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J M COOPER

Showing results (141-150 of 186) with videos related to

Pageof 19
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Human Molecular Genetics|November 7, 2000
Expression of mutant alpha-synuclein causes increased susceptibility to dopamine toxicityS J Tabrizi, M Orth, J M Wilkinson, et al.
Brain : a Journal of Neurology|February 25, 2000
Cytochrome oxidase immunohistochemistry: clues for genetic mechanismsS Rahman, B D Lake, J W Taanman, et al.
Optics Express|February 12, 2014
Aerosol droplet optical trap loading using surface acoustic wave nebulizationS Anand, J Nylk, S L Neale, et al.
Annals of Neurology|December 1, 1989
Mitochondrial myopathies: clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNAI J Holt, A E Harding, J M Cooper, et al.
Lab on a Chip|December 10, 2015
Assessment of biocompatibility of 3D printed photopolymers using zebrafish embryo toxicity assaysN P Macdonald, F Zhu, C J Hall, 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.
Pageof 19

Showing results (141-150 of 186) with videos related to

Sort By:
Pageof 19
Human Molecular Genetics|November 7, 2000
Expression of mutant alpha-synuclein causes increased susceptibility to dopamine toxicityS J Tabrizi, M Orth, J M Wilkinson, et al.
Brain : a Journal of Neurology|February 25, 2000
Cytochrome oxidase immunohistochemistry: clues for genetic mechanismsS Rahman, B D Lake, J W Taanman, et al.
Optics Express|February 12, 2014
Aerosol droplet optical trap loading using surface acoustic wave nebulizationS Anand, J Nylk, S L Neale, et al.
Annals of Neurology|December 1, 1989
Mitochondrial myopathies: clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNAI J Holt, A E Harding, J M Cooper, et al.
Lab on a Chip|December 10, 2015
Assessment of biocompatibility of 3D printed photopolymers using zebrafish embryo toxicity assaysN P Macdonald, F Zhu, C J Hall, 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.
Pageof 19