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Previous Next 		Contents: Volume 17, Number 12, 15 June 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

Bredford Kerr, Matías Alvarez-Saavedra, Mauricio A. Sáez, Alexandra Saona, and Juan I. Young
Defective body-weight regulation, motor control and abnormal social interactions in Mecp2 hypomorphic mice
Human Molecular Genetics Advance Access published on March 4, 2008
Hum. Mol. Genet. 2008 17: 1707-1717; doi:10.1093/hmg/ddn061 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Rodney C. Samaco, John D. Fryer, Jun Ren, Sharyl Fyffe, Hsiao-Tuan Chao, Yaling Sun, John J. Greer, Huda Y. Zoghbi, and Jeffrey L. Neul
A partial loss of function allele of Methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndrome
Human Molecular Genetics Advance Access published on March 4, 2008
Hum. Mol. Genet. 2008 17: 1718-1727; doi:10.1093/hmg/ddn062 [Abstract] [Full Text] [PDF] [Request Permissions]  

Jody B. Proescher, Marjatta Son, Jeffrey L. Elliott, and Valeria C. Culotta
Biological effects of CCS in the absence of SOD1 enzyme activation: implications for disease in a mouse model for ALS
Human Molecular Genetics Advance Access published on March 12, 2008
Hum. Mol. Genet. 2008 17: 1728-1737; doi:10.1093/hmg/ddn063 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Barbara Beyer, Charlotte Deleuze, Verity A. Letts, Connie L. Mahaffey, Rebecca M. Boumil, Timothy A. Lew, John R. Huguenard, and Wayne N. Frankel
Absence seizures in C3H/HeJ and knockout mice caused by mutation of the AMPA receptor subunit Gria4
Human Molecular Genetics Advance Access published on March 3, 2008
Hum. Mol. Genet. 2008 17: 1738-1749; doi:10.1093/hmg/ddn064 [Abstract] [FREE Full Text] [PDF] [Supplementary Data]   OPEN ACCESS ARTICLE  

Sabine Hein, Peter Schönfeld, Stefan Kahlert, and Georg Reiser
Toxic effects of X-linked adrenoleukodystrophy-associated, very long chain fatty acids on glial cells and neurons from rat hippocampus in culture
Human Molecular Genetics Advance Access published on March 14, 2008
Hum. Mol. Genet. 2008 17: 1750-1761; doi:10.1093/hmg/ddn066 [Abstract] [Full Text] [PDF] [Request Permissions]  

Stéphane Fourcade, Jone López-Erauskin, Jorge Galino, Carine Duval, Alba Naudi, Mariona Jove, Stephan Kemp, Francesc Villarroya, Isidre Ferrer, Reinald Pamplona, Manuel Portero-Otin, and Aurora Pujol
Early oxidative damage underlying neurodegeneration in X-adrenoleukodystrophy
Human Molecular Genetics Advance Access published on March 14, 2008
Hum. Mol. Genet. 2008 17: 1762-1773; doi:10.1093/hmg/ddn085 [Abstract] [Full Text] [PDF] [Request Permissions]  

Junghee Lee, Sean Hagerty, Kerry A. Cormier, Jinho Kim, Andrew L. Kung, Robert J. Ferrante, and Hoon Ryu
Monoallele deletion of CBP leads to pericentromeric heterochromatin condensation through ESET expression and histone H3 (K9) methylation
Human Molecular Genetics Advance Access published on March 4, 2008
Hum. Mol. Genet. 2008 17: 1774-1782; doi:10.1093/hmg/ddn067 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Howard J. Edenberg, Jun Wang, Huijun Tian, Sirisha Pochareddy, Xiaoling Xuei, Leah Wetherill, Alison Goate, Tony Hinrichs, Samuel Kuperman, John I. Nurnberger, Jr, Marc Schuckit, Jay A. Tischfield, and Tatiana Foroud
A regulatory variation in OPRK1, the gene encoding the {kappa}-opioid receptor, is associated with alcohol dependence
Human Molecular Genetics Advance Access published on March 4, 2008
Hum. Mol. Genet. 2008 17: 1783-1789; doi:10.1093/hmg/ddn068 [Abstract] [FREE Full Text] [PDF] [Supplementary Data]   OPEN ACCESS ARTICLE  

Hideyuki Mototani, Aritoshi Iida, Masahiro Nakajima, Tatsuya Furuichi, Yoshinari Miyamoto, Tatsuhiko Tsunoda, Akihiro Sudo, Akihiro Kotani, Atsumasa Uchida, Kouichi Ozaki, Yoshiya Tanaka, Yusuke Nakamura, Toshihiro Tanaka, Kohei Notoya, and Shiro Ikegawa
A functional SNP in EDG2 increases susceptibility to knee osteoarthritis in Japanese
Human Molecular Genetics Advance Access published on March 6, 2008
Hum. Mol. Genet. 2008 17: 1790-1797; doi:10.1093/hmg/ddn069 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

