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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.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.Neurology|October 30, 2016
FGF21 is a biomarker for mitochondrial translation and mtDNA maintenance disordersJenni M Lehtonen, Saara Forsström, Emanuela Bottani, et al.Proceedings of the National Academy of Sciences of the United States of America|July 31, 2013
Targeting proximal tubule mitochondrial dysfunction attenuates the renal disease of methylmalonic acidemiaIrini Manoli, Justin R Sysol, Lingli Li, et al.Neurology|March 20, 2025
Natural History of Patients With Mitochondrial ATPase Deficiency Due to Pathogenic Variants of MT-ATP6 and MT-ATP8Sara Carli, Anna Levarlet, Daria Diodato, et al.European Journal of Human Genetics : EJHG|May 3, 2024
COQ7 defect causes prenatal onset of mitochondrial CoQ10 deficiency with cardiomyopathy and gastrointestinal obstructionIlaria Pettenuzzo, Sara Carli, Ana Sánchez-Cuesta, et al.Cell Death and Differentiation|July 15, 2020
Defective endoplasmic reticulum-mitochondria contacts and bioenergetics in SEPN1-related myopathyAnne Filipe, Alexander Chernorudskiy, Sandrine Arbogast, et al.Annals of Neurology|May 25, 2019
Deoxynucleoside Therapy for Thymidine Kinase 2-Deficient MyopathyCristina Domínguez-González, Marcos Madruga-Garrido, Fabiola Mavillard, et al.American Journal of Human Genetics|October 15, 2013
Macrocytic anemia and mitochondriopathy resulting from a defect in sideroflexin 4Gordon J Hildick-Smith, Jeffrey D Cooney, Caterina Garone, et al.Pageof 15