Minding the gap: the underground functions of BRCA1 and BRCA2 at stalled replication forks - Wikidata - wikimedia - TriplyDB

Minding the gap: the underground functions of BRCA1 and BRCA2 at stalled replication forks

Minding the gap: the underground functions of BRCA1 and BRCA2 at stalled replication forks

http://www.wikidata.org/entity/Q28294399

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The UBXN1 protein associates with autoubiquitinated forms of the BRCA1 tumor suppressor and inhibits its enzymatic function The MMS22L-TONSL complex mediates recovery from replication stress and homologous recombination Molding BRCA2 function through its interacting partners BRCA2 acts as a RAD51 loader to facilitate telomere replication and capping A chromatin-dependent role of the fragile X mental retardation protein FMRP in the DNA damage response Double strand break repair functions of histone H2AX Genetic evidence for single-strand lesions initiating Nbs1-dependent homologous recombination in diversification of Ig v in chicken B lymphocytes.Lympho-vascular invasion in BRCA related breast cancer compared to sporadic controls.GEMIN2 promotes accumulation of RAD51 at double-strand breaks in homologous recombination Slip-sliding away: serial changes and homoplasy in repeat number in the Drosophila yakuba homolog of human cancer susceptibility gene BRCA2 Wild-type BRCA1, but not mutated BRCA1, regulates the expression of the nuclear form of beta-catenin Cell cycle-dependent induction of homologous recombination by a tightly regulated I-SceI fusion protein.Significance of the Fanconi anemia FANCD2 protein in sporadic and metastatic human breast cancer BRCA1 controls homologous recombination at Tus/Ter-stalled mammalian replication forks Mechanisms of double-strand break repair in somatic mammalian cells.Targeting abnormal DNA double strand break repair in cancer S100A11 plays a role in homologous recombination and genome maintenance by influencing the persistence of RAD51 in DNA repair foci.Roles of the Werner syndrome RecQ helicase in DNA replication.Synthetic lethality of PARP inhibition in cancers lacking BRCA1 and BRCA2 mutations.BRCA1 is required for postreplication repair after UV-induced DNA damage A protective role for BRCA2 at stalled replication forks.Distinct roles of FANCO/RAD51C protein in DNA damage signaling and repair: implications for Fanconi anemia and breast cancer susceptibility.BRCA1 tumor suppressor network: focusing on its tail.Complex Breakpoints and Template Switching Associated with Non-canonical Termination of Homologous Recombination in Mammalian Cells.Lack of MRE11-RAD50-NBS1 (MRN) complex detection occurs frequently in low-grade epithelial ovarian cancer.Implication of BRCA2 -26G>A 5' untranslated region polymorphism in susceptibility to sporadic breast cancer and its modulation by p53 codon 72 Arg>Pro polymorphism The basal-like mammary carcinomas induced by Brca1 or Bard1 inactivation implicate the BRCA1/BARD1 heterodimer in tumor suppression.Mutagenic and recombinagenic responses to defective DNA polymerase delta are facilitated by the Rev1 protein in pol3-t mutants of Saccharomyces cerevisiae.Ku protein levels, localization and association to replication origins in different stages of breast tumor progression.E3 ligase activity of BRCA1 is not essential for mammalian cell viability or homology-directed repair of double-strand DNA breaks.Spatial separation of replisome arrest sites influences homologous recombination quality at a Tus/Ter-mediated replication fork barrier.BRCA1 and BRCA2: different roles in a common pathway of genome protection.The Fanconi anemia protein interaction network: casting a wide net.Molecular evolution of a Drosophila homolog of human BRCA2.Functional interaction between the Fanconi Anemia D2 protein and proliferating cell nuclear antigen (PCNA) via a conserved putative PCNA interaction motif.RAD51C: a novel cancer susceptibility gene is linked to Fanconi anemia and breast cancer.Hereditary gynaecological malignancies: advances in screening and treatment.Mycobacterium tuberculosis RecG protein but not RuvAB or RecA protein is efficient at remodeling the stalled replication forks: implications for multiple mechanisms of replication restart in mycobacteria Deciphering the Code of the Cancer Genome: Mechanisms of Chromosome Rearrangement.Double-strand break repair-independent role for BRCA2 in blocking stalled replication fork degradation by MRE11.

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Minding the gap: the underground functions of BRCA1 and BRCA2 at stalled replication forks

http://www.wikidata.org/entity/Q28294399

description

2007 nî lūn-bûn

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2007 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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2007 թվականի հուլիսին հրատարակված գիտական հոդված

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年论文

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Minding the gap: the undergrou ...... 2 at stalled replication forks

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Minding the gap: the undergrou ...... 2 at stalled replication forks

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Minding the gap: the undergrou ...... 2 at stalled replication forks

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Ganesh Nagaraju

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Ralph Scully

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P2860

Stable interaction between the products of the BRCA1 and BRCA2 tumor suppressor genes in mitotic and meiotic cells

Interaction between the product of the breast cancer susceptibility gene BRCA2 and DSS1, a protein functionally conserved from yeast to mammals

Functional interaction of BRCA1-associated BARD1 with polyadenylation factor CstF-50

The Hallmarks of Cancer

BRCA1 is associated with a human SWI/SNF-related complex: linking chromatin remodeling to breast cancer

BACH1, a novel helicase-like protein, interacts directly with BRCA1 and contributes to its DNA repair function

The BRCT domain is a phospho-protein binding domain

ATM activation by DNA double-strand breaks through the Mre11-Rad50-Nbs1 complex

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

Regulation of BRCC, a holoenzyme complex containing BRCA1 and BRCA2, by a signalosome-like subunit and its role in DNA repair

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