BRCA1 is required for postreplication repair after UV-induced DNA damage - Wikidata - wikimedia - TriplyDB

BRCA1 is required for postreplication repair after UV-induced DNA damage

BRCA1 is required for postreplication repair after UV-induced DNA damage

http://www.wikidata.org/entity/Q35434721

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Targeting DNA Replication Stress for Cancer Therapy Genomic scars as biomarkers of homologous recombination deficiency and drug response in breast and ovarian cancers USP45 deubiquitylase controls ERCC1-XPF endonuclease-mediated DNA damage responses BRCA1 deficiency exacerbates estrogen-induced DNA damage and genomic instability BRCA1 controls homologous recombination at Tus/Ter-stalled mammalian replication forks Chronic treatment with cisplatin induces replication-dependent sister chromatid recombination to confer cisplatin-resistant phenotype in nasopharyngeal carcinoma.BRCA1 pathway function in basal-like breast cancer cells.Systematic screening reveals a role for BRCA1 in the response to transcription-associated DNA damage Repair of naturally occurring mismatches can induce mutations in flanking DNA.Constitutional and somatic deletions of the Williams-Beuren syndrome critical region in non-Hodgkin lymphoma The chromatin remodeling protein BRG1 modulates BRCA1 response to UV irradiation by regulating ATR/ATM activation.FANC pathway promotes UV-induced stalled replication forks recovery by acting both upstream and downstream Polη and Rev1.BRCA1 haploinsufficiency for replication stress suppression in primary cells PARP1-driven poly-ADP-ribosylation regulates BRCA1 function in homologous recombination-mediated DNA repair.Tumor mutation burden forecasts outcome in ovarian cancer with BRCA1 or BRCA2 mutations.BRCA1 recruitment to transcriptional pause sites is required for R-loop-driven DNA damage repair.Key mediators of somatic ATR signaling localize to unpaired chromosomes in spermatocytes.BRCA1 regulates PIG3-mediated apoptosis in a p53-dependent manner.Oncogenic BRAF(V600E) Induces Clastogenesis and UVB Hypersensitivity BRCA1 tumor suppressor network: focusing on its tail.Repair of transposable phage Mu DNA insertions begins only when the E. coli replisome collides with the transpososome A porcine model system of BRCA1 driven breast cancer.Mechanism of release and fate of excised oligonucleotides during nucleotide excision repair Replication fork stability confers chemoresistance in BRCA-deficient cells Mechanisms of BRCA1 tumor suppression Augmented generation of protein fragments during wakefulness as the molecular cause of sleep: a hypothesis.BRCA1 inhibits AR-mediated proliferation of breast cancer cells through the activation of SIRT1 The role of BRCA1 in homologous recombination repair in response to replication stress: significance in tumorigenesis and cancer therapy PARI overexpression promotes genomic instability and pancreatic tumorigenesis.BRCA1 in the DNA damage response and at telomeres FANCJ at the FORK.RING domain-deficient BRCA1 promotes PARP inhibitor and platinum resistance.Spatial separation of replisome arrest sites influences homologous recombination quality at a Tus/Ter-mediated replication fork barrier.BRCA1/FANCD2/BRG1-Driven DNA Repair Stabilizes the Differentiation State of Human Mammary Epithelial Cells.Physiological modulation of endogenous BRCA1 p220 abundance suppresses DNA damage during the cell cycle Loss of BRCA1 or BRCA2 markedly increases the rate of base substitution mutagenesis and has distinct effects on genomic deletions.BRCA1-regulated RRM2 expression protects glioblastoma cells from endogenous replication stress and promotes tumorigenicity.Loss of Caenorhabditis elegans BRCA1 promotes genome stability during replication in smc-5 mutants Links between genome integrity and BRCA1 tumor suppression.Proteomic identification of a direct role for cyclin d1 in DNA damage repair.

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BRCA1 is required for postreplication repair after UV-induced DNA damage

http://www.wikidata.org/entity/Q35434721

description

2011 nî lūn-bûn

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2011 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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BRCA1 is required for postreplication repair after UV-induced DNA damage

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BRCA1 is required for postreplication repair after UV-induced DNA damage

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BRCA1 is required for postreplication repair after UV-induced DNA damage

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BRCA1 is required for postreplication repair after UV-induced DNA damage

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BRCA1 is required for postreplication repair after UV-induced DNA damage

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BRCA1 is required for postreplication repair after UV-induced DNA damage

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J.MOLCEL.2011.09.002

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BRCA1 is required for postreplication repair after UV-induced DNA damage

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David M Livingston

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Guillaume O Adelmant

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Jarrod A Marto

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Jean Feunteun

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Jenna Nguyen

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Ralph Scully

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Sarah J Hill

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Shailja Pathania

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P2860

Three DNA polymerases, recruited by different mechanisms, carry out NER repair synthesis in human cells

Interaction between human MCM7 and Rad17 proteins is required for replication checkpoint signaling

Functional uncoupling of MCM helicase and DNA polymerase activities activates the ATR-dependent checkpoint.

Loading of the human 9-1-1 checkpoint complex onto DNA by the checkpoint clamp loader hRad17-replication factor C complex in vitro

Direct DNA binding by Brca1

Replication protein A-mediated recruitment and activation of Rad17 complexes

The comings and goings of nucleotide excision repair factors on damaged DNA

Regulation of ATR substrate selection by Rad17-dependent loading of Rad9 complexes onto chromatin

Sensing DNA damage through ATRIP recognition of RPA-ssDNA complexes

A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1

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235-251

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2

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