Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Florin Sasarman

Showing results (11-20 of 30) with videos related to

Pageof 3
Sort By:
Cell Metabolism|March 12, 2013
The mitochondrial RNA-binding protein GRSF1 localizes to RNA granules and is required for posttranscriptional mitochondrial gene expressionHana Antonicka, Florin Sasarman, Tamiko Nishimura, et al.
Human Molecular Genetics|September 13, 2014
Tissue-specific responses to the LRPPRC founder mutation in French Canadian Leigh SyndromeFlorin Sasarman, Tamiko Nishimura, Hana Antonicka, et al.
Human Molecular Genetics|May 20, 2014
The arginine methyltransferase NDUFAF7 is essential for complex I assembly and early vertebrate embryogenesisOlga Zurita Rendón, Lissiene Silva Neiva, Florin Sasarman, et al.
Molecular Biology of the Cell|March 5, 2010
LRPPRC and SLIRP interact in a ribonucleoprotein complex that regulates posttranscriptional gene expression in mitochondriaFlorin Sasarman, Catherine Brunel-Guitton, Hana Antonicka, et al.
Journal of Inherited Metabolic Disease|December 23, 2015
Biosynthesis of glycosaminoglycans: associated disorders and biochemical testsFlorin Sasarman, Catalina Maftei, Philippe M Campeau, et al.
American Journal of Human Genetics|January 17, 2012
Mutations in C12orf62, a factor that couples COX I synthesis with cytochrome c oxidase assembly, cause fatal neonatal lactic acidosisWoranontee Weraarpachai, Florin Sasarman, Tamiko Nishimura, et al.
The Journal of Biological Chemistry|March 8, 2006
The P174L mutation in human Sco1 severely compromises Cox17-dependent metallation but does not impair copper bindingPaul A Cobine, Fabien Pierrel, Scot C Leary, et al.
American Journal of Human Genetics|October 2, 2012
An RMND1 Mutation causes encephalopathy associated with multiple oxidative phosphorylation complex deficiencies and a mitochondrial translation defectAlexandre Janer, Hana Antonicka, Emilie Lalonde, et al.
Nature Genetics|June 9, 2009
Mutation in TACO1, encoding a translational activator of COX I, results in cytochrome c oxidase deficiency and late-onset Leigh syndromeWoranontee Weraarpachai, Hana Antonicka, Florin Sasarman, et al.
Cell|December 25, 2012
MITRAC links mitochondrial protein translocation to respiratory-chain assembly and translational regulationDavid U Mick, Sven Dennerlein, Heike Wiese, et al.
Pageof 3

Showing results (11-20 of 30) with videos related to

Sort By:
Pageof 3
Cell Metabolism|March 12, 2013
The mitochondrial RNA-binding protein GRSF1 localizes to RNA granules and is required for posttranscriptional mitochondrial gene expressionHana Antonicka, Florin Sasarman, Tamiko Nishimura, et al.
Human Molecular Genetics|September 13, 2014
Tissue-specific responses to the LRPPRC founder mutation in French Canadian Leigh SyndromeFlorin Sasarman, Tamiko Nishimura, Hana Antonicka, et al.
Human Molecular Genetics|May 20, 2014
The arginine methyltransferase NDUFAF7 is essential for complex I assembly and early vertebrate embryogenesisOlga Zurita Rendón, Lissiene Silva Neiva, Florin Sasarman, et al.
Molecular Biology of the Cell|March 5, 2010
LRPPRC and SLIRP interact in a ribonucleoprotein complex that regulates posttranscriptional gene expression in mitochondriaFlorin Sasarman, Catherine Brunel-Guitton, Hana Antonicka, et al.
Journal of Inherited Metabolic Disease|December 23, 2015
Biosynthesis of glycosaminoglycans: associated disorders and biochemical testsFlorin Sasarman, Catalina Maftei, Philippe M Campeau, et al.
American Journal of Human Genetics|January 17, 2012
Mutations in C12orf62, a factor that couples COX I synthesis with cytochrome c oxidase assembly, cause fatal neonatal lactic acidosisWoranontee Weraarpachai, Florin Sasarman, Tamiko Nishimura, et al.
The Journal of Biological Chemistry|March 8, 2006
The P174L mutation in human Sco1 severely compromises Cox17-dependent metallation but does not impair copper bindingPaul A Cobine, Fabien Pierrel, Scot C Leary, et al.
American Journal of Human Genetics|October 2, 2012
An RMND1 Mutation causes encephalopathy associated with multiple oxidative phosphorylation complex deficiencies and a mitochondrial translation defectAlexandre Janer, Hana Antonicka, Emilie Lalonde, et al.
Nature Genetics|June 9, 2009
Mutation in TACO1, encoding a translational activator of COX I, results in cytochrome c oxidase deficiency and late-onset Leigh syndromeWoranontee Weraarpachai, Hana Antonicka, Florin Sasarman, et al.
Cell|December 25, 2012
MITRAC links mitochondrial protein translocation to respiratory-chain assembly and translational regulationDavid U Mick, Sven Dennerlein, Heike Wiese, et al.
Pageof 3