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Previous Next 		Contents: Volume 17, Number 7, 1 April 2008   [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

Rosemary E. Teresi, Sarah M. Planchon, Kristin A. Waite, and Charis Eng
Regulation of the PTEN promoter by statins and SREBP
Human Molecular Genetics Advance Access published on December 7, 2007
Hum. Mol. Genet. 2008 17: 919-928; doi:10.1093/hmg/ddm364 [Abstract] [Full Text] [PDF] [Request Permissions]  

Fanggeng Zou, Rangaraj K. Gopalraj, Johann Lok, Haiyan Zhu, I-Fang Ling, James F. Simpson, H. Michael Tucker, Jeremiah F. Kelly, Samuel G. Younkin, Dennis W. Dickson, Ronald C. Petersen, Neill R. Graff-Radford, David A. Bennett, Julia E. Crook, Steven G. Younkin, and Steven Estus
Sex-dependent association of a common low-density lipoprotein receptor polymorphism with RNA splicing efficiency in the brain and Alzheimer’s disease
Human Molecular Genetics Advance Access published on December 8, 2007
Hum. Mol. Genet. 2008 17: 929-935; doi:10.1093/hmg/ddm365 [Abstract] [Full Text] [PDF] [Request Permissions]  

Jincheng Yan, Shi Chen, Yingze Zhang, Xiaohong Li, Yan Li, Xiaohua Wu, Jin Yuan, Alexander G. Robling, Reuben Karpur, Rebecca J. Chan, and Feng-Chun Yang
Rac1 mediates the osteoclast gains-in-function induced by haploinsufficiency of Nf1
Human Molecular Genetics Advance Access published on December 18, 2007
Hum. Mol. Genet. 2008 17: 936-948; doi:10.1093/hmg/ddm366 [Abstract] [Full Text] [PDF] [Request Permissions]  

Lyndsay M. Murray, Laura H. Comley, Derek Thomson, Nick Parkinson, Kevin Talbot, and Thomas H. Gillingwater
Selective vulnerability of motor neurons and dissociation of pre- and post-synaptic pathology at the neuromuscular junction in mouse models of spinal muscular atrophy
Human Molecular Genetics Advance Access published on December 8, 2007
Hum. Mol. Genet. 2008 17: 949-962; doi:10.1093/hmg/ddm367 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Howard J. Edenberg, Xiaoling Xuei, Leah Flury Wetherill, Laura Bierut, Kathleen Bucholz, Danielle M. Dick, Victor Hesselbrock, Sam Kuperman, Bernice Porjesz, Marc A. Schuckit, Jay A. Tischfield, Laura A. Almasy, J.I. Nurnberger, Jr, and Tatiana Foroud
Association of NFKB1, which encodes a subunit of the transcription factor NF-{kappa}B, with alcohol dependence
Human Molecular Genetics Advance Access published on December 12, 2007
Hum. Mol. Genet. 2008 17: 963-970; doi:10.1093/hmg/ddm368 [Abstract] [FREE Full Text] [PDF]   OPEN ACCESS ARTICLE  

Kylee L. Spencer, Michael A. Hauser, Lana M. Olson, Silke Schmidt, William K. Scott, Paul Gallins, Anita Agarwal, Eric A. Postel, Margaret A. Pericak-Vance, and Jonathan L. Haines
Deletion of CFHR3 and CFHR1 genes in age-related macular degeneration
Human Molecular Genetics Advance Access published on December 15, 2007
Hum. Mol. Genet. 2008 17: 971-977; doi:10.1093/hmg/ddm369 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Laura A. Lettice, Alison E. Hill, Paul S. Devenney, and Robert E. Hill
Point mutations in a distant sonic hedgehog cis-regulator generate a variable regulatory output responsible for preaxial polydactyly
Human Molecular Genetics Advance Access published on December 21, 2007
Hum. Mol. Genet. 2008 17: 978-985; doi:10.1093/hmg/ddm370 [Abstract] [FREE Full Text] [PDF] [Supplementary Data]   OPEN ACCESS ARTICLE  

