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Mitochondrion|June 5, 2021
Characterization of neutral sphingomyelinase activity and isoform expression in rodent skeletal muscle mitochondriaSebastian Silvera, Jennifer A Wilkinson, Paul J LeBlancMitochondrion|June 8, 2021
Placental mitochondrial DNA mutational load and perinatal outcomes: Findings from a multi-ethnic pregnancy cohortWhitney Cowell, Kelly Brunst, Elena Colicino, et al.Mitochondrion|December 13, 2022
Paternal aging impacts mitochondrial DNA content and telomere length in mouse embryosJun Ito, Mio Kageyama, Shunsuke Hara, et al.Mitochondrion|November 25, 2022
The longest-lived metazoan, Arctica islandica, exhibits high mitochondrial H2O2 removal capacitiesDaniel Munro, Enrique Rodríguez, Pierre U BlierMitochondrion|July 1, 2021
Neurological & psychological aspects of Barth syndrome: Clinical manifestations and potential pathogenic mechanismsMelissa Olivar-Villanueva, Mindong Ren, Colin K L PhoonMitochondrion|January 7, 2021
Mitochondrial calcium in command of juggling myriads of cellular functionsSabita Singh, Ulaganathan MabalirajanMitochondrion|January 7, 2021
The involvement of autophagy in the maintenance of endothelial homeostasis: The role of mitochondriaDorota DymkowskaMitochondrion|July 17, 2021
High-resolution mass spectrometric analysis of cardiolipin profiles in Barth syndromeSeul Kee Byeon, Madan Gopal Ramarajan, Anil K Madugundu, et al.Mitochondrion|July 17, 2021
Plasma lactate responses during and after submaximal handgrip exercise are not diagnostically helpful in mitochondrial myopathyNicoline Løkken, Sofie Vinther Skriver, Tahmina Khawajazada, et al.Mitochondrion|July 12, 2021
Defective complex III mitochondrial respiratory chain due to a novel variant in CYC1 gene masquerades acute demyelinating syndrome or Leber hereditary optic neuropathyErfan Heidari, Maryam Rasoulinezhad, Neda Pak, et al.Pageof 198