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John M Land

Showing results (21-30 of 29) with videos related to

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Biology Open|August 17, 2013
Nrf2 impacts cellular bioenergetics by controlling substrate availability for mitochondrial respirationKira M Holmström, Liam Baird, Ying Zhang, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|October 2, 2012
Poor maternal nutrition followed by accelerated postnatal growth leads to alterations in DNA damage and repair, oxidative and nitrosative stress, and oxidative defense capacity in rat heartJane L Tarry-Adkins, Malgorzata S Martin-Gronert, Denise S Fernandez-Twinn, et al.
Molecular Genetics and Metabolism|June 27, 2006
Phenotypic variability of mitochondrial disease caused by a nuclear mutation in complex IIAlistair T Pagnamenta, Iain P Hargreaves, Andrew J Duncan, et al.
Neuromuscular Disorders : NMD|December 19, 2009
A novel mitochondrial MTND5 frameshift mutation causing isolated complex I deficiency, renal failure and myopathyCharlotte L Alston, Monika Morak, Christopher Reid, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 8, 2013
Novel C12orf65 mutations in patients with axonal neuropathy and optic atrophyArianna Tucci, Yo-Tsen Liu, Elisabeth Preza, et al.
Plos One|August 23, 2011
Uncovering genomic causes of co-morbidity in epilepsy: gene-driven phenotypic characterization of rare microdeletionsDalia Kasperavičiūtė, Claudia B Catarino, Krishna Chinthapalli, et al.
Orphanet Journal of Rare Diseases|July 9, 2013
SURF1 deficiency: a multi-centre natural history studyYehani Wedatilake, Ruth M Brown, Robert McFarland, et al.
JAMA Neurology|October 9, 2013
COX10 mutations resulting in complex multisystem mitochondrial disease that remains stable into adulthoodRobert D S Pitceathly, Jan-Willem Taanman, Shamima Rahman, et al.
Brain : a Journal of Neurology|November 21, 2013
Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2A Reghan Foley, Manoj P Menezes, Amelie Pandraud, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Biology Open|August 17, 2013
Nrf2 impacts cellular bioenergetics by controlling substrate availability for mitochondrial respirationKira M Holmström, Liam Baird, Ying Zhang, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|October 2, 2012
Poor maternal nutrition followed by accelerated postnatal growth leads to alterations in DNA damage and repair, oxidative and nitrosative stress, and oxidative defense capacity in rat heartJane L Tarry-Adkins, Malgorzata S Martin-Gronert, Denise S Fernandez-Twinn, et al.
Molecular Genetics and Metabolism|June 27, 2006
Phenotypic variability of mitochondrial disease caused by a nuclear mutation in complex IIAlistair T Pagnamenta, Iain P Hargreaves, Andrew J Duncan, et al.
Neuromuscular Disorders : NMD|December 19, 2009
A novel mitochondrial MTND5 frameshift mutation causing isolated complex I deficiency, renal failure and myopathyCharlotte L Alston, Monika Morak, Christopher Reid, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 8, 2013
Novel C12orf65 mutations in patients with axonal neuropathy and optic atrophyArianna Tucci, Yo-Tsen Liu, Elisabeth Preza, et al.
Plos One|August 23, 2011
Uncovering genomic causes of co-morbidity in epilepsy: gene-driven phenotypic characterization of rare microdeletionsDalia Kasperavičiūtė, Claudia B Catarino, Krishna Chinthapalli, et al.
Orphanet Journal of Rare Diseases|July 9, 2013
SURF1 deficiency: a multi-centre natural history studyYehani Wedatilake, Ruth M Brown, Robert McFarland, et al.
JAMA Neurology|October 9, 2013
COX10 mutations resulting in complex multisystem mitochondrial disease that remains stable into adulthoodRobert D S Pitceathly, Jan-Willem Taanman, Shamima Rahman, et al.
Brain : a Journal of Neurology|November 21, 2013
Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2A Reghan Foley, Manoj P Menezes, Amelie Pandraud, et al.
Pageof 3