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Previous Next 		Contents: Volume 16, Number 5, 1 March 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

William Hennah, Liisa Tomppo, Tero Hiekkalinna, Outi M. Palo, Helena Kilpinen, Jesper Ekelund, Annamari Tuulio-Henriksson, Kaisa Silander, Timo Partonen, Tiina Paunio, Joseph D. Terwilliger, Jouko Lönnqvist, and Leena Peltonen
Families with the risk allele of DISC1 reveal a link between schizophrenia and another component of the same molecular pathway, NDE1
Human Molecular Genetics Advance Access published on December 21, 2006
Hum. Mol. Genet. 2007 16: 453-462; doi:10.1093/hmg/ddl462 [Abstract] [FREE Full Text] [PDF]   OPEN ACCESS ARTICLE  

Scott J. Hebbring, Araba A. Adjei, Janel L. Baer, Gregory D. Jenkins, Jianping Zhang, Julie M. Cunningham, Daniel J. Schaid, Richard M. Weinshilboum, and Stephen N. Thibodeau
Human SULT1A1 gene: copy number differences and functional implications
Human Molecular Genetics Advance Access published on December 22, 2006
Hum. Mol. Genet. 2007 16: 463-470; doi:10.1093/hmg/ddl468 [Abstract] [FREE Full Text] [PDF]   OPEN ACCESS ARTICLE  

Vidyullatha Vasireddy, Yoshikazu Uchida, Norman Salem, Jr, Soo Yeon Kim, Md Nawajesh Ali Mandal, Geereddy Bhanuprakash Reddy, Ravi Bodepudi, Nathan L. Alderson, Johnie C. Brown, Hiroko Hama, Andrzej Dlugosz, Peter M. Elias, Walter M. Holleran, and Radha Ayyagari
Loss of functional ELOVL4 depletes very long-chain fatty acids (≥C28) and the unique {omega}-O-acylceramides in skin leading to neonatal death
Human Molecular Genetics Advance Access published on January 5, 2007
Hum. Mol. Genet. 2007 16: 471-482; doi:10.1093/hmg/ddl480 [Abstract] [FREE Full Text] [PDF]   OPEN ACCESS ARTICLE  

Ming-Chang Chiang, Hui-Mei Chen, Yi-Hsin Lee, Hao-Hung Chang, Yi-Chih Wu, Bing-Wen Soong, Chiung-Mei Chen, Yih-Ru Wu, Chin-San Liu, Dau-Ming Niu, Jer-Yuarn Wu, Yuan-Tsong Chen, and Yijuang Chern
Dysregulation of C/EBP{alpha} by mutant Huntingtin causes the urea cycle deficiency in Huntington's disease
Human Molecular Genetics Advance Access published on January 9, 2007
Hum. Mol. Genet. 2007 16: 483-498; doi:10.1093/hmg/ddl481 [Abstract] [Full Text] [PDF] [Request Permissions]  

Chen-Hung Ting, Chiao-Wei Lin, Shin-Lan Wen, Hsiu-Mei Hsieh-Li, and Hung Li
Stat5 constitutive activation rescues defects in spinal muscular atrophy
Human Molecular Genetics Advance Access published on January 12, 2007
Hum. Mol. Genet. 2007 16: 499-514; doi:10.1093/hmg/ddl482 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Kathryn D. Rodgers, Takako Sasaki, Attila Aszodi, and Olena Jacenko
Reduced perlecan in mice results in chondrodysplasia resembling Schwartz–Jampel syndrome
Human Molecular Genetics Advance Access published on January 9, 2007
Hum. Mol. Genet. 2007 16: 515-528; doi:10.1093/hmg/ddl484 [Abstract] [Full Text] [PDF] [Request Permissions]  

Dominique Massey-Harroche, Marie-Hélène Delgrossi, Lydie Lane-Guermonprez, Jean-Pierre Arsanto, Jean-Paul Borg, Marc Billaud, and André Le Bivic
Evidence for a molecular link between the tuberous sclerosis complex and the Crumbs complex
Human Molecular Genetics Advance Access published on January 18, 2007
Hum. Mol. Genet. 2007 16: 529-536; doi:10.1093/hmg/ddl485 [Abstract] [Full Text] [PDF] [Request Permissions]  

James M. Wilkins, Lorraine Southam, Andrew J. Price, Zehra Mustafa, Andrew Carr, and John Loughlin
Extreme context specificity in differential allelic expression
Human Molecular Genetics Advance Access published on January 12, 2007
Hum. Mol. Genet. 2007 16: 537-546; doi:10.1093/hmg/ddl488 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Bastiaan T. Heijmans, Dennis Kremer, Elmar W. Tobi, Dorret I. Boomsma, and P. Eline Slagboom
Heritable rather than age-related environmental and stochastic factors dominate variation in DNA methylation of the human IGF2/H19 locus
Human Molecular Genetics Advance Access published on March 5, 2007
Hum. Mol. Genet. 2007 16: 547-554; doi:10.1093/hmg/ddm010 [Abstract] [Full Text] [PDF] [Request Permissions]  

Olivier Blard, Sébastien Feuillette, Jacqueline Bou, Boris Chaumette, Thierry Frébourg, Dominique Campion, and Magalie Lecourtois
Cytoskeleton proteins are modulators of mutant tau-induced neurodegeneration in Drosophila
Human Molecular Genetics Advance Access published on February 19, 2007
Hum. Mol. Genet. 2007 16: 555-566; doi:10.1093/hmg/ddm011 [Abstract] [Full Text] [PDF] [Request Permissions]  

Andrew J. Sharp, Rebecca R. Selzer, Joris A. Veltman, Stefania Gimelli, Giorgio Gimelli, Pasquale Striano, Antonietta Coppola, Regina Regan, Sue M. Price, Nine V. Knoers, Peggy S. Eis, Han G. Brunner, Raoul C. Hennekam, Samantha J.L. Knight, Bert B.A. de Vries, Orsetta Zuffardi, and Evan E. Eichler
Characterization of a recurrent 15q24 microdeletion syndrome
Human Molecular Genetics Advance Access published on March 14, 2007
Hum. Mol. Genet. 2007 16: 567-572; doi:10.1093/hmg/ddm016 [Abstract] [FREE Full Text] [PDF] [Supplementary Data]   OPEN ACCESS ARTICLE  

Nadia Bogdanova, Jürgen Horst, Marcin Chlystun, Peter J.P. Croucher, Almut Nebel, Axel Bohring, Albena Todorova, Stefan Schreiber, Volker Gerke, Michael Krawczak, and Arseni Markoff
A common haplotype of the annexin A5 (ANXA5) gene promoter is associated with recurrent pregnancy loss
Human Molecular Genetics Advance Access published on March 5, 2007
Hum. Mol. Genet. 2007 16: 573-578; doi:10.1093/hmg/ddm017 [Abstract] [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.