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Journal of Biochemistry|June 30, 2026
BNIP3/NIX-dependent mitophagy: molecular mechanisms and physiological rolesTamara Ginevskaia, Takayuki Mito, Keiichi Inoue, et al.
G3 (Bethesda, Md.)|July 16, 2013
Mitochondrial DNA with a large-scale deletion causes two distinct mitochondrial disease phenotypes in miceShun Katada, Takayuki Mito, Emi Ogasawara, et al.
Biochemical and Biophysical Research Communications|June 15, 2015
A somatic T15091C mutation in the Cytb gene of mouse mitochondrial DNA dominantly induces respiration defectsChisato Hayashi, Gaku Takibuchi, Akinori Shimizu, et al.
Biochemical and Biophysical Research Communications|February 28, 2015
G7731A mutation in mouse mitochondrial tRNALys regulates late-onset disorders in transmitochondrial miceAkinori Shimizu, Takayuki Mito, Osamu Hashizume, et al.
Clinical and Translational Medicine|July 18, 2025
PDK4 and nutrient responses explain muscle specific manifestation in mitochondrial diseaseSwagat Pradhan, Takayuki Mito, Nahid A Khan, et al.
Scientific Reports|November 7, 2019
Disruption of the mouse Shmt2 gene confers embryonic anaemia via foetal liver-specific metabolomic disordersHaruna Tani, Takayuki Mito, Vidya Velagapudi, et al.
Cell Metabolism|January 14, 2022
Mosaic dysfunction of mitophagy in mitochondrial muscle diseaseTakayuki Mito, Amy E Vincent, Julie Faitg, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 5, 2019
Acquired Expression of Mutant <i>Mitofusin 2</i> Causes Progressive Neurodegeneration and Abnormal BehaviorKaori Ishikawa, Satoshi Yamamoto, Satoko Hattori, et al.
Biochemical and Biophysical Research Communications|September 19, 2015
Mouse somatic mutation orthologous to MELAS A3302G mutation in the mitochondrial tRNA(Leu(UUR)) gene confers respiration defectsAkinori Shimizu, Shunkei Enoki, Kaori Ishikawa, et al.
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