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Previous Next 		Contents: Volume 16, Number 21, 1 November 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

Masashi Demura, Regina M. Martin, Makio Shozu, Siby Sebastian, Kazuto Takayama, Wei-Tong Hsu, Roger A. Schultz, Kirk Neely, Michael Bryant, Berenice B. Mendonca, Keiichi Hanaki, Susumu Kanzaki, David B. Rhoads, Madhusmita Misra, and Serdar E. Bulun
Regional rearrangements in chromosome 15q21 cause formation of cryptic promoters for the CYP19 (aromatase) gene
Human Molecular Genetics Advance Access published on June 21, 2007
Hum. Mol. Genet. 2007 16: 2529-2541; doi:10.1093/hmg/ddm145 [Abstract] [FREE Full Text] [PDF]   OPEN ACCESS ARTICLE  

Hisato Kobayashi, Akiko Sato, Eiko Otsu, Hitoshi Hiura, Chisako Tomatsu, Takafumi Utsunomiya, Hiroyuki Sasaki, Nobuo Yaegashi, and Takahiro Arima
Aberrant DNA methylation of imprinted loci in sperm from oligospermic patients
Human Molecular Genetics Advance Access published on July 17, 2007
Hum. Mol. Genet. 2007 16: 2542-2551; doi:10.1093/hmg/ddm187 [Abstract] [FREE Full Text] [PDF] [Supplementary Data]   OPEN ACCESS ARTICLE  

Behrooz Z. Alizadeh, Gustavo Valdigem, Marieke J.H. Coenen, Alexandra Zhernakova, Barbara Franke, Alienke Monsuur, Piet L.C.M. van Riel, Pilar Barrera, Timothy R.D.J. Radstake, Bart O. Roep, Cisca Wijmenga, and Bobby P.C. Koeleman
Association analysis of functional variants of the FcgRIIa and FcgRIIIa genes with type 1 diabetes, celiac disease and rheumatoid arthritis
Human Molecular Genetics Advance Access published on July 25, 2007
Hum. Mol. Genet. 2007 16: 2552-2559; doi:10.1093/hmg/ddm194 [Abstract] [Full Text] [PDF] [Request Permissions]  

Melanie Babcock, Svetlana Yatsenko, Janet Hopkins, Matthew Brenton, Qing Cao, Pieter de Jong, Pawel Stankiewicz, James R. Lupski, James M Sikela, and Bernice E. Morrow
Hominoid lineage specific amplification of low-copy repeats on 22q11.2 (LCR22s) associated with velo-cardio-facial/digeorge syndrome
Human Molecular Genetics Advance Access published on August 3, 2007
Hum. Mol. Genet. 2007 16: 2560-2571; doi:10.1093/hmg/ddm197 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Nina Bosch, Mario Cáceres, Maria Francesca Cardone, Anna Carreras, Ester Ballana, Mariano Rocchi, Lluís Armengol, and Xavier Estivill
Characterization and evolution of the novel gene family FAM90A in primates originated by multiple duplication and rearrangement events
Human Molecular Genetics Advance Access published on August 7, 2007
Hum. Mol. Genet. 2007 16: 2572-2582; doi:10.1093/hmg/ddm209 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Chang-Yi Cui, Makoto Kunisada, Diana Esibizione, Sergei I. Grivennikov, Yulan Piao, Sergei A. Nedospasov, and David Schlessinger
Lymphotoxin-ß regulates periderm differentiation during embryonic skin development
Human Molecular Genetics Advance Access published on August 1, 2007
Hum. Mol. Genet. 2007 16: 2583-2590; doi:10.1093/hmg/ddm210 [Abstract] [FREE Full Text] [PDF] [Supplementary Data]   OPEN ACCESS ARTICLE  

