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Previous Next 		Contents: Volume 17, Number 4, 14 February 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

Hui Wei, Sung-Jo Kim, Zhongjian Zhang, Pei-Chih Tsai, Krystyna E. Wisniewski, and Anil B. Mukherjee
ER and oxidative stresses are common mediators of apoptosis in both neurodegenerative and non-neurodegenerative lysosomal storage disorders and are alleviated by chemical chaperones
Human Molecular Genetics Advance Access published on November 7, 2007
Hum. Mol. Genet. 2008 17: 469-477; doi:10.1093/hmg/ddm324 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Thierry Brun, Kai Hui Hu He, Roberto Lupi, Bernhard Boehm, Anne Wojtusciszyn, Nadine Sauter, Marc Donath, Piero Marchetti, Kathrin Maedler, and Benoit R. Gauthier
The diabetes-linked transcription factor Pax4 is expressed in human pancreatic islets and is activated by mitogens and GLP-1
Human Molecular Genetics Advance Access published on November 7, 2007
Hum. Mol. Genet. 2008 17: 478-489; doi:10.1093/hmg/ddm325 [Abstract] [Full Text] [PDF] [Request Permissions]  

Fred B. Berry, Jonathan M. Skarie, Farideh Mirzayans, Yannick Fortin, Thomas J. Hudson, Vincent Raymond, Brian A. Link, and Michael A. Walter
FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1A
Human Molecular Genetics Advance Access published on November 9, 2007
Hum. Mol. Genet. 2008 17: 490-505; doi:10.1093/hmg/ddm326 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Helina Tadesse, Julie Deschênes-Furry, Sophie Boisvenue, and Jocelyn Côté
KH-type splicing regulatory protein interacts with survival motor neuron protein and is misregulated in spinal muscular atrophy
Human Molecular Genetics Advance Access published on November 12, 2007
Hum. Mol. Genet. 2008 17: 506-524; doi:10.1093/hmg/ddm327 [Abstract] [Full Text] [PDF] [Request Permissions]  

Patricia A. Gongal and Andrew J. Waskiewicz
Zebrafish model of holoprosencephaly demonstrates a key role for TGIF in regulating retinoic acid metabolism
Human Molecular Genetics Advance Access published on November 12, 2007
Hum. Mol. Genet. 2008 17: 525-538; doi:10.1093/hmg/ddm328 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Radoslaw Dobrowolski, Philipp Sasse, Jan W. Schrickel, Marcus Watkins, Jung-Sun Kim, Mindaugas Rackauskas, Clemens Troatz, Alexander Ghanem, Klaus Tiemann, Joachim Degen, Feliksas F. Bukauskas, Roberto Civitelli, Thorsten Lewalter, Bernd K. Fleischmann, and Klaus Willecke
The conditional connexin43G138R mouse mutant represents a new model of hereditary oculodentodigital dysplasia in humans
Human Molecular Genetics Advance Access published on November 13, 2007
Hum. Mol. Genet. 2008 17: 539-554; doi:10.1093/hmg/ddm329 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Nigel M. Williams, Beate Glaser, Nadine Norton, Hywel Williams, Timothy Pierce, Valentina Moskvina, Stephen Monks, Jurgen Del Favero, Dirk Goossens, Dan Rujescu, Ina Giegling, George Kirov, Nicholas Craddock, Kieran C. Murphy, Michael C. O'Donovan, and Michael J. Owen
Strong evidence that GNB1L is associated with schizophrenia
Human Molecular Genetics Advance Access published on November 13, 2007
Hum. Mol. Genet. 2008 17: 555-566; doi:10.1093/hmg/ddm330 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Andrew E. Fry, Michael J. Griffiths, Sarah Auburn, Mahamadou Diakite, Julian T. Forton, Angela Green, Anna Richardson, Jonathan Wilson, Muminatou Jallow, Fatou Sisay-Joof, Margaret Pinder, Norbert Peshu, Thomas N. Williams, Kevin Marsh, Malcolm E. Molyneux, Terrie E. Taylor, Kirk A. Rockett, and Dominic P. Kwiatkowski
Common variation in the ABO glycosyltransferase is associated with susceptibility to severe Plasmodium falciparum malaria
Human Molecular Genetics Advance Access published on November 13, 2007
Hum. Mol. Genet. 2008 17: 567-576; doi:10.1093/hmg/ddm331 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Mamoru Kato, Fuyuki Miya, Yonehiro Kanemura, Toshihiro Tanaka, Yusuke Nakamura, and Tatsuhiko Tsunoda
Recombination rates of genes expressed in human tissues
Human Molecular Genetics Advance Access published on November 13, 2007
Hum. Mol. Genet. 2008 17: 577-586; doi:10.1093/hmg/ddm332 [Abstract] [FREE Full Text] [PDF] [Supplementary Data]   OPEN ACCESS ARTICLE  

