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Human Molecular Genetics|May 31, 2015
Mitochondrial respiratory dysfunction caused by a heteroplasmic mitochondrial DNA mutation blocks cellular reprogrammingMutsumi Yokota, Hideyuki Hatakeyama, Saki Okabe, et al.
Cell Death & Disease|January 13, 2017
Mitochondrial respiratory dysfunction disturbs neuronal and cardiac lineage commitment of human iPSCsMutsumi Yokota, Hideyuki Hatakeyama, Yasuha Ono, et al.
Plos One|August 25, 2021
Melanocyte progenitor cells reside in human subcutaneous adipose tissueYuri Ikeda, Akino Wada, Toshio Hasegawa, et al.
Experimental Animals|July 28, 2011
Nuclear but not mitochondrial DNA involvement in respiratory complex I defects found in senescence-accelerated mouse strain, SAMP8Hirotake Imanishi, Mutsumi Yokota, Masayuki Mori, et al.
Journal of Cell Science|May 12, 2019
Peroxisomes control mitochondrial dynamics and the mitochondrion-dependent apoptosis pathwayHideaki Tanaka, Tomohiko Okazaki, Saeko Aoyama, et al.
Scientific Reports|July 24, 2020
Insulin2<sup>Q104del</sup> (Kuma) mutant mice develop diabetes with dominant inheritanceDaisuke Sakano, Airi Inoue, Takayuki Enomoto, et al.
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