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L A Bindoff

Showing results (21-30 of 58) with videos related to

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American Journal of Human Genetics|June 1, 1997
Intracellular mitochondrial triplasmy in a patient with two heteroplasmic base changesS K Bidooki, M A Johnson, Z Chrzanowska-Lightowlers, et al.
Lancet (London, England)|July 1, 1989
Mitochondrial function in Parkinson's diseaseL A Bindoff, M Birch-Machin, N E Cartlidge, 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.
European Journal of Neurology|November 22, 2007
Opsoclonus myoclonus syndrome in two cases with neuroborreliosisG O Skeie, G Eldøen, B S Skeie, 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.
Progress in Clinical and Biological Research|January 1, 1992
Combined defect of long-chain 3-hydroxyacyl-CoA dehydrogenase, 2-enoyl-CoA hydratase and 3-oxoacyl-CoA thiolaseS Jackson, R S Kler, K Bartlett, et al.
European Journal of Biochemistry|January 15, 1994
Molecular cloning and expression of a cDNA encoding human electron transfer flavoprotein-ubiquinone oxidoreductaseS I Goodman, K M Axtell, L A Bindoff, et al.
Pageof 6

Showing results (21-30 of 58) with videos related to

Sort By:
Pageof 6
American Journal of Human Genetics|June 1, 1997
Intracellular mitochondrial triplasmy in a patient with two heteroplasmic base changesS K Bidooki, M A Johnson, Z Chrzanowska-Lightowlers, et al.
Lancet (London, England)|July 1, 1989
Mitochondrial function in Parkinson's diseaseL A Bindoff, M Birch-Machin, N E Cartlidge, 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.
European Journal of Neurology|November 22, 2007
Opsoclonus myoclonus syndrome in two cases with neuroborreliosisG O Skeie, G Eldøen, B S Skeie, 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.
Progress in Clinical and Biological Research|January 1, 1992
Combined defect of long-chain 3-hydroxyacyl-CoA dehydrogenase, 2-enoyl-CoA hydratase and 3-oxoacyl-CoA thiolaseS Jackson, R S Kler, K Bartlett, et al.
European Journal of Biochemistry|January 15, 1994
Molecular cloning and expression of a cDNA encoding human electron transfer flavoprotein-ubiquinone oxidoreductaseS I Goodman, K M Axtell, L A Bindoff, et al.
Pageof 6