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DiMauro

Showing results (681-690 of 942) with videos related to

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Neurology|February 5, 1999
A double mutation (A8296G and G8363A) in the mitochondrial DNA tRNA (Lys) gene associated with myoclonus epilepsy with ragged-red fibersJ Arenas, Y Campos, B Bornstein, et al.
Neurology|November 18, 1998
Missense mutation in the mtDNA cytochrome b gene in a patient with myopathyA L Andreu, C Bruno, S Shanske, et al.
Biochemical and Biophysical Research Communications|October 11, 2005
hCOX18 and hCOX19: two human genes involved in cytochrome c oxidase assemblySabrina Sacconi, Eva Trevisson, Francesca Pistollato, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 31, 2008
Respiratory chain dysfunction and oxidative stress correlate with severity of primary CoQ10 deficiencyCatarina M Quinzii, Luis C López, Jakob Von-Moltke, et al.
Gene|January 1, 1987
Isolation of a cDNA clone encoding subunit IV of human cytochrome c oxidaseM Zeviani, M Nakagawa, J Herbert, et al.
Journal of Dairy Science|May 23, 2012
Prediction of genomic breeding values for dairy traits in Italian Brown and Simmental bulls using a principal component approachM A Pintus, G Gaspa, E L Nicolazzi, et al.
Molecular Genetics and Metabolism|March 20, 2016
Functional cellular analyses reveal energy metabolism defect and mitochondrial DNA depletion in a case of mitochondrial aconitase deficiencyRoa Sadat, Emanuele Barca, Ruchi Masand, et al.
Neurology|March 10, 2004
Late-onset cerebellar ataxia with hypogonadism and muscle coenzyme Q10 deficiencyM Gironi, C Lamperti, R Nemni, et al.
Journal of the Neurological Sciences|June 17, 1999
The mitochondrial DNA A3243G mutation in Portugal: clinical and molecular studies in 5 familiesL Vilarinho, F M Santorelli, I Coelho, et al.
Journal of the Neurological Sciences|July 13, 1999
A new mitochondrial DNA mutation (A3288G) in the tRNA(Leu(UUR)) gene associated with familial myopathyG M Hadjigeorgiou, S H Kim, K H Fischbeck, et al.
Pageof 95

Showing results (681-690 of 942) with videos related to

Sort By:
Pageof 95
Neurology|February 5, 1999
A double mutation (A8296G and G8363A) in the mitochondrial DNA tRNA (Lys) gene associated with myoclonus epilepsy with ragged-red fibersJ Arenas, Y Campos, B Bornstein, et al.
Neurology|November 18, 1998
Missense mutation in the mtDNA cytochrome b gene in a patient with myopathyA L Andreu, C Bruno, S Shanske, et al.
Biochemical and Biophysical Research Communications|October 11, 2005
hCOX18 and hCOX19: two human genes involved in cytochrome c oxidase assemblySabrina Sacconi, Eva Trevisson, Francesca Pistollato, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 31, 2008
Respiratory chain dysfunction and oxidative stress correlate with severity of primary CoQ10 deficiencyCatarina M Quinzii, Luis C López, Jakob Von-Moltke, et al.
Gene|January 1, 1987
Isolation of a cDNA clone encoding subunit IV of human cytochrome c oxidaseM Zeviani, M Nakagawa, J Herbert, et al.
Journal of Dairy Science|May 23, 2012
Prediction of genomic breeding values for dairy traits in Italian Brown and Simmental bulls using a principal component approachM A Pintus, G Gaspa, E L Nicolazzi, et al.
Molecular Genetics and Metabolism|March 20, 2016
Functional cellular analyses reveal energy metabolism defect and mitochondrial DNA depletion in a case of mitochondrial aconitase deficiencyRoa Sadat, Emanuele Barca, Ruchi Masand, et al.
Neurology|March 10, 2004
Late-onset cerebellar ataxia with hypogonadism and muscle coenzyme Q10 deficiencyM Gironi, C Lamperti, R Nemni, et al.
Journal of the Neurological Sciences|June 17, 1999
The mitochondrial DNA A3243G mutation in Portugal: clinical and molecular studies in 5 familiesL Vilarinho, F M Santorelli, I Coelho, et al.
Journal of the Neurological Sciences|July 13, 1999
A new mitochondrial DNA mutation (A3288G) in the tRNA(Leu(UUR)) gene associated with familial myopathyG M Hadjigeorgiou, S H Kim, K H Fischbeck, et al.
Pageof 95