L A Bindoff|D M Turnbull - JoVE Visualize

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Annals of Neurology|January 1, 1993

Cytochrome c oxidase activity in single muscle fibers: assay techniques and diagnostic applicationsM A Johnson, L A Bindoff, D M Turnbull

Biochemical and Biophysical Research Communications|October 15, 1993

An antisense oligodeoxynucleotide approach to investigate the function of the nuclear-encoded subunits of human cytochrome c oxidaseZ M Chrzanowska-Lightowlers, D M Turnbull, L A Bindoff, et al.

Annals of Neurology|November 1, 1990

Absence of immunoreactive enzyme protein in short-chain acylcoenzyme A dehydrogenase deficiencyL Farnsworth, I M Shepherd, M A Johnson, et al.

Human Genetics|September 1, 1992

Mitochondrial gene segregation in mammals: is the bottleneck always narrow?N Howell, S Halvorson, I Kubacka, et al.

Journal of the Neurological Sciences|August 11, 1991

Respiratory chain abnormalities in skeletal muscle from patients with Parkinson's diseaseL A Bindoff, M A Birch-Machin, N E Cartlidge, et al.

Biochemical Medicine and Metabolic Biology|February 1, 1994

An evaluation of the measurement of the activities of complexes I-IV in the respiratory chain of human skeletal muscle mitochondriaM A Birch-Machin, H L Briggs, A A Saborido, et al.

Revue Neurologique|January 1, 1991

Deficiency of the pyruvate dehydrogenase complex and of mitochondrial fatty acid oxidationL A Bindoff, M A Birch-Machin, S Jackson, et al.

Biochemical and Biophysical Research Communications|September 15, 1989

Multiple defects of the respiratory chain including complex II in a family with myopathy and encephalopathyC Desnuelle, M Birch-Machin, J F Pellissier, et al.

American Journal of Human Genetics|February 1, 1997

A new mtDNA mutation showing accumulation with time and restriction to skeletal muscleK Weber, J N Wilson, L Taylor, et al.

Journal of the Neurological Sciences|November 1, 1989

Familial intermittent ataxia due to a defect of the E1 component of pyruvate dehydrogenase complexL A Bindoff, M A Birch-Machin, L Farnsworth, et al.

Pageof 22

Showing results (1-10 of 220) with videos related to

Sort By:

Pageof 22

Annals of Neurology|January 1, 1993

Cytochrome c oxidase activity in single muscle fibers: assay techniques and diagnostic applicationsM A Johnson, L A Bindoff, D M Turnbull

Biochemical and Biophysical Research Communications|October 15, 1993

An antisense oligodeoxynucleotide approach to investigate the function of the nuclear-encoded subunits of human cytochrome c oxidaseZ M Chrzanowska-Lightowlers, D M Turnbull, L A Bindoff, et al.

Annals of Neurology|November 1, 1990

Absence of immunoreactive enzyme protein in short-chain acylcoenzyme A dehydrogenase deficiencyL Farnsworth, I M Shepherd, M A Johnson, et al.

Human Genetics|September 1, 1992

Mitochondrial gene segregation in mammals: is the bottleneck always narrow?N Howell, S Halvorson, I Kubacka, et al.

Journal of the Neurological Sciences|August 11, 1991

Respiratory chain abnormalities in skeletal muscle from patients with Parkinson's diseaseL A Bindoff, M A Birch-Machin, N E Cartlidge, et al.

Biochemical Medicine and Metabolic Biology|February 1, 1994

An evaluation of the measurement of the activities of complexes I-IV in the respiratory chain of human skeletal muscle mitochondriaM A Birch-Machin, H L Briggs, A A Saborido, et al.

Revue Neurologique|January 1, 1991

Deficiency of the pyruvate dehydrogenase complex and of mitochondrial fatty acid oxidationL A Bindoff, M A Birch-Machin, S Jackson, et al.

Biochemical and Biophysical Research Communications|September 15, 1989

Multiple defects of the respiratory chain including complex II in a family with myopathy and encephalopathyC Desnuelle, M Birch-Machin, J F Pellissier, et al.

American Journal of Human Genetics|February 1, 1997

A new mtDNA mutation showing accumulation with time and restriction to skeletal muscleK Weber, J N Wilson, L Taylor, et al.

Journal of the Neurological Sciences|November 1, 1989

Familial intermittent ataxia due to a defect of the E1 component of pyruvate dehydrogenase complexL A Bindoff, M A Birch-Machin, L Farnsworth, et al.

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