Xeroderma pigmentosum group C protein complex is the initiator of global genome nucleotide excision repair - Wikidata - wikimedia - TriplyDB

Xeroderma pigmentosum group C protein complex is the initiator of global genome nucleotide excision repair

Xeroderma pigmentosum group C protein complex is the initiator of global genome nucleotide excision repair

http://www.wikidata.org/entity/Q24312736

about

Dynamic interaction of TTDA with TFIIH is stabilized by nucleotide excision repair in living cells Human single-stranded DNA binding proteins are essential for maintaining genomic stability The xeroderma pigmentosum group C protein complex XPC-HR23B plays an important role in the recruitment of transcription factor IIH to damaged DNA 3-Methyladenine-DNA glycosylase (MPG protein) interacts with human RAD23 proteins XAB2, a novel tetratricopeptide repeat protein involved in transcription-coupled DNA repair and transcription Cloning of a human homolog of the yeast nucleotide excision repair gene MMS19 and interaction with transcription repair factor TFIIH via the XPB and XPD helicases Strong functional interactions of TFIIH with XPC and XPG in human DNA nucleotide excision repair, without a preassembled repairosome Centrosome protein centrin 2/caltractin 1 is part of the xeroderma pigmentosum group C complex that initiates global genome nucleotide excision repair Translocation of Cockayne syndrome group A protein to the nuclear matrix: possible relevance to transcription-coupled DNA repair Defining the function of xeroderma pigmentosum group F protein in psoralen interstrand cross-link-mediated DNA repair and mutagenesis Centrin 2 stimulates nucleotide excision repair by interacting with xeroderma pigmentosum group C protein.Influence of XPB helicase on recruitment and redistribution of nucleotide excision repair proteins at sites of UV-induced DNA damage Structural basis of UV DNA-damage recognition by the DDB1-DDB2 complex DNA nucleotide excision repair-dependent signaling to checkpoint activation Regulation of global genome nucleotide excision repair by SIRT1 through xeroderma pigmentosum C Xeroderma pigmentosum group C protein interacts physically and functionally with thymine DNA glycosylase Global genome repair is required to activate KIN17, a UVC-responsive gene involved in DNA replication.DNA damage triggers nucleotide excision repair-dependent monoubiquitylation of histone H2A Nucleotide excision repair- and polymerase eta-mediated error-prone removal of mitomycin C interstrand cross-links Significance analysis of microarrays applied to the ionizing radiation response The role of altered nucleotide excision repair and UVB-induced DNA damage in melanomagenesis A novel regulation mechanism of DNA repair by damage-induced and RAD23-dependent stabilization of xeroderma pigmentosum group C protein The comings and goings of nucleotide excision repair factors on damaged DNA Nucleotide Excision Repair, Genome Stability, and Human Disease: New Insight from Model Systems Human XPC-hHR23B interacts with XPA-RPA in the recognition of triplex-directed psoralen DNA interstrand crosslinks.DNA repair factor XPC is modified by SUMO-1 and ubiquitin following UV irradiation Melanocortin 1 Receptor: Structure, Function, and Regulation Global-genome Nucleotide Excision Repair Controlled by Ubiquitin/Sumo Modifiers Host nucleotide polymorphism in hepatitis B virus-associated hepatocellular carcinoma Xeroderma pigmentosum group C sensor: unprecedented recognition strategy and tight spatiotemporal regulation Nucleotide excision repair in eukaryotes Recognition of Damaged DNA for Nucleotide Excision Repair: A Correlated Motion Mechanism with a Mismatched cis-syn Thymine Dimer Lesion.Involvement of global genome repair, transcription coupled repair, and chromatin remodeling in UV DNA damage response changes during development Interactions of human nucleotide excision repair protein XPA with DNA and RPA70 Delta C327: chemical shift mapping and 15N NMR relaxation studies DNA-repair protein hHR23a alters its protein structure upon binding proteasomal subunit S5a Damaged DNA induced UV-damaged DNA-binding protein (UV-DDB) dimerization and its roles in chromatinized DNA repair Structural and functional evidence that Rad4 competes with Rad2 for binding to the Tfb1 subunit of TFIIH in NER Preferential binding of yeast Rad4.Rad23 complex to damaged DNA.Rad4-Rad23 interaction with SWI/SNF links ATP-dependent chromatin remodeling with nucleotide excision repair.XPC: Going where no DNA damage sensor has gone before

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P2860

Xeroderma pigmentosum group C protein complex is the initiator of global genome nucleotide excision repair

http://www.wikidata.org/entity/Q24312736

description

1998 nî lūn-bûn

@nan

1998 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

1998 թվականի օգոստոսին հրատարակված գիտական հոդված

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1998年の論文

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1998年論文

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1998年論文

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1998年論文

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name

Xeroderma pigmentosum group C ...... ome nucleotide excision repair

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Xeroderma pigmentosum group C ...... ome nucleotide excision repair

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Xeroderma pigmentosum group C ...... ome nucleotide excision repair

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Xeroderma pigmentosum group C ...... ome nucleotide excision repair

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Xeroderma pigmentosum group C ...... ome nucleotide excision repair

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Xeroderma pigmentosum group C ...... ome nucleotide excision repair

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Xeroderma pigmentosum group C ...... ome nucleotide excision repair

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Xeroderma pigmentosum group C ...... ome nucleotide excision repair

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Xeroderma pigmentosum group C ...... ome nucleotide excision repair

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nucleotide-excision repair

XPC complex subunit, DNA damage recognition and repair factor

RAD23 homolog B, nucleotide excision repair protein