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C M Sue

Showing results (21-30 of 44) with videos related to

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Human Reproduction (Oxford, England)|March 14, 2019
Public attitudes towards novel reproductive technologies: a citizens' jury on mitochondrial donationA J Newson, S de Lacey, D K Dowling, et al.
Journal of Child Neurology|December 7, 2000
G8363A mutation in the mitochondrial DNA transfer ribonucleic acidLys gene: another cause of Leigh syndromeA Shtilbans, S Shanske, S Goodman, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1993
Mitochondrial encephalomyopathy: variable clinical expression within a single kindredD Crimmins, J G Morris, G L Walker, et al.
Neuromuscular Disorders : NMD|November 2, 1999
Manifesting heterozygotes in a Japanese family with a novel mutation in the muscle-specific phosphoglycerate mutase (PGAM-M) geneG M Hadjigeorgiou, N Kawashima, C Bruno, et al.
Annals of Neurology|June 9, 1999
Exercise intolerance due to a nonsense mutation in the mtDNA ND4 geneA L Andreu, K Tanji, C Bruno, et al.
Journal of Child Neurology|July 17, 2001
A5814G mutation in mitochondrial DNA can cause mitochondrial myopathy and cardiomyopathyC Karadimas, K Tanji, M Geremek, et al.
Human Genetics|September 15, 2000
Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHMK L Friend, D Crimmins, T G Phan, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 14, 1998
Neuroradiological features of six kindreds with MELAS tRNA(Leu) A2343G point mutation: implications for pathogenesisC M Sue, D S Crimmins, Y S Soo, et al.
Annals of Neurology|March 20, 1998
Cochlear origin of hearing loss in MELAS syndromeC M Sue, L J Lipsett, D S Crimmins, et al.
American Journal of Human Genetics|August 12, 1999
A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IVC Bruno, A Martinuzzi, Y Tang, et al.
Pageof 5

Showing results (21-30 of 44) with videos related to

Sort By:
Pageof 5
Human Reproduction (Oxford, England)|March 14, 2019
Public attitudes towards novel reproductive technologies: a citizens' jury on mitochondrial donationA J Newson, S de Lacey, D K Dowling, et al.
Journal of Child Neurology|December 7, 2000
G8363A mutation in the mitochondrial DNA transfer ribonucleic acidLys gene: another cause of Leigh syndromeA Shtilbans, S Shanske, S Goodman, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1993
Mitochondrial encephalomyopathy: variable clinical expression within a single kindredD Crimmins, J G Morris, G L Walker, et al.
Neuromuscular Disorders : NMD|November 2, 1999
Manifesting heterozygotes in a Japanese family with a novel mutation in the muscle-specific phosphoglycerate mutase (PGAM-M) geneG M Hadjigeorgiou, N Kawashima, C Bruno, et al.
Annals of Neurology|June 9, 1999
Exercise intolerance due to a nonsense mutation in the mtDNA ND4 geneA L Andreu, K Tanji, C Bruno, et al.
Journal of Child Neurology|July 17, 2001
A5814G mutation in mitochondrial DNA can cause mitochondrial myopathy and cardiomyopathyC Karadimas, K Tanji, M Geremek, et al.
Human Genetics|September 15, 2000
Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHMK L Friend, D Crimmins, T G Phan, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 14, 1998
Neuroradiological features of six kindreds with MELAS tRNA(Leu) A2343G point mutation: implications for pathogenesisC M Sue, D S Crimmins, Y S Soo, et al.
Annals of Neurology|March 20, 1998
Cochlear origin of hearing loss in MELAS syndromeC M Sue, L J Lipsett, D S Crimmins, et al.
American Journal of Human Genetics|August 12, 1999
A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IVC Bruno, A Martinuzzi, Y Tang, et al.
Pageof 5