Calpain 3 participates in sarcomere remodeling by acting upstream of the ubiquitin–proteasome pathway

By Kramerova Irina   Kudryashova Elena   Venkatraman Gayathri   Spencer Melissa J.  

Human Molecular Genetics, Vol. 14, Iss. 15, 2005-08 ,pp. : 2125-2134

Oxford University Press

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Calpain 3 participates in sarcomere remodeling by acting upstream of the ubiquitin-proteasome pathway

By Kramerova I.   Kudryashova E.   Venkatraman G.   Spencer M.J.  

Human Molecular Genetics, Vol. 16, Iss. 8, 2007-04 ,pp. : 1006-1006

Oxford University Press

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A null mutation in the cystatin M/E gene of ichq mice causes juvenile lethality and defects in epidermal cornification

By Zeeuwen P.L.J.M.  

Human Molecular Genetics, Vol. 11, Iss. 23, 2002-11 ,pp. : 2867-2875

Oxford University Press

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Myopathy phenotype of transgenic mice expressing active site-mutated inactive p94 skeletal muscle-specific calpain, the gene product responsible for limb girdle muscular dystrophy type 2A

By Tagawa Kazuhiko  

Human Molecular Genetics, Vol. 9, Iss. 9, 2000-05 ,pp. : 1393-1402

Oxford University Press

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A mutation in NFkB interacting protein 1 results in cardiomyopathy and abnormal skin development in wa3 mice

By Herron Bruce J.  

Human Molecular Genetics, Vol. 14, Iss. 5, 2005-03 ,pp. : 667-677

Oxford University Press

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