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Nucleic Acids Research|July 29, 2016
Near-complete elimination of mutant mtDNA by iterative or dynamic dose-controlled treatment with mtZFNsPayam A Gammage, Edoardo Gaude, Lindsey Van Haute, et al.
The Journal of Biological Chemistry|January 14, 2017
The Pseudouridine Synthase RPUSD4 Is an Essential Component of Mitochondrial RNA GranulesSofia Zaganelli, Pedro Rebelo-Guiomar, Kinsey Maundrell, et al.
Nature Communications|May 2, 2018
Linear mitochondrial DNA is rapidly degraded by components of the replication machineryViktoriya Peeva, Daniel Blei, Genevieve Trombly, et al.
Molecular Cell|November 14, 2021
Balancing of mitochondrial translation through METTL8-mediated m<sup>3</sup>C modification of mitochondrial tRNAsEva Schöller, James Marks, Virginie Marchand, et al.
JIMD Reports|May 8, 2023
Severe neonatal onset neuroregression with paroxysmal dystonia and apnoea: Expanding the phenotypic and genotypic spectrum of <i>CARS2</i>-related mitochondrial diseaseJessie Poquérusse, Melinda Nolan, David R Thorburn, et al.
Nucleic Acids Research|July 6, 2019
NSUN2 introduces 5-methylcytosines in mammalian mitochondrial tRNAsLindsey Van Haute, Song-Yi Lee, Beverly J McCann, et al.
Elife|December 23, 2021
Disruption of the TCA cycle reveals an ATF4-dependent integration of redox and amino acid metabolismDylan Gerard Ryan, Ming Yang, Hiran A Prag, et al.
Orphanet Journal of Rare Diseases|July 3, 2016
TRNT1 deficiency: clinical, biochemical and molecular genetic featuresYehani Wedatilake, Rojeen Niazi, Elisa Fassone, et al.
Molecular Cell|August 31, 2022
The human mitochondrial genome contains a second light strand promoterBenedict G Tan, Christian D Mutti, Yonghong Shi, et al.
Human Molecular Genetics|October 4, 2017
Defective mitochondrial rRNA methyltransferase MRM2 causes MELAS-like clinical syndromeCaterina Garone, Aaron R D'Souza, Cristina Dallabona, et al.
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