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Nucleic Acids Research|May 6, 2021
DNA polymerase gamma mutations that impair holoenzyme stability cause catalytic subunit depletionPedro Silva-Pinheiro, Carlos Pardo-Hernández, Aurelio Reyes, et al.Cell Death & Disease|March 12, 2024
Genome-wide CRISPR/Cas9 screen shows that loss of GET4 increases mitochondria-endoplasmic reticulum contact sites and is neuroprotectiveEmma L Wilson, Yizhou Yu, Nuno S Leal, et al.Journal of Medical Genetics|May 23, 2020
Mutation in the MICOS subunit gene <i>APOO</i> (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic featuresCristiane Benincá, Vanessa Zanette, Michele Brischigliaro, et al.Nature|September 24, 2025
Ribonucleotide incorporation into mitochondrial DNA drives inflammationAmir Bahat, Dusanka Milenkovic, Eileen Cors, et al.Redox Biology|August 12, 2022
Rapid and selective generation of H<sub>2</sub>S within mitochondria protects against cardiac ischemia-reperfusion injuryJan Lj Miljkovic, Nils Burger, Justyna M Gawel, et al.Cell Chemical Biology|February 5, 2019
Selective Disruption of Mitochondrial Thiol Redox State in Cells and In VivoLee M Booty, Justyna M Gawel, Filip Cvetko, et al.Nature|March 8, 2023
Fumarate induces vesicular release of mtDNA to drive innate immunityVincent Zecchini, Vincent Paupe, Irene Herranz-Montoya, et al.Nature Communications|September 14, 2021
SMARCA4/2 loss inhibits chemotherapy-induced apoptosis by restricting IP3R3-mediated Ca<sup>2+</sup> flux to mitochondriaYibo Xue, Jordan L Morris, Kangning Yang, et al.Nature Communications|November 20, 2025
An inherited mitochondrial DNA mutation remodels inflammatory cytokine responses in macrophages and in vivo in miceEloïse Marques, Stephen P Burr, Alva M Casey, et al.Brain : a Journal of Neurology|June 19, 2022
TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegiaLuis Carlos Tábara, Fatema Al-Salmi, Reza Maroofian, et al.Pageof 7