Nico Ruf, Sylvia Bähring, Danuta Galetzka, Galyna Pliushch, Friedrich C. Luft, Peter Nürnberg, Thomas Haaf, Gavin Kelsey, and Ulrich Zechner
Sequence-based bioinformatic prediction and QUASEP identify genomic imprinting of the KCNK9 potassium channel gene in mouse and human
Human Molecular Genetics Advance Access published on August 17, 2007
Hum. Mol. Genet. 2007 16: 2591-2599; doi:10.1093/hmg/ddm216 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Randy Singh Atwal, Jianrun Xia, Deborah Pinchev, Jillian Taylor, Richard M. Epand, and Ray Truant
Huntingtin has a membrane association signal that can modulate huntingtin aggregation, nuclear entry and toxicity
Human Molecular Genetics Advance Access published on August 18, 2007
Hum. Mol. Genet. 2007 16: 2600-2615; doi:10.1093/hmg/ddm217 [Abstract] [FREE Full Text] [PDF] [Supplementary Data]   OPEN ACCESS ARTICLE  

Shu-Yang Xie, Zhao-Rui Ren, Jing-Zhi Zhang, Xin-Bin Guo, Qing-Xue Wang, Shu Wang, Dan Lin, Xiu-Li Gong, Wei Li, Shu-Zhen Huang, Fanyi Zeng, and Yi-Tao Zeng
Restoration of the balanced {alpha}/ß-globin gene expression in ß654-thalassemia mice using combined RNAi and antisense RNA approach
Human Molecular Genetics Advance Access published on August 22, 2007
Hum. Mol. Genet. 2007 16: 2616-2625; doi:10.1093/hmg/ddm218 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Airong Li, Zhongcong Xie, Yuanlin Dong, Kenneth M. McKay, Mary L. McKee, and Rudolph E. Tanzi
Isolation and characterization of the Drosophila ubiquilin ortholog dUbqln: in vivo interaction with early-onset Alzheimer disease genes
Human Molecular Genetics Advance Access published on August 18, 2007
Hum. Mol. Genet. 2007 16: 2626-2639; doi:10.1093/hmg/ddm219 [Abstract] [Full Text] [PDF] [Request Permissions]  

Peter Gustavsson, Nicholas D.E. Greene, Dina Lad, Erwin Pauws, Sandra C.P. de Castro, Philip Stanier, and Andrew J. Copp
Increased expression of Grainyhead-like-3 rescues spina bifida in a folate-resistant mouse model
Human Molecular Genetics Advance Access published on August 24, 2007
Hum. Mol. Genet. 2007 16: 2640-2646; doi:10.1093/hmg/ddm221 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

RETRACTION Back

May Christine V. Malicdan, Satoru Noguchi, Ikuya Nonaka, Yukiko K. Hayashi, and Ichizo Nishino
A Gne knockout mouse expressing human V572L mutation develops features similar to distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy
Human Molecular Genetics Advance Access published on September 25, 2007
Hum. Mol. Genet. 2007 16: 2647; doi:10.1093/hmg/ddm231 [Extract] [Full Text] [PDF] [Request Permissions]  

CORRIGENDUM Back

Umrao R. Monani, Michael Sendtner, Daniel D. Coovert, D. William Parsons, Catia Andreassi, Thanh T. Le, Sibylle Jablonka, Berthold Schrank, Wilfried Rossoll, Thomas W. Prior, Glenn E. Morris, and Arthur H.M. Burghes
The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn–/– mice and results in a mouse with spinal muscular atrophy
Hum. Mol. Genet. 2007 16: 2648; doi:10.1093/hmg/ddm236 [Extract] [Full Text] [PDF] [Request Permissions]  

Africa Fernandez-L, Eva M. Garrido-Martin, Francisco Sanz-Rodriguez, Miguel Pericacho, Alicia Rodriguez-Barbero, Nelida Eleno, Jose M. Lopez-Novoa, Anette Düwell, Miguel A. Vega, Carmelo Bernabeu, and Luisa M. Botella
Gene expression fingerprinting for human hereditary hemorrhagic telangiectasia
Human Molecular Genetics Advance Access published on September 26, 2007
Hum. Mol. Genet. 2007 16: 2649; doi:10.1093/hmg/ddm250 [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.