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Pediatric Nephrology (Berlin, Germany)
|
August 1, 1995
Neonatal Fanconi syndrome due to deficiency of complex III of the respiratory chain
A 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)) mutation
M 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 proteasome
B-Y Zeng, M M Iravani, S-T Lin, et al.
Advances in Neurology
|
July 20, 1999
Antiparkinsonian activity of adenosine A2A antagonists in experimental models
Y 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 space
A 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 ataxia
R 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 rejection
R 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 Mice
N 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 muscle
J 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 disease
A R Curtis, C Fey, C M Morris, et al.
Page
of 30
Search research articles
Search
Showing results (281-290 of 292) with videos related to
Sort By:
Page
of 30
Pediatric Nephrology (Berlin, Germany)
|
August 1, 1995
Neonatal Fanconi syndrome due to deficiency of complex III of the respiratory chain
A 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)) mutation
M 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 proteasome
B-Y Zeng, M M Iravani, S-T Lin, et al.
Advances in Neurology
|
July 20, 1999
Antiparkinsonian activity of adenosine A2A antagonists in experimental models
Y 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 space
A 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 ataxia
R 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 rejection
R 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 Mice
N 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 muscle
J 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 disease
A R Curtis, C Fey, C M Morris, et al.
Page
of 30