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Ali Naini

Showing results (31-40 of 52) with videos related to

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American Journal of Medical Genetics. Part A|March 3, 2009
Longitudinal changes of mtDNA A3243G mutation load and level of functioning in MELASMahsa Mehrazin, Sara Shanske, Petra Kaufmann, et al.
Neuromuscular Disorders : NMD|October 26, 2002
Molecular genetic study of myophosphorylase deficiency (McArdle's disease) in two Yemenite-Jewish familiesGeorgios M Hadjigeorgiou, Menachem Sadeh, Olimpia Musumeci, et al.
Molecular Genetics and Metabolism|February 12, 2026
Rhabdomyolysis due to mtDNA pathogenic variants: Report of a subject with a novel MT-CO3 variant and review of the literatureEmanuele Barca, Nuri Jacoby, Ali Naini, et al.
Resuscitation|April 3, 2012
Coenzyme Q10 levels are low and associated with increased mortality in post-cardiac arrest patientsMichael N Cocchi, Brandon Giberson, Katherine Berg, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 19, 2003
Cyclooxygenase-2 is instrumental in Parkinson's disease neurodegenerationPeter Teismann, Kim Tieu, Dong-Kug Choi, et al.
Brain Pathology (Zurich, Switzerland)|September 28, 2004
A pathogenic peripherin gene mutation in a patient with amyotrophic lateral sclerosisConrad L Leung, Cui Zhen He, Petra Kaufmann, et al.
Child Neurology Open|May 16, 2017
A De Novo Mutation in <i>MTND6</i> Causes Generalized Dystonia in 2 Unrelated ChildrenYasemin Gulcan Kurt, Jorida Çoku, H Orhan Akman, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 31, 2008
Respiratory chain dysfunction and oxidative stress correlate with severity of primary CoQ10 deficiencyCatarina M Quinzii, Luis C López, Jakob Von-Moltke, et al.
Integrative Cancer Therapies|November 20, 2025
Phase I Randomized, Placebo-Controlled, Cross-Over Dose-Finding Study of Coenzyme Q10 on Doxorubicin Pharmacokinetics during Breast Cancer TreatmentHeather Greenlee, Katherine D Crew, Matthew Maurer, et al.
Human Molecular Genetics|May 16, 2015
Lack of aprataxin impairs mitochondrial functions via downregulation of the APE1/NRF1/NRF2 pathwayBeatriz Garcia-Diaz, Emanuele Barca, Andrea Balreira, et al.
Pageof 6

Showing results (31-40 of 52) with videos related to

Sort By:
Pageof 6
American Journal of Medical Genetics. Part A|March 3, 2009
Longitudinal changes of mtDNA A3243G mutation load and level of functioning in MELASMahsa Mehrazin, Sara Shanske, Petra Kaufmann, et al.
Neuromuscular Disorders : NMD|October 26, 2002
Molecular genetic study of myophosphorylase deficiency (McArdle's disease) in two Yemenite-Jewish familiesGeorgios M Hadjigeorgiou, Menachem Sadeh, Olimpia Musumeci, et al.
Molecular Genetics and Metabolism|February 12, 2026
Rhabdomyolysis due to mtDNA pathogenic variants: Report of a subject with a novel MT-CO3 variant and review of the literatureEmanuele Barca, Nuri Jacoby, Ali Naini, et al.
Resuscitation|April 3, 2012
Coenzyme Q10 levels are low and associated with increased mortality in post-cardiac arrest patientsMichael N Cocchi, Brandon Giberson, Katherine Berg, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 19, 2003
Cyclooxygenase-2 is instrumental in Parkinson's disease neurodegenerationPeter Teismann, Kim Tieu, Dong-Kug Choi, et al.
Brain Pathology (Zurich, Switzerland)|September 28, 2004
A pathogenic peripherin gene mutation in a patient with amyotrophic lateral sclerosisConrad L Leung, Cui Zhen He, Petra Kaufmann, et al.
Child Neurology Open|May 16, 2017
A De Novo Mutation in <i>MTND6</i> Causes Generalized Dystonia in 2 Unrelated ChildrenYasemin Gulcan Kurt, Jorida Çoku, H Orhan Akman, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 31, 2008
Respiratory chain dysfunction and oxidative stress correlate with severity of primary CoQ10 deficiencyCatarina M Quinzii, Luis C López, Jakob Von-Moltke, et al.
Integrative Cancer Therapies|November 20, 2025
Phase I Randomized, Placebo-Controlled, Cross-Over Dose-Finding Study of Coenzyme Q10 on Doxorubicin Pharmacokinetics during Breast Cancer TreatmentHeather Greenlee, Katherine D Crew, Matthew Maurer, et al.
Human Molecular Genetics|May 16, 2015
Lack of aprataxin impairs mitochondrial functions via downregulation of the APE1/NRF1/NRF2 pathwayBeatriz Garcia-Diaz, Emanuele Barca, Andrea Balreira, et al.
Pageof 6