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Mitochondrion|June 4, 2017
Metabolomics of mitochondrial diseaseKarien Esterhuizen, Francois H van der Westhuizen, Roan LouwMitochondrion|March 16, 2010
Succinate dehydrogenase - Assembly, regulation and role in human diseaseJared Rutter, Dennis R Winge, Joshua D SchiffmanMitochondrion|March 10, 2010
Left ventricular noncompaction is associated with mutations in the mitochondrial genomeSha Tang, Anjan Batra, Yu Zhang, et al.Mitochondrion|January 12, 2010
Mitochondrial localization of human FAD synthetase isoform 1Enza Maria Torchetti, Carmen Brizio, Matilde Colella, et al.Mitochondrion|January 19, 2010
Regulation of mitochondrial ribosomal protein S29 (MRPS29) expression by a 5'-upstream open reading frameMin-Joon Han, Daniel T Chiu, Emine C KocMitochondrion|December 26, 2009
Isolation of mitochondria for biogenetical studies: An updateErika Fernández-Vizarra, Gustavo Ferrín, Acisclo Pérez-Martos, et al.Mitochondrion|August 22, 2016
Mitochondrial tRNA mutations in 2070 Chinese Han subjects with hypertensionLing Xue, Meng Wang, Haiying Li, et al.Mitochondrion|July 9, 2017
Recessive mutation in EXOSC3 associates with mitochondrial dysfunction and pontocerebellar hypoplasiaGudrun Schottmann, Sylvie Picker-Minh, Jana Marie Schwarz, et al.Mitochondrion|July 4, 2017
Functional nanosome for enhanced mitochondria-targeted gene delivery and expressionYoonhee Bae, Min Kyo Jung, Su Jeong Song, et al.Mitochondrion|July 5, 2017
MPV17 hepatocerebral mitochondrial DNA depletion syndrome presenting as acute flaccid paralysis - A case reportAnjan Pyal, Arumugam Paramasivam, Angamuthu Kannan Meena, et al.Pageof 198