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Previous Next 		Contents: Volume 15, Number 6, 15 March 2006   [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

Huiping Zhang, Xingguang Luo, Henry R. Kranzler, Jaakko Lappalainen, Bao-Zhu Yang, Evgeny Krupitsky, Edwin Zvartau, and Joel Gelernter
Association between two µ-opioid receptor gene (OPRM1) haplotype blocks and drug or alcohol dependence
Human Molecular Genetics Advance Access published on February 13, 2006
Hum. Mol. Genet. 2006 15: 807-819; doi:10.1093/hmg/ddl024 [Abstract] [FREE Full Text] [PDF] [Supplementary Material]   OPEN ACCESS ARTICLE  

Takahiro Kawakami, Tokuhiro Chano, Kahori Minami, Hidetoshi Okabe, Yusaku Okada, and Keisei Okamoto
Imprinted DLK1 is a putative tumor suppressor gene and inactivated by epimutation at the region upstream of GTL2 in human renal cell carcinoma
Human Molecular Genetics Advance Access published on January 26, 2006
Hum. Mol. Genet. 2006 15: 821-830; doi:10.1093/hmg/ddl001 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

J. Peter McPherson, M. Prakash Hande, Anuradha Poonepalli, Benedicte Lemmers, Elzbieta Zablocki, Eva Migon, Amro Shehabeldin, Annaliza Porras, Jana Karaskova, Bisera Vukovic, Jeremy Squire, and Razqallah Hakem
A role for Brca1 in chromosome end maintenance
Human Molecular Genetics Advance Access published on January 30, 2006
Hum. Mol. Genet. 2006 15: 831-838; doi:10.1093/hmg/ddl002 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Lina S. Correa-Cerro, Christopher A. Wassif, Lisa Kratz, Georgina F. Miller, Jeeva P. Munasinghe, Alexander Grinberg, Steven J. Fliesler, and Forbes D. Porter
Development and characterization of a hypomorphic Smith–Lemli–Opitz syndrome mouse model and efficacy of simvastatin therapy
Human Molecular Genetics Advance Access published on January 30, 2006
Hum. Mol. Genet. 2006 15: 839-851; doi:10.1093/hmg/ddl003 [Abstract] [FREE Full Text] [PDF] [Supplementary Material] [Request Permissions]  

Colin A. Baron, Clifford G. Tepper, Stephenie Y. Liu, Ryan R. Davis, Nicholas J. Wang, N. Carolyn Schanen, and Jeffrey P. Gregg
Genomic and functional profiling of duplicated chromosome 15 cell lines reveal regulatory alterations in UBE3A-associated ubiquitin–proteasome pathway processes
Human Molecular Genetics Advance Access published on January 30, 2006
Hum. Mol. Genet. 2006 15: 853-869; doi:10.1093/hmg/ddl004 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Atsuko Kasahara, Kaori Ishikawa, Makiko Yamaoka, Masahito Ito, Naoki Watanabe, Miho Akimoto, Akitsugu Sato, Kazuto Nakada, Hitoshi Endo, Yoko Suda, Shinichi Aizawa, and Jun-Ichi Hayashi
Generation of trans-mitochondrial mice carrying homoplasmic mtDNAs with a missense mutation in a structural gene using ES cells
Human Molecular Genetics Advance Access published on January 31, 2006
Hum. Mol. Genet. 2006 15: 871-881; doi:10.1093/hmg/ddl005 [Abstract] [FREE Full Text] [PDF]   OPEN ACCESS ARTICLE  

Yukiko Kuroda, Takao Mitsui, Makoto Kunishige, Masayuki Shono, Masashi Akaike, Hiroyuki Azuma, and Toshio Matsumoto
Parkin enhances mitochondrial biogenesis in proliferating cells
Human Molecular Genetics Advance Access published on January 31, 2006
Hum. Mol. Genet. 2006 15: 883-895; doi:10.1093/hmg/ddl006 [Abstract] [FREE Full Text] [PDF] [Supplementary Material] [Request Permissions]  

