Mutational spectrum analysis of RNase H(35) deficient Saccharomyces cerevisiae using fluorescence-based directed termination PCR.
about
Idling by DNA polymerase delta maintains a ligatable nick during lagging-strand DNA replicationPCNA directs type 2 RNase H activity on DNA replication and repair substratesMechanisms employed by Escherichia coli to prevent ribonucleotide incorporation into genomic DNA by Pol VThe deletion of rnhB in Mycobacterium smegmatis does not affect the level of RNase HII substrates or influence genome stabilityProcessing ribonucleotides incorporated during eukaryotic DNA replication.Abundant ribonucleotide incorporation into DNA by yeast replicative polymerases.Genome instability due to ribonucleotide incorporation into DNA.Okazaki fragment maturation in yeast. I. Distribution of functions between FEN1 AND DNA2.Mutagenic processing of ribonucleotides in DNA by yeast topoisomerase IFluorescence-based directed termination PCR: direct mutation characterization without sequencing.Excision of misincorporated ribonucleotides in DNA by RNase H (type 2) and FEN-1 in cell-free extracts.A genome-wide screen for Saccharomyces cerevisiae deletion mutants that affect telomere length.Ribonucleotide triggered DNA damage and RNA-DNA damage responsesHuman DNA polymerase ε is able to efficiently extend from multiple consecutive ribonucleotides.Topoisomerase 1-mediated removal of ribonucleotides from nascent leading-strand DNAMismatch repair-independent tandem repeat sequence instability resulting from ribonucleotide incorporation by DNA polymerase ε.Flexibility of eukaryotic Okazaki fragment maturation through regulated strand displacement synthesisRibonucleotides and Transcription-Associated Mutagenesis in Yeast.Polynucleotide phosphorylase plays an important role in the generation of spontaneous mutations in Escherichia coli.RNA∶DNA hybrids initiate quasi-palindrome-associated mutations in highly transcribed yeast DNA.Roles of SGS1, MUS81, and RAD51 in the repair of lagging-strand replication defects in Saccharomyces cerevisiae.Missed cleavage opportunities by FEN1 lead to Okazaki fragment maturation via the long-flap pathway.
P2860
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P2860
Mutational spectrum analysis of RNase H(35) deficient Saccharomyces cerevisiae using fluorescence-based directed termination PCR.
description
2000 nî lūn-bûn
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2000 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
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2000 թվականի սեպտեմբերին հրատարակված գիտական հոդված
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2000年の論文
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2000年論文
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2000年論文
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2000年論文
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2000年論文
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2000年論文
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name
Mutational spectrum analysis o ...... ased directed termination PCR.
@ast
Mutational spectrum analysis o ...... ased directed termination PCR.
@en
type
label
Mutational spectrum analysis o ...... ased directed termination PCR.
@ast
Mutational spectrum analysis o ...... ased directed termination PCR.
@en
prefLabel
Mutational spectrum analysis o ...... ased directed termination PCR.
@ast
Mutational spectrum analysis o ...... ased directed termination PCR.
@en
P2093
P2860
P356
P1476
Mutational spectrum analysis o ...... ased directed termination PCR.
@en
P2093
P2860
P304
P356
10.1093/NAR/28.18.3649
P407
P577
2000-09-01T00:00:00Z