Replication fork assembly at recombination intermediates is required for bacterial growth. - Wikidata - wikimedia - TriplyDB

Replication fork assembly at recombination intermediates is required for bacterial growth.

Replication fork assembly at recombination intermediates is required for bacterial growth.

http://www.wikidata.org/entity/Q36443290

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Inhibition of mutation and combating the evolution of antibiotic resistance Structural insight into the DNA-binding mode of the primosomal proteins PriA, PriB, and DnaT Reductive genome evolution in Buchnera aphidicola Historical overview: searching for replication help in all of the rec places Allele specific synthetic lethality between priC and dnaAts alleles at the permissive temperature of 30 degrees C in E. coli K-12 A new role for translation initiation factor 2 in maintaining genome integrity Genetic and biochemical assays reveal a key role for replication restart proteins in group II intron retrohoming The importance of repairing stalled replication forks Role of PriA in replication fork reactivation in Escherichia coli.The breast cancer susceptibility gene, BRCA2: at the crossroads between DNA replication and recombination?PriA and phage T4 gp59: factors that promote DNA replication on forked DNA substrates microreview.Recombinational repair and restart of damaged replication forks.Integration of foreign DNA during natural transformation of Acinetobacter sp. by homology-facilitated illegitimate recombination.Break-induced DNA replication Replication fork collapse at replication terminator sequences.Mu insertions are repaired by the double-strand break repair pathway of Escherichia coli Rescue of arrested replication forks by homologous recombination Recombination and replication.Escherichia coli cells with increased levels of DnaA and deficient in recombinational repair have decreased viability.Evidence that stationary-phase hypermutation in the Escherichia coli chromosome is promoted by recombination.Inhibition of bacterial DNA replication by zinc mobilization during nitrosative stress.Double-strand-break repair recombination in Escherichia coli: physical evidence for a DNA replication mechanism in vivo.Mechanisms of replication fork restart in Escherichia coli.Interplay between DNA replication, recombination and repair based on the structure of RecG helicase.Structural basis of the 3'-end recognition of a leading strand in stalled replication forks by PriA.Replication Restart after Replication-Transcription Conflicts Requires RecA in Bacillus subtilis.Cellular characterization of the primosome and rep helicase in processing and restoration of replication following arrest by UV-induced DNA damage in Escherichia coli.DNA repair and genome maintenance in Bacillus subtilis.Bacteriophage replication modules.DNA damage differentially activates regional chromosomal loci for Tn7 transposition in Escherichia coli Effects of mutations involving cell division, recombination, and chromosome dimer resolution on a priA2::kan mutant.Rescue of stalled replication forks by RecG: simultaneous translocation on the leading and lagging strand templates supports an active DNA unwinding model of fork reversal and Holliday junction formation Formation of Holliday junctions by regression of nascent DNA in intermediates containing stalled replication forks: RecG stimulates regression even when the DNA is negatively supercoiled DNA damage responses in prokaryotes: regulating gene expression, modulating growth patterns, and manipulating replication forks.Genetic analysis of repair and damage tolerance mechanisms for DNA-protein cross-links in Escherichia coli.Recruitment to stalled replication forks of the PriA DNA helicase and replisome-loading activities is essential for survival.Helicases that underpin replication of protein-bound DNA in Escherichia coli.Replication fork dynamics and the DNA damage response.Stabilization of a stalled replication fork by concerted actions of two helicases.A dnaT mutant with phenotypes similar to those of a priA2::kan mutant in Escherichia coli K-12.

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P2860

Replication fork assembly at recombination intermediates is required for bacterial growth.

http://www.wikidata.org/entity/Q36443290

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1999 nî lūn-bûn

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Replication fork assembly at r ...... required for bacterial growth.

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Replication fork assembly at r ...... required for bacterial growth.

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

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Replication fork assembly at r ...... required for bacterial growth.

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P2093

J Liu

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

K J Marians

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L Xu

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S J Sandler

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P2860

Differential suppression of priA2::kan phenotypes in Escherichia coli K-12 by mutations in priA, lexA, and dnaC

Escherichia coli replication factor Y, a component of the primosome, can act as a DNA helicase

Interaction of Escherichia coli dnaB and dnaC(D) gene products in vitro

The DNA replication priming protein, PriA, is required for homologous recombination and double-strand break repair

Prokaryotic DNA replication.

Dissecting the functional role of PriA protein-catalysed primosome assembly in Escherichia coli DNA replication.

Escherichia coli PriA protein is essential for inducible and constitutive stable DNA replication.

Coupling of a replicative polymerase and helicase: a tau-DnaB interaction mediates rapid replication fork movement.

Inactivation of the Escherichia coli priA DNA replication protein induces the SOS response.

Enzymology of DNA in replication in prokaryotes.

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3552-3555

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10.1073/PNAS.96.7.3552

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7

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22331

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