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M J Jackson

Showing results (281-290 of 292) with videos related to

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Pediatric Nephrology (Berlin, Germany)|August 1, 1995
Neonatal Fanconi syndrome due to deficiency of complex III of the respiratory chainA A Morris, R W Taylor, M A Birch-Machin, et al.
Diabetes Care|November 1, 1995
Insulin and proinsulin secretion in subjects with abnormal glucose tolerance and a mitochondrial tRNA(Leu(UUR)) mutationM Walker, R W Taylor, M W Stewart, et al.
The European Journal of Neuroscience|April 21, 2006
MPTP treatment of common marmosets impairs proteasomal enzyme activity and decreases expression of structural and regulatory elements of the 26S proteasomeB-Y Zeng, M M Iravani, S-T Lin, et al.
Advances in Neurology|July 20, 1999
Antiparkinsonian activity of adenosine A2A antagonists in experimental modelsY Kuwana, S Shiozaki, T Kanda, et al.
American Journal of Physiology. Cell Physiology|April 13, 2004
Role of mitochondrial superoxide dismutase in contraction-induced generation of reactive oxygen species in skeletal muscle extracellular spaceA McArdle, J van der Meulen, G L Close, et al.
Annals of Neurology|February 1, 1996
Deficiency of complex II of the mitochondrial respiratory chain in late-onset optic atrophy and ataxiaR W Taylor, M A Birch-Machin, J Schaefer, et al.
Transplantation Proceedings|March 27, 2001
Effects of angiotensin-converting-enzyme inhibitors on progression to end-stage renal failure in chronic vascular rejectionR Rustom, M T Paraoan, R A Sells, et al.
Eneuro|February 22, 2023
Deletion of <i>Sod1</i> in Motor Neurons Exacerbates Age-Related Changes in Axons and Neuromuscular Junctions in MiceN Pollock, P C Macpherson, C A Staunton, et al.
Free Radical Biology & Medicine|February 15, 2014
Lifelong training preserves some redox-regulated adaptive responses after an acute exercise stimulus in aged human skeletal muscleJ N Cobley, G K Sakellariou, D J Owens, et al.
Nature Genetics|July 5, 2001
Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia diseaseA R Curtis, C Fey, C M Morris, et al.
Pageof 30

Showing results (281-290 of 292) with videos related to

Sort By:
Pageof 30
Pediatric Nephrology (Berlin, Germany)|August 1, 1995
Neonatal Fanconi syndrome due to deficiency of complex III of the respiratory chainA A Morris, R W Taylor, M A Birch-Machin, et al.
Diabetes Care|November 1, 1995
Insulin and proinsulin secretion in subjects with abnormal glucose tolerance and a mitochondrial tRNA(Leu(UUR)) mutationM Walker, R W Taylor, M W Stewart, et al.
The European Journal of Neuroscience|April 21, 2006
MPTP treatment of common marmosets impairs proteasomal enzyme activity and decreases expression of structural and regulatory elements of the 26S proteasomeB-Y Zeng, M M Iravani, S-T Lin, et al.
Advances in Neurology|July 20, 1999
Antiparkinsonian activity of adenosine A2A antagonists in experimental modelsY Kuwana, S Shiozaki, T Kanda, et al.
American Journal of Physiology. Cell Physiology|April 13, 2004
Role of mitochondrial superoxide dismutase in contraction-induced generation of reactive oxygen species in skeletal muscle extracellular spaceA McArdle, J van der Meulen, G L Close, et al.
Annals of Neurology|February 1, 1996
Deficiency of complex II of the mitochondrial respiratory chain in late-onset optic atrophy and ataxiaR W Taylor, M A Birch-Machin, J Schaefer, et al.
Transplantation Proceedings|March 27, 2001
Effects of angiotensin-converting-enzyme inhibitors on progression to end-stage renal failure in chronic vascular rejectionR Rustom, M T Paraoan, R A Sells, et al.
Eneuro|February 22, 2023
Deletion of <i>Sod1</i> in Motor Neurons Exacerbates Age-Related Changes in Axons and Neuromuscular Junctions in MiceN Pollock, P C Macpherson, C A Staunton, et al.
Free Radical Biology & Medicine|February 15, 2014
Lifelong training preserves some redox-regulated adaptive responses after an acute exercise stimulus in aged human skeletal muscleJ N Cobley, G K Sakellariou, D J Owens, et al.
Nature Genetics|July 5, 2001
Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia diseaseA R Curtis, C Fey, C M Morris, et al.
Pageof 30