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L A Bindoff

Showing results (31-40 of 58) with videos related to

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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.
Brain : a Journal of Neurology|April 1, 1995
Presentation and clinical investigation of mitochondrial respiratory chain disease. A study of 51 patientsM J Jackson, J A Schaefer, M A Johnson, et al.
Diabetes Care|July 1, 1994
Biochemical and molecular studies of mitochondrial function in diabetes insipidus, diabetes mellitus, optic atrophy, and deafnessM J Jackson, L A Bindoff, K Weber, et al.
Annals of Neurology|September 1, 1996
MELAS associated with a mutation in the valine transfer RNA gene of mitochondrial DNAR W Taylor, P F Chinnery, F Haldane, et al.
American Journal of Human Genetics|November 1, 1991
Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigreesN Howell, L A Bindoff, D A McCullough, et al.
Gut|December 15, 2000
Mitochondrial enteropathy: the primary pathology may not be within the gastrointestinal tractP F Chinnery, S Jones, L Sviland, et al.
The Journal of Clinical Investigation|October 1, 1992
Combined enzyme defect of mitochondrial fatty acid oxidationS Jackson, R S Kler, K Bartlett, et al.
Diabetes Care|February 1, 1995
Insulin sensitivity and mitochondrial gene mutationM Walker, R W Taylor, M W Stewart, et al.
The Journal of Biological Chemistry|September 15, 1993
Abnormal RNA processing associated with a novel tRNA mutation in mitochondrial DNA. A potential disease mechanismL A Bindoff, N Howell, J Poulton, et al.
Pageof 6

Showing results (31-40 of 58) with videos related to

Sort By:
Pageof 6
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.
Brain : a Journal of Neurology|April 1, 1995
Presentation and clinical investigation of mitochondrial respiratory chain disease. A study of 51 patientsM J Jackson, J A Schaefer, M A Johnson, et al.
Diabetes Care|July 1, 1994
Biochemical and molecular studies of mitochondrial function in diabetes insipidus, diabetes mellitus, optic atrophy, and deafnessM J Jackson, L A Bindoff, K Weber, et al.
Annals of Neurology|September 1, 1996
MELAS associated with a mutation in the valine transfer RNA gene of mitochondrial DNAR W Taylor, P F Chinnery, F Haldane, et al.
American Journal of Human Genetics|November 1, 1991
Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigreesN Howell, L A Bindoff, D A McCullough, et al.
Gut|December 15, 2000
Mitochondrial enteropathy: the primary pathology may not be within the gastrointestinal tractP F Chinnery, S Jones, L Sviland, et al.
The Journal of Clinical Investigation|October 1, 1992
Combined enzyme defect of mitochondrial fatty acid oxidationS Jackson, R S Kler, K Bartlett, et al.
Diabetes Care|February 1, 1995
Insulin sensitivity and mitochondrial gene mutationM Walker, R W Taylor, M W Stewart, et al.
The Journal of Biological Chemistry|September 15, 1993
Abnormal RNA processing associated with a novel tRNA mutation in mitochondrial DNA. A potential disease mechanismL A Bindoff, N Howell, J Poulton, et al.
Pageof 6