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Previous Next 		Contents: Volume 15, Number 24, 15 December 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

Lydia E. Matesic, Diana C. Haines, Neal G. Copeland, and Nancy A. Jenkins
Itch genetically interacts with Notch1 in a mouse autoimmune disease model
Human Molecular Genetics Advance Access published on November 9, 2006
Hum. Mol. Genet. 2006 15: 3485-3497; doi:10.1093/hmg/ddl425 [Abstract] [FREE Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Joel Gelernter, Yi Yu, Roger Weiss, Kathleen Brady, Carolien Panhuysen, Bao-zhu Yang, Henry R. Kranzler, and Lindsay Farrer
Haplotype spanning TTC12 and ANKK1, flanked by the DRD2 and NCAM1 loci, is strongly associated to nicotine dependence in two distinct American populations
Human Molecular Genetics Advance Access published on November 3, 2006
Hum. Mol. Genet. 2006 15: 3498-3507; doi:10.1093/hmg/ddl426 [Abstract] [FREE Full Text] [PDF]   OPEN ACCESS ARTICLE  

Chenzhong Kuang, Yan Xiao, Ling Yang, Qian Chen, Zhenzhen Wang, Simon J. Conway, and Yan Chen
Intragenic deletion of Tgif causes defectsin brain development
Human Molecular Genetics Advance Access published on November 2, 2006
Hum. Mol. Genet. 2006 15: 3508-3519; doi:10.1093/hmg/ddl427 [Abstract] [FREE Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Cherie Stayner, Diana M. Iglesias, Paul R. Goodyer, Lana Ellis, Greg Germino, Jing Zhou, and Michael R. Eccles
Pax2 gene dosage influences cystogenesis in autosomal dominant polycystic kidney disease
Human Molecular Genetics Advance Access published on November 2, 2006
Hum. Mol. Genet. 2006 15: 3520-3528; doi:10.1093/hmg/ddl428 [Abstract] [FREE Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Tara M. Caffrey, Catharine Joachim, Silvia Paracchini, Margaret M. Esiri, and Richard Wade-Martins
Haplotype-specific expression of exon 10 at the human MAPT locus
Human Molecular Genetics Advance Access published on November 3, 2006
Hum. Mol. Genet. 2006 15: 3529-3537; doi:10.1093/hmg/ddl429 [Abstract] [FREE Full Text] [PDF] [Supplementary Data]   OPEN ACCESS ARTICLE  

Rodolfo A. Rey, Marcela Venara, Régis Coutant, Jean-Baptiste Trabut, Stéphanie Rouleau, Najiba Lahlou, Charles Sultan, Jean-Marie Limal, Jean-Yves Picard, and Serge Lumbroso
Unexpected mosaicism of R201H-GNAS1 mutant-bearing cells in the testes underlie macro-orchidism without sexual precocity in McCune–Albright syndrome
Human Molecular Genetics Advance Access published on November 13, 2006
Hum. Mol. Genet. 2006 15: 3538-3543; doi:10.1093/hmg/ddl430 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Anne Tarrade, Coralie Fassier, Sabrina Courageot, Delphine Charvin, Jérémie Vitte, Leticia Peris, Alain Thorel, Etienne Mouisel, Nuria Fonknechten, Natacha Roblot, Danielle Seilhean, Andrée Diérich, Jean Jacques Hauw, and Judith Melki
A mutation of spastin is responsible for swellings and impairment of transport in a region of axon characterized by changes in microtubule composition
Human Molecular Genetics Advance Access published on November 13, 2006
Hum. Mol. Genet. 2006 15: 3544-3558; doi:10.1093/hmg/ddl431 [Abstract] [FREE Full Text] [PDF] [Supplementary Data]   OPEN ACCESS ARTICLE  

Jeremy D. Rhodes, Darren G. Monckton, John P. McAbney, Alan R. Prescott, and George Duncan
Increased SK3 expression in DM1 lens cells leads to impaired growth through a greater calcium-induced fragility
Human Molecular Genetics Advance Access published on November 13, 2006
Hum. Mol. Genet. 2006 15: 3559-3568; doi:10.1093/hmg/ddl432 [Abstract] [FREE Full Text] [PDF]   OPEN ACCESS ARTICLE  

Hsiao-Jung Kao, Ching-Feng Cheng, Yen-Hui Chen, Shuen-Iu Hung, Cheng-Chih Huang, David Millington, Tateki Kikuchi, Jer-Yuarn Wu, and Yuan-Tsong Chen
ENU mutagenesis identifies mice with cardiac fibrosis and hepatic steatosis caused by a mutation in the mitochondrial trifunctional protein ß-subunit
Human Molecular Genetics Advance Access published on November 20, 2006
Hum. Mol. Genet. 2006 15: 3569-3577; doi:10.1093/hmg/ddl433 [Abstract] [FREE Full Text] [PDF]   OPEN ACCESS ARTICLE  

Eugenia Trushina, Raman Deep Singh, Roy B. Dyer, Sheng Cao, Vijay H. Shah, Robert G. Parton, Richard E. Pagano, and Cynthia T. McMurray
Mutant huntingtin inhibits clathrin-independent endocytosis and causes accumulation of cholesterol in vitro and in vivo
Hum. Mol. Genet. 2006 15: 3578-3591; doi:10.1093/hmg/ddl434 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

CORRIGENDUM Back

Zoe Kemp, Luis Carvajal-Carmona, Sarah Spain, Ella Barclay, Margaret Gorman, Lynn Martin, Emma Jaeger, Neil Brooks, D. Timothy Bishop, Huw Thomas, Ian Tomlinson, Elli Papaemmanuil, Emily Webb, Gabrielle S. Sellick, Wendy Wood, Gareth Evans, Anneke Lucassen, Eamonn R. Maher, Richard S. Houlston, and the ColoRectal tumour Gene Identification (CoRGI) Study Consortium
Evidence for a colorectal cancer susceptibility locus on chromosome 3q21–q24 from a high-density SNP genome-wide linkage scan
Hum. Mol. Genet. 2006 15: 3592; doi:10.1093/hmg/ddl435 [Extract] [FREE 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.