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DiMauro

Showing results (851-860 of 942) with videos related to

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Neurology|November 19, 2011
Natural history of MELAS associated with mitochondrial DNA m.3243A>G genotypeP Kaufmann, K Engelstad, Y Wei, et al.
Brain : a Journal of Neurology|October 9, 2012
Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletionsDario Ronchi, Caterina Garone, Andreina Bordoni, et al.
JAMA Neurology|February 10, 2015
Deep intronic GBE1 mutation in manifesting heterozygous patients with adult polyglucosan body diseaseH Orhan Akman, Or Kakhlon, Jorida Coku, et al.
Molecular Genetics and Metabolism|May 23, 2022
Time to harmonize mitochondrial syndrome nomenclature and classification: A consensus from the North American Mitochondrial Disease Consortium (NAMDC)Valentina Emmanuele, Jaya Ganesh, Georgirene Vladutiu, et al.
Bioorganic & Medicinal Chemistry Letters|December 18, 2007
N-(3-(phenylcarbamoyl)arylpyrimidine)-5-carboxamides as potent and selective inhibitors of Lck: structure, synthesis and SARHolly L Deak, John R Newcomb, Joseph J Nunes, et al.
The Journal of Pediatrics|August 4, 1999
The mitochondrial DNA C3303T mutation can cause cardiomyopathy and/or skeletal myopathyC Bruno, D M Kirby, Y Koga, et al.
Antioxidants (Basel, Switzerland)|May 27, 2023
Online Home-Based Physical Activity Counteracts Changes of Redox-Status Biomarkers and Fitness Profiles during Treatment Programs in Postsurgery Female Breast Cancer PatientsChantalle Moulton, Elisa Grazioli, Cristina Antinozzi, 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.
Mitochondrion|January 13, 2010
Extensive screening system using suspension array technology to detect mitochondrial DNA point mutationsYutaka Nishigaki, Hitomi Ueno, Jorida Coku, et al.
BMC Structural Biology|March 20, 2009
Rational mutagenesis to support structure-based drug design: MAPKAP kinase 2 as a case studyMaria A Argiriadi, Silvino Sousa, David Banach, et al.
Pageof 95

Showing results (851-860 of 942) with videos related to

Sort By:
Pageof 95
Neurology|November 19, 2011
Natural history of MELAS associated with mitochondrial DNA m.3243A>G genotypeP Kaufmann, K Engelstad, Y Wei, et al.
Brain : a Journal of Neurology|October 9, 2012
Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletionsDario Ronchi, Caterina Garone, Andreina Bordoni, et al.
JAMA Neurology|February 10, 2015
Deep intronic GBE1 mutation in manifesting heterozygous patients with adult polyglucosan body diseaseH Orhan Akman, Or Kakhlon, Jorida Coku, et al.
Molecular Genetics and Metabolism|May 23, 2022
Time to harmonize mitochondrial syndrome nomenclature and classification: A consensus from the North American Mitochondrial Disease Consortium (NAMDC)Valentina Emmanuele, Jaya Ganesh, Georgirene Vladutiu, et al.
Bioorganic & Medicinal Chemistry Letters|December 18, 2007
N-(3-(phenylcarbamoyl)arylpyrimidine)-5-carboxamides as potent and selective inhibitors of Lck: structure, synthesis and SARHolly L Deak, John R Newcomb, Joseph J Nunes, et al.
The Journal of Pediatrics|August 4, 1999
The mitochondrial DNA C3303T mutation can cause cardiomyopathy and/or skeletal myopathyC Bruno, D M Kirby, Y Koga, et al.
Antioxidants (Basel, Switzerland)|May 27, 2023
Online Home-Based Physical Activity Counteracts Changes of Redox-Status Biomarkers and Fitness Profiles during Treatment Programs in Postsurgery Female Breast Cancer PatientsChantalle Moulton, Elisa Grazioli, Cristina Antinozzi, 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.
Mitochondrion|January 13, 2010
Extensive screening system using suspension array technology to detect mitochondrial DNA point mutationsYutaka Nishigaki, Hitomi Ueno, Jorida Coku, et al.
BMC Structural Biology|March 20, 2009
Rational mutagenesis to support structure-based drug design: MAPKAP kinase 2 as a case studyMaria A Argiriadi, Silvino Sousa, David Banach, et al.
Pageof 95