Skip Navigation

Receive this page by email each issue: [Sign up for eTOCs]

Cover Image
[Cover Caption] 
Other Issues:
Previous 		Contents: Volume 18, Number 24, 15 December 2009   [Index by Author] 

Down ARTICLES
Down ASSOCIATION STUDIES ARTICLES
Down CORRIGENDA
Down FRONT-MATTER/BACK-MATTER


[Search ALL Issues]

Table of Contents (PDF)

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

Xinhua Yu, Lena Wester-Rosenlöf, Ulrike Gimsa, Stephanie-Anna Holzhueter, Andreia Marques, Ludwig Jonas, Kristin Hagenow, Manfred Kunz, Horst Nizze, Markus Tiedge, Rikard Holmdahl, and Saleh M. Ibrahim
The mtDNA nt7778 G/T polymorphism affects autoimmune diseases and reproductive performance in the mouse
Human Molecular Genetics Advance Access published on September 16, 2009
Hum. Mol. Genet. 2009 18: 4689-4698; doi:10.1093/hmg/ddp432 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Tõnis Org, Ana Rebane, Kai Kisand, Martti Laan, Uku Haljasorg, Reidar Andreson, and Pärt Peterson
AIRE activated tissue specific genes have histone modifications associated with inactive chromatin
Human Molecular Genetics Advance Access published on September 10, 2009
Hum. Mol. Genet. 2009 18: 4699-4710; doi:10.1093/hmg/ddp433 [Abstract] [FREE Full Text] [PDF] [Supplementary Data]   Creative Commons License OPEN ACCESS  

Marion Delous, Nathan E. Hellman, Helori-Maël Gaudé, Flora Silbermann, André Le Bivic, Rémi Salomon, Corinne Antignac, and Sophie Saunier
Nephrocystin-1 and nephrocystin-4 are required for epithelial morphogenesis and associate with PALS1/PATJ and Par6
Human Molecular Genetics Advance Access published on September 14, 2009
Hum. Mol. Genet. 2009 18: 4711-4723; doi:10.1093/hmg/ddp434 [Abstract] [FREE Full Text] [PDF] [Supplementary Data]   Creative Commons License OPEN ACCESS  

Salah Azzi, Sylvie Rossignol, Virginie Steunou, Theo Sas, Nathalie Thibaud, Fabienne Danton, Maryline Le Jule, Claudine Heinrichs, Sylvie Cabrol, Christine Gicquel, Yves Le Bouc, and Irene Netchine
Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci
Human Molecular Genetics Advance Access published on September 14, 2009
Hum. Mol. Genet. 2009 18: 4724-4733; doi:10.1093/hmg/ddp435 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Daniel Tattersall, Claire A. Scott, Colin Gray, Daniel Zicha, and David P. Kelsell
EKV mutant connexin 31 associated cell death is mediated by ER stress
Human Molecular Genetics Advance Access published on September 14, 2009
Hum. Mol. Genet. 2009 18: 4734-4745; doi:10.1093/hmg/ddp436 [Abstract] [FREE Full Text] [PDF] [Supplementary Data]   Creative Commons License OPEN ACCESS  

Sylvie Grandemange, Stephan Soler, and Isabelle Touitou
Expression of the familial Mediterranean fever gene is regulated by nonsense-mediated decay
Human Molecular Genetics Advance Access published on September 15, 2009
Hum. Mol. Genet. 2009 18: 4746-4755; doi:10.1093/hmg/ddp437 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Patricia Lopes Pereira, Laetitia Magnol, Ignasi Sahún, Véronique Brault, Arnaud Duchon, Paola Prandini, Agnès Gruart, Jean-Charles Bizot, Bernadette Chadefaux-Vekemans, Samuel Deutsch, Fabrice Trovero, José María Delgado-García, Stylianos E. Antonarakis, Mara Dierssen, and Yann Herault
A new mouse model for the trisomy of the Abcg1–U2af1 region reveals the complexity of the combinatorial genetic code of down syndrome
Human Molecular Genetics Advance Access published on September 26, 2009
Hum. Mol. Genet. 2009 18: 4756-4769; doi:10.1093/hmg/ddp438 [Abstract] [FREE Full Text] [PDF] [Supplementary Data]   Creative Commons License OPEN ACCESS  

