Possible association of BLM in decreasing DNA double strand breaks during DNA replication - Test2 - elhamkhani - TriplyDB

Possible association of BLM in decreasing DNA double strand breaks during DNA replication

Possible association of BLM in decreasing DNA double strand breaks during DNA replication

http://www.wikidata.org/entity/Q35115298

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Rif1 provides a new DNA-binding interface for the Bloom syndrome complex to maintain normal replication UV-induced replication arrest in the xeroderma pigmentosum variant leads to DNA double-strand breaks, gamma -H2AX formation, and Mre11 relocalization Homologous recombination: from model organisms to human disease.Eme1 is involved in DNA damage processing and maintenance of genomic stability in mammalian cells RMI, a new OB-fold complex essential for Bloom syndrome protein to maintain genome stability Manipulating mitotic recombination in the zebrafish embryo through RecQ helicases Opposing roles for DNA structure-specific proteins Rad1, Msh2, Msh3, and Sgs1 in yeast gene targeting.The Bloom's syndrome protein (BLM) interacts with MLH1 but is not required for DNA mismatch repair Functional link between BLM defective in Bloom's syndrome and the ataxia-telangiectasia-mutated protein, ATM Potential role for the BLM helicase in recombinational repair via a conserved interaction with RAD51 Enhanced genomic instability and defective postreplication repair in RAD18 knockout mouse embryonic stem cells Essential roles of BCCIP in mouse embryonic development and structural stability of chromosomes Chromosome instability and defective recombinational repair in knockout mutants of the five Rad51 paralogs Novel pro- and anti-recombination activities of the Bloom's syndrome helicase.Topoisomerase IIIalpha is required for normal proliferation and telomere stability in alternative lengthening of telomeres.RTEL1 contributes to DNA replication and repair and telomere maintenance.Meiotic chromosome synapsis-promoting proteins antagonize the anti-crossover activity of sgs1.The MER3 helicase involved in meiotic crossing over is stimulated by single-stranded DNA-binding proteins and unwinds DNA in the 3' to 5' direction.Mechanisms by which Bloom protein can disrupt recombination intermediates of Okazaki fragment maturation.The G-quadruplex ligand telomestatin impairs binding of topoisomerase IIIalpha to G-quadruplex-forming oligonucleotides and uncaps telomeres in ALT cells Functional relationships of FANCC to homologous recombination, translesion synthesis, and BLM The chicken as a model for large-scale analysis of vertebrate gene function.Manipulating the mammalian genome by homologous recombination Genetic interactions between BLM and DNA ligase IV in human cells.Mobile D-loops are a preferred substrate for the Bloom's syndrome helicase.BLM helicase stimulates the ATPase and chromatin-remodeling activities of RAD54.BLM helicase-dependent transport of p53 to sites of stalled DNA replication forks modulates homologous recombination Werner protein cooperates with the XRCC4-DNA ligase IV complex in end-processing RecQ helicases: suppressors of tumorigenesis and premature aging.The BLM dissolvasome in DNA replication and repair.Chromosomes and cancer cells.Mechanisms of leukemia translocations Identification and analysis of new proteins involved in the DNA damage response network of Fanconi anemia and Bloom syndrome.Genome instability and embryonic developmental defects in RMI1 deficient mice.Hitting the bull's eye: novel directed cancer therapy through helicase-targeted synthetic lethality.Possible anti-recombinogenic role of Bloom's syndrome helicase in double-strand break processing Bloom syndrome complex promotes FANCM recruitment to stalled replication forks and facilitates both repair and traverse of DNA interstrand crosslinks Rad54, the motor of homologous recombination.Single-molecule studies reveal reciprocating of WRN helicase core along ssDNA during DNA unwinding.RecQ helicases; at the crossroad of genome replication, repair, and recombination.

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P2860

Possible association of BLM in decreasing DNA double strand breaks during DNA replication

http://www.wikidata.org/entity/Q35115298

description

2000 nî lūn-bûn

@nan

2000 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2000 թվականի հուլիսին հրատարակված գիտական հոդված

@hy

2000年の論文

@ja

2000年論文

@yue

2000年論文

@zh-hant

2000年論文

@zh-hk

2000年論文

@zh-mo

2000年論文

@zh-tw

2000年论文

@wuu

name

Possible association of BLM in decreasing DNA double strand breaks during DNA replication

@ast

Possible association of BLM in decreasing DNA double strand breaks during DNA replication

@en

type

label

Possible association of BLM in decreasing DNA double strand breaks during DNA replication

@ast

Possible association of BLM in decreasing DNA double strand breaks during DNA replication

@en

prefLabel

Possible association of BLM in decreasing DNA double strand breaks during DNA replication

@ast

Possible association of BLM in decreasing DNA double strand breaks during DNA replication

@en

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P1433

The EMBO Journal

P1476

Possible association of BLM in decreasing DNA double strand breaks during DNA replication

@en

P2093

Enomoto T

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

Katada T

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

Masuko T

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

Narita Y

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Seki M

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

Sonoda E

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

Takeda S

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

Wang W

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

Yamada K

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P2860

Cloning of two new human helicase genes of the RecQ family: biological significance of multiple species in higher eukaryotes

Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome

Mutations of a novel human RAD54 homologue, RAD54B, in primary cancer

Molecular cloning of cDNA encoding human DNA helicase Q1 which has homology to Escherichia coli Rec Q helicase and localization of the gene at chromosome 12p12

The Werner syndrome protein is a DNA helicase

The Bloom's syndrome gene product is a 3'-5' DNA helicase

The Bloom's syndrome gene product is homologous to RecQ helicases

Bloom's and Werner's syndrome genes suppress hyperrecombination in yeast sgs1 mutant: implication for genomic instability in human diseases

Cloning and characterization of RECQL, a potential human homologue of the Escherichia coli DNA helicase RecQ

Drosophila and human RecQ5 exist in different isoforms generated by alternative splicing

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3428-3435

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scholarly article

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10.1093/EMBOJ/19.13.3428

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13

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19

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2000-07-01T00:00:00Z

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12439430

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10880455

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313960

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