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Previous Next 		Contents: Volume 16, Number 12, 15 June 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

Jodi Dufner-Beattie, Benjamin P. Weaver, Jim Geiser, Mehmet Bilgen, Melissa Larson, Wenhao Xu, and Glen K. Andrews
The mouse acrodermatitis enteropathica gene Slc39a4 (Zip4) is essential for early development and heterozygosity causes hypersensitivity to zinc deficiency
Human Molecular Genetics Advance Access published on May 4, 2007
Hum. Mol. Genet. 2007 16: 1391-1399; doi:10.1093/hmg/ddm088 [Abstract] [Full Text] [PDF] [Request Permissions]  

Neil Ashley, Susan Adams, Abdelhamid Slama, Massimo Zeviani, Anu Suomalainen, Antonio L. Andreu, Robert K. Naviaux, and Joanna Poulton
Defects in maintenance of mitochondrial DNA are associated with intramitochondrial nucleotide imbalances
Human Molecular Genetics Advance Access published on May 3, 2007
Hum. Mol. Genet. 2007 16: 1400-1411; doi:10.1093/hmg/ddm090 [Abstract] [FREE Full Text] [PDF] [Supplementary Data]   OPEN ACCESS ARTICLE  

Theodosios Kyriakou, David E. Pontefract, Enrique Viturro, Conrad P. Hodgkinson, Ross C. Laxton, Neda Bogari, George Cooper, Michael Davies, Joel Giblett, Ian N.M. Day, Iain A. Simpson, Christiane Albrecht, and Shu Ye
Functional polymorphism in ABCA1 influences age of symptom onset in coronary artery disease patients
Human Molecular Genetics Advance Access published on April 5, 2007
Hum. Mol. Genet. 2007 16: 1412-1422; doi:10.1093/hmg/ddm091 [Abstract] [FREE Full Text] [PDF]   OPEN ACCESS ARTICLE  

Tom Van de Putte, Annick Francis, Luc Nelles, Leo A. van Grunsven, and Danny Huylebroeck
Neural crest-specific removal of Zfhx1b in mouse leads to a wide range of neurocristopathies reminiscent of Mowat–Wilson syndrome
Human Molecular Genetics Advance Access published on May 3, 2007
Hum. Mol. Genet. 2007 16: 1423-1436; doi:10.1093/hmg/ddm093 [Abstract] [Full Text] [PDF] [Request Permissions]  

Peter T.E. Wootton, Nupur L. Arora, Fotios Drenos, Simon R. Thompson, Jackie A. Cooper, Jeffrey W. Stephens, Steven J. Hurel, Eva Hurt-Camejo, Olov Wiklund, Steve E. Humphries, and Philippa J. Talmud
Tagging SNP haplotype analysis of the secretory PLA2-V gene, PLA2G5, shows strong association with LDL and oxLDL levels, suggesting functional distinction from sPLA2-IIA: results from the UDACS study
Hum. Mol. Genet. 2007 16: 1437-1444; doi:10.1093/hmg/ddm094 [Abstract] [Full Text] [PDF] [Request Permissions]  

Vasanta Subramanian and Ying Feng
A new role for angiogenin in neurite growth and pathfinding: implications for amyotrophic lateral sclerosis
Human Molecular Genetics Advance Access published on April 27, 2007
Hum. Mol. Genet. 2007 16: 1445-1453; doi:10.1093/hmg/ddm095 [Abstract] [Full Text] [PDF] [Request Permissions]  

Xi Huang, Ying Litingtung, and Chin Chiang
Ectopic sonic hedgehog signaling impairs telencephalic dorsal midline development: implication for human holoprosencephaly
Human Molecular Genetics Advance Access published on April 27, 2007
Hum. Mol. Genet. 2007 16: 1454-1468; doi:10.1093/hmg/ddm096 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Matthew J. Huentelman, Andreas Papassotiropoulos, David W. Craig, Frederic J. Hoerndli, John V. Pearson, Kim-Dung Huynh, Jason Corneveaux, Jürgen Hänggi, Christian R.A. Mondadori, Andreas Buchmann, Eric M. Reiman, Katharina Henke, Dominique J.-F. de Quervain, and Dietrich A. Stephan
Calmodulin-binding transcription activator 1 (CAMTA1) alleles predispose human episodic memory performance
Human Molecular Genetics Advance Access published on April 30, 2007
Hum. Mol. Genet. 2007 16: 1469-1477; doi:10.1093/hmg/ddm097 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Mischa G. Vrouwe, Elhaam Elghalbzouri-Maghrani, Matty Meijers, Peter Schouten, Barbara C. Godthelp, Zahurul A. Bhuiyan, Egbert J. Redeker, Marcel M. Mannens, Leon H.F. Mullenders, Albert Pastink, and Firouz Darroudi
Increased DNA damage sensitivity of Cornelia de Lange syndrome cells: evidence for impaired recombinational repair
Human Molecular Genetics Advance Access published on April 27, 2007
Hum. Mol. Genet. 2007 16: 1478-1487; doi:10.1093/hmg/ddm098 [Abstract] [Full Text] [PDF] [Request Permissions]  

Antje Brockschmidt, Unda Todt, Soojin Ryu, Alexander Hoischen, Christina Landwehr, Stefanie Birnbaum, Wilhelm Frenck, Bernhard Radlwimmer, Peter Lichter, Hartmut Engels, Wolfgang Driever, Christian Kubisch, and Ruthild G. Weber
Severe mental retardation with breathing abnormalities (Pitt–Hopkins syndrome) is caused by haploinsufficiency of the neuronal bHLH transcription factor TCF4
Human Molecular Genetics Advance Access published on May 3, 2007
Hum. Mol. Genet. 2007 16: 1488-1494; doi:10.1093/hmg/ddm099 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Chris D. Pacheco, Robin Kunkel, and Andrew P. Lieberman
Autophagy in Niemann–Pick C disease is dependent upon Beclin-1 and responsive to lipid trafficking defects
Human Molecular Genetics Advance Access published on April 27, 2007
Hum. Mol. Genet. 2007 16: 1495-1503; doi:10.1093/hmg/ddm100 [Abstract] [Full Text] [PDF] [Request Permissions]  

Joanne E. Curran, Matthew P. Johnson, Thomas D. Dyer, Harald H.H. Göring, Jack W. Kent, Jac C. Charlesworth, Anthony J. Borg, Jeremy B.M. Jowett, Shelley A. Cole, Jean W. MacCluer, Ahmed H. Kissebah, Eric K. Moses, and John Blangero
Genetic determinants of mitochondrial content
Human Molecular Genetics Advance Access published on April 27, 2007
Hum. Mol. Genet. 2007 16: 1504-1514; doi:10.1093/hmg/ddm101 [Abstract] [Full Text] [PDF] [Supplementary Data] [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.