Genet. 2006 15: 1690-1703; doi:10.1093/hmg/ddl092 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Paulo S. Pereira, Alexandra Teixeira, Sofia Pinho, Paulo Ferreira, Joana Fernandes, Carla Oliveira, Raquel Seruca, Gianpaolo Suriano, and Fernando Casares
E-cadherin missense mutations, associated with hereditary diffuse gastric cancer (HDGC) syndrome, display distinct invasive behaviors and genetic interactions with the Wnt and Notch pathways in Drosophila epithelia
Human Molecular Genetics Advance Access published on April 6, 2006
Hum. Mol. Genet. 2006 15: 1704-1712; doi:10.1093/hmg/ddl093 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Maria Björkqvist, Åsa Petersén, Karl Bacos, Jeremy Isaacs, Per Norlén, Joana Gil, Natalija Popovic, Frank Sundler, Gillian P. Bates, Sarah J. Tabrizi, Patrik Brundin, and Hindrik Mulder
Progressive alterations in the hypothalamic-pituitary-adrenal axis in the R6/2 transgenic mouse model of Huntington's disease
Human Molecular Genetics Advance Access published on April 13, 2006
Hum. Mol. Genet. 2006 15: 1713-1721; doi:10.1093/hmg/ddl094 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Hiroyuki Akagawa, Atsushi Tajima, Yoshiko Sakamoto, Boris Krischek, Taku Yoneyama, Hidetoshi Kasuya, Hideaki Onda, Tomokatsu Hori, Motoo Kubota, Toshio Machida, Naokatsu Saeki, Akira Hata, Kazunari Hashiguchi, Eizou Kimura, Chul-Jin Kim, Tae-Ki Yang, Jong-Young Lee, Kuchan Kimm, and Ituro Inoue
A haplotype spanning two genes, ELN and LIMK1, decreases their transcripts and confers susceptibility to intracranial aneurysms
Human Molecular Genetics Advance Access published on April 12, 2006
Hum. Mol. Genet. 2006 15: 1722-1734; doi:10.1093/hmg/ddl096 [Abstract] [FREE Full Text] [PDF]   OPEN ACCESS ARTICLE  

Marina Ciullo, Céline Bellenguez, Vincenza Colonna, Teresa Nutile, Antonietta Calabria, Rosalinda Pacente, Gianluigi Iovino, Bruno Trimarco, Catherine Bourgain, and M. Graziella Persico
New susceptibility locus for hypertension on chromosome 8q by efficient pedigree-breaking in an Italian isolate
Human Molecular Genetics Advance Access published on April 12, 2006
Hum. Mol. Genet. 2006 15: 1735-1743; doi:10.1093/hmg/ddl097 [Abstract] [FREE Full Text] [PDF]   OPEN ACCESS ARTICLE  

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.