Histone deacetylases (HDACs) in XPC gene silencing and bladder cancer. - Wikidata - wikimedia - TriplyDB

Histone deacetylases (HDACs) in XPC gene silencing and bladder cancer.

Histone deacetylases (HDACs) in XPC gene silencing and bladder cancer.

http://www.wikidata.org/entity/Q38335802

about

Over-expression of deubiquitinating enzyme USP14 in lung adenocarcinoma promotes proliferation through the accumulation of β-catenin Overexpression of deubiquitinating enzyme USP28 promoted non-small cell lung cancer growth Evaluation of cell death pathways initiated by antitumor drugs melatonin and valproic acid in bladder cancer cells.The role of XPC: implications in cancer and oxidative DNA damage HDAC4: mechanism of regulation and biological functions Chromatin remodeling, cell proliferation and cell death in valproic acid-treated HeLa cells Expression of histone deacetylases 1, 2 and 3 in urothelial bladder cancer Chemotherapy in advanced bladder cancer: current status and future The cAMP responsive element binding protein 1 transactivates epithelial membrane protein 2, a potential tumor suppressor in the urinary bladder urothelial carcinoma The Nucleotide Excision Repair Pathway Limits L1 Retrotransposition Histone deacetylases and mechanisms of regulation of gene expression MIIP remodels Rac1-mediated cytoskeleton structure in suppression of endometrial cancer metastasis.Molecular mechanisms of cisplatin resistance in bladder cancer.Sp1 and the 'hallmarks of cancer'.Knockdown of HDAC1 expression suppresses invasion and induces apoptosis in glioma cells HDAC inhibition suppresses bladder cancer cell adhesion to collagen under flow conditions.Upregulation of miR-520b promotes ovarian cancer growth.Clinicopathological significance and prognostic value of Xeroderma pigmentosum complementary group C (XPC) expression in sporadic breast cancer patients.HDAC inhibition as a treatment concept to combat temsirolimus-resistant bladder cancer cells.Genetic determinants for chemo- and radiotherapy resistance in bladder cancer.Epigenetic Treatment Options in Urothelial Carcinoma.

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P2860

Histone deacetylases (HDACs) in XPC gene silencing and bladder cancer.

http://www.wikidata.org/entity/Q38335802

description

2011 nî lūn-bûn

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2011年の論文

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年學術文章

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2011年學術文章

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2011年學術文章

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name

Histone deacetylases (HDACs) in XPC gene silencing and bladder cancer.

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Histone deacetylases (HDACs) in XPC gene silencing and bladder cancer.

@en

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Histone deacetylases (HDACs) in XPC gene silencing and bladder cancer.

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Journal of Hematology & Oncology

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Histone deacetylases (HDACs) in XPC gene silencing and bladder cancer.

@en

P2093

Gan Wang

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Judith Abrams

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Le Wang

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Xiaoxin S Xu

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P2860

The xeroderma pigmentosum group C protein complex XPC-HR23B plays an important role in the recruitment of transcription factor IIH to damaged DNA

Strong functional interactions of TFIIH with XPC and XPG in human DNA nucleotide excision repair, without a preassembled repairosome

Recognition of RNA polymerase II and transcription bubbles by XPG, CSB, and TFIIH: insights for transcription-coupled repair and Cockayne Syndrome

Reconstitution of human excision nuclease with recombinant XPF-ERCC1 complex

XPG endonuclease makes the 3' incision in human DNA nucleotide excision repair

HDAC4 represses p21(WAF1/Cip1) expression in human cancer cells through a Sp1-dependent, p53-independent mechanism

Sp1 and Sp3 recruit histone deacetylase to repress transcription of human telomerase reverse transcriptase (hTERT) promoter in normal human somatic cells

Molecular mechanisms of mammalian DNA repair and the DNA damage checkpoints

A multistep damage recognition mechanism for global genomic nucleotide excision repair

Valproic acid induces functional heat-shock protein 70 via Class I histone deacetylase inhibition in cortical neurons: a potential role of Sp1 acetylation

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10.1186/1756-8722-4-17

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