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Previous Next 		Contents: Volume 16, Number 3, 1 February 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

Benjamin A. Raby, Manuel E. Soto-Quiros, Lydiana Avila, Stephen L. Lake, Amy Murphy, Catherine Liang, Eduardo Fournier, Mitzi Spesny, Jody S. Sylvia, Andrei Verner, Thomas J. Hudson, Barbara J. Klanderman, Nelson B. Freimer, Edwin K. Silverman, and Juan C. Celedón
Sex-specific linkage to total serum immunoglobulin E in families of children with asthma in Costa Rica
Human Molecular Genetics Advance Access published on December 1, 2006
Hum. Mol. Genet. 2007 16: 243-253; doi:10.1093/hmg/ddl447 [Abstract] [FREE Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Angela Sparago, Silvia Russo, Flavia Cerrato, Serena Ferraiuolo, Pierangela Castorina, Angelo Selicorni, Christine Schwienbacher, Massimo Negrini, Giovanni Battista Ferrero, Margherita Cirillo Silengo, Cecilia Anichini, Lidia Larizza, and Andrea Riccio
Mechanisms causing imprinting defects in familial Beckwith–Wiedemann syndrome with Wilms' tumour
Human Molecular Genetics Advance Access published on December 11, 2006
Hum. Mol. Genet. 2007 16: 254-264; doi:10.1093/hmg/ddl448 [Abstract] [FREE Full Text] [PDF]   OPEN ACCESS ARTICLE  

Asif Ali, Paul T. Christie, Irina V. Grigorieva, Brian Harding, Hilde Van Esch, S. Faisal Ahmed, Maria Bitner-Glindzicz, Eberhard Blind, Catherine Bloch, Patricia Christin, Peter Clayton, Jozef Gecz, Brigitte Gilbert-Dussardier, Encarna Guillen-Navarro, Anna Hackett, Isil Halac, Geoffrey N. Hendy, Fiona Lalloo, Christoph J. Mache, Zulf Mughal, Albert C.M. Ong, Choni Rinat, Nicholas Shaw, Sarah F. Smithson, John Tolmie, Jacques Weill, M. Andrew Nesbit, and Rajesh V. Thakker
Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factor
Human Molecular Genetics Advance Access published on January 8, 2007
Hum. Mol. Genet. 2007 16: 265-275; doi:10.1093/hmg/ddl454 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

H. Fagman, J. Liao, J. Westerlund, L. Andersson, B.E. Morrow, and M. Nilsson
The 22q11 deletion syndrome candidate gene Tbx1 determines thyroid size and positioning
Human Molecular Genetics Advance Access published on December 12, 2006
Hum. Mol. Genet. 2007 16: 276-285; doi:10.1093/hmg/ddl455 [Abstract] [FREE Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Yong-Gang Yao, Felicia M. Ellison, J. Philip McCoy, Jichun Chen, and Neal S. Young
Age-dependent accumulation of mtDNA mutations in murine hematopoietic stem cells is modulated by the nuclear genetic background
Human Molecular Genetics Advance Access published on December 21, 2006
Hum. Mol. Genet. 2007 16: 286-294; doi:10.1093/hmg/ddl457 [Abstract] [FREE Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Purnima Desai Sundar, Chang-En Yu, Weiva Sieh, Ellen Steinbart, Ralph M. Garruto, Kiyomitsu Oyanagi, Ulla-Katrina Craig, Thomas D. Bird, Ellen M. Wijsman, Douglas R. Galasko, and Gerard D. Schellenberg
Two sites in the MAPT region confer genetic risk for Guam ALS/PDC and dementia
Human Molecular Genetics Advance Access published on December 21, 2006
Hum. Mol. Genet. 2007 16: 295-306; doi:10.1093/hmg/ddl463 [Abstract] [FREE Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Mark A. Jobling, Iek Chi C. Lo, Daniel J. Turner, Georgina R. Bowden, Andrew C. Lee, Yali Xue, Denise Carvalho-Silva, Matthew E. Hurles, Susan M. Adams, Yuet Meng Chang, Thirsa Kraaijenbrink, Jürgen Henke, Ginevra Guanti, Brian McKeown, Roland A.H. van Oorschot, R. John Mitchell, Peter de Knijff, Chris Tyler-Smith, and Emma J. Parkin
Structural variation on the short arm of the human Y chromosome: recurrent multigene deletions encompassing Amelogenin Y
Human Molecular Genetics Advance Access published on December 22, 2006
Hum. Mol. Genet. 2007 16: 307-316; doi:10.1093/hmg/ddl465 [Abstract] [FREE Full Text] [PDF] [Supplementary Data]   OPEN ACCESS ARTICLE  

Jae-Woong Chang, Hyunwoo Choi, Hyun-Ji Kim, Dong-Gyu Jo, Young-Jun Jeon, Jee-Yeon Noh, Woo Jin Park, and Yong-Keun Jung
Neuronal vulnerability of CLN3 deletion to calcium-induced cytotoxicity is mediated by calsenilin
Human Molecular Genetics Advance Access published on December 22, 2006
Hum. Mol. Genet. 2007 16: 317-326; doi:10.1093/hmg/ddl466 [Abstract] [FREE Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Christopher T. Esapa, Adrian Waite, Matthew Locke, Matthew A. Benson, Michaela Kraus, R.A. Jeffrey McIlhinney, Roy V. Sillitoe, Philip W. Beesley, and Derek J. Blake
SGCE missense mutations that cause myoclonus-dystonia syndrome impair {varepsilon}-sarcoglycan trafficking to the plasma membrane: modulation by ubiquitination and torsinA
Human Molecular Genetics Advance Access published on January 2, 2007
Hum. Mol. Genet. 2007 16: 327-342; doi:10.1093/hmg/ddl472 [Abstract] [FREE Full Text] [PDF] [Supplementary Data]   OPEN ACCESS ARTICLE  

Anne L. Hancock, Keith W. Brown, Kim Moorwood, Hanlim Moon, Claes Holmgren, Sudhanshu H. Mardikar, Anthony R. Dallosso, Elena Klenova, Dmitri Loukinov, Rolf Ohlsson, Victor V. Lobanenkov, and Karim Malik
A CTCF-binding silencer regulates the imprinted genes AWT1 and WT1-AS and exhibits sequential epigenetic defects during Wilms' tumourigenesis
Human Molecular Genetics Advance Access published on January 8, 2007
Hum. Mol. Genet. 2007 16: 343-354; doi:10.1093/hmg/ddl478 [Abstract] [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.