Xi-Qin Ding, Cynthia S. Harry, Yumiko Umino, Alexander V. Matveev, Steven J. Fliesler, and Robert B. Barlow
Impaired cone function and cone degeneration resulting from CNGB3 deficiency: down-regulation of CNGA3 biosynthesis as a potential mechanism
Human Molecular Genetics Advance Access published on September 17, 2009
Hum. Mol. Genet. 2009 18: 4770-4780; doi:10.1093/hmg/ddp440 [Abstract] [Full Text] [PDF] [Request Permissions]  

Priya S. Kishnani, Tzu-Po Chuang, Deeksha Bali, Dwight Koeberl, Stephanie Austin, David A. Weinstein, Elaine Murphy, Ying-Ting Chen, Keri Boyette, Chu-Hao Liu, Yuan-Tsong Chen, and Ling-Hui Li
Chromosomal and genetic alterations in human hepatocellular adenomas associated with type Ia glycogen storage disease
Human Molecular Genetics Advance Access published on September 16, 2009
Hum. Mol. Genet. 2009 18: 4781-4790; doi:10.1093/hmg/ddp441 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Alice R. Clark, Gregory M. Sawyer, Stephen P. Robertson, and Andrew J. Sutherland-Smith
Skeletal dysplasias due to filamin A mutations result from a gain-of-function mechanism distinct from allelic neurological disorders
Human Molecular Genetics Advance Access published on September 22, 2009
Hum. Mol. Genet. 2009 18: 4791-4800; doi:10.1093/hmg/ddp442 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Glen M. Borchert, Brian L. Gilmore, Ryan M. Spengler, Yi Xing, William Lanier, Debashish Bhattacharya, and Beverly L. Davidson
Adenosine deamination in human transcripts generates novel microRNA binding sites
Human Molecular Genetics Advance Access published on September 23, 2009
Hum. Mol. Genet. 2009 18: 4801-4807; doi:10.1093/hmg/ddp443 [Abstract] [FREE Full Text] [PDF] [Supplementary Data]   Creative Commons License OPEN ACCESS  

Hyang-Min Byun, Kimberly D. Siegmund, Fei Pan, Daniel J. Weisenberger, Gary Kanel, Peter W. Laird, and Allen S. Yang
Epigenetic profiling of somatic tissues from human autopsy specimens identifies tissue- and individual-specific DNA methylation patterns
Human Molecular Genetics Advance Access published on September 23, 2009
Hum. Mol. Genet. 2009 18: 4808-4817; doi:10.1093/hmg/ddp445 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Nilva K. Cervigne, Patricia P. Reis, Jerry Machado, Bekim Sadikovic, Grace Bradley, Natalie Naranjo Galloni, Melania Pintilie, Igor Jurisica, Bayardo Perez-Ordonez, Ralph Gilbert, Patrick Gullane, Jonathan Irish, and Suzanne Kamel-Reid
Identification of a microRNA signature associated with progression of leukoplakia to oral carcinoma
Human Molecular Genetics Advance Access published on September 23, 2009
Hum. Mol. Genet. 2009 18: 4818-4829; doi:10.1093/hmg/ddp446 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Tanya L. Henshall, Ben Tucker, Amanda L. Lumsden, Svanhild Nornes, Michael T. Lardelli, and Robert I. Richards
Selective neuronal requirement for huntingtin in the developing zebrafish
Human Molecular Genetics Advance Access published on September 29, 2009
Hum. Mol. Genet. 2009 18: 4830-4842; doi:10.1093/hmg/ddp455 [Abstract] [FREE Full Text] [PDF]   Creative Commons License OPEN ACCESS  

Joonil Jung, Kexiang Xu, Derek Lessing, and Nancy M. Bonini
Preventing Ataxin-3 protein cleavage mitigates degeneration in a Drosophila model of SCA3
Human Molecular Genetics Advance Access published on September 25, 2009
Hum. Mol. Genet. 2009 18: 4843-4852; doi:10.1093/hmg/ddp456 [Abstract] [FREE Full Text] [PDF] [Supplementary Data]   Creative Commons License OPEN ACCESS  

