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DiMauro

Showing results (791-800 of 942) with videos related to

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Neurology|April 11, 2008
Is muscle glycogenolysis impaired in X-linked phosphorylase b kinase deficiency?M C Ørngreen, H J Schelhaas, T D Jeppesen, et al.
Physical Review Letters|July 27, 2019
Disentangling Spectral Phases of Interfering Autoionizing States from Attosecond Interferometric MeasurementsLou Barreau, C Leon M Petersson, Markus Klinker, et al.
Neurology|August 24, 2005
Infantile encephalomyopathy and nephropathy with CoQ10 deficiency: a CoQ10-responsive conditionL Salviati, S Sacconi, L Murer, et al.
Journal of the Neurological Sciences|March 4, 2008
A novel tRNA(Val) mitochondrial DNA mutation causing MELASKurenai Tanji, Petra Kaufmann, Ali B Naini, et al.
The Journal of Chemical Physics|May 17, 2019
Probing the interplay between geometric and electronic-structure features via high-harmonic spectroscopyT T Gorman, T D Scarborough, P M Abanador, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Structure-based design of 2-aminopyridine oxazolidinones as potent and selective tankyrase inhibitorsHongbing Huang, Angel Guzman-Perez, Lisa Acquaviva, et al.
ACS Central Science|January 27, 2025
NSF NeXUS: A New Model for Accessing the Frontiers of Ultrafast ScienceL Robert Baker, Louis F DiMauro, Claudia Turro, et al.
American Journal of Medical Genetics|May 26, 1999
Maternally inherited nonsyndromic hearing lossR A Friedman, Y Bykhovskaya, C M Sue, et al.
Journal of Medical Genetics|January 8, 2008
Further pitfalls in the diagnosis of mtDNA mutations: homoplasmic mt-tRNA mutationsH A L Tuppen, F Fattori, R Carrozzo, et al.
Journal of the Neurological Sciences|October 7, 2008
Neonatal mitochondrial encephaloneuromyopathy due to a defect of mitochondrial protein synthesisClaudia C Ferreiro-Barros, Célia H Tengan, Mário H Barros, et al.
Pageof 95

Showing results (791-800 of 942) with videos related to

Sort By:
Pageof 95
Neurology|April 11, 2008
Is muscle glycogenolysis impaired in X-linked phosphorylase b kinase deficiency?M C Ørngreen, H J Schelhaas, T D Jeppesen, et al.
Physical Review Letters|July 27, 2019
Disentangling Spectral Phases of Interfering Autoionizing States from Attosecond Interferometric MeasurementsLou Barreau, C Leon M Petersson, Markus Klinker, et al.
Neurology|August 24, 2005
Infantile encephalomyopathy and nephropathy with CoQ10 deficiency: a CoQ10-responsive conditionL Salviati, S Sacconi, L Murer, et al.
Journal of the Neurological Sciences|March 4, 2008
A novel tRNA(Val) mitochondrial DNA mutation causing MELASKurenai Tanji, Petra Kaufmann, Ali B Naini, et al.
The Journal of Chemical Physics|May 17, 2019
Probing the interplay between geometric and electronic-structure features via high-harmonic spectroscopyT T Gorman, T D Scarborough, P M Abanador, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Structure-based design of 2-aminopyridine oxazolidinones as potent and selective tankyrase inhibitorsHongbing Huang, Angel Guzman-Perez, Lisa Acquaviva, et al.
ACS Central Science|January 27, 2025
NSF NeXUS: A New Model for Accessing the Frontiers of Ultrafast ScienceL Robert Baker, Louis F DiMauro, Claudia Turro, et al.
American Journal of Medical Genetics|May 26, 1999
Maternally inherited nonsyndromic hearing lossR A Friedman, Y Bykhovskaya, C M Sue, et al.
Journal of Medical Genetics|January 8, 2008
Further pitfalls in the diagnosis of mtDNA mutations: homoplasmic mt-tRNA mutationsH A L Tuppen, F Fattori, R Carrozzo, et al.
Journal of the Neurological Sciences|October 7, 2008
Neonatal mitochondrial encephaloneuromyopathy due to a defect of mitochondrial protein synthesisClaudia C Ferreiro-Barros, Célia H Tengan, Mário H Barros, et al.
Pageof 95