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C M Sue

Showing results (31-40 of 44) with videos related to

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Annals of Neurology|January 23, 1999
A nonsense mutation (G15059A) in the cytochrome b gene in a patient with exercise intolerance and myoglobinuriaA L Andreu, C Bruno, T C Dunne, et al.
Neurology|September 12, 2000
Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNAC L Karadimas, P Greenstein, C M Sue, et al.
The Journal of Pediatrics|June 4, 1999
Infantile encephalopathy associated with the MELAS A3243G mutationC M Sue, C Bruno, A L Andreu, et al.
Neurology|June 17, 1999
Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNA(Ser(UCN)) geneC M Sue, K Tanji, G Hadjigeorgiou, et al.
American Journal of Medical Genetics|May 26, 1999
Maternally inherited nonsyndromic hearing lossR A Friedman, Y Bykhovskaya, C M Sue, et al.
Stem Cell Research|October 27, 2023
Generation of the iPSC line FINi002-A from a male Parkinson's disease patient carrying compound heterozygous mutations in the PRKN geneC Pavan, J Jin, S Jong, et al.
Parkinsonism & Related Disorders|January 17, 2012
A DNA resequencing array for genes involved in Parkinson's diseaseE J Wilkins, J P Rubio, K E Kotschet, et al.
European Journal of Neurology|July 21, 2012
Glucocerebrosidase mutations in a Serbian Parkinson's disease populationK R Kumar, A Ramirez, A Göbel, et al.
Annals of Neurology|May 11, 2000
Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2C M Sue, C Karadimas, N Checcarelli, et al.
Endocrine-Related Cancer|March 14, 2014
Overexpression of miR-210 is associated with SDH-related pheochromocytomas, paragangliomas, and gastrointestinal stromal tumoursV H M Tsang, T Dwight, D E Benn, et al.
Pageof 5

Showing results (31-40 of 44) with videos related to

Sort By:
Pageof 5
Annals of Neurology|January 23, 1999
A nonsense mutation (G15059A) in the cytochrome b gene in a patient with exercise intolerance and myoglobinuriaA L Andreu, C Bruno, T C Dunne, et al.
Neurology|September 12, 2000
Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNAC L Karadimas, P Greenstein, C M Sue, et al.
The Journal of Pediatrics|June 4, 1999
Infantile encephalopathy associated with the MELAS A3243G mutationC M Sue, C Bruno, A L Andreu, et al.
Neurology|June 17, 1999
Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNA(Ser(UCN)) geneC M Sue, K Tanji, G Hadjigeorgiou, et al.
American Journal of Medical Genetics|May 26, 1999
Maternally inherited nonsyndromic hearing lossR A Friedman, Y Bykhovskaya, C M Sue, et al.
Stem Cell Research|October 27, 2023
Generation of the iPSC line FINi002-A from a male Parkinson's disease patient carrying compound heterozygous mutations in the PRKN geneC Pavan, J Jin, S Jong, et al.
Parkinsonism & Related Disorders|January 17, 2012
A DNA resequencing array for genes involved in Parkinson's diseaseE J Wilkins, J P Rubio, K E Kotschet, et al.
European Journal of Neurology|July 21, 2012
Glucocerebrosidase mutations in a Serbian Parkinson's disease populationK R Kumar, A Ramirez, A Göbel, et al.
Annals of Neurology|May 11, 2000
Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2C M Sue, C Karadimas, N Checcarelli, et al.
Endocrine-Related Cancer|March 14, 2014
Overexpression of miR-210 is associated with SDH-related pheochromocytomas, paragangliomas, and gastrointestinal stromal tumoursV H M Tsang, T Dwight, D E Benn, et al.
Pageof 5