Mutations in human DNA polymerase γ confer unique mechanisms of catalytic deficiency that mirror the disease severity in mitochondrial disorder patients.
about
Probing the molecular mechanism of action of the HIV-1 reverse transcriptase inhibitor 4'-ethynyl-2-fluoro-2'-deoxyadenosine (EFdA) using pre-steady-state kineticsAlpers disease mutations in human DNA polymerase gamma cause catalytic defects in mitochondrial DNA replication by distinct mechanismsThe DNA Polymerase Gamma R953C Mutant Is Associated with Antiretroviral Therapy-Induced Mitochondrial ToxicityYeast cells expressing the human mitochondrial DNA polymerase reveal correlations between polymerase fidelity and human disease progressionNeurotoxicity of cytarabine (Ara-C) in dorsal root ganglion neurons originates from impediment of mtDNA synthesis and compromise of mitochondrial function.
P2860
Mutations in human DNA polymerase γ confer unique mechanisms of catalytic deficiency that mirror the disease severity in mitochondrial disorder patients.
description
2012 nî lūn-bûn
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2012年の論文
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name
Mutations in human DNA polymer ...... tochondrial disorder patients.
@ast
Mutations in human DNA polymer ...... tochondrial disorder patients.
@en
type
label
Mutations in human DNA polymer ...... tochondrial disorder patients.
@ast
Mutations in human DNA polymer ...... tochondrial disorder patients.
@en
prefLabel
Mutations in human DNA polymer ...... tochondrial disorder patients.
@ast
Mutations in human DNA polymer ...... tochondrial disorder patients.
@en
P2093
P2860
P356
P1476
Mutations in human DNA polymer ...... tochondrial disorder patients.
@en
P2093
Christal D Sohl
Karen S Anderson
Rajesh Kasiviswanathan
William C Copeland
P2860
P304
P356
10.1093/HMG/DDS509
P577
2012-12-03T00:00:00Z