Yohei Kirino, Takehiro Yasukawa, Sanna K. Marjavaara, Howard T. Jacobs, Ian J. Holt, Kimitsuna Watanabe, and Tsutomu Suzuki
Acquisition of the wobble modification in mitochondrial tRNALeu(CUN) bearing the G12300A mutation suppresses the MELAS molecular defect
Human Molecular Genetics Advance Access published on January 30, 2006
Hum. Mol. Genet. 2006 15: 897-904; doi:10.1093/hmg/ddl007 [Abstract] [FREE Full Text] [PDF] [Supplementary Material] [Request Permissions]  

Fred B. Berry, Matthew A. Lines, J. Martin Oas, Tim Footz, D. Alan Underhill, Philip J. Gage, and Michael A. Walter
Functional interactions between FOXC1 and PITX2 underlie the sensitivity to FOXC1 gene dose in Axenfeld–Rieger syndrome and anterior segment dysgenesis
Human Molecular Genetics Advance Access published on January 31, 2006
Hum. Mol. Genet. 2006 15: 905-919; doi:10.1093/hmg/ddl008 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Youssef A. Elhaji, Ileana Stoica, Sheldon Dennis, Enrico O. Purisima, and Mark A. Trifiro
Impaired helix 12 dynamics due to proline 892 substitutions in the androgen receptor are associated with complete androgen insensitivity
Human Molecular Genetics Advance Access published on January 31, 2006
Hum. Mol. Genet. 2006 15: 921-931; doi:10.1093/hmg/ddl009 [Abstract] [FREE Full Text] [PDF] [Supplementary Material] [Request Permissions]  

Clelia Tiziana Storlazzi, Thoas Fioretos, Cecilia Surace, Angelo Lonoce, Angela Mastrorilli, Bodil Strömbeck, Pietro D'Addabbo, Francesco Iacovelli, Crescenzio Minervini, Anna Aventin, Nicole Dastugue, Christa Fonatsch, Anne Hagemeijer, Martine Jotterand, Dominique Mühlematter, Marina Lafage-Pochitaloff, Florence Nguyen-Khac, Claudia Schoch, Marilyn L. Slovak, Arabella Smith, Francesc Solè, Nadine Van Roy, Bertil Johansson, and Mariano Rocchi
MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene
Human Molecular Genetics Advance Access published on February 1, 2006
Hum. Mol. Genet. 2006 15: 933-942; doi:10.1093/hmg/ddl010 [Abstract] [FREE Full Text] [PDF] [Supplementary Material] [Request Permissions]  

Takahiro Sasaki, Takahiro Gotow, Motoko Shiozaki, Fumika Sakaue, Taro Saito, Jean-Pierre Julien, Yasuo Uchiyama, and Shin-Ichi Hisanaga
Aggregate formation and phosphorylation of neurofilament-L Pro22 Charcot–Marie–Tooth disease mutants
Human Molecular Genetics Advance Access published on February 1, 2006
Hum. Mol. Genet. 2006 15: 943-952; doi:10.1093/hmg/ddl011 [Abstract] [FREE Full Text] [PDF] [Supplementary Material] [Request Permissions]  

Corinne Pondarré, Brendan B. Antiochos, Dean R. Campagna, Stephen L. Clarke, Eric L. Greer, Kathryn M. Deck, Alice McDonald, An-Ping Han, Amy Medlock, Jeffery L. Kutok, Sheila A. Anderson, Richard S. Eisenstein, and Mark D. Fleming
The mitochondrial ATP-binding cassette transporter Abcb7 is essential in mice and participates in cytosolic iron–sulfur cluster biogenesis
Human Molecular Genetics Advance Access published on February 8, 2006
Hum. Mol. Genet. 2006 15: 953-964; doi:10.1093/hmg/ddl012 [Abstract] [FREE Full Text] [PDF] [Supplementary Material] [Request Permissions]  

