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Previous Next 		Contents: Volume 17, Number 3, 1 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

Stéphane Thifault, Seda Ondrej, Yulin Sun, Anny Fortin, Emil Skamene, Robert Lalonde, Johanne Tremblay, and Pavel Hamet
Genetic determinants of emotionality and stress response in AcB/BcA recombinant congenic mice and in silico evidence of convergence with cardiovascular candidate genes
Human Molecular Genetics Advance Access published on October 3, 2007
Hum. Mol. Genet. 2008 17: 331-344; doi:10.1093/hmg/ddm277 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Toshiaki Takahashi, Shinya Kikuchi, Shinichi Katada, Yoshitaka Nagai, Masatoyo Nishizawa, and Osamu Onodera
Soluble polyglutamine oligomers formed prior to inclusion body formation are cytotoxic
Human Molecular Genetics Advance Access published on October 18, 2007
Hum. Mol. Genet. 2008 17: 345-356; doi:10.1093/hmg/ddm311 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Veerle Labarque, Kathleen Freson, Chantal Thys, Christine Wittevrongel, Marc F. Hoylaerts, Rita De Vos, Nathalie Goemans, and Chris Van Geet
Increased Gs signalling in platelets and impaired collagen activation, due to a defect in the dystrophin gene, result in increased blood loss during spinal surgery
Human Molecular Genetics Advance Access published on November 1, 2007
Hum. Mol. Genet. 2008 17: 357-366; doi:10.1093/hmg/ddm312 [Abstract] [FREE Full Text] [PDF] [Supplementary Data]   OPEN ACCESS ARTICLE  

Scott A. Detmer, Christine Vande Velde, Don W. Cleveland, and David C. Chan
Hindlimb gait defects due to motor axon loss and reduced distal muscles in a transgenic mouse model of Charcot–Marie–Tooth type 2A
Human Molecular Genetics Advance Access published on October 24, 2007
Hum. Mol. Genet. 2008 17: 367-375; doi:10.1093/hmg/ddm314 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Joana Branco, Ismael Al-Ramahi, Lubna Ukani, Alma M. Pérez, Pedro Fernandez-Funez, Diego Rincón-Limas, and Juan Botas
Comparative analysis of genetic modifiers in Drosophila points to common and distinct mechanisms of pathogenesis among polyglutamine diseases
Human Molecular Genetics Advance Access published on November 5, 2007
Hum. Mol. Genet. 2008 17: 376-390; doi:10.1093/hmg/ddm315 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Joomyeong Kim and Jeong Do Kim
In vivo YY1 knockdown effects on genomic imprinting
Human Molecular Genetics Advance Access published on October 31, 2007
Hum. Mol. Genet. 2008 17: 391-401; doi:10.1093/hmg/ddm316 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Svanhild Nornes, Morgan Newman, Giuseppe Verdile, Simon Wells, Cristi L. Stoick-Cooper, Ben Tucker, Inna Frederich-Sleptsova, Ralph Martins, and Michael Lardelli
Interference with splicing of Presenilin transcripts has potent dominant negative effects on Presenilin activity
Human Molecular Genetics Advance Access published on November 2, 2007
Hum. Mol. Genet. 2008 17: 402-412; doi:10.1093/hmg/ddm317 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

C. Fava, M. Montagnana, L. Rosberg, P. Burri, P. Almgren, A. Jönsson, P. Wanby, G. Lippi, P. Minuz, L.U. Hulthèn, M. Aurell, and O. Melander
Subjects heterozygous for genetic loss of function of the thiazide-sensitive cotransporter have reduced blood pressure
Human Molecular Genetics Advance Access published on November 1, 2007
Hum. Mol. Genet. 2008 17: 413-418; doi:10.1093/hmg/ddm318 [Abstract] [FREE Full Text] [PDF]   OPEN ACCESS ARTICLE  

Thanaset Senawong, Janyaporn Phuchareon, Osamu Ohara, Frank McCormick, Katherine A. Rauen, and Osamu Tetsu
Germline mutations of MEK in cardio-facio-cutaneous syndrome are sensitive to MEK and RAF inhibition: implications for therapeutic options
Human Molecular Genetics Advance Access published on November 2, 2007
Hum. Mol. Genet. 2008 17: 419-430; doi:10.1093/hmg/ddm319 [Abstract] [Full Text] [PDF] [Request Permissions]  

Jeanne M.M. Tan, Esther S.P. Wong, Donald S. Kirkpatrick, Olga Pletnikova, Han Seok Ko, Shiam-Peng Tay, Michelle W.L. Ho, Juan Troncoso, Steven P. Gygi, Michael K. Lee, Valina L. Dawson, Ted M. Dawson, and Kah-Leong Lim
Lysine 63-linked ubiquitination promotes the formation and autophagic clearance of protein inclusions associated with neurodegenerative diseases
Human Molecular Genetics Advance Access published on November 1, 2007
Hum. Mol. Genet. 2008 17: 431-439; doi:10.1093/hmg/ddm320 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Giuseppe Esposito, Jaime Imitola, Jie Lu, Daniele De Filippis, Caterina Scuderi, Vijay S. Ganesh, Rebecca Folkerth, Jonathan Hecht, Soojung Shin, Teresa Iuvone, Jonathan Chesnut, Luca Steardo, and Volney Sheen
Genomic and functional profiling of human Down syndrome neural progenitors implicates S100B and aquaporin 4 in cell injury
Human Molecular Genetics Advance Access published on November 5, 2007
Hum. Mol. Genet. 2008 17: 440-457; doi:10.1093/hmg/ddm322 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

George Kirov, Dilihan Gumus, Wei Chen, Nadine Norton, Lyudmila Georgieva, Murat Sari, Michael C O’Donovan, Fikret Erdogan, Michael J Owen, Hans-Hilger Ropers, and Reinhard Ullmann
Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia
Human Molecular Genetics Advance Access published on November 6, 2007
Hum. Mol. Genet. 2008 17: 458-465; doi:10.1093/hmg/ddm323 [Abstract] [Full Text] [PDF] [Request Permissions]  

ERRATA Back

Dalila Pinto, Christian Marshall, Lars Feuk, and Stephen W. Scherer
Copy-number variation in control population cohorts
Human Molecular Genetics Advance Access published on November 28, 2007
Hum. Mol. Genet. 2008 17: 466-467; doi:10.1093/hmg/ddm321 [Extract] [Full Text] [PDF] [Request Permissions]  

Sebastian Kandert, Yvonne Lüke, Tobias Kleinhenz, Sascha Neumann, Wenshu Lu, Verena M. Jaeger, Martina Munck, Manfred Wehnert, Clemens R. Müller, Zhongjun Zhou, Angelika A. Noegel, Marie-Christine Dabauvalle, and Iakowos Karakesisoglou
Nesprin-2 giant safeguards nuclear envelope architecture in LMNA S143F progeria cells
Human Molecular Genetics Advance Access published on November 24, 2007
Hum. Mol. Genet. 2008 17: 468; doi:10.1093/hmg/ddm338 [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.