Opa3, a novel regulator of mitochondrial function, controls thermogenesis and abdominal fat mass in a mouse model for Costeff syndrome

By Wells Timothy   Davies Jennifer R.   Guschina Irina A.   Ball Daniel J.   Davies Jeffrey S.   Davies Vanessa J.   Evans Bronwen A. J.   Votruba Marcela  

Human Molecular Genetics, Vol. 21, Iss. 22, 2012-11 ,pp. : 4836-4844

Oxford University Press

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A novel deletion in the GTPase domain of OPA1 causes defects in mitochondrial morphology and distribution, but not in function

By Spinazzi Marco   Cazzola Silvia   Bortolozzi Mario   Baracca Alessandra   Loro Emanuele   Casarin Alberto   Solaini Giancarlo   Sgarbi Gianluca   Casalena Gabriella   Cenacchi Giovanna   Malena Adriana   Frezza Christian   Carrara Franco   Angelini Corrado   Scorrano Luca   Salviati Leonardo   Vergani Lodovica  

Human Molecular Genetics, Vol. 17, Iss. 21, 2008-11 ,pp. : 3291-3302

Oxford University Press

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Widespread expression of the Supv3L1 mitochondrial RNA helicase in the mouse

By Paul Erin  

Transgenic Research, Vol. 19, Iss. 4, 2010-08 ,pp. : 691-701

Springer Publishing Company

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LETM1 , deleted in WolfHirschhorn syndrome is required for normal mitochondrial morphology and cellular viability

By Dimmer Kai Stefan   Navoni Francesca   Casarin Alberto   Trevisson Eva   Endele Sabine   Winterpacht Andreas   Salviati Leonardo   Scorrano Luca  

Human Molecular Genetics, Vol. 17, Iss. 2, 2008-01 ,pp. : 201-214

Oxford University Press

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Mitochondrial DNA polymerase gamma is essential for mammalian embryogenesis

By Hance Nicole   Ekstrand Mats I.   Trifunovic Aleksandra  

Human Molecular Genetics, Vol. 14, Iss. 13, 2005-07 ,pp. : 1775-1783

Oxford University Press

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