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Massimo Zeviani

Showing results (251-260 of 289) with videos related to

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EMBO Molecular Medicine|April 14, 2019
miR-181a/b downregulation exerts a protective action on mitochondrial disease modelsAlessia Indrieri, Sabrina Carrella, Alessia Romano, et al.
Human Reproduction (Oxford, England)|January 27, 2017
PGD for the m.14487 T>C mitochondrial DNA mutation resulted in the birth of a healthy boySuzanne C E H Sallevelt, Joseph C F M Dreesen, Marion Drüsedau, et al.
Cell Metabolism|May 13, 2014
Pharmacological Inhibition of poly(ADP-ribose) polymerases improves fitness and mitochondrial function in skeletal muscleEija Pirinen, Carles Cantó, Young Suk Jo, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|July 11, 2013
Decreased in vitro mitochondrial function is associated with enhanced brain metabolism, blood flow, and memory in Surf1-deficient miceAi-Ling Lin, Daniel A Pulliam, Sathyaseelan S Deepa, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|February 26, 2017
Down-regulation of the mitochondrial aspartate-glutamate carrier isoform 1 AGC1 inhibits proliferation and N-acetylaspartate synthesis in Neuro2A cellsEmanuela Profilo, Luis Emiliano Peña-Altamira, Mariangela Corricelli, et al.
American Journal of Ophthalmology|June 8, 2014
Early macular retinal ganglion cell loss in dominant optic atrophy: genotype-phenotype correlationPiero Barboni, Giacomo Savini, Maria Lucia Cascavilla, et al.
Lancet (London, England)|August 18, 2004
Risk of developing a mitochondrial DNA deletion disorderPatrick F Chinnery, Salvatore DiMauro, Sara Shanske, et al.
Human Mutation|August 10, 2013
MTO1 mutations are associated with hypertrophic cardiomyopathy and lactic acidosis and cause respiratory chain deficiency in humans and yeastEnrico Baruffini, Cristina Dallabona, Federica Invernizzi, et al.
Neurology|October 30, 2016
FGF21 is a biomarker for mitochondrial translation and mtDNA maintenance disordersJenni M Lehtonen, Saara Forsström, Emanuela Bottani, et al.
Cell Metabolism|October 5, 2022
Two independent respiratory chains adapt OXPHOS performance to glycolytic switchErika Fernández-Vizarra, Sandra López-Calcerrada, Ana Sierra-Magro, et al.
Pageof 29

Showing results (251-260 of 289) with videos related to

Sort By:
Pageof 29
EMBO Molecular Medicine|April 14, 2019
miR-181a/b downregulation exerts a protective action on mitochondrial disease modelsAlessia Indrieri, Sabrina Carrella, Alessia Romano, et al.
Human Reproduction (Oxford, England)|January 27, 2017
PGD for the m.14487 T>C mitochondrial DNA mutation resulted in the birth of a healthy boySuzanne C E H Sallevelt, Joseph C F M Dreesen, Marion Drüsedau, et al.
Cell Metabolism|May 13, 2014
Pharmacological Inhibition of poly(ADP-ribose) polymerases improves fitness and mitochondrial function in skeletal muscleEija Pirinen, Carles Cantó, Young Suk Jo, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|July 11, 2013
Decreased in vitro mitochondrial function is associated with enhanced brain metabolism, blood flow, and memory in Surf1-deficient miceAi-Ling Lin, Daniel A Pulliam, Sathyaseelan S Deepa, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|February 26, 2017
Down-regulation of the mitochondrial aspartate-glutamate carrier isoform 1 AGC1 inhibits proliferation and N-acetylaspartate synthesis in Neuro2A cellsEmanuela Profilo, Luis Emiliano Peña-Altamira, Mariangela Corricelli, et al.
American Journal of Ophthalmology|June 8, 2014
Early macular retinal ganglion cell loss in dominant optic atrophy: genotype-phenotype correlationPiero Barboni, Giacomo Savini, Maria Lucia Cascavilla, et al.
Lancet (London, England)|August 18, 2004
Risk of developing a mitochondrial DNA deletion disorderPatrick F Chinnery, Salvatore DiMauro, Sara Shanske, et al.
Human Mutation|August 10, 2013
MTO1 mutations are associated with hypertrophic cardiomyopathy and lactic acidosis and cause respiratory chain deficiency in humans and yeastEnrico Baruffini, Cristina Dallabona, Federica Invernizzi, et al.
Neurology|October 30, 2016
FGF21 is a biomarker for mitochondrial translation and mtDNA maintenance disordersJenni M Lehtonen, Saara Forsström, Emanuela Bottani, et al.
Cell Metabolism|October 5, 2022
Two independent respiratory chains adapt OXPHOS performance to glycolytic switchErika Fernández-Vizarra, Sandra López-Calcerrada, Ana Sierra-Magro, et al.
Pageof 29