Increased mitochondrial Ca 2 and decreased sarcoplasmic reticulum Ca 2 in mitochondrial myopathy

By Aydin Jan   Andersson Daniel C.   Hnninen Sandra L.   Wredenberg Anna   Tavi Pasi   Park Chan Bae   Larsson Nils-Gran   Bruton Joseph D.   Westerblad Hkan  

Human Molecular Genetics, Vol. 18, Iss. 2, 2009-01 ,pp. : 278-288

Oxford University Press

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Fine-tuning in Ca 2+ homeostasis underlies progression of cardiomyopathy in myocytes derived from genetically modified embryonic stem cells

By Grey Corinne   Méry Annabelle   Pucéat Michel  

Human Molecular Genetics, Vol. 14, Iss. 10, 2005-05 ,pp. : 1367-1377

Oxford University Press

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Loss of CHK1 function impedes DNA damage-induced FANCD2 monoubiquitination but normalizes the abnormal G2 arrest in Fanconi anemia

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Human Molecular Genetics, Vol. 17, Iss. 5, 2008-03 ,pp. : 679-689

Oxford University Press

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Abnormal association of mutant huntingtin with synaptic vesicles inhibits glutamate release

By Li H.   Wyman T.   Yu Z-X.   Li S-H.   Li X-J.  

Human Molecular Genetics, Vol. 12, Iss. 16, 2003-08 ,pp. : 2021-2030

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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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