David Meyre, Morgane Farge, Cécile Lecoeur, Christine Proenca, Emmanuelle Durand, Frédéric Allegaert, Jean Tichet, Michel Marre, Beverley Balkau, Jacques Weill, Jérôme Delplanque, and Philippe Froguel
R125W coding variant in TBC1D1 confers risk for familial obesity and contributes to linkage on chromosome 4p14 in the French population
Human Molecular Genetics Advance Access published on March 5, 2008
Hum. Mol. Genet. 2008 17: 1798-1802; doi:10.1093/hmg/ddn070 [Abstract] [Full Text] [PDF] [Request Permissions]  

Yong-Jun Liu, Xiao-Gang Liu, Liang Wang, Christian Dina, Han Yan, Jian-Feng Liu, Shawn Levy, Christopher J. Papasian, Betty M. Drees, James J. Hamilton, David Meyre, Jerome Delplanque, Yu-Fang Pei, Lei Zhang, Robert R. Recker, Philippe Froguel, and Hong-Wen Deng
Genome-wide association scans identified CTNNBL1 as a novel gene for obesity
Human Molecular Genetics Advance Access published on March 5, 2008
Hum. Mol. Genet. 2008 17: 1803-1813; doi:10.1093/hmg/ddn072 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Sabrina Sacconi, Leonardo Salviati, Yutaka Nishigaki, Winsome F. Walker, Evelyn Hernandez-Rosa, Eva Trevisson, Severine Delplace, Claude Desnuelle, Sara Shanske, Michio Hirano, Eric A. Schon, Eduardo Bonilla, Darryl C. De Vivo, Salvatore DiMauro, and Mercy M. Davidson
A functionally dominant mitochondrial DNA mutation
Human Molecular Genetics Advance Access published on March 12, 2008
Hum. Mol. Genet. 2008 17: 1814-1820; doi:10.1093/hmg/ddn073 [Abstract] [Full Text] [PDF] [Request Permissions]  

Kylee L. Spencer, Lana M. Olson, Brent M. Anderson, Nathalie Schnetz-Boutaud, William K. Scott, Paul Gallins, Anita Agarwal, Eric A. Postel, Margaret A. Pericak-Vance, and Jonathan L. Haines
C3 R102G polymorphism increases risk of age-related macular degeneration
Human Molecular Genetics Advance Access published on March 6, 2008
Hum. Mol. Genet. 2008 17: 1821-1824; doi:10.1093/hmg/ddn075 [Abstract] [Full Text] [PDF] [Request Permissions]  

Gareth N. Corry, Michael J. Hendzel, and D. Alan Underhill
Subnuclear localization and mobility are key indicators of PAX3 dysfunction in Waardenburg syndrome
Human Molecular Genetics Advance Access published on March 5, 2008
Hum. Mol. Genet. 2008 17: 1825-1837; doi:10.1093/hmg/ddn076 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Valeska B. Guzman, Anatoly Yambartsev, Amador Goncalves-Primo, Ismael D.C.G. Silva, Carmen R.N. Carvalho, Julisa C.L. Ribalta, Luiz Ricardo Goulart, Natalia Shulzhenko, Maria Gerbase-DeLima, and Andrey Morgun
New approach reveals CD28 and IFNG gene interaction in the susceptibility to cervical cancer
Human Molecular Genetics Advance Access published on March 12, 2008
Hum. Mol. Genet. 2008 17: 1838-1844; doi:10.1093/hmg/ddn077 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Paola Bartoccioni, Mònica Rius, Antonio Zorzano, Manuel Palacín, and Josep Chillarón
Distinct classes of trafficking rBAT mutants cause the type I cystinuria phenotype
Human Molecular Genetics Advance Access published on March 10, 2008
Hum. Mol. Genet. 2008 17: 1845-1854; doi:10.1093/hmg/ddn080 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Yanchao Huang, Antoine de Morrée, Alexandra van Remoortere, Kate Bushby, Rune R. Frants, Johan Tden Dunnen, and Silvère M. van der Maarel
Calpain 3 is a modulator of the dysferlin protein complex in skeletal muscle
Human Molecular Genetics Advance Access published on March 11, 2008
Hum. Mol. Genet. 2008 17: 1855-1866; doi:10.1093/hmg/ddn081 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Ingrid Meulenbelt, Josine L. Min, Steffan Bos, Naghmeh Riyazi, Jeanine J. Houwing-Duistermaat, Henk-Jan van der Wijk, Herman M. Kroon, Masahiro Nakajima, Shiro Ikegawa, André G. Uitterlinden, Joyce B.J. van Meurs, Wendy M. van der Deure, Theo J. Visser, Albert B. Seymour, Nico Lakenberg, Ruud van der Breggen, Dennis Kremer, Cornelia M. van Duijn, Margreet Kloppenburg, John Loughlin, and P. Eline Slagboom
Identification of DIO2 as a new susceptibility locus for symptomatic osteoarthritis
Human Molecular Genetics Advance Access published on March 11, 2008
Hum. Mol. Genet. 2008 17: 1867-1875; doi:10.1093/hmg/ddn082 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

ERRATUM Back

Jincheng Yan, Shi Chen, Yingze Zhang, Xiaohong Li, Yan Li, Xiaohua Wu, Jin Yuan, Alexander G. Robling, Reuben Kapur, 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 April 29, 2008
Hum. Mol. Genet. 2008 17: 1876; doi:10.1093/hmg/ddn103 [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.