Targeted disruption of hepatic frataxin expression causes impaired mitochondrial function, decreased life span and tumor growth in mice

By Thierbach René   Schulz Tim J.   Voigt Anja   Mietzner Brun   Drewes Gunnar   von Kleist-Retzow Jürgen-Christoph   Wiesner Rudolf J.   Magnuson Mark A.   Puccio Hélène   Pfeiffer Andreas F.H.   Steinberg Pablo   Ristow Michael  

Human Molecular Genetics, Vol. 14, Iss. 24, 2005-12 ,pp. : 3857-3864

Oxford University Press

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Targeted disruption of the Epm2a gene causes formation of Lafora inclusion bodies, neurodegeneration, ataxia, myoclonus epilepsy and impaired behavioral response in mice

By Amano K.  

Human Molecular Genetics, Vol. 11, Iss. 11, 2002-05 ,pp. : 1251-1262

Oxford University Press

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Reduction in frataxin causes progressive accumulation of mitochondrial damage

By Karthikeyan Gopalakrishnan  

Human Molecular Genetics, Vol. 12, Iss. 24, 2003-12 ,pp. : 3331-3342

Oxford University Press

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Frataxin expression rescues mitochondrial dysfunctions in FRDA cells

By Lonnerdal B.  

Human Molecular Genetics, Vol. 10, Iss. 19, 2001-09 ,pp. : 2099-2107

Oxford University Press

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Disruption of the WFS1 gene in mice causes progressive -cell loss and impaired stimulus–secretion coupling in insulin secretion

By Ishihara Hisamitsu   Takeda Satoshi   Tamura Akira   Takahashi Rui   Yamaguchi Suguru   Takei Daisuke   Yamada Takahiro   Inoue Hiroshi   Soga Hiroyuki   Katagiri Hideki   Tanizawa Yukio   Oka Yoshitomo  

Human Molecular Genetics, Vol. 13, Iss. 11, 2004-06 ,pp. : 1159-1170

Oxford University Press

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