Giuseppe Gasparre, Eric Hervouet, Elodie de Laplanche, Jocelyne Demont, Lucia Fiammetta Pennisi, Marc Colombel, Florence Mège-Lechevallier, Jean-Yves Scoazec, Elena Bonora, Roel Smeets, Jan Smeitink, Vladimir Lazar, James Lespinasse, Sophie Giraud, Catherine Godinot, Giovanni Romeo, and Hélène Simonnet
Clonal expansion of mutated mitochondrial DNA is associated with tumor formation and complex I deficiency in the benign renal oncocytoma
Human Molecular Genetics Advance Access published on December 21, 2007
Hum. Mol. Genet. 2008 17: 986-995; doi:10.1093/hmg/ddm371 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Martin Götte, Dorothe Spillmann, George W. Yip, Elly Versteeg, Frank G. Echtermeyer, Toin H. van Kuppevelt, and Ludwig Kiesel
Changes in heparan sulfate are associated with delayed wound repair, altered cell migration, adhesion and contractility in the galactosyltransferase I (ß4GalT-7) deficient form of Ehlers–Danlos syndrome
Human Molecular Genetics Advance Access published on December 24, 2007
Hum. Mol. Genet. 2008 17: 996-1009; doi:10.1093/hmg/ddm372 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Lara Moumné, Aurélie Dipietromaria, Frank Batista, Ayhan Kocer, Marc Fellous, Eric Pailhoux, and Reiner A. Veitia
Differential aggregation and functional impairment induced by polyalanine expansions in FOXL2, a transcription factor involved in cranio-facial and ovarian development
Human Molecular Genetics Advance Access published on December 24, 2007
Hum. Mol. Genet. 2008 17: 1010-1019; doi:10.1093/hmg/ddm373 [Abstract] [Full Text] [PDF] [Request Permissions]  

Damien J. Keating, Daphne Dubach, Mark P. Zanin, Yong Yu, Katherine Martin, Yu-Feng Zhao, Chen Chen, Sílvia Porta, Maria L. Arbonés, Laureane Mittaz, and Melanie A. Pritchard
DSCR1/RCAN1 regulates vesicle exocytosis and fusion pore kinetics: implications for Down syndrome and Alzheimer's disease
Human Molecular Genetics Advance Access published on January 7, 2008
Hum. Mol. Genet. 2008 17: 1020-1030; doi:10.1093/hmg/ddm374 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Xue-Yuan Dong, Carmen Rodriguez, Peng Guo, Xiaodong Sun, Jeffrey T. Talbot, Wei Zhou, John Petros, Qunna Li, Robert L. Vessella, Adam S. Kibel, Victoria L. Stevens, Eugenia E. Calle, and Jin-Tang Dong
SnoRNA U50 is a candidate tumor-suppressor gene at 6q14.3 with a mutation associated with clinically significant prostate cancer
Human Molecular Genetics Advance Access published on January 17, 2008
Hum. Mol. Genet. 2008 17: 1031-1042; doi:10.1093/hmg/ddm375 [Abstract] [Full Text] [PDF] [Request Permissions]  

Inkeri Tiala, Janica Wakkinen, Sari Suomela, Pauli Puolakkainen, Raija Tammi, Sofi Forsberg, Ola Rollman, Kati Kainu, Björn Rozell, Juha Kere, Ulpu Saarialho-Kere, and Outi Elomaa
The PSORS1 locus gene CCHCR1 affects keratinocyte proliferation in transgenic mice
Human Molecular Genetics Advance Access published on January 3, 2008
Hum. Mol. Genet. 2008 17: 1043-1051; doi:10.1093/hmg/ddm377 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Florian Herb, Thorsten Thye, Stefan Niemann, Edmund N.L. Browne, Margaret A. Chinbuah, John Gyapong, Ivy Osei, Ellis Owusu-Dabo, Oliver Werz, Sabine Rüsch-Gerdes, Rolf D. Horstmann, and Christian G. Meyer
ALOX5 variants associated with susceptibility to human pulmonary tuberculosis
Human Molecular Genetics Advance Access published on January 3, 2008
Hum. Mol. Genet. 2008 17: 1052-1060; doi:10.1093/hmg/ddm378 [Abstract] [Full Text] [PDF] [Request Permissions]  

CORRIGENDUM Back

Brett T. Chiquet, Andrew C. Lidral, Samuel Stal, John B. Mulliken, Lina M. Moreno, Mauricio Arcos-Burgos, Consuelo Valencia-Ramirez, Susan H. Blanton, and Jacqueline T. Hecht
CRISPLD2: a novel NSCLP candidate gene
Human Molecular Genetics Advance Access published on February 6, 2008
Hum. Mol. Genet. 2008 17: 1061; doi:10.1093/hmg/ddn010 [Extract] [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.