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Replication and recombination intersect
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
10753777
retrieved
29 July 2017
review article
1 reference
stated in
Europe PubMed Central
title
Replication and recombination intersect
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
10753777
retrieved
29 July 2017
author name string
K J Marians
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
10753777
retrieved
29 July 2017
publication date
1 April 2000
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stated in
Europe PubMed Central
PubMed ID
10753777
retrieved
29 July 2017
published in
Current Opinion in Genetics & Development
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stated in
Europe PubMed Central
PubMed ID
10753777
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29 July 2017
volume
10
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stated in
Europe PubMed Central
PubMed ID
10753777
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29 July 2017
page(s)
151-156
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Europe PubMed Central
PubMed ID
10753777
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29 July 2017
issue
2
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Europe PubMed Central
PubMed ID
10753777
retrieved
29 July 2017
cites work
DNA double-strand breaks caused by replication arrest
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https://api.crossref.org/works/10.1016%2FS0959-437X%2800%2900059-9
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RuvAB acts at arrested replication forks
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Processing of recombination intermediates by the RuvABC proteins
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Spontaneous mitotic recombination in mms8-1, an allele of the CDC9 gene of Saccharomyces cerevisiae
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Chromosomal rearrangements occur in S. cerevisiae rfa1 mutator mutants due to mutagenic lesions processed by double-strand-break repair
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A novel mutation avoidance mechanism dependent on S. cerevisiae RAD27 is distinct from DNA mismatch repair
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A checkpoint regulates the rate of progression through S phase in S. cerevisiae in response to DNA damage.
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Aanlysis of the frequency and distribution of sister chromatid exchanges in cultured human lymphocytes
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Sister chromatid exchange in human chromosomes from normal individuals and patients with ataxia telangiectasia
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Sister chromatid exchanges are mediated by homologous recombination in vertebrate cells
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What to do at an end: DNA double-strand-break repair
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Gatekeepers of recombination
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7 January 2021
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Recombination and recombination-dependent DNA replication in bacteriophage T4.
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Recombination-dependent DNA replication stimulated by double-strand breaks in bacteriophage T4.
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DNA or RNA priming of bacteriophage G4 DNA synthesis by Escherichia coli dnaG protein
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Prokaryotic DNA replication
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Inactivation of the Escherichia coli priA DNA replication protein induces the SOS response
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Replication deficiencies in priA mutants of Escherichia coli lacking the primosomal replication n' protein
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Escherichia coli PriA protein is essential for inducible and constitutive stable DNA replication.
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The DNA replication priming protein, PriA, is required for homologous recombination and double-strand break repair
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Dissecting the functional role of PriA protein-catalysed primosome assembly in Escherichia coli DNA replication
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The DNA replication protein PriA and the recombination protein RecG bind D-loops.
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Two modes of PriA binding to DNA.
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Replication fork assembly at recombination intermediates is required for bacterial growth
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Role of PriA in replication fork reactivation in Escherichia coli
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Recovery of DNA replication in UV-irradiated Escherichia coli requires both excision repair and recF protein function
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Degradation of individual chromosomes in recA mutants of Escherichia coli
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Double-strand break repair in the absence of RAD51 in yeast: a possible role for break-induced DNA replication
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Double-strand break repair in yeast requires both leading and lagging strand DNA polymerases
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Homology-directed repair is a major double-strand break repair pathway in mammalian cells
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Double-strand break repair by interchromosomal recombination: suppression of chromosomal translocations
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Mammalian XRCC2 promotes the repair of DNA double-strand breaks by homologous recombination
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XRCC3 promotes homology-directed repair of DNA damage in mammalian cells
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Brca1 controls homology-directed DNA repair
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Correction of chromosomal instability and sensitivity to diverse mutagens by a cloned cDNA of the XRCC3 DNA repair gene
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XRCC2 and XRCC3, new human Rad51-family members, promote chromosome stability and protect against DNA cross-links and other damages
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Association of BRCA1 with Rad51 in mitotic and meiotic cells
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Centrosome amplification and a defective G2-M cell cycle checkpoint induce genetic instability in BRCA1 exon 11 isoform-deficient cells
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A mutation in mouse rad51 results in an early embryonic lethal that is suppressed by a mutation in p53
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Targeted disruption of the Rad51 gene leads to lethality in embryonic mice
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Homologous recombination and non-homologous end-joining pathways of DNA double-strand break repair have overlapping roles in the maintenance of chromosomal integrity in vertebrate cells
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Double-strand-break repair recombination in Escherichia coli: physical evidence for a DNA replication mechanism in vivo
1 reference
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reference URL
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Identifiers
DOI
10.1016/S0959-437X(00)00059-9
1 reference
stated in
Europe PubMed Central
PubMed ID
10753777
retrieved
29 July 2017
PubMed ID
10753777
1 reference
stated in
Europe PubMed Central
PubMed ID
10753777
retrieved
29 July 2017
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