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Contents: Volume 15, Number 16, 15 August 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

Yan Guo, Dong-Hai Xiong, Tie-Lin Yang, Yan-Fang Guo, Robert R. Recker, and Hong-Wen Deng
Polymorphisms of estrogen-biosynthesis genes CYP17 and CYP19 may influence age at menarche: a genetic association study in Caucasian females
Human Molecular Genetics Advance Access published on June 16, 2006
Hum. Mol. Genet. 2006 15: 2401-2408; doi:10.1093/hmg/ddl155 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Xiaoyan Zhong and Randall N. Pittman
Ataxin-3 binds VCP/p97 and regulates retrotranslocation of ERAD substrates
Human Molecular Genetics Advance Access published on July 5, 2006
Hum. Mol. Genet. 2006 15: 2409-2420; doi:10.1093/hmg/ddl164 [Abstract] [FREE Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Feng-Chun Yang, Shi Chen, Travis Clegg, Xiaohong Li, Trent Morgan, Selina A. Estwick, Jin Yuan, Waleed Khalaf, Sarah Burgin, Jeff Travers, Luis F. Parada, David A. Ingram, and D. Wade Clapp
Nf1+/– mast cells induce neurofibroma like phenotypes through secreted TGF-ß signaling
Human Molecular Genetics Advance Access published on July 11, 2006
Hum. Mol. Genet. 2006 15: 2421-2437; doi:10.1093/hmg/ddl165 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Susanne Lucae, Daria Salyakina, Nicholas Barden, Mario Harvey, Bernard Gagné, Michel Labbé, Elisabeth B. Binder, Manfred Uhr, Marcelo Paez-Pereda, Inge Sillaber, Marcus Ising, Tanja Brückl, Roselind Lieb, Florian Holsboer, and Bertram Müller-Myhsok
P2RX7, a gene coding for a purinergic ligand-gated ion channel, is associated with major depressive disorder
Human Molecular Genetics Advance Access published on July 5, 2006
Hum. Mol. Genet. 2006 15: 2438-2445; doi:10.1093/hmg/ddl166 [Abstract] [FREE Full Text] [PDF] [Supplementary Data]   OPEN ACCESS ARTICLE  

Matthias Riemenschneider, Lidija Konta, Patricia Friedrich, Sandra Schwarz, Kevin Taddei, Frauke Neff, Alessandro Padovani, Heike Kölsch, Simon M. Laws, Norman Klopp, Heike Bickeböller, Stefan Wagenpfeil, Jakob C. Mueller, Albert Rosenberger, Janine Diehl-Schmid, Silvana Archetti, Nicola Lautenschlager, Barbara Borroni, Ulrich Müller, Thomas Illig, Reinhard Heun, Rupert Egensperger, Jürgen Schlegel, Hans Förstl, Ralph N. Martins the German Sib-Pair Study Group, and Alexander Kurz
A functional polymorphism within plasminogen activator urokinase (PLAU) is associated with Alzheimer's disease
Human Molecular Genetics Advance Access published on July 6, 2006
Hum. Mol. Genet. 2006 15: 2446-2456; doi:10.1093/hmg/ddl167 [Abstract] [FREE Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Alan W. Hart, Joanne E. Morgan, Jürgen Schneider, Katrine West, Lisa McKie, Shoumo Bhattacharya, Ian J. Jackson, and Sally H. Cross
Cardiac malformations and midline skeletal defects in mice lacking filamin A
Human Molecular Genetics Advance Access published on July 6, 2006
Hum. Mol. Genet. 2006 15: 2457-2467; doi:10.1093/hmg/ddl168 [Abstract] [FREE Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Qing Song, John W. Cole, Jeffrey R. O'Connell, Oscar C. Stine, Margaret Gallagher, Wayne H. Giles, Braxton D. Mitchell, Marcella A. Wozniak, Barney J. Stern, John D. Sorkin, Patrick F. McArdle, Adam C. Naj, Qin Xu, Gary H. Gibbons, and Steven J. Kittner
Phosphodiesterase 4D polymorphisms and the risk of cerebral infarction in a biracial population: the Stroke Prevention in Young Women Study
Human Molecular Genetics Advance Access published on July 11, 2006
Hum. Mol. Genet. 2006 15: 2468-2478; doi:10.1093/hmg/ddl169 [Abstract] [FREE Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Yuexia Wang, Alan J. Herron, and Howard J. Worman
Pathology and nuclear abnormalities in hearts of transgenic mice expressing M371K lamin A encoded by an LMNA mutation causing Emery–Dreifuss muscular dystrophy
Human Molecular Genetics Advance Access published on July 6, 2006
Hum. Mol. Genet. 2006 15: 2479-2489; doi:10.1093/hmg/ddl170 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Philip J. Smith, Chaolin Zhang, Jinhua Wang, Shern L. Chew, Michael Q. Zhang, and Adrian R. Krainer
An increased specificity score matrix for the prediction of SF2/ASF-specific exonic splicing enhancers
Human Molecular Genetics Advance Access published on July 6, 2006
Hum. Mol. Genet. 2006 15: 2490-2508; doi:10.1093/hmg/ddl171 [Abstract] [FREE Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Valerie L.R.M. Verstraeten, Jos L.V. Broers, Maurice A.M. van Steensel, Sophie Zinn-Justin, Frans C.S. Ramaekers, Peter M. Steijlen, Miriam Kamps, Helma J.H. Kuijpers, Diane Merckx, Hubert J.M. Smeets, Raoul C.M. Hennekam, Carlo L.M. Marcelis, and Arthur van den Wijngaard
Compound heterozygosity for mutations in LMNA causes a progeria syndrome without prelamin A accumulation
Human Molecular Genetics Advance Access published on July 6, 2006
Hum. Mol. Genet. 2006 15: 2509-2522; doi:10.1093/hmg/ddl172 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Terrence F. Satterfield and Leo J. Pallanck
Ataxin-2 and its Drosophila homolog, ATX2, physically assemble with polyribosomes
Human Molecular Genetics Advance Access published on July 11, 2006
Hum. Mol. Genet. 2006 15: 2523-2532; doi:10.1093/hmg/ddl173 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Lydia Urak, Martha Feucht, Nahid Fathi, Kurt Hornik, and Karoline Fuchs
A GABRB3 promoter haplotype associated with childhood absence epilepsy impairs transcriptional activity
Human Molecular Genetics Advance Access published on July 11, 2006
Hum. Mol. Genet. 2006 15: 2533-2541; doi:10.1093/hmg/ddl174 [Abstract] [FREE 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.