Pages that link to "Q24293340"
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The following pages link to Functional human mitochondrial DNA polymerase gamma forms a heterotrimer (Q24293340):
Displaying 50 items.
- DNA polymerase gamma, catalytic subunit (Q21101133) (← links)
- DNA polymerase gamma 2, accessory subunit (Q21101142) (← links)
- Antimutator alleles of yeast DNA polymerase gamma modulate the balance between DNA synthesis and excision (Q21134954) (← links)
- Twinkle mutations associated with autosomal dominant progressive external ophthalmoplegia lead to impaired helicase function and in vivo mtDNA replication stalling (Q24310134) (← links)
- Human DNA2 is a mitochondrial nuclease/helicase for efficient processing of DNA replication and repair intermediates (Q24312975) (← links)
- Structural insight into processive human mitochondrial DNA synthesis and disease-related polymerase mutations (Q24336678) (← links)
- The EM structure of human DNA polymerase gamma reveals a localized contact between the catalytic and accessory subunits (Q24338797) (← links)
- Mutant POLG2 disrupts DNA polymerase gamma subunits and causes progressive external ophthalmoplegia (Q24546476) (← links)
- Mitochondrial DNA replication and disease: insights from DNA polymerase γ mutations (Q24612561) (← links)
- DNA polymerase γ and disease: what we have learned from yeast (Q26825324) (← links)
- Functional roles of the N- and C-terminal regions of the human mitochondrial single-stranded DNA-binding protein (Q28475950) (← links)
- Polg2 is essential for mammalian embryogenesis and is required for mtDNA maintenance (Q28510356) (← links)
- Manganese superoxide dismutase is a mitochondrial fidelity protein that protects Polγ against UV-induced inactivation (Q28594641) (← links)
- Epilepsy due to mutations in the mitochondrial polymerase gamma (POLG) gene: A clinical and molecular genetic review. (Q30248334) (← links)
- Mitochondrial DNA depletion and fatal infantile hepatic failure due to mutations in the mitochondrial polymerase γ (POLG) gene: a combined morphological/enzyme histochemical and immunocytochemical/biochemical and molecular genetic study (Q30447289) (← links)
- The role of mitochondrial DNA mutations in mammalian aging (Q33275295) (← links)
- Each monomer of the dimeric accessory protein for human mitochondrial DNA polymerase has a distinct role in conferring processivity (Q33569793) (← links)
- A mechanistic view of human mitochondrial DNA polymerase gamma: providing insight into drug toxicity and mitochondrial disease (Q33756066) (← links)
- Molecular and biochemical characterisation of a novel mutation in POLG associated with Alpers syndrome (Q33793596) (← links)
- Functional analysis of H. sapiens DNA polymerase gamma spacer mutation W748S with and without common variant E1143G. (Q33814578) (← links)
- Mitochondrial genome maintenance in health and disease. (Q33821051) (← links)
- Functional analysis of mutant mitochondrial DNA polymerase proteins involved in human disease. (Q33918516) (← links)
- Replication pauses of the wild-type and mutant mitochondrial DNA polymerase gamma: a simulation study (Q34085612) (← links)
- Ribonucleotide discrimination and reverse transcription by the human mitochondrial DNA polymerase. (Q34202531) (← links)
- Overexpression of DNA polymerase zeta reduces the mitochondrial mutability caused by pathological mutations in DNA polymerase gamma in yeast (Q34217894) (← links)
- Role of Histidine 932 of the Human Mitochondrial DNA Polymerase in Nucleotide Discrimination and Inherited Disease (Q34232186) (← links)
- Polymorphisms in DNA polymerase γ affect the mtDNA stability and the NRTI-induced mitochondrial toxicity in Saccharomyces cerevisiae (Q35024623) (← links)
- Biochemical analysis of human POLG2 variants associated with mitochondrial disease. (Q35090101) (← links)
- Evolution of the metazoan mitochondrial replicase. (Q35569785) (← links)
- Modulation of the W748S mutation in DNA polymerase gamma by the E1143G polymorphismin mitochondrial disorders (Q35606895) (← links)
- Clustering of Alpers disease mutations and catalytic defects in biochemical variants reveal new features of molecular mechanism of the human mitochondrial replicase, Pol γ. (Q35620870) (← links)
- Identification of a Mitochondrial DNA Polymerase Affecting Cardiotoxicity of Sunitinib Using a Genome-Wide Screening on S. pombe Deletion Library (Q35781121) (← links)
- Mechanism of interaction of human mitochondrial DNA polymerase γ with the novel nucleoside reverse transcriptase inhibitor 4'-ethynyl-2-fluoro-2'-deoxyadenosine indicates a low potential for host toxicity. (Q35806294) (← links)
- Developing master keys to brain pathology, cancer and aging from the structural biology of proteins controlling reactive oxygen species and DNA repair. (Q35865533) (← links)
- Yeast model analysis of novel polymerase gamma variants found in patients with autosomal recessive mitochondrial disease. (Q35929393) (← links)
- Binding parameters and thermodynamics of the interaction of the human cytomegalovirus DNA polymerase accessory protein, UL44, with DNA: implications for the processivity mechanism (Q35945415) (← links)
- Base Excision Repair in the Mitochondria. (Q35988349) (← links)
- POLG2 disease variants: analyses reveal a dominant negative heterodimer, altered mitochondrial localization and impaired respiratory capacity. (Q35999327) (← links)
- Mitochondrial Single-stranded DNA-binding Proteins Stimulate the Activity of DNA Polymerase γ by Organization of the Template DNA. (Q36323420) (← links)
- The ageing mitochondrial genome (Q36360675) (← links)
- Mitochondrial DNA copy number is regulated in a tissue specific manner by DNA methylation of the nuclear-encoded DNA polymerase gamma A (Q36368773) (← links)
- Mapping 136 pathogenic mutations into functional modules in human DNA polymerase γ establishes predictive genotype-phenotype correlations for the complete spectrum of POLG syndromes. (Q36394823) (← links)
- Biolayer Interferometry: A Novel Method to Elucidate Protein-Protein and Protein-DNA Interactions in the Mitochondrial DNA Replisome (Q36435698) (← links)
- Comparative purification strategies for Drosophila and human mitochondrial DNA replication proteins: DNA polymerase gamma and mitochondrial single-stranded DNA-binding protein (Q36435729) (← links)
- A novel processive mechanism for DNA synthesis revealed by structure, modeling and mutagenesis of the accessory subunit of human mitochondrial DNA polymerase (Q36435827) (← links)
- Progressive external ophthalmoplegia and vision and hearing loss in a patient with mutations in POLG2 and OPA1. (Q36625859) (← links)
- Mutations in human DNA polymerase γ confer unique mechanisms of catalytic deficiency that mirror the disease severity in mitochondrial disorder patients (Q36626862) (← links)
- Roles of DNA polymerases in replication, repair, and recombination in eukaryotes. (Q36687824) (← links)
- Removal of oxidative DNA damage via FEN1-dependent long-patch base excision repair in human cell mitochondria (Q36845992) (← links)
- Mitochondrial transcription termination factor 1 directs polar replication fork pausing (Q37076313) (← links)