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Rejuvenation Research
|
August 22, 2007
Mitochondria in aging and Alzheimer's disease
P J Crouch, K Cimdins, J A Duce, et al.
Pharmacology & Therapeutics
|
June 12, 2016
Emerging Mitochondrial Therapeutic Targets in Optic Neuropathies
M 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 mutation
M 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 dystonia
A 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 translocator
B H Graham, K G Waymire, B Cottrell, et al.
Eye (London, England)
|
January 7, 2017
Targeting retinal ganglion cell recovery
J G Crowston, E T Fahy, L Fry, et al.
Mitochondrion
|
July 20, 2010
Xenomitochondrial mice: investigation into mitochondrial compensatory mechanisms
M V Cannon, D A Dunn, M H Irwin, et al.
Journal of Bioenergetics and Biomembranes
|
September 21, 2004
Development and initial characterization of xenomitochondrial mice
I A Trounce, M McKenzie, C A Cassar, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
Rejuvenation Research
|
August 22, 2007
Mitochondria in aging and Alzheimer's disease
P J Crouch, K Cimdins, J A Duce, et al.
Pharmacology & Therapeutics
|
June 12, 2016
Emerging Mitochondrial Therapeutic Targets in Optic Neuropathies
M 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 mutation
M 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 dystonia
A 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 translocator
B H Graham, K G Waymire, B Cottrell, et al.
Eye (London, England)
|
January 7, 2017
Targeting retinal ganglion cell recovery
J G Crowston, E T Fahy, L Fry, et al.
Mitochondrion
|
July 20, 2010
Xenomitochondrial mice: investigation into mitochondrial compensatory mechanisms
M V Cannon, D A Dunn, M H Irwin, et al.
Journal of Bioenergetics and Biomembranes
|
September 21, 2004
Development and initial characterization of xenomitochondrial mice
I A Trounce, M McKenzie, C A Cassar, et al.
Page
of 1