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K Tanji

Showing results (81-90 of 90) 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 New England Journal of Medicine|September 30, 1999
Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNAA L Andreu, M G Hanna, H Reichmann, 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.
Annals of Neurology|June 1, 1996
Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: a study of 56 patientsF M Santorelli, M Sciacco, K Tanji, et al.
Neurology|June 20, 1998
Clinical manifestations of mitochondrial DNA depletionT H Vu, M Sciacco, K Tanji, 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.
Nature|September 6, 2000
Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease)I Nishino, J Fu, K Tanji, et al.
Neuroreport|December 1, 2001
Interleukin-1beta stimulates galectin-9 expression in human astrocytesH Yoshida, T Imaizumi, M Kumagai, et al.
Nature Genetics|November 5, 1999
Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly geneL C Papadopoulou, C M Sue, M M Davidson, et al.
Pageof 9

Showing results (81-90 of 90) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 90 results.
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 New England Journal of Medicine|September 30, 1999
Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNAA L Andreu, M G Hanna, H Reichmann, 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.
Annals of Neurology|June 1, 1996
Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: a study of 56 patientsF M Santorelli, M Sciacco, K Tanji, et al.
Neurology|June 20, 1998
Clinical manifestations of mitochondrial DNA depletionT H Vu, M Sciacco, K Tanji, 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.
Nature|September 6, 2000
Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease)I Nishino, J Fu, K Tanji, et al.
Neuroreport|December 1, 2001
Interleukin-1beta stimulates galectin-9 expression in human astrocytesH Yoshida, T Imaizumi, M Kumagai, et al.
Nature Genetics|November 5, 1999
Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly geneL C Papadopoulou, C M Sue, M M Davidson, et al.
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