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Mitochondrion|October 17, 2021
Identification of a novel m.3955G > A variant in MT-ND1 associated with Leigh syndromeManting Xu, Robert Kopajtich, Matthias Elstner, et al.
Mitochondrion|September 30, 2021
Diagnosis of primary mitochondrial disorders -Emphasis on myopathological aspectsNarayanappa Gayathri, Sekar Deepha, Shivani Sharma
Mitochondrion|May 3, 2022
Flavonoid quercetin abolish paxilline inhibition of the mitochondrial BKCa channelRafał Paweł Kampa, Aleksandra Gliździńska, Adam Szewczyk, et al.
Mitochondrion|July 10, 2019
Mitochondrial dysfunction in neurodegenerative diseases and drug targets via apoptotic signalingYuanbo Wu, Meiqiao Chen, Jielong Jiang
Mitochondrion|September 10, 2018
Mitochondrial dysfunction caused by m.2336T>C mutation with hypertrophic cardiomyopathy in cybrid cell linesDan Li, Yaping Sun, Qianqian Zhuang, et al.
Mitochondrion|February 26, 2022
Fighting Parkinson's disease: The return of the mitochondriaKevin Zambrano, Diego Barba, Karina Castillo, et al.
Mitochondrion|September 2, 2008
Naturally occurring mitochondrial DNA heteroplasmy in the MRL mousePaweł Sachadyn, Xiang-Ming Zhang, Lise Desquenne Clark, et al.
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