Fuli Yu, Alon Keinan, Hua Chen, Russell J. Ferland, Robert S. Hill, Andre A. Mignault, Christopher A. Walsh, and David Reich
Detecting natural selection by empirical comparison to random regions of the genome
Human Molecular Genetics Advance Access published on September 25, 2009
Hum. Mol. Genet. 2009 18: 4853-4867; doi:10.1093/hmg/ddp457 [Abstract] [FREE Full Text] [PDF] [Supplementary Data]   Creative Commons License OPEN ACCESS  

Cole J. Ferguson, Guy M. Lenk, and Miriam H. Meisler
Defective autophagy in neurons and astrocytes from mice deficient in PI(3,5)P2
Human Molecular Genetics Advance Access published on September 29, 2009
Hum. Mol. Genet. 2009 18: 4868-4878; doi:10.1093/hmg/ddp460 [Abstract] [FREE Full Text] [PDF] [Supplementary Data]   Creative Commons License OPEN ACCESS  

ASSOCIATION STUDIES ARTICLES Back

Lina M. Moreno, Maria Adela Mansilla, Steve A. Bullard, Margaret E. Cooper, Tamara D. Busch, Junichiro Machida, Marla K. Johnson, David Brauer, Katherine Krahn, Sandy Daack-Hirsch, Jamie L'Heureux, Consuelo Valencia-Ramirez, Dora Rivera, Ana Maria López, Manuel A. Moreno, Anne Hing, Edward J. Lammer, Marilyn Jones, Kaare Christensen, Rolv T. Lie, Astanand Jugessur, Allen J. Wilcox, Peter Chines, Elizabeth Pugh, Kim Doheny, Mauricio Arcos-Burgos, Mary L. Marazita, Jeffrey C. Murray, and Andrew C. Lidral
FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate
Human Molecular Genetics Advance Access published on September 24, 2009
Hum. Mol. Genet. 2009 18: 4879-4896; doi:10.1093/hmg/ddp444 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Yang Li, Wen-Jing Wang, Huiqing Cao, Jiehua Lu, Chong Wu, Fang-Yuan Hu, Jian Guo, Ling Zhao, Fan Yang, Yi-Xin Zhang, Wei Li, Gu-Yan Zheng, Hanbin Cui, Xiaomin Chen, Zhiming Zhu, Hongbo He, Birong Dong, Xianming Mo, Yi Zeng, and Xiao-Li Tian
Genetic association of FOXO1A and FOXO3A with longevity trait in Han Chinese populations
Human Molecular Genetics Advance Access published on September 29, 2009
Hum. Mol. Genet. 2009 18: 4897-4904; doi:10.1093/hmg/ddp459 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

CORRIGENDA Back

Neil Ashley, Anthony O'Rourke, Conrad Smith, Susan Adams, Vasantha Gowda, Massimo Zeviani, Garry K. Brown, Carl Fratter, and Joanna Poulton
Depletion of mitochondrial DNA in fibroblast cultures from patients with POLG1 mutations is a consequence of catalytic mutations
Human Molecular Genetics Advance Access published on October 13, 2009
Hum. Mol. Genet. 2009 18: 4905-4906; doi:10.1093/hmg/ddp458 [Extract] [Full Text] [PDF] [Request Permissions]  

Catherine Deveault, Jian Hua Qian, Wafaa Chebaro, Asangla Ao, Lucy Gilbert, Amira Mehio, Rabia Khan, Seang Lin Tan, Anita Wischmeijer, Philippe Coullin, Xing Xie, and Rima Slim
NLRP7 mutations in women with diploid androgenetic and triploid moles: a proposed mechanism for mole formation
Human Molecular Genetics Advance Access published on October 13, 2009
Hum. Mol. Genet. 2009 18: 4907; doi:10.1093/hmg/ddp461 [Extract] [Full Text] [PDF] [Request Permissions]  

FRONT-MATTER/BACK-MATTER Back

Cover Page
Hum. Mol. Genet. 2009 18: NP; doi:10.1093/hmg/ddp492 [PDF] [Request Permissions]  

Editorial Board
Hum. Mol. Genet. 2009 18: NP; doi:10.1093/hmg/ddp493 [PDF] [Request Permissions]  

Subscription Page
Hum. Mol. Genet. 2009 18: NP; doi:10.1093/hmg/ddp494 [PDF] [Request Permissions]  

Contents Page
Hum. Mol. Genet. 2009 18: NP; doi:10.1093/hmg/ddp491 [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.