Rebecca Lee Yean Wong, Bogdan J. Wlodarczyk, Kyung Soo Min, Melissa L. Scott, Susan Kartiko, Wei Yu, Michelle Y. Merriweather, Peter Vogel, Brian P. Zambrowicz, and Richard H. Finnell
Mouse Fkbp8 activity is required to inhibit cell death and establish dorso-ventral patterning in the posterior neural tube
Human Molecular Genetics Advance Access published on November 13, 2007
Hum. Mol. Genet. 2008 17: 587-601; doi:10.1093/hmg/ddm333 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Andreas Weihofen, Beth Ostaszewski, Yasufumi Minami, and Dennis J. Selkoe
Pink1 Parkinson mutations, the Cdc37/Hsp90 chaperones and Parkin all influence the maturation or subcellular distribution of Pink1
Human Molecular Genetics Advance Access published on November 14, 2007
Hum. Mol. Genet. 2008 17: 602-616; doi:10.1093/hmg/ddm334 [Abstract] [FREE Full Text] [PDF] [Supplementary Data]   OPEN ACCESS ARTICLE  

Norihiro Kato, Toshiyuki Miyata, Yasuharu Tabara, Tomohiro Katsuya, Kazuyuki Yanai, Hironori Hanada, Kei Kamide, Jun Nakura, Katsuhiko Kohara, Fumihiko Takeuchi, Hiroyuki Mano, Michio Yasunami, Akinori Kimura, Yoshikuni Kita, Hirotsugu Ueshima, Tomohiro Nakayama, Masayoshi Soma, Akira Hata, Akihiro Fujioka, Yuhei Kawano, Kazuwa Nakao, Akihiro Sekine, Teruhiko Yoshida, Yusuke Nakamura, Takao Saruta, Toshio Ogihara, Sumio Sugano, Tetsuro Miki, and Hitonobu Tomoike
High-density association study and nomination of susceptibility genes for hypertension in the Japanese National Project
Human Molecular Genetics Advance Access published on November 14, 2007
Hum. Mol. Genet. 2008 17: 617-627; doi:10.1093/hmg/ddm335 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Ravinesh A. Kumar, Samer KaraMohamed, Jyotsna Sudi, Donald F. Conrad, Camille Brune, Judith A. Badner, T. Conrad Gilliam, Norma J. Nowak, Edwin H. Cook, Jr, William B. Dobyns, and Susan L. Christian
Recurrent 16p11.2 microdeletions in autism
Human Molecular Genetics Advance Access published on December 21, 2007
Hum. Mol. Genet. 2008 17: 628-638; doi:10.1093/hmg/ddm376 [Abstract] [FREE Full Text] [PDF] [Supplementary Data]   OPEN ACCESS ARTICLE  

CORRIGENDUM Back

Hélène Sebban-Benin, Alessandra Pescatore, Francesca Fusco, Valérie Pascuale, Jérémie Gautheron, Shoji Yamaoka, Anne Moncla, Matilde Valeria Ursini, and Gilles Courtois
Identification of TRAF6-dependent NEMO polyubiquitination sites through analysis of a new NEMO mutation causing incontinentia pigmenti
Human Molecular Genetics Advance Access published on December 5, 2007
Hum. Mol. Genet. 2008 17: 639; doi:10.1093/hmg/ddm345 [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.