Reconstitution of a eukaryotic replisome reveals suppression mechanisms that define leading/lagging strand operation. - Wikidata - awgldk - TriplyDB

Reconstitution of a eukaryotic replisome reveals suppression mechanisms that define leading/lagging strand operation.

Reconstitution of a eukaryotic replisome reveals suppression mechanisms that define leading/lagging strand operation.

http://www.wikidata.org/entity/Q35550942

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The Eukaryotic Replisome Goes Under the Microscope The architecture of a eukaryotic replisome.Reconsidering DNA Polymerases at the Replication Fork in Eukaryotes PDIP46 (DNA polymerase δ interacting protein 46) is an activating factor for human DNA polymerase δ Eukaryotic genome instability in light of asymmetric DNA replication A panoply of errors: polymerase proofreading domain mutations in cancer CMG-Pol epsilon dynamics suggests a mechanism for the establishment of leading-strand synthesis in the eukaryotic replisome.Mutations in the Non-Catalytic Subunit Dpb2 of DNA Polymerase Epsilon Affect the Nrm1 Branch of the DNA Replication Checkpoint.Replication Protein A Prohibits Diffusion of the PCNA Sliding Clamp along Single-Stranded DNA.Dpb11 may function with RPA and DNA to initiate DNA replication Insights into the Initiation of Eukaryotic DNA Replication.The eukaryotic CMG helicase pumpjack and integration into the replisome.Chromosome Duplication in Saccharomyces cerevisiae.Reconstitution of a eukaryotic replisome reveals the mechanism of asymmetric distribution of DNA polymerases Quality control mechanisms exclude incorrect polymerases from the eukaryotic replication fork.The [4Fe4S] cluster of human DNA primase functions as a redox switch using DNA charge transport Human mismatch repair system balances mutation rates between strands by removing more mismatches from the lagging strand.Evolution of replication machines.DNA Polymerases Divide the Labor of Genome Replication.POLD1: Central mediator of DNA replication and repair, and implication in cancer and other pathologies Forging Ahead through Darkness: PCNA, Still the Principal Conductor at the Replication Fork.Eukaryotic Translesion DNA Synthesis on the Leading and Lagging Strands: Unique Detours around the Same Obstacle Human CTF18-RFC clamp-loader complexed with non-synthesising DNA polymerase ε efficiently loads the PCNA sliding clamp.Genetic Networks Required to Coordinate Chromosome Replication by DNA Polymerases α, δ, and ε in Saccharomyces cerevisiae.How the Eukaryotic Replisome Achieves Rapid and Efficient DNA Replication.Roles of human POLD1 and POLD3 in genome stability.Action of CMG with strand-specific DNA blocks supports an internal unwinding mode for the eukaryotic replicative helicase.In vitro Assays for Eukaryotic Leading/Lagging Strand DNA Replication.Single-Molecule DNA Polymerase Dynamics at a Bacterial Replisome in Live Cells.Bacillus subtilis DNA polymerases, PolC and DnaE, are required for both leading and lagging strand synthesis in SPP1 origin-dependent DNA replication.Germline PMS2 and somatic POLE exonuclease mutations cause hypermutability of the leading DNA strand in biallelic mismatch repair deficiency syndrome brain tumours.Single-molecule visualization of Saccharomyces cerevisiae leading-strand synthesis reveals dynamic interaction between MTC and the replisome.The Eukaryotic CMG Helicase at the Replication Fork: Emerging Architecture Reveals an Unexpected Mechanism.Architecture of the Saccharomyces cerevisiae Replisome.Chromatin Constrains the Initiation and Elongation of DNA Replication.Alternative clamp loaders/unloaders.The Human Replicative Helicase, the CMG Complex, as a Target for Anti-cancer Therapy.The Initial Response of a Eukaryotic Replisome to DNA Damage.Histone H2A-H2B binding by Pol α in the eukaryotic replisome contributes to the maintenance of repressive chromatin Bacterial and Eukaryotic Replisome Machines

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P2860

Reconstitution of a eukaryotic replisome reveals suppression mechanisms that define leading/lagging strand operation.

http://www.wikidata.org/entity/Q35550942

description

2015 nî lūn-bûn

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2015 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2015 թվականի ապրիլին հրատարակված գիտական հոդված

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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name

Reconstitution of a eukaryotic ...... ding/lagging strand operation.

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Reconstitution of a eukaryotic ...... ding/lagging strand operation.

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type

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Reconstitution of a eukaryotic ...... ding/lagging strand operation.

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Reconstitution of a eukaryotic ...... ding/lagging strand operation.

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prefLabel

Reconstitution of a eukaryotic ...... ding/lagging strand operation.

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Reconstitution of a eukaryotic ...... ding/lagging strand operation.

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Reconstitution of a eukaryotic ...... ading/lagging strand operation

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P2093

Dan Zhang

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

Grant D Schauer

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

Jeff Finkelstein

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

Nina Y Yao

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

Olga Yurieva

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P2860

Isolation of the Cdc45/Mcm2-7/GINS (CMG) complex, a candidate for the eukaryotic DNA replication fork helicase

Yeast DNA polymerase epsilon participates in leading-strand DNA replication

Physical Interactions between Mcm10, DNA, and DNA Polymerase

A Ctf4 trimer couples the CMG helicase to DNA polymerase α in the eukaryotic replisome.

Structural basis for processive DNA synthesis by yeast DNA polymerase ɛ

Global analysis of protein expression in yeast

GINS maintains association of Cdc45 with MCM in replisome progression complexes at eukaryotic DNA replication forks.

A key role for Ctf4 in coupling the MCM2-7 helicase to DNA polymerase alpha within the eukaryotic replisome.

DNA polymerase delta is highly processive with proliferating cell nuclear antigen and undergoes collision release upon completing DNA.

The quaternary structure of DNA polymerase epsilon from Saccharomyces cerevisiae.

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10.7554/ELIFE.04988

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4

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Lance D Langston

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25871847

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