Cell cycle regulation of the endogenous wild type Bloom's syndrome DNA helicase - sprookjes - yvandenbroek - TriplyDB

Cell cycle regulation of the endogenous wild type Bloom's syndrome DNA helicase

Cell cycle regulation of the endogenous wild type Bloom's syndrome DNA helicase

http://www.wikidata.org/entity/Q28138117

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Regulation and localization of the Bloom syndrome protein in response to DNA damage Colocalization, physical, and functional interaction between Werner and Bloom syndrome proteins BLAP75, an essential component of Bloom's syndrome protein complexes that maintain genome integrity MPS1-dependent mitotic BLM phosphorylation is important for chromosome stability The RecQ DNA helicases in DNA repair RMI, a new OB-fold complex essential for Bloom syndrome protein to maintain genome stability BLAP18/RMI2, a novel OB-fold-containing protein, is an essential component of the Bloom helicase-double Holliday junction dissolvasome The Bloom's syndrome helicase (BLM) interacts physically and functionally with p12, the smallest subunit of human DNA polymerase delta Telomere and ribosomal DNA repeats are chromosomal targets of the bloom syndrome DNA helicase The C-terminal domain of the Bloom syndrome DNA helicase is essential for genomic stability Functions of Ubiquitin and SUMO in DNA Replication and Replication Stress Functional interaction of p53 and BLM DNA helicase in apoptosis 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 The broken genome: genetic and pharmacologic approaches to breaking DNA Association of BLM and BRCA1 during Telomere Maintenance in ALT Cells Unwinding protein complexes in ALTernative telomere maintenance.Selective cleavage of BLM, the bloom syndrome protein, during apoptotic cell death.RecQ helicases: guardian angels of the DNA replication fork.Regulation of BLM Nucleolar Localization The role of post-translational modifications in fine-tuning BLM helicase function during DNA repair Werner protein protects nonproliferating cells from oxidative DNA damage Sgs1 truncations induce genome rearrangements but suppress detrimental effects of BLM overexpression in Saccharomyces cerevisiae.The yeast Sgs1 helicase is differentially required for genomic and ribosomal DNA replication.RecQ helicases: suppressors of tumorigenesis and premature aging.DNA end resection is needed for the repair of complex lesions in G1-phase human cells.DNA polymerase stabilization at stalled replication forks requires Mec1 and the RecQ helicase Sgs1.Structure and function of RecQ DNA helicases.Protein degradation pathways regulate the functions of helicases in the DNA damage response and maintenance of genomic stability The human RecQ helicases BLM and RECQL4 cooperate to preserve genome stability.The BLM helicase contributes to telomere maintenance through processing of late-replicating intermediate structures Bloom's syndrome protein is required for correct relocalization of RAD50/MRE11/NBS1 complex after replication fork arrest Accumulation and Phosphorylation of RecQ-Mediated Genome Instability Protein 1 (RMI1) at Serine 284 and Serine 292 during Mitosis.Bloom syndrome cells undergo p53-dependent apoptosis and delayed assembly of BRCA1 and NBS1 repair complexes at stalled replication forks.hSSB1 associates with and promotes stability of the BLM helicase Non-Bloom syndrome-associated partial and total loss-of-function variants of BLM helicase.The BLM dissolvasome in DNA replication and repair.Monopolar spindle 1 (MPS1) protein-dependent phosphorylation of RecQ-mediated genome instability protein 2 (RMI2) at serine 112 is essential for BLM-Topo III α-RMI1-RMI2 (BTR) protein complex function upon spindle assembly checkpoint (SAC) activatio Possible anti-recombinogenic role of Bloom's syndrome helicase in double-strand break processing Bloom's Syndrome: Clinical Spectrum, Molecular Pathogenesis, and Cancer Predisposition.

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Cell cycle regulation of the endogenous wild type Bloom's syndrome DNA helicase

http://www.wikidata.org/entity/Q28138117

description

2000 nî lūn-bûn

@nan

2000 թուականի Մայիսին հրատարակուած գիտական յօդուած

@hyw

2000 թվականի մայիսին 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

Cell cycle regulation of the endogenous wild type Bloom's syndrome DNA helicase

@ast

Cell cycle regulation of the endogenous wild type Bloom's syndrome DNA helicase

@en

Cell cycle regulation of the endogenous wild type Bloom's syndrome DNA helicase

@nl

type

label

Cell cycle regulation of the endogenous wild type Bloom's syndrome DNA helicase

@ast

Cell cycle regulation of the endogenous wild type Bloom's syndrome DNA helicase

@en

Cell cycle regulation of the endogenous wild type Bloom's syndrome DNA helicase

@nl

prefLabel

Cell cycle regulation of the endogenous wild type Bloom's syndrome DNA helicase

@ast

Cell cycle regulation of the endogenous wild type Bloom's syndrome DNA helicase

@en

Cell cycle regulation of the endogenous wild type Bloom's syndrome DNA helicase

@nl

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Cell cycle regulation of the endogenous wild type Bloom's syndrome DNA helicase

@en

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Ababou M

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Amor-Guéret M

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Delic J

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Dutertre S

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Jaulin C

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Onclercq R

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P2860

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

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

Geminin, an inhibitor of DNA replication, is degraded during mitosis

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

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

Structure and functions of the 20S and 26S proteasomes

Sgs1: a eukaryotic homolog of E. coli RecQ that interacts with topoisomerase II in vivo and is required for faithful chromosome segregation.

The yeast type I topoisomerase Top3 interacts with Sgs1, a DNA helicase homolog: a potential eukaryotic reverse gyrase

Inhibitors of the proteasome block the degradation of most cell proteins and the generation of peptides presented on MHC class I molecules

E3-ubiquitin ligase/E6-AP links multicopy maintenance protein 7 to the ubiquitination pathway by a novel motif, the L2G box

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2731-2738

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scholarly article

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1644400

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10.1038/SJ.ONC.1203595

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23

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19

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1019516625

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