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C Greaves

Showing results (101-110 of 118) with videos related to

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Molecular Metabolism|April 7, 2022
Mitochondrial complex I subunit deficiency promotes pancreatic α-cell proliferationXuefei Yu, Catherine Arden, Rolando Berlinguer-Palmini, et al.
Investigative Ophthalmology & Visual Science|February 19, 2010
Mitochondrial DNA defects and selective extraocular muscle involvement in CPEOLaura C Greaves, Patrick Yu-Wai-Man, Emma L Blakely, et al.
The Journal of Experimental Medicine|December 3, 2014
Bmi1 enhances skeletal muscle regeneration through MT1-mediated oxidative stress protection in a mouse model of dystrophinopathyValentina Di Foggia, Xinyu Zhang, Danilo Licastro, et al.
Cell Stem Cell|December 4, 2014
SCNT-derived ESCs with mismatched mitochondria trigger an immune response in allogeneic hostsTobias Deuse, Dong Wang, Mandy Stubbendorff, et al.
Circulation|June 17, 1997
Early versus delayed angiotensin-converting enzyme inhibition therapy in acute myocardial infarction. The healing and early afterload reducing therapy trialM A Pfeffer, S C Greaves, J M Arnold, et al.
Plos Genetics|September 19, 2014
Clonal expansion of early to mid-life mitochondrial DNA point mutations drives mitochondrial dysfunction during human ageingLaura C Greaves, Marco Nooteboom, Joanna L Elson, et al.
The Journal of Clinical Investigation|November 5, 2003
Mitochondrial DNA mutations in human colonic crypt stem cellsRobert W Taylor, Martin J Barron, Gillian M Borthwick, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 13, 2006
Mitochondrial DNA mutations are established in human colonic stem cells, and mutated clones expand by crypt fissionLaura C Greaves, Sean L Preston, Paul J Tadrous, et al.
Hepatology (Baltimore, Md.)|March 25, 2009
Locating the stem cell niche and tracing hepatocyte lineages in human liverTariq G Fellous, Shahriar Islam, Paul J Tadrous, et al.
Clinical Science (London, England : 1979)|January 29, 2015
Novel MTND1 mutations cause isolated exercise intolerance, complex I deficiency and increased assembly factor expressionGrainne S Gorman, Emma L Blakely, Hue-Tran Hornig-Do, et al.
Pageof 12

Showing results (101-110 of 118) with videos related to

Sort By:
Pageof 12
Molecular Metabolism|April 7, 2022
Mitochondrial complex I subunit deficiency promotes pancreatic α-cell proliferationXuefei Yu, Catherine Arden, Rolando Berlinguer-Palmini, et al.
Investigative Ophthalmology & Visual Science|February 19, 2010
Mitochondrial DNA defects and selective extraocular muscle involvement in CPEOLaura C Greaves, Patrick Yu-Wai-Man, Emma L Blakely, et al.
The Journal of Experimental Medicine|December 3, 2014
Bmi1 enhances skeletal muscle regeneration through MT1-mediated oxidative stress protection in a mouse model of dystrophinopathyValentina Di Foggia, Xinyu Zhang, Danilo Licastro, et al.
Cell Stem Cell|December 4, 2014
SCNT-derived ESCs with mismatched mitochondria trigger an immune response in allogeneic hostsTobias Deuse, Dong Wang, Mandy Stubbendorff, et al.
Circulation|June 17, 1997
Early versus delayed angiotensin-converting enzyme inhibition therapy in acute myocardial infarction. The healing and early afterload reducing therapy trialM A Pfeffer, S C Greaves, J M Arnold, et al.
Plos Genetics|September 19, 2014
Clonal expansion of early to mid-life mitochondrial DNA point mutations drives mitochondrial dysfunction during human ageingLaura C Greaves, Marco Nooteboom, Joanna L Elson, et al.
The Journal of Clinical Investigation|November 5, 2003
Mitochondrial DNA mutations in human colonic crypt stem cellsRobert W Taylor, Martin J Barron, Gillian M Borthwick, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 13, 2006
Mitochondrial DNA mutations are established in human colonic stem cells, and mutated clones expand by crypt fissionLaura C Greaves, Sean L Preston, Paul J Tadrous, et al.
Hepatology (Baltimore, Md.)|March 25, 2009
Locating the stem cell niche and tracing hepatocyte lineages in human liverTariq G Fellous, Shahriar Islam, Paul J Tadrous, et al.
Clinical Science (London, England : 1979)|January 29, 2015
Novel MTND1 mutations cause isolated exercise intolerance, complex I deficiency and increased assembly factor expressionGrainne S Gorman, Emma L Blakely, Hue-Tran Hornig-Do, et al.
Pageof 12