DDB2 decides cell fate following DNA damage. - Wikidata - awgldk - TriplyDB

DDB2 decides cell fate following DNA damage.

DDB2 decides cell fate following DNA damage.

http://www.wikidata.org/entity/Q37249918

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Circadian control of XPA and excision repair of cisplatin-DNA damage by cryptochrome and HERC2 ubiquitin ligase The yin-yang of DNA damage response: roles in tumorigenesis and cellular senescence.Chromatin retention of DNA damage sensors DDB2 and XPC through loss of p97 segregase causes genotoxicity.NRIP/DCAF6 stabilizes the androgen receptor protein by displacing DDB2 from the CUL4A-DDB1 E3 ligase complex in prostate cancer.Interplay between Mdm2 and HIPK2 in the DNA damage response.α-N-methylation of damaged DNA-binding protein 2 (DDB2) and its function in nucleotide excision repair.Damaged DNA-binding protein 2 (DDB2) protects against UV irradiation in human cells and Drosophila.RETRACTED: DDB2, an essential mediator of premature senescence DDB2 suppresses tumorigenicity by limiting the cancer stem cell population in ovarian cancer.Similar nucleotide excision repair capacity in melanocytes and melanoma cells New insights into the link between DNA damage and apoptosis.The deubiquitinating protein USP24 interacts with DDB2 and regulates DDB2 stability.DDB2 increases radioresistance of NSCLC cells by enhancing DNA damage responses.High-throughput screening identifies aclacinomycin as a radiosensitizer of EGFR-mutant non-small cell lung cancer Regulators of global genome repair do not respond to DNA damaging therapy but correlate with survival in melanoma.Coordination between p21 and DDB2 in the cellular response to UV radiation.Functional regulation of the DNA damage-recognition factor DDB2 by ubiquitination and interaction with xeroderma pigmentosum group C protein.p21 cooperates with DDB2 protein in suppression of ultraviolet ray-induced skin malignancies.Inhibition of MDM2 by RG7388 confers hypersensitivity to X-radiation in xenograft models of childhood sarcoma.Combination of Aβ Secretion and Oxidative Stress in an Alzheimer-Like Cell Line Leads to the Over-Expression of the Nucleotide Excision Repair Proteins DDB2 and XPC Transcriptomic features of Pecten maximus oocyte quality and maturation.Damaged DNA binding protein 2 in reactive oxygen species (ROS) regulation and premature senescence Radiation dose effect of DNA repair-related gene expression in mouse white blood cells.Tumor regression by phenethyl isothiocyanate involves DDB2.Nucleotide excision repair deficiency in melanoma in response to UVA.A novel cis-acting element from the 3'UTR of DNA damage-binding protein 2 mRNA links transcriptional and post-transcriptional regulation of gene expression DDB2 suppresses epithelial-to-mesenchymal transition in colon cancer.DDB2 (damaged-DNA binding protein 2) in nucleotide excision repair and DNA damage response.DNA damage-binding complex recruits HDAC1 to repress Bcl-2 transcription in human ovarian cancer cells.COP9 signalosome function in the DDR.Integration of DNA damage and repair with murine double-minute 2 (Mdm2) in tumorigenesis.Genetic architecture of acne vulgaris.UVB-Induced p21 degradation promotes apoptosis of human keratinocytes.A DDB2 mutant protein unable to interact with PCNA promotes cell cycle progression of human transformed embryonic kidney cells.Damaged-DNA Binding Protein-2 Drives Apoptosis Following DNA Damage.DDB2 association with PCNA is required for its degradation after UV-induced DNA damage.Identification of epigenetically altered genes and potential gene targets in melanoma using bioinformatic methods.Sequential decitabine and carboplatin treatment increases the DNA repair protein XPC, increases apoptosis and decreases proliferation in melanoma.DDB2 represses ovarian cancer cell dedifferentiation by suppressing ALDH1A1.DDB2 regulates Epithelial-to-Mesenchymal Transition (EMT) in Oral/Head and Neck Squamous Cell Carcinoma

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DDB2 decides cell fate following DNA damage.

http://www.wikidata.org/entity/Q37249918

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 16 June 2009

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

DDB2 decides cell fate following DNA damage.

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DDB2 decides cell fate following DNA damage.

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type

label

DDB2 decides cell fate following DNA damage.

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DDB2 decides cell fate following DNA damage.

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prefLabel

DDB2 decides cell fate following DNA damage.

@en

DDB2 decides cell fate following DNA damage.

@nl

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PNAS.0812254106

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Proceedings of the National Academy of Sciences of the United States of America

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DDB2 decides cell fate following DNA damage.

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Dragana Kopanja

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Nilotpal Roy

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Pradip Raychaudhuri

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Srilata Bagchi

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Tanya Stoyanova

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P2860

p53 has a direct apoptogenic role at the mitochondria

PCNA-dependent regulation of p21 ubiquitylation and degradation via the CRL4Cdt2 ubiquitin ligase complex.

PUMA couples the nuclear and cytoplasmic proapoptotic function of p53

Mutations specific to the xeroderma pigmentosum group E Ddb- phenotype

Sequential binding of UV DNA damage binding factor and degradation of the p48 subunit as early events after UV irradiation.

p53 Binds and activates the xeroderma pigmentosum DDB2 gene in humans but not mice.

WAF1, a potential mediator of p53 tumor suppression

Sustained activation of the JNK cascade and rapamycin-induced apoptosis are suppressed by p53/p21(Cip1)

Histone H3 and H4 ubiquitylation by the CUL4-DDB-ROC1 ubiquitin ligase facilitates cellular response to DNA damage

A short mitochondrial form of p19ARF induces autophagy and caspase-independent cell death

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10690-10695

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scholarly article

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10.1073/PNAS.0812254106

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26

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106

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2009-06-16T00:00:00Z

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26306401

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19541625

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2705559

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