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。Characterizing the mitochondrial DNA polymerase gamma interactome by BioID identifies Ruvbl2 localizes to the mitochondria
Sanduni U. Liyanage et al.
MITOCHONDRION (2017)
Nucleotide pools dictate the identity and frequency of ribonucleotide incorporation in mitochondrial DNA
Anna-Karin Berglund et al.
PLOS GENETICS (2017)
Structural Impact of Single Ribonucleotide Residues in DNA
Marina Evich et al.
CHEMBIOCHEM (2016)
Mitochondrial DNA repair and replication proteins revealed by targeted chemical probes
Simon Wisnovsky et al.
NATURE CHEMICAL BIOLOGY (2016)
MPV17 Loss Causes Deoxynucleotide Insufficiency and Slow DNA Replication in Mitochondria
Ilaria Dalla Rosa et al.
PLOS GENETICS (2016)
Mitochondrial diseases
Grainne S. Gorman et al.
NATURE REVIEWS DISEASE PRIMERS (2016)
Genome-wide mapping of embedded ribonucleotides and other noncanonical nucleotides using emRiboSeq and EndoSeq
James Ding et al.
NATURE PROTOCOLS (2015)
Deoxyribonucleotide metabolism, mutagenesis and cancer
Christopher K. Mathews
NATURE REVIEWS CANCER (2015)
Administration of deoxyribonucleosides or inhibition of their catabolism as a pharmacological approach for mitochondrial DNA depletion syndrome
Yolanda Camara et al.
HUMAN MOLECULAR GENETICS (2014)
RNA intrusions change DNA elastic properties and structure
Hsiang-Chih Chiu et al.
NANOSCALE (2014)
MTH1 inhibition eradicates cancer by preventing sanitation of the dNTP pool
Helge Gad et al.
NATURE (2014)
PrimPol, an Archaic Primase/Polymerase Operating in Human Cells
Sara Garcia-Gomez et al.
MOLECULAR CELL (2013)
transparent, a gene affecting stripe formation in Zebrafish, encodes the mitochondrial protein Mpv17 that is required for iridophore survival
Jana Krauss et al.
BIOLOGY OPEN (2013)
MPV17 Mutations Causing Adult-Onset Multisystemic Disorder With Multiple Mitochondrial DNA Deletions
Caterina Garone et al.
ARCHIVES OF NEUROLOGY (2012)
Enzymatic Removal of Ribonucleotides from DNA Is Essential for Mammalian Genome Integrity and Development
Martin A. M. Reijns et al.
CELL (2012)
MPV17 mutation causes neuropathy and leukoencephalopathy with multiple mtDNA deletions in muscle
Emma L. Blakely et al.
NEUROMUSCULAR DISORDERS (2012)
Ribonucleotide Discrimination and Reverse Transcription by the Human Mitochondrial DNA Polymerase
Rajesh Kasiviswanathan et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2011)
Nucleoside Triphosphate Pool Asymmetry in Mammalian Mitochondria
Linda J. Wheeler et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2011)
The Sequence Alignment/Map format and SAMtools
Heng Li et al.
BIOINFORMATICS (2009)
Early-onset liver mtDNA depletion and late-onset proteinuric nephropathy in Mpv17 knockout mice
Carlo Viscomi et al.
HUMAN MOLECULAR GENETICS (2009)
Analyzing real-time PCR data by the comparative C-T method
Thomas D. Schmittgen et al.
NATURE PROTOCOLS (2008)
Mutation of RRM2B, encoding p53-controlled ribonucleotide reductase (p53R2), causes severe mitochondrial DNA depletion
Alice Bourdon et al.
NATURE GENETICS (2007)
MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA depletion
A Spinazzola et al.
NATURE GENETICS (2006)
DNA precursor asymmetries in mammalian tissue mitochondria and possible contribution to mutagenesis through reduced replication fidelity
SW Song et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)
Biased incorporation of ribonucleotides on the mitochondrial L-strand accounts for apparent strand-asymmetric DNA replication
MY Yang et al.
CELL (2002)
The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA
H Mandel et al.
NATURE GENETICS (2001)
Role of adenine nucleotide translocator 1 in mtDNA maintenance
J Kaukonen et al.
SCIENCE (2000)
分享论文
