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I A Trounce

Showing results (1-10 of 8) with videos related to

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Rejuvenation Research|August 22, 2007
Mitochondria in aging and Alzheimer's diseaseP J Crouch, K Cimdins, J A Duce, et al.
Pharmacology & Therapeutics|June 12, 2016
Emerging Mitochondrial Therapeutic Targets in Optic NeuropathiesM I G Lopez Sanchez, J G Crowston, D A Mackey, et al.
The Journal of Biological Chemistry|September 8, 2000
Functional analysis of lymphoblast and cybrid mitochondria containing the 3460, 11778, or 14484 Leber's hereditary optic neuropathy mitochondrial DNA mutationM D Brown, I A Trounce, A S Jun, et al.
Molecular and Cellular Biology|March 1, 1996
Use of transmitochondrial cybrids to assign a complex I defect to the mitochondrial DNA-encoded NADH dehydrogenase subunit 6 gene mutation at nucleotide pair 14459 that causes Leber hereditary optic neuropathy and dystoniaA S Jun, I A Trounce, M D Brown, et al.
Nature Genetics|July 1, 1997
A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocatorB H Graham, K G Waymire, B Cottrell, et al.
Eye (London, England)|January 7, 2017
Targeting retinal ganglion cell recoveryJ G Crowston, E T Fahy, L Fry, et al.
Mitochondrion|July 20, 2010
Xenomitochondrial mice: investigation into mitochondrial compensatory mechanismsM V Cannon, D A Dunn, M H Irwin, et al.
Journal of Bioenergetics and Biomembranes|September 21, 2004
Development and initial characterization of xenomitochondrial miceI A Trounce, M McKenzie, C A Cassar, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Rejuvenation Research|August 22, 2007
Mitochondria in aging and Alzheimer's diseaseP J Crouch, K Cimdins, J A Duce, et al.
Pharmacology & Therapeutics|June 12, 2016
Emerging Mitochondrial Therapeutic Targets in Optic NeuropathiesM I G Lopez Sanchez, J G Crowston, D A Mackey, et al.
The Journal of Biological Chemistry|September 8, 2000
Functional analysis of lymphoblast and cybrid mitochondria containing the 3460, 11778, or 14484 Leber's hereditary optic neuropathy mitochondrial DNA mutationM D Brown, I A Trounce, A S Jun, et al.
Molecular and Cellular Biology|March 1, 1996
Use of transmitochondrial cybrids to assign a complex I defect to the mitochondrial DNA-encoded NADH dehydrogenase subunit 6 gene mutation at nucleotide pair 14459 that causes Leber hereditary optic neuropathy and dystoniaA S Jun, I A Trounce, M D Brown, et al.
Nature Genetics|July 1, 1997
A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocatorB H Graham, K G Waymire, B Cottrell, et al.
Eye (London, England)|January 7, 2017
Targeting retinal ganglion cell recoveryJ G Crowston, E T Fahy, L Fry, et al.
Mitochondrion|July 20, 2010
Xenomitochondrial mice: investigation into mitochondrial compensatory mechanismsM V Cannon, D A Dunn, M H Irwin, et al.
Journal of Bioenergetics and Biomembranes|September 21, 2004
Development and initial characterization of xenomitochondrial miceI A Trounce, M McKenzie, C A Cassar, et al.
Pageof 1