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C T Moraes

Showing results (41-50 of 88) with videos related to

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Brain Pathology (Zurich, Switzerland)|April 1, 1992
Disorders associated with depletion of mitochondrial DNAE Ricci, C T Moraes, S Servidei, et al.
Biochimica Et Biophysica Acta|July 17, 1992
The mitochondrial tRNA(Leu)(UUR)) mutation in MELAS: a model for pathogenesisE A Schon, Y Koga, M Davidson, et al.
Neurologic Clinics|August 1, 1990
Mitochondrial encephalomyopathiesS DiMauro, E Bonilla, A Lombes, et al.
Brain Pathology (Zurich, Switzerland)|April 1, 1992
New morphological approaches to the study of mitochondrial encephalomyopathiesE Bonilla, M Sciacco, K Tanji, et al.
Mutation Research|October 23, 1997
Oxidative phosphorylation dysfunction does not increase the rate of accumulation of age-related mtDNA deletions in skeletal muscleC H Tengan, A A Gabbai, S Shanske, et al.
Science (New York, N.Y.)|April 21, 1989
A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNAE A Schon, R Rizzuto, C T Moraes, et al.
Human Mutation|January 1, 1996
Identification of a mutation in the mitochondrial tRNA(Cys) gene associated with mitochondrial encephalopathyG Manfredi, E A Schon, E Bonilla, et al.
American Journal of Human Genetics|March 1, 1990
Transcription and translation of deleted mitochondrial genomes in Kearns-Sayre syndrome: implications for pathogenesisH Nakase, C T Moraes, R Rizzuto, et al.
Molecular and Cellular Biology|March 1, 1991
Replication-competent human mitochondrial DNA lacking the heavy-strand promoter regionC T Moraes, F Andreetta, E Bonilla, et al.
Neuromuscular Disorders : NMD|September 21, 2000
A novel myopathy-associated mitochondrial DNA mutation altering the conserved size of the tRNA(Gln) anticodon loopR Dey, C H Tengan, M P Morita, et al.
Pageof 9

Showing results (41-50 of 88) with videos related to

Sort By:
Pageof 9
Brain Pathology (Zurich, Switzerland)|April 1, 1992
Disorders associated with depletion of mitochondrial DNAE Ricci, C T Moraes, S Servidei, et al.
Biochimica Et Biophysica Acta|July 17, 1992
The mitochondrial tRNA(Leu)(UUR)) mutation in MELAS: a model for pathogenesisE A Schon, Y Koga, M Davidson, et al.
Neurologic Clinics|August 1, 1990
Mitochondrial encephalomyopathiesS DiMauro, E Bonilla, A Lombes, et al.
Brain Pathology (Zurich, Switzerland)|April 1, 1992
New morphological approaches to the study of mitochondrial encephalomyopathiesE Bonilla, M Sciacco, K Tanji, et al.
Mutation Research|October 23, 1997
Oxidative phosphorylation dysfunction does not increase the rate of accumulation of age-related mtDNA deletions in skeletal muscleC H Tengan, A A Gabbai, S Shanske, et al.
Science (New York, N.Y.)|April 21, 1989
A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNAE A Schon, R Rizzuto, C T Moraes, et al.
Human Mutation|January 1, 1996
Identification of a mutation in the mitochondrial tRNA(Cys) gene associated with mitochondrial encephalopathyG Manfredi, E A Schon, E Bonilla, et al.
American Journal of Human Genetics|March 1, 1990
Transcription and translation of deleted mitochondrial genomes in Kearns-Sayre syndrome: implications for pathogenesisH Nakase, C T Moraes, R Rizzuto, et al.
Molecular and Cellular Biology|March 1, 1991
Replication-competent human mitochondrial DNA lacking the heavy-strand promoter regionC T Moraes, F Andreetta, E Bonilla, et al.
Neuromuscular Disorders : NMD|September 21, 2000
A novel myopathy-associated mitochondrial DNA mutation altering the conserved size of the tRNA(Gln) anticodon loopR Dey, C H Tengan, M P Morita, et al.
Pageof 9