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Mitochondrion|November 21, 2012
Developing outcome measures for pediatric mitochondrial disorders: which complaints and limitations are most burdensome to patients and their parents?Saskia Koene, Saskia B Wortmann, Maaike C de Vries, et al.Mitochondrion|February 5, 2014
Rare POLG1 CAG variants do not influence Parkinson's disease or polymerase gamma functionSteven R Bentley, Jianguo Shan, Michael Todorovic, et al.Mitochondrion|June 3, 2026
Mitochondrial dysfunction in muscle cells induced by snoring vibrationsPer Stål, Roine El-Habta, Yu-Cheng Qian, et al.Mitochondrion|May 25, 2010
Fish as a model in investigations about the relationship between oxygen consumption and hydroxyl radical production in permeabilized muscle fibersH Mortelette, C Moisan, P Sébert, et al.Mitochondrion|June 18, 2018
Is there a mutation gradient along vertebrate mitochondrial genome mediated by genome replication?Xuhua XiaMitochondrion|December 31, 2019
Mitochondrial haplogroups and lifespan in a population isolateJoseph Bonner, Rachel Fisher, Ellen Wilch, et al.Mitochondrion|November 8, 2005
Longevity-associated mitochondrial DNA 5178 C/A polymorphism is associated with fasting plasma glucose levels and glucose tolerance in Japanese menAkatsuki Kokaze, Mamoru Ishikawa, Naomi Matsunaga, et al.Mitochondrion|May 9, 2007
Analysis of coenzyme Q in human blood and tissuesBruce A Barshop, Jon A GangoitiMitochondrion|June 27, 2026
DNM1L depletion leads to accelerated heteroplasmy shifting of m.10191C allele through ATG7-dependent pathwaysMelissa Geng, Dahai Wang, Sam Kavoosi, et al.Mitochondrion|July 30, 2019
Alterations of complex IV in the tissues of a septic mouse modelXue Yang, Guo-Ping Lu, Xiao-Di Cai, et al.Pageof 198