E2F1 localizes to sites of UV-induced DNA damage to enhance nucleotide excision repair. - Wikidata - wikimedia - TriplyDB

E2F1 localizes to sites of UV-induced DNA damage to enhance nucleotide excision repair.

E2F1 localizes to sites of UV-induced DNA damage to enhance nucleotide excision repair.

http://www.wikidata.org/entity/Q33562595

about

Implication of posttranslational histone modifications in nucleotide excision repair Transcriptional and Posttranslational Regulation of Nucleotide Excision Repair: The Guardian of the Genome against Ultraviolet Radiation E2F1 promotes the recruitment of DNA repair factors to sites of DNA double-strand breaks XPA-mediated regulation of global nucleotide excision repair by ATR Is p53-dependent and occurs primarily in S-phase.GCN5 and E2F1 stimulate nucleotide excision repair by promoting H3K9 acetylation at sites of damage.Communication: UV photoionization of cytosine catalyzed by Ag(+).The p38 MAPK-MK2 axis regulates E2F1 and FOXM1 expression after epirubicin treatment.E2F1 and p53 transcription factors as accessory factors for nucleotide excision repair.E2F1 Transcription Factor Regulates O-linked N-acetylglucosamine (O-GlcNAc) Transferase and O-GlcNAcase Expression.RNF126 promotes homologous recombination via regulation of E2F1-mediated BRCA1 expression Transcriptional and nontranscriptional functions of E2F1 in response to DNA damage.Tumorigenicity analysis of heterogeneous dental stem cells and its self-modification for chromosome instability.ATM and p53 regulate FOXM1 expression via E2F in breast cancer epirubicin treatment and resistance RB localizes to DNA double-strand breaks and promotes DNA end resection and homologous recombination through the recruitment of BRG1.Molecular mechanisms of ultraviolet radiation-induced DNA damage and repair.Autophagy and genomic integrity.Role of Purα in the cellular response to ultraviolet-C radiation.Xeroderma pigmentosum group C protein interacts with histones: regulation by acetylated states of histone H3.E2F1 and E2F2 induction in response to DNA damage preserves genomic stability in neuronal cells.The PIM-2 kinase is an essential component of the ultraviolet damage response that acts upstream to E2F-1 and ATM E2F1 interactions with hHR23A inhibit its degradation and promote DNA repair.The Retinoblastoma (RB) Tumor Suppressor: Pushing Back against Genome Instability on Multiple Fronts.E2F1 responds to ultraviolet radiation by directly stimulating DNA repair and suppressing carcinogenesis.p53: Guardian of pancreatic epithelial identity.E2F1: A new role in the DNA damage response.A new role for E2F1 in DNA repair: all for the greater good.Hormone-induced DNA damage response and repair mediated by cyclin D1 in breast and prostate cancer.E2F1 regulates p53R2 gene expression in p53-deficient cells.Inhibition of E2F1 activity and cell cycle progression by arsenic via retinoblastoma protein.An E2F7-dependent transcriptional program modulates DNA damage repair and genomic stability.

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P2860

E2F1 localizes to sites of UV-induced DNA damage to enhance nucleotide excision repair.

http://www.wikidata.org/entity/Q33562595

description

2010 nî lūn-bûn

@nan

2010 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

2010年の論文

@ja

2010年論文

@yue

2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

name

E2F1 localizes to sites of UV-induced DNA damage to enhance nucleotide excision repair.

@ast

E2F1 localizes to sites of UV-induced DNA damage to enhance nucleotide excision repair.

@en

E2F1 localizes to sites of UV-induced DNA damage to enhance nucleotide excision repair.

@nl

type

label

E2F1 localizes to sites of UV-induced DNA damage to enhance nucleotide excision repair.

@ast

E2F1 localizes to sites of UV-induced DNA damage to enhance nucleotide excision repair.

@en

E2F1 localizes to sites of UV-induced DNA damage to enhance nucleotide excision repair.

@nl

prefLabel

E2F1 localizes to sites of UV-induced DNA damage to enhance nucleotide excision repair.

@ast

E2F1 localizes to sites of UV-induced DNA damage to enhance nucleotide excision repair.

@en

E2F1 localizes to sites of UV-induced DNA damage to enhance nucleotide excision repair.

@nl

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JBC.M110.121939

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Journal of Biological Chemistry

P1476

E2F1 localizes to sites of UV-induced DNA damage to enhance nucleotide excision repair.

@en

P2093

Anup K Biswas

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

David L Mitchell

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

Feng Zhu

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

Jie Chen

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

Ruifeng Guo

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

Thomas R Berton

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

P2860

Cockayne syndrome A and B proteins differentially regulate recruitment of chromatin remodeling and repair factors to stalled RNA polymerase II in vivo

ATM and ATR substrate analysis reveals extensive protein networks responsive to DNA damage

DNA nucleotide excision repair-dependent signaling to checkpoint activation

Proapoptotic function of the retinoblastoma tumor suppressor protein

DDB, a putative DNA repair protein, can function as a transcriptional partner of E2F1.

TopBP1 recruits Brg1/Brm to repress E2F1-induced apoptosis, a novel pRb-independent and E2F1-specific control for cell survival

Regulation of E2F1 by BRCT domain-containing protein TopBP1

Differential role of RB in response to UV and IR damage.

Sensing DNA damage through ATRIP recognition of RPA-ssDNA complexes

A splicing mutation affecting expression of ataxia-telangiectasia and Rad3-related protein (ATR) results in Seckel syndrome

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19308-19315

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scholarly article

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10.1074/JBC.M110.121939

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25

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285

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David G. Johnson

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2010-04-22T00:00:00Z

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20413589

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2885209

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