Oligonucleotide transformation of yeast reveals mismatch repair complexes to be differentially active on DNA replication strands. - Test2 - elhamkhani - TriplyDB

Oligonucleotide transformation of yeast reveals mismatch repair complexes to be differentially active on DNA replication strands.

Oligonucleotide transformation of yeast reveals mismatch repair complexes to be differentially active on DNA replication strands.

http://www.wikidata.org/entity/Q36090192

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Genetic spell-checking: gene editing using single-stranded DNA oligonucleotides Postreplicative mismatch repair.Replicative DNA polymerase δ but not ε proofreads errors in Cis and in Trans DNA repair mechanisms and the bypass of DNA damage in Saccharomyces cerevisiae A 'Semi-Protected Oligonucleotide Recombination' Assay for DNA Mismatch Repair in vivo Suggests Different Modes of Repair for Lagging Strand Mismatches.Eukaryotic Mismatch Repair in Relation to DNA Replication Yeast oligo-mediated genome engineering (YOGE).Engineering ecosystems and synthetic ecologies.In vivo bypass of 8-oxodG.Transformation with oligonucleotides creating clustered changes in the yeast genome Differential correction of lagging-strand replication errors made by DNA polymerases {alpha} and {delta}An end for mismatch repair.Deciphering the rules by which 5'-UTR sequences affect protein expression in yeast.Different roles of eukaryotic MutS and MutL complexes in repair of small insertion and deletion loops in yeast.Quantifying the contributions of base selectivity, proofreading and mismatch repair to nuclear DNA replication in Saccharomyces cerevisiae.Mismatch repair-dependent mutagenesis in nondividing cells.Human postmeiotic segregation 2 exhibits biased repair at tetranucleotide microsatellite sequences LNA modification of single-stranded DNA oligonucleotides allows subtle gene modification in mismatch-repair-proficient cells.Cell-cycle and DNA damage regulation of the DNA mismatch repair protein Msh2 occurs at the transcriptional and post-transcriptional level.Absence of MutSβ leads to the formation of slipped-DNA for CTG/CAG contractions at primate replication forks.Progress and prospects: oligonucleotide-directed gene modification in mouse embryonic stem cells: a route to therapeutic application.Effect of sequence context and direction of replication on AP site bypass in Saccharomyces cerevisiae.Synthesis of DNA fragments in yeast by one-step assembly of overlapping oligonucleotides.Precise Editing at DNA Replication Forks Enables Multiplex Genome Engineering in Eukaryotes.Mispaired rNMPs in DNA are mutagenic and are targets of mismatch repair and RNases H.

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P2860

Oligonucleotide transformation of yeast reveals mismatch repair complexes to be differentially active on DNA replication strands.

http://www.wikidata.org/entity/Q36090192

description

2007 nî lūn-bûn

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2007年の論文

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Oligonucleotide transformation ...... ve on DNA replication strands.

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Oligonucleotide transformation ...... ve on DNA replication strands.

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type

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Oligonucleotide transformation ...... ve on DNA replication strands.

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Oligonucleotide transformation ...... ve on DNA replication strands.

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Oligonucleotide transformation ...... ve on DNA replication strands.

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Oligonucleotide transformation ...... ve on DNA replication strands.

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PNAS.0704695104

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Proceedings of the National Academy of Sciences of the United States of America

P1476

Oligonucleotide transformation ...... ve on DNA replication strands.

@en

P2093

Gaobin Bao

http://www.w3.org/2001/XMLSchema#string

Gray F Crouse

http://www.w3.org/2001/XMLSchema#string

Jason W Reeves

http://www.w3.org/2001/XMLSchema#string

Sue Jinks-Robertson

http://www.w3.org/2001/XMLSchema#string

Yoke W Kow

http://www.w3.org/2001/XMLSchema#string

P2860

Functional interaction of proliferating cell nuclear antigen with MSH2-MSH6 and MSH2-MSH3 complexes

Phage annealing proteins promote oligonucleotide-directed mutagenesis in Escherichia coli and mouse ES cells

Mutagenic effects of abasic and oxidized abasic lesions in Saccharomyces cerevisiae.

A system of shuttle vectors and yeast host strains designed for efficient manipulation of DNA in Saccharomyces cerevisiae

Functional characterization of the S. cerevisiae genome by gene deletion and parallel analysis

Discrete in vivo roles for the MutL homologs Mlh2p and Mlh3p in the removal of frameshift intermediates in budding yeast.

Analysis of the proteins involved in the in vivo repair of base-base mismatches and four-base loops formed during meiotic recombination in the yeast Saccharomyces cerevisiae.

The Saccharomyces cerevisiae MLH3 gene functions in MSH3-dependent suppression of frameshift mutations.

Eukaryotic DNA mismatch repair.

Functional specificity of MutL homologs in yeast: evidence for three Mlh1-based heterocomplexes with distinct roles during meiosis in recombination and mismatch correction.

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11352-11357

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scholarly article

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10.1073/PNAS.0704695104

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104

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17592146

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2040902

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