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Human Molecular Genetics|January 30, 2004
Differences in assembly or stability of complex I and other mitochondrial OXPHOS complexes in inherited complex I deficiencyCristina Ugalde, Rolf J R J Janssen, Lambert P van den Heuvel, et al.
Human Molecular Genetics|January 30, 2004
The complex genetic epidemiology of prostate cancerDaniel J Schaid
Human Molecular Genetics|February 7, 2004
Genetic dissection of myocilin glaucomaGordon Gong, Omofolasade Kosoko-Lasaki, Gleb R Haynatzki, et al.
Human Molecular Genetics|November 14, 2003
A palindrome-mediated mechanism distinguishes translocations involving LCR-B of chromosome 22q11.2Anthony L Gotter, Tamim H Shaikh, Marcia L Budarf, et al.
Human Molecular Genetics|November 14, 2003
Interference of Crx-dependent transcription by ataxin-7 involves interaction between the glutamine regions and requires the ataxin-7 carboxy-terminal region for nuclear localizationShiming Chen, Guang-Hua Peng, Xuejiao Wang, et al.
Human Molecular Genetics|November 14, 2003
ND5 is a hot-spot for multiple atypical mitochondrial DNA deletions in mitochondrial neurogastrointestinal encephalomyopathyYutaka Nishigaki, Ramon Marti, Michio Hirano
Human Molecular Genetics|January 15, 2004
Muscleblind protein, MBNL1/EXP, binds specifically to CHHG repeatsYoshihiro Kino, Daisuke Mori, Yoko Oma, et al.
Human Molecular Genetics|June 17, 2004
Structural and functional consequences of glutamine tract variation in the androgen receptorGrant Buchanan, Miao Yang, Albert Cheong, et al.
Human Molecular Genetics|June 17, 2004
Evidence for a dominant-negative effect in ACTA1 nemaline myopathy caused by abnormal folding, aggregation and altered polymerization of mutant actin isoformsBiljana Ilkovski, Kristen J Nowak, Ana Domazetovska, et al.
Human Molecular Genetics|April 2, 2004
Disruption of the WFS1 gene in mice causes progressive beta-cell loss and impaired stimulus-secretion coupling in insulin secretionHisamitsu Ishihara, Satoshi Takeda, Akira Tamura, et al.
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