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Brian H Robinson

Showing results (51-60 of 57) with videos related to

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Clinical Chemistry|September 6, 2005
Automated spectrophotometric analysis of mitochondrial respiratory chain complex enzyme activities in cultured skin fibroblastsKaren A Kramer, Devin Oglesbee, Stacy J Hartman, et al.
Journal of Medical Genetics|January 27, 2011
LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiencyFrançois-Guillaume Debray, Charles Morin, Annie Janvier, et al.
Journal of Materials Science. Materials in Medicine|August 3, 2014
Synthesis, physiochemical characterization, and biocompatibility of a chitosan/dextran-based hydrogel for postsurgical adhesion preventionJaydee D Cabral, Marina Roxburgh, Zheng Shi, et al.
Pediatric Neurology|June 13, 2009
Rolandic mitochondrial encephalomyelopathy and MT-ND3 mutationsKlaus G E Werner, Chantal F Morel, Adam Kirton, et al.
Plos One|March 8, 2013
Genome-wide association analysis identifies a mutation in the thiamine transporter 2 (SLC19A3) gene associated with Alaskan Husky encephalopathyKaren M Vernau, Jonathan A Runstadler, Emily A Brown, et al.
Cancer Cell|November 19, 2011
Inhibition of mitochondrial translation as a therapeutic strategy for human acute myeloid leukemiaMarko Skrtić, Shrivani Sriskanthadevan, Bozhena Jhas, et al.
Brain : a Journal of Neurology|December 17, 2013
Variant non ketotic hyperglycinemia is caused by mutations in LIAS, BOLA3 and the novel gene GLRX5Peter R Baker, Marisa W Friederich, Michael A Swanson, et al.
Pageof 6

Showing results (51-60 of 57) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 57 results.
Clinical Chemistry|September 6, 2005
Automated spectrophotometric analysis of mitochondrial respiratory chain complex enzyme activities in cultured skin fibroblastsKaren A Kramer, Devin Oglesbee, Stacy J Hartman, et al.
Journal of Medical Genetics|January 27, 2011
LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiencyFrançois-Guillaume Debray, Charles Morin, Annie Janvier, et al.
Journal of Materials Science. Materials in Medicine|August 3, 2014
Synthesis, physiochemical characterization, and biocompatibility of a chitosan/dextran-based hydrogel for postsurgical adhesion preventionJaydee D Cabral, Marina Roxburgh, Zheng Shi, et al.
Pediatric Neurology|June 13, 2009
Rolandic mitochondrial encephalomyelopathy and MT-ND3 mutationsKlaus G E Werner, Chantal F Morel, Adam Kirton, et al.
Plos One|March 8, 2013
Genome-wide association analysis identifies a mutation in the thiamine transporter 2 (SLC19A3) gene associated with Alaskan Husky encephalopathyKaren M Vernau, Jonathan A Runstadler, Emily A Brown, et al.
Cancer Cell|November 19, 2011
Inhibition of mitochondrial translation as a therapeutic strategy for human acute myeloid leukemiaMarko Skrtić, Shrivani Sriskanthadevan, Bozhena Jhas, et al.
Brain : a Journal of Neurology|December 17, 2013
Variant non ketotic hyperglycinemia is caused by mutations in LIAS, BOLA3 and the novel gene GLRX5Peter R Baker, Marisa W Friederich, Michael A Swanson, et al.
Pageof 6