相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Defective Mitophagy in XPA via PARP-1 Hyperactivation and NAD+/SIRT1 Reduction
Evandro Fei Fang et al.
CELL (2014)
Ribonucleotides in DNA: Origins, repair and consequences
Jessica S. Williams et al.
DNA REPAIR (2014)
Mitochondrial genome maintenance in health and disease
William C. Copeland et al.
DNA REPAIR (2014)
Overexpression of DNA ligase III in mitochondria protects cells against oxidative stress and improves mitochondrial DNA base excision repair
Mansour Akbari et al.
DNA REPAIR (2014)
Intrinsic mitochondrial DNA repair defects in Ataxia Telangiectasia
Nilesh K. Sharma et al.
DNA REPAIR (2014)
Aprataxin resolves adenylated RNA-DNA junctions to maintain genome integrity
Percy Tumbale et al.
NATURE (2014)
Role of polymerase β in complementing aprataxin deficiency during abasic-site base excision repair
Melike Caglayan et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2014)
A novel diagnostic tool reveals mitochondrial pathology in human diseases and aging
Morten Scheibye-Knudsen et al.
AGING-US (2013)
The role of mitochondria in aging
Ana Bratic et al.
JOURNAL OF CLINICAL INVESTIGATION (2013)
Modulation of DNA base excision repair during neuronal differentiation
Peter Sykora et al.
NEUROBIOLOGY OF AGING (2013)
Mitochondrial dysfunction in ataxia-telangiectasia
Yasmine A. Valentin-Vega et al.
BLOOD (2012)
Enzymatic Removal of Ribonucleotides from DNA Is Essential for Mammalian Genome Integrity and Development
Martin A. M. Reijns et al.
CELL (2012)
Mitochondria: In Sickness and in Health
Jodi Nunnari et al.
CELL (2012)
Cockayne syndrome group B protein prevents the accumulation of damaged mitochondria by promoting mitochondrial autophagy
Morten Scheibye-Knudsen et al.
JOURNAL OF EXPERIMENTAL MEDICINE (2012)
Ribonucleotide Discrimination and Reverse Transcription by the Human Mitochondrial DNA Polymerase
Rajesh Kasiviswanathan et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2011)
Ataxia with oculomotor apraxia type1 (AOA1): novel and recurrent aprataxin mutations, coenzyme Q10 analyses, and clinical findings in Italian patients
Barbara Castellotti et al.
NEUROGENETICS (2011)
Aprataxin localizes to mitochondria and preserves mitochondrial function
Peter Sykora et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
DNA polymerase β-dependent long patch base excision repair in living cells
Kenjiro Asagoshi et al.
DNA REPAIR (2010)
Genetic interactions between HNT3/Aprataxin and RAD27/FEN1 suggest parallel pathways for 5′ end processing during base excision repair
James M. Daley et al.
DNA REPAIR (2010)
Mitochondrial base excision repair assays
Scott Maynard et al.
METHODS (2010)
Short-patch single-strand break repair in ataxia oculomotor apraxia-1
John J. Reynolds et al.
BIOCHEMICAL SOCIETY TRANSACTIONS (2009)
Synergistic decrease of DNA single-strand break repair rates in mouse neural cells lacking both Tdp1 and aprataxin
Sherif F. El-Khamisy et al.
DNA REPAIR (2009)
Extracts of proliferating and non-proliferating human cells display different base excision pathways and repair fidelity
Mansour Akbari et al.
DNA REPAIR (2009)
Ribonuclease H: the enzymes in eukaryotes
Susana M. Cerritelli et al.
FEBS JOURNAL (2009)
Defective DNA Ligation during Short-Patch Single-Strand Break Repair in Ataxia Oculomotor Apraxia 1
John J. Reynolds et al.
MOLECULAR AND CELLULAR BIOLOGY (2009)
Mitochondrial base excision repair of uracil and AP sites takes place by single-nucleotide insertion and long-patch DNA synthesis
Mansour Akbari et al.
DNA REPAIR (2008)
Long patch base excision repair in mammalian mitochondrial Genomes
Bartosz Szczesny et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
Removal of oxidative DNA damage via FEN1-dependent long-patch base excision repair in human cell mitochondria
Pingfang Liu et al.
MOLECULAR AND CELLULAR BIOLOGY (2008)
Terminally differentiated muscle cells are defective in base excision DNA repair and hypersensitive to oxygen injury
Laura Narciso et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Actions of aprataxin in multiple DNA repair pathways
Ulrich Rass et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2007)
The neurodegenerative disease protein aprataxin resolves abortive DNA ligation intermediates
Ivan Ahel et al.
NATURE (2006)
Aprataxin forms a discrete branch in the HIT (histidine triad) superfamily of proteins with both DNA/RNA binding and nucleotide hydrolase activities
Amanda W. Kijas et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
The FHA domain of aprataxin interacts with the C-terminal region of XRCC1
H Date et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2004)
The ataxia-oculomotor apraxia 1 gene product has a role distinct from ATM and interacts with the DNA strand break repair proteins XRCC1 and XRCC4
PM Clements et al.
DNA REPAIR (2004)
Aprataxin, a novel protein that protects against genotoxic stress
N Gueven et al.
HUMAN MOLECULAR GENETICS (2004)
A new XRCC1-Containing complex and its role in cellular survival of methyl methanesulfonate treatment
H Luo et al.
MOLECULAR AND CELLULAR BIOLOGY (2004)
Characterization of novel reverse transcriptase and other RNA-associated catalytic activities by human DNA polymerase γ -: Importance in mitochondrial DNA replication
E Murakami et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Biased incorporation of ribonucleotides on the mitochondrial L-strand accounts for apparent strand-asymmetric DNA replication
MY Yang et al.
CELL (2002)
The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxin
MC Moreira et al.
NATURE GENETICS (2001)
Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene
H Date et al.
NATURE GENETICS (2001)
Mitochondrial DNA ligase III function is independent of xrcc1
U Lakshmipathy et al.
NUCLEIC ACIDS RESEARCH (2000)
FEN1 stimulation of DNA polymerase β mediates an excision step in mammalian long patch base excision repair
R Prasad et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
分享论文