Angela Hodges, Andrew D. Strand, Aaron K. Aragaki, Alexandre Kuhn, Thierry Sengstag, Gareth Hughes, Lyn A. Elliston, Cathy Hartog, Darlene R. Goldstein, Doris Thu, Zane R. Hollingsworth, Francois Collin, Beth Synek, Peter A. Holmans, Anne B. Young, Nancy S. Wexler, Mauro Delorenzi, Charles Kooperberg, Sarah J. Augood, Richard L.M. Faull, James M. Olson, Lesley Jones, and Ruth Luthi-Carter
Regional and cellular gene expression changes in human Huntington's disease brain
Human Molecular Genetics Advance Access published on February 8, 2006
Hum. Mol. Genet. 2006 15: 965-977; doi:10.1093/hmg/ddl013 [Abstract] [FREE Full Text] [PDF] [Supplementary Material] [Request Permissions]  

Colleen J. Saunders, Stavroulla L. Xenophontos, Marios A. Cariolou, Lakis C. Anastassiades, Timothy D. Noakes, and Malcolm Collins
The bradykinin ß2 receptor (BDKRB2) and endothelial nitric oxide synthase 3 (NOS3) genes and endurance performance during Ironman Triathlons
Human Molecular Genetics Advance Access published on February 6, 2006
Hum. Mol. Genet. 2006 15: 979-987; doi:10.1093/hmg/ddl014 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Chun Guo, Michael Willem, Alexander Werner, Gennadij Raivich, Michael Emerson, Ludwig Neyses, and Ulrike Mayer
Absence of {alpha}7 integrin in dystrophin-deficient mice causes a myopathy similar to Duchenne muscular dystrophy
Human Molecular Genetics Advance Access published on February 13, 2006
Hum. Mol. Genet. 2006 15: 989-998; doi:10.1093/hmg/ddl018 [Abstract] [FREE Full Text] [PDF]   OPEN ACCESS ARTICLE  

A. Disset, C.F. Bourgeois, N. Benmalek, M. Claustres, J. Stevenin, and Sylvie Tuffery-Giraud
An exon skipping-associated nonsense mutation in the dystrophin gene uncovers a complex interplay between multiple antagonistic splicing elements
Human Molecular Genetics Advance Access published on February 6, 2006
Hum. Mol. Genet. 2006 15: 999-1013; doi:10.1093/hmg/ddl015 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Ophélia Maertens, Hans Prenen, Maria Debiec-Rychter, Agnieszka Wozniak, Raf Sciot, Patrick Pauwels, Ivo De Wever, Joris R. Vermeesch, Thomas de Raedt, Anne De Paepe, Frank Speleman, Allan van Oosterom, Ludwine Messiaen, and Eric Legius
Molecular pathogenesis of multiple gastrointestinal stromal tumors in NF1 patients
Human Molecular Genetics Advance Access published on February 6, 2006
Hum. Mol. Genet. 2006 15: 1015-1023; doi:10.1093/hmg/ddl016 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Hongmin Wang, Precious J. Lim, Chaobo Yin, Matthias Rieckher, Bruce E. Vogel, and Mervyn J. Monteiro
Suppression of polyglutamine-induced toxicity in cell and animal models of Huntington's disease by ubiquilin
Human Molecular Genetics Advance Access published on February 6, 2006
Hum. Mol. Genet. 2006 15: 1025-1041; doi:10.1093/hmg/ddl017 [Abstract] [FREE Full Text] [PDF] [Supplementary Material] [Request Permissions]  

Jennifer A. Kearney, Yan Yang, Barbara Beyer, Sarah K. Bergren, Lieve Claes, Peter DeJonghe, and Wayne N. Frankel
Severe epilepsy resulting from genetic interaction between Scn2a and Kcnq2
Human Molecular Genetics Advance Access published on February 7, 2006
Hum. Mol. Genet. 2006 15: 1043-1048; doi:10.1093/hmg/ddl019 [Abstract] [FREE Full Text] [PDF] [Supplementary Material] [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.