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Julian Ostrovsky

Showing results (11-20 of 16) with videos related to

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Plos One|July 30, 2013
Primary respiratory chain disease causes tissue-specific dysregulation of the global transcriptome and nutrient-sensing signaling networkZhe Zhang, Mai Tsukikawa, Min Peng, et al.
Human Molecular Genetics|January 23, 2019
Pre-clinical evaluation of cysteamine bitartrate as a therapeutic agent for mitochondrial respiratory chain diseaseSujay Guha, Chigoziri Konkwo, Manuela Lavorato, et al.
EMBO Molecular Medicine|May 14, 2011
Probucol ameliorates renal and metabolic sequelae of primary CoQ deficiency in Pdss2 mutant miceMarni J Falk, Erzsebet Polyak, Zhe Zhang, et al.
Journal of Molecular Biology|February 19, 2014
Mitochondrial DNA variant in COX1 subunit significantly alters energy metabolism of geographically divergent wild isolates in Caenorhabditis elegansStephen D Dingley, Erzsebet Polyak, Julian Ostrovsky, et al.
Nature Genetics|July 31, 2012
NMNAT1 mutations cause Leber congenital amaurosisMarni J Falk, Qi Zhang, Eiko Nakamaru-Ogiso, et al.
American Journal of Human Genetics|September 3, 2013
Mutations in FBXL4, encoding a mitochondrial protein, cause early-onset mitochondrial encephalomyopathyXiaowu Gai, Daniele Ghezzi, Mark A Johnson, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Plos One|July 30, 2013
Primary respiratory chain disease causes tissue-specific dysregulation of the global transcriptome and nutrient-sensing signaling networkZhe Zhang, Mai Tsukikawa, Min Peng, et al.
Human Molecular Genetics|January 23, 2019
Pre-clinical evaluation of cysteamine bitartrate as a therapeutic agent for mitochondrial respiratory chain diseaseSujay Guha, Chigoziri Konkwo, Manuela Lavorato, et al.
EMBO Molecular Medicine|May 14, 2011
Probucol ameliorates renal and metabolic sequelae of primary CoQ deficiency in Pdss2 mutant miceMarni J Falk, Erzsebet Polyak, Zhe Zhang, et al.
Journal of Molecular Biology|February 19, 2014
Mitochondrial DNA variant in COX1 subunit significantly alters energy metabolism of geographically divergent wild isolates in Caenorhabditis elegansStephen D Dingley, Erzsebet Polyak, Julian Ostrovsky, et al.
Nature Genetics|July 31, 2012
NMNAT1 mutations cause Leber congenital amaurosisMarni J Falk, Qi Zhang, Eiko Nakamaru-Ogiso, et al.
American Journal of Human Genetics|September 3, 2013
Mutations in FBXL4, encoding a mitochondrial protein, cause early-onset mitochondrial encephalomyopathyXiaowu Gai, Daniele Ghezzi, Mark A Johnson, et al.
Pageof 2