BCCIP regulates homologous recombination by distinct domains and suppresses spontaneous DNA damage. - Test2 - elhamkhani - TriplyDB

BCCIP regulates homologous recombination by distinct domains and suppresses spontaneous DNA damage.

BCCIP regulates homologous recombination by distinct domains and suppresses spontaneous DNA damage.

http://www.wikidata.org/entity/Q36328985

about

LYRIC/AEG-1 overexpression modulates BCCIPalpha protein levels in prostate tumor cells BCCIP associates with the receptor protein tyrosine phosphatase PTPmu Requirement of mouse BCCIP for neural development and progenitor proliferation Identification of the DNA repair defects in a case of Dubowitz syndrome Essential roles of BCCIP in mouse embryonic development and structural stability of chromosomes Regulation of spindle integrity and mitotic fidelity by BCCIP Alterations of BCCIP, a BRCA2 interacting protein, in astrocytomas Involvement of Caveolin-1 in repair of DNA damage through both homologous recombination and non-homologous end joining The over-expression of the β2 catalytic subunit of the proteasome decreases homologous recombination and impairs DNA double-strand break repair in human cells.BCCIP as a prognostic marker for radiotherapy of laryngeal cancer.Revealing the Molecular Portrait of Triple Negative Breast Tumors in an Understudied Population through Omics Analysis of Formalin-Fixed and Paraffin-Embedded Tissues.Prognostic values of filamin-A status for topoisomerase II poison chemotherapy FH535 inhibited metastasis and growth of pancreatic cancer cells.The β-isoform of BCCIP promotes ADP release from the RAD51 presynaptic filament and enhances homologous DNA pairing.The cytoskeleton protein filamin-A is required for an efficient recombinational DNA double strand break repair.BCCIP is required for the nuclear localization of the p21 protein.Celecoxib enhances the radiosensitivity of HCT116 cells in a COX-2 independent manner by up-regulating BCCIP.High Expression of BCCIP β Can Promote Proliferation of Esophageal Squamous Cell Carcinoma.Filamin-A as a marker and target for DNA damage based cancer therapy.Distinct RAD51 associations with RAD52 and BCCIP in response to DNA damage and replication stress.Filamin A expression predicts early recurrence of hepatocellular carcinoma after hepatectomy.BCCIP suppresses tumor initiation but is required for tumor progression Roles of BCCIP deficiency in mammary tumorigenesis.BCCIPβ modulates the ribosomal and extraribosomal function of S7 through a direct interaction.

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P2860

BCCIP regulates homologous recombination by distinct domains and suppresses spontaneous DNA damage.

http://www.wikidata.org/entity/Q36328985

description

2007 nî lūn-bûn

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2007年の論文

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2007年学术文章

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2007年学术文章

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2007年学术文章

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2007年學術文章

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name

BCCIP regulates homologous rec ...... resses spontaneous DNA damage.

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BCCIP regulates homologous rec ...... resses spontaneous DNA damage.

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type

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BCCIP regulates homologous rec ...... resses spontaneous DNA damage.

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BCCIP regulates homologous rec ...... resses spontaneous DNA damage.

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BCCIP regulates homologous rec ...... resses spontaneous DNA damage.

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BCCIP regulates homologous rec ...... resses spontaneous DNA damage.

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Nucleic Acids Research

P1476

BCCIP regulates homologous rec ...... presses spontaneous DNA damage

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P2093

Huimei Lu

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

Jac A Nickoloff

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Jingyin Yue

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Zhiyuan Shen

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P2860

TOK-1, a novel p21Cip1-binding protein that cooperatively enhances p21-dependent inhibitory activity toward CDK2 kinase

The SET domain protein Metnase mediates foreign DNA integration and links integration to nonhomologous end-joining repair

CDK-dependent phosphorylation of BRCA2 as a regulatory mechanism for recombinational repair

Differential effects of Rad52p overexpression on gene targeting and extrachromosomal homologous recombination in a human cell line

BLAP75/RMI1 promotes the BLM-dependent dissolution of homologous recombination intermediates

The BRCA2-interacting protein BCCIP functions in RAD51 and BRCA2 focus formation and homologous recombinational repair

Deficiency of human BRCA2 leads to impaired homologous recombination but maintains normal nonhomologous end joining

Abrogation of the transactivation activity of p53 by BCCIP down-regulation

A simplified system for generating recombinant adenoviruses

BRCA2 function in DNA binding and recombination from a BRCA2-DSS1-ssDNA structure

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