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DiMauro

Showing results (581-590 of 942) with videos related to

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Animal : an International Journal of Animal Bioscience|November 3, 2016
Estimates of heritability and genetic correlations for milk coagulation properties and individual laboratory cheese yield in Sarda ewesA Puledda, G Gaspa, M G Manca, et al.
Neuromuscular Disorders : NMD|January 1, 1993
Atypical clinical presentations associated with the MELAS mutation at position 3243 of human mitochondrial DNAC T Moraes, F Ciacci, G Silvestri, et al.
Muscle & Nerve|January 1, 1979
Lipid storage myopathy, ichthyosis, and steatorrheaA Miranda, S DiMauro, A Eastwood, et al.
Biochemical and Biophysical Research Communications|November 22, 1995
A novel mitochondrial DNA point mutation associated with mitochondrial encephalocardiomyopathyF M Santorelli, S C Mak, M Vàzquez-Acevedo, et al.
Annals of Neurology|August 1, 1997
Association of myopathy with large-scale mitochondrial DNA duplications and deletions: which is pathogenic?G Manfredi, T Vu, E Bonilla, et al.
Journal of the Neurological Sciences|February 18, 2011
Recurrent myoglobinuria in a sporadic patient with a novel mitochondrial DNA tRNA(Ile) mutationValentina Emmanuele, Evangelia Sotiriou, Maryam Shirazi, et al.
Plos One|August 7, 2010
Treatment of CoQ(10) deficient fibroblasts with ubiquinone, CoQ analogs, and vitamin C: time- and compound-dependent effectsLuis C López, Catarina M Quinzii, Estela Area, et al.
Optics Letters|September 29, 2017
High-order harmonic generations in intense MIR fields by cascade three-wave mixing in a fractal-poled LiNbO<sub>3</sub> photonic crystalHyunwook Park, Antoine Camper, Kyle Kafka, et al.
American Journal of Human Genetics|December 23, 2006
Leigh syndrome with nephropathy and CoQ10 deficiency due to decaprenyl diphosphate synthase subunit 2 (PDSS2) mutationsLuis Carlos López, Markus Schuelke, Catarina M Quinzii, et al.
American Journal of Medical Genetics. Part A|September 17, 2004
Varying loads of the mitochondrial DNA A3243G mutation in different tissues: implications for diagnosisSara Shanske, Jacklyn Pancrudo, Petra Kaufmann, et al.
Pageof 95

Showing results (581-590 of 942) with videos related to

Sort By:
Pageof 95
Animal : an International Journal of Animal Bioscience|November 3, 2016
Estimates of heritability and genetic correlations for milk coagulation properties and individual laboratory cheese yield in Sarda ewesA Puledda, G Gaspa, M G Manca, et al.
Neuromuscular Disorders : NMD|January 1, 1993
Atypical clinical presentations associated with the MELAS mutation at position 3243 of human mitochondrial DNAC T Moraes, F Ciacci, G Silvestri, et al.
Muscle & Nerve|January 1, 1979
Lipid storage myopathy, ichthyosis, and steatorrheaA Miranda, S DiMauro, A Eastwood, et al.
Biochemical and Biophysical Research Communications|November 22, 1995
A novel mitochondrial DNA point mutation associated with mitochondrial encephalocardiomyopathyF M Santorelli, S C Mak, M Vàzquez-Acevedo, et al.
Annals of Neurology|August 1, 1997
Association of myopathy with large-scale mitochondrial DNA duplications and deletions: which is pathogenic?G Manfredi, T Vu, E Bonilla, et al.
Journal of the Neurological Sciences|February 18, 2011
Recurrent myoglobinuria in a sporadic patient with a novel mitochondrial DNA tRNA(Ile) mutationValentina Emmanuele, Evangelia Sotiriou, Maryam Shirazi, et al.
Plos One|August 7, 2010
Treatment of CoQ(10) deficient fibroblasts with ubiquinone, CoQ analogs, and vitamin C: time- and compound-dependent effectsLuis C López, Catarina M Quinzii, Estela Area, et al.
Optics Letters|September 29, 2017
High-order harmonic generations in intense MIR fields by cascade three-wave mixing in a fractal-poled LiNbO<sub>3</sub> photonic crystalHyunwook Park, Antoine Camper, Kyle Kafka, et al.
American Journal of Human Genetics|December 23, 2006
Leigh syndrome with nephropathy and CoQ10 deficiency due to decaprenyl diphosphate synthase subunit 2 (PDSS2) mutationsLuis Carlos López, Markus Schuelke, Catarina M Quinzii, et al.
American Journal of Medical Genetics. Part A|September 17, 2004
Varying loads of the mitochondrial DNA A3243G mutation in different tissues: implications for diagnosisSara Shanske, Jacklyn Pancrudo, Petra Kaufmann, et al.
Pageof 95