Human mitochondrial DNA replication machinery and disease.
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Mitochondrial CardiomyopathiesSending Out an SOS: Mitochondria as a Signaling HubPathogenicity in POLG syndromes: DNA polymerase gamma pathogenicity prediction server and database.A domain in human EXOG converts apoptotic endonuclease to DNA-repair exonuclease.DNA polymerases in the mitochondria: A critical review of the evidence.Inherited mitochondrial genomic instability and chemical exposures.Mitochondrial Mutations in Cardiac Disorders.Mitochondrial Neurogastrointestinal Encephalomyopathy Caused by Thymidine Phosphorylase Enzyme Deficiency: From Pathogenesis to Emerging Therapeutic Options.Cellular and population level processes influence the rate, accumulation and observed frequency of inherited and somatic mtDNA mutations.DNA Damage Tolerance by Eukaryotic DNA Polymerase and Primase PrimPol.Live imaging reveals the dynamics and regulation of mitochondrial nucleoids during the cell cycle in Fucci2-HeLa cells.Off-Target Effects of Drugs that Disrupt Human Mitochondrial DNA Maintenance.Nuclear genes involved in mitochondrial diseases caused by instability of mitochondrial DNA.Asymmetric Ataxia, Depression, Memory Loss, Epilepsy, and Axonal Neuropathy Associated with A Heterozygous DNA Polymerase Gamma Variant of Uncertain Significance, c1370G>a (R457Q).Mitochondrial retrograde signaling in the nervous system.Mitochondrial DNA damage and reactive oxygen species in neurodegenerative disease.A multi-systemic mitochondrial disorder due to a dominant p.Y955H disease variant in DNA polymerase gamma.Pharmacological Inhibition of Necroptosis Protects from Dopaminergic Neuronal Cell Death in Parkinson's Disease Models.Mice lacking the mitochondrial exonuclease MGME1 accumulate mtDNA deletions without developing progeria.Autophagy balances mtDNA synthesis and degradation by DNA polymerase POLG during starvation.The C-terminal tail of the NEIL1 DNA glycosylase interacts with the human mitochondrial single-stranded DNA binding protein.Neurotoxicity of cytarabine (Ara-C) in dorsal root ganglion neurons originates from impediment of mtDNA synthesis and compromise of mitochondrial function.Analysis of mtDNA/nDNA Ratio in Mice.
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Human mitochondrial DNA replication machinery and disease.
description
article científic
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article scientifique
@fr
articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on 08 April 2016
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Human mitochondrial DNA replication machinery and disease.
@en
Human mitochondrial DNA replication machinery and disease.
@nl
type
label
Human mitochondrial DNA replication machinery and disease.
@en
Human mitochondrial DNA replication machinery and disease.
@nl
prefLabel
Human mitochondrial DNA replication machinery and disease.
@en
Human mitochondrial DNA replication machinery and disease.
@nl
P2860
P1476
Human mitochondrial DNA replication machinery and disease.
@en
P2093
Matthew J Young
P2860
P356
10.1016/J.GDE.2016.03.005
P577
2016-04-08T00:00:00Z