Congenital myopathy-causing tropomyosin mutations induce thin filament dysfunction via distinct physiological mechanisms

By Ochala Julien   Gokhin David S.   Pénisson-Besnier Isabelle   Quijano-Roy Susana   Monnier Nicole   Lunardi Joël   Romero Norma B.   Fowler Velia M.  

Human Molecular Genetics, Vol. 21, Iss. 20, 2012-10 ,pp. : 4473-4485

Oxford University Press

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Somatodendritic accumulation of misfolded SOD1-L126Z in motor neurons mediates degeneration: αB-crystallin modulates aggregation

By Wang Jiou  

Human Molecular Genetics, Vol. 14, Iss. 16, 2005-08 ,pp. : 2335-2347

Oxford University Press

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Parkin is recruited into aggresomes in a stress-specific manner: over-expression of parkin reduces aggresome formation but can be dissociated from parkin's effect on neuronal survival

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Human Molecular Genetics, Vol. 13, Iss. 1, 2004-01 ,pp. : 117-135

Oxford University Press

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Breakpoint Diversity Illustrates Distinct Mechanisms for Robertsonian Translocation Formation

By Page Scott L.   Shin Jong-Chul   Han Jin-Yeong   Andy Choo K. H.   Shaffer Lisa G.  

Human Molecular Genetics, Vol. 5, Iss. 9, 1996-01 ,pp. : 1279-1288

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Heterodimer formation of wild-type and amyotrophic lateral sclerosis-causing mutant Cu/Zn-superoxide dismutase induces toxicity independent of protein aggregation

By Witan Heidrun   Kern Andreas   Koziollek-Drechsler Ingrid   Wade Rebecca   Behl Christian   Clement Albrecht M.  

Human Molecular Genetics, Vol. 17, Iss. 10, 2008-05 ,pp. : 1373-1385

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