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Florin Sasarman

Showing results (1-10 of 30) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|June 11, 2009
Oxidative phosphorylation: synthesis of mitochondrially encoded proteins and assembly of individual structural subunits into functional holoenzyme complexesScot C Leary, Florin Sasarman
Methods in Molecular Biology (Clifton, N.J.)|January 5, 2012
Radioactive labeling of mitochondrial translation products in cultured cellsFlorin Sasarman, Eric A Shoubridge
The Canadian Journal of Cardiology|November 1, 2015
Mitochondrial Diseases and CardiomyopathiesCatherine Brunel-Guitton, Alina Levtova, Florin Sasarman
Human Molecular Genetics|August 30, 2008
The A3243G tRNALeu(UUR) MELAS mutation causes amino acid misincorporation and a combined respiratory chain assembly defect partially suppressed by overexpression of EFTu and EFG2Florin Sasarman, Hana Antonicka, Eric A Shoubridge
Human Molecular Genetics|June 21, 2002
Nuclear genetic control of mitochondrial translation in skeletal muscle revealed in patients with mitochondrial myopathyFlorin Sasarman, George Karpati, Eric A Shoubridge
Human Molecular Genetics|September 6, 2011
The 2-thiouridylase function of the human MTU1 (TRMU) enzyme is dispensable for mitochondrial translationFlorin Sasarman, Hana Antonicka, Rita Horvath, et al.
Human Mutation|April 17, 2012
A novel mutation in YARS2 causes myopathy with lactic acidosis and sideroblastic anemiaFlorin Sasarman, Tamiko Nishimura, Isabelle Thiffault, et al.
Molecular Biology of the Cell|November 23, 2012
The conserved interaction of C7orf30 with MRPL14 promotes biogenesis of the mitochondrial large ribosomal subunit and mitochondrial translationStephen Fung, Tamiko Nishimura, Florin Sasarman, et al.
Human Molecular Genetics|April 25, 2006
The molecular basis for tissue specificity of the oxidative phosphorylation deficiencies in patients with mutations in the mitochondrial translation factor EFG1Hana Antonicka, Florin Sasarman, Nancy G Kennaway, et al.
Human Molecular Genetics|April 2, 2009
Human SCO2 is required for the synthesis of CO II and as a thiol-disulphide oxidoreductase for SCO1Scot C Leary, Florin Sasarman, Tamiko Nishimura, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Methods in Molecular Biology (Clifton, N.J.)|June 11, 2009
Oxidative phosphorylation: synthesis of mitochondrially encoded proteins and assembly of individual structural subunits into functional holoenzyme complexesScot C Leary, Florin Sasarman
Methods in Molecular Biology (Clifton, N.J.)|January 5, 2012
Radioactive labeling of mitochondrial translation products in cultured cellsFlorin Sasarman, Eric A Shoubridge
The Canadian Journal of Cardiology|November 1, 2015
Mitochondrial Diseases and CardiomyopathiesCatherine Brunel-Guitton, Alina Levtova, Florin Sasarman
Human Molecular Genetics|August 30, 2008
The A3243G tRNALeu(UUR) MELAS mutation causes amino acid misincorporation and a combined respiratory chain assembly defect partially suppressed by overexpression of EFTu and EFG2Florin Sasarman, Hana Antonicka, Eric A Shoubridge
Human Molecular Genetics|June 21, 2002
Nuclear genetic control of mitochondrial translation in skeletal muscle revealed in patients with mitochondrial myopathyFlorin Sasarman, George Karpati, Eric A Shoubridge
Human Molecular Genetics|September 6, 2011
The 2-thiouridylase function of the human MTU1 (TRMU) enzyme is dispensable for mitochondrial translationFlorin Sasarman, Hana Antonicka, Rita Horvath, et al.
Human Mutation|April 17, 2012
A novel mutation in YARS2 causes myopathy with lactic acidosis and sideroblastic anemiaFlorin Sasarman, Tamiko Nishimura, Isabelle Thiffault, et al.
Molecular Biology of the Cell|November 23, 2012
The conserved interaction of C7orf30 with MRPL14 promotes biogenesis of the mitochondrial large ribosomal subunit and mitochondrial translationStephen Fung, Tamiko Nishimura, Florin Sasarman, et al.
Human Molecular Genetics|April 25, 2006
The molecular basis for tissue specificity of the oxidative phosphorylation deficiencies in patients with mutations in the mitochondrial translation factor EFG1Hana Antonicka, Florin Sasarman, Nancy G Kennaway, et al.
Human Molecular Genetics|April 2, 2009
Human SCO2 is required for the synthesis of CO II and as a thiol-disulphide oxidoreductase for SCO1Scot C Leary, Florin Sasarman, Tamiko Nishimura, et al.
Pageof 3