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Contents: Volume 16, Number 14, 15 July 2007   [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

Lirong Zhu, Karine G. Harutyunyan, Jian Lan Peng, Jun Wang, Robert J. Schwartz, and John W. Belmont
Identification of a novel role of ZIC3 in regulating cardiac development
Human Molecular Genetics Advance Access published on April 27, 2007
Hum. Mol. Genet. 2007 16: 1649-1660; doi:10.1093/hmg/ddm106 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Jie Lu, Gewei Lian, Robert Lenkinski, Alec De Grand, R. Roy Vaid, Thomas Bryce, Marina Stasenko, Adele Boskey, Christopher Walsh, and Volney Sheen
Filamin B mutations cause chondrocyte defects in skeletal development
Human Molecular Genetics Advance Access published on May 17, 2007
Hum. Mol. Genet. 2007 16: 1661-1675; doi:10.1093/hmg/ddm114 [Abstract] [Full Text] [PDF] [Request Permissions]  

Takahiro Nakamura, Dongquan Shi, Maria Tzetis, Julio Rodriguez-Lopez, Yoshinari Miyamoto, Aspasia Tsezou, Antonio Gonzalez, Qing Jiang, Naoyuki Kamatani, John Loughlin, and Shiro Ikegawa
Meta-analysis of association between the ASPN D-repeat and osteoarthritis
Human Molecular Genetics Advance Access published on May 20, 2007
Hum. Mol. Genet. 2007 16: 1676-1681; doi:10.1093/hmg/ddm115 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Yuhei Nishimura, Christa L. Martin, Araceli Vazquez-Lopez, Sarah J. Spence, Ana Isabel Alvarez-Retuerto, Marian Sigman, Corinna Steindler, Sandra Pellegrini, N. Carolyn Schanen, Stephen T. Warren, and Daniel H. Geschwind
Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways
Human Molecular Genetics Advance Access published on May 21, 2007
Hum. Mol. Genet. 2007 16: 1682-1698; doi:10.1093/hmg/ddm116 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Antonella Comitato, Carmine Spampanato, Christina Chakarova, Daniela Sanges, Shomi S. Bhattacharya, and Valeria Marigo
Mutations in splicing factor PRPF3, causing retinal degeneration, form detrimental aggregates in photoreceptor cells
Human Molecular Genetics Advance Access published on May 20, 2007
Hum. Mol. Genet. 2007 16: 1699-1707; doi:10.1093/hmg/ddm118 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Sarah L. Lambourne, Trevor Humby, Anthony R. Isles, Piers C. Emson, Maria G. Spillantini, and Lawrence S. Wilkinson
Impairments in impulse control in mice transgenic for the human FTDP-17 tauV337M mutation are exacerbated by age
Human Molecular Genetics Advance Access published on May 20, 2007
Hum. Mol. Genet. 2007 16: 1708-1719; doi:10.1093/hmg/ddm119 [Abstract] [Full Text] [PDF] [Request Permissions]  

Mara Angelini, Stefano Cannata, Valentina Mercaldo, Luisa Gibello, Claudio Santoro, Irma Dianzani, and Fabrizio Loreni
Missense mutations associated with Diamond–Blackfan anemia affect the assembly of ribosomal protein S19 into the ribosome
Human Molecular Genetics Advance Access published on May 20, 2007
Hum. Mol. Genet. 2007 16: 1720-1727; doi:10.1093/hmg/ddm120 [Abstract] [Full Text] [PDF] [Request Permissions]  

Matthew P. Leighton, Seema Nundlall, Tobias Starborg, Roger S. Meadows, Farhana Suleman, Lynette Knowles, Raimund Wagener, David J. Thornton, Karl E. Kadler, Raymond P. Boot-Handford, and Michael D. Briggs
Decreased chondrocyte proliferation and dysregulated apoptosis in the cartilage growth plate are key features of a murine model of epiphyseal dysplasia caused by a matn3 mutation
Human Molecular Genetics Advance Access published on May 21, 2007
Hum. Mol. Genet. 2007 16: 1728-1741; doi:10.1093/hmg/ddm121 [Abstract] [FREE Full Text] [PDF] [Supplementary Data]   OPEN ACCESS ARTICLE  

Taru Muranen, Mikaela Grönholm, Aurelie Lampin, Dominique Lallemand, Fang Zhao, Marco Giovannini, and Olli Carpén
The tumor suppressor merlin interacts with microtubules and modulates Schwann cell microtubule cytoskeleton
Human Molecular Genetics Advance Access published on June 12, 2007
Hum. Mol. Genet. 2007 16: 1742-1751; doi:10.1093/hmg/ddm122 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Gen Wen, Jennifer Wessel, Weidong Zhou, Georg B. Ehret, Fangwen Rao, Mats Stridsberg, Sushil K. Mahata, Peter M. Gent, Madhusudan Das, Richard S. Cooper, Aravinda Chakravarti, Huilin Zhou, Nicholas J. Schork, Daniel T. O'Connor, and Bruce A. Hamilton
An ancestral variant of Secretogranin II confers regulation by PHOX2 transcription factors and association with hypertension
Human Molecular Genetics Advance Access published on June 21, 2007
Hum. Mol. Genet. 2007 16: 1752-1764; doi:10.1093/hmg/ddm123 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Haiyan Zhu, H. Michael Tucker, Karrie E. Grear, James F. Simpson, Alisa K. Manning, L. Adrienne Cupples, and Steven Estus
A common polymorphism decreases low-density lipoprotein receptor exon 12 splicing efficiency and associates with increased cholesterol
Human Molecular Genetics Advance Access published on May 21, 2007
Hum. Mol. Genet. 2007 16: 1765-1772; doi:10.1093/hmg/ddm124 [Abstract] [Full Text] [PDF] [Request Permissions]  

Emma N. Hilton, Forbes D.C. Manson, Jill E. Urquhart, Jennifer J. Johnston, Anne M. Slavotinek, Peter Hedera, Eva-Lena Stattin, Ann Nordgren, Leslie G. Biesecker, and Graeme C.M. Black
Left-sided embryonic expression of the BCL-6 corepressor, BCOR, is required for vertebrate laterality determination
Human Molecular Genetics Advance Access published on May 21, 2007
Hum. Mol. Genet. 2007 16: 1773-1782; doi:10.1093/hmg/ddm125 [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.