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J M Cooper

Showing results (181-190 of 222) with videos related to

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Biochemical Society Transactions|August 1, 1990
Biochemical and molecular aspects of human mitochondrial respiratory chain disordersJ M Cooper, A H Schapira, I J Holt, et al.
American Journal of Human Genetics|May 1, 1995
Congenital encephalomyopathy and adult-onset myopathy and diabetes mellitus: different phenotypic associations of a new heteroplasmic mtDNA tRNA glutamic acid mutationM G Hanna, I Nelson, M G Sweeney, et al.
Glia|December 20, 2022
Chronic demyelination of rabbit lesions is attributable to failed oligodendrocyte progenitor cell repopulationJames J M Cooper, Jessie J Polanco, Darpan Saraswat, et al.
Human Molecular Genetics|June 1, 1997
Molecular mechanisms in mitochondrial DNA depletion syndromeJ W Taanman, A G Bodnar, J M Cooper, et al.
Cardiovascular Research|September 15, 2001
Cardiac energetics are abnormal in Friedreich ataxia patients in the absence of cardiac dysfunction and hypertrophy: an in vivo 31P magnetic resonance spectroscopy studyR Lodi, B Rajagopalan, A M Blamire, et al.
Revue Neurologique|January 1, 1991
The molecular pathology of human respiratory chain defectsJ A Morgan-Hughes, J M Cooper, A H Schapira, et al.
The Journal of Thoracic and Cardiovascular Surgery|March 1, 1993
Evaluation of lung metabolism during successful twenty-four-hour canine lung preservationH Date, A Matsumura, J K Manchester, et al.
Journal of the Neurological Sciences|July 17, 1998
Mitochondrial function, GSH and iron in neurodegeneration and Lewy body diseasesM Gu, A D Owen, S E Toffa, et al.
Pain and Therapy|April 29, 2017
Prevalence and Incidence Trends for Diagnosed Prescription Opioid Use Disorders in the United KingdomAndrew J M Cooper, Jenna Willis, Janice Fuller, et al.
Journal of Neurochemistry|December 1, 1990
Anatomic and disease specificity of NADH CoQ1 reductase (complex I) deficiency in Parkinson's diseaseA H Schapira, V M Mann, J M Cooper, et al.
Pageof 23

Showing results (181-190 of 222) with videos related to

Sort By:
Pageof 23
Biochemical Society Transactions|August 1, 1990
Biochemical and molecular aspects of human mitochondrial respiratory chain disordersJ M Cooper, A H Schapira, I J Holt, et al.
American Journal of Human Genetics|May 1, 1995
Congenital encephalomyopathy and adult-onset myopathy and diabetes mellitus: different phenotypic associations of a new heteroplasmic mtDNA tRNA glutamic acid mutationM G Hanna, I Nelson, M G Sweeney, et al.
Glia|December 20, 2022
Chronic demyelination of rabbit lesions is attributable to failed oligodendrocyte progenitor cell repopulationJames J M Cooper, Jessie J Polanco, Darpan Saraswat, et al.
Human Molecular Genetics|June 1, 1997
Molecular mechanisms in mitochondrial DNA depletion syndromeJ W Taanman, A G Bodnar, J M Cooper, et al.
Cardiovascular Research|September 15, 2001
Cardiac energetics are abnormal in Friedreich ataxia patients in the absence of cardiac dysfunction and hypertrophy: an in vivo 31P magnetic resonance spectroscopy studyR Lodi, B Rajagopalan, A M Blamire, et al.
Revue Neurologique|January 1, 1991
The molecular pathology of human respiratory chain defectsJ A Morgan-Hughes, J M Cooper, A H Schapira, et al.
The Journal of Thoracic and Cardiovascular Surgery|March 1, 1993
Evaluation of lung metabolism during successful twenty-four-hour canine lung preservationH Date, A Matsumura, J K Manchester, et al.
Journal of the Neurological Sciences|July 17, 1998
Mitochondrial function, GSH and iron in neurodegeneration and Lewy body diseasesM Gu, A D Owen, S E Toffa, et al.
Pain and Therapy|April 29, 2017
Prevalence and Incidence Trends for Diagnosed Prescription Opioid Use Disorders in the United KingdomAndrew J M Cooper, Jenna Willis, Janice Fuller, et al.
Journal of Neurochemistry|December 1, 1990
Anatomic and disease specificity of NADH CoQ1 reductase (complex I) deficiency in Parkinson's diseaseA H Schapira, V M Mann, J M Cooper, et al.
Pageof 23