Mitochondrial DNA maintenance defects: potential therapeutic strategies
- 6 July 2022
- journal article
- review article
- Published by Elsevier in Molecular Genetics and Metabolism
- Vol. 137 (1-2) , 40-48
Abstract
No abstract availableKeywords
This publication has 100 references indexed in Scilit:
- Mitochondrial Fusion Proteins and Human DiseasesNeurology Research International, 2013
- TWINKLE is an essential mitochondrial helicase required for synthesis of nascent D-loop strands and complete mtDNA replicationHuman Molecular Genetics, 2013
- Nicotinamide-induced MitophagyJournal of Biological Chemistry, 2012
- Early-onset severe neuromuscular phenotype associated with compound heterozygosity for OPA1 mutationsMolecular Genetics and Metabolism, 2011
- Mitochondrial Fusion Is Required for mtDNA Stability in Skeletal Muscle and Tolerance of mtDNA MutationsCell, 2010
- Unbalanced deoxynucleotide pools cause mitochondrial DNA instability in thymidine phosphorylase-deficient miceHuman Molecular Genetics, 2008
- Mitochondrial DNA polymerase-γ and human diseaseHuman Molecular Genetics, 2006
- Molecular, Functional, and Pathological Aspects of the Mitochondrial ADP/ATP CarrierPhysiology, 2006
- DNA Polymerase γ, The Mitochondrial ReplicaseAnnual Review of Biochemistry, 2004
- Cloning of the cDNA and Chromosome Localization of the Gene for Human Thymidine Kinase 2Journal of Biological Chemistry, 1997