Identical defects in DNA repair in xeroderma pigmentosum group G and rodent ERCC group 5
about
P1343
Conserved residues of human XPG protein important for nuclease activity and function in nucleotide excision repairHuman exonuclease 1 functionally complements its yeast homologues in DNA recombination, RNA primer removal, and mutation avoidancePurification and cloning of a nucleotide excision repair complex involving the xeroderma pigmentosum group C protein and a human homologue of yeast RAD23Ultraviolet-induced movement of the human DNA repair protein, Xeroderma pigmentosum type G, in the nucleusHuman DNA repair excision nuclease. Analysis of the roles of the subunits involved in dual incisions by using anti-XPG and anti-ERCC1 antibodiesCorrection of xeroderma pigmentosum repair defect by basal transcription factor BTF2 (TFIIH)Human ERCC5 cDNA-cosmid complementation for excision repair and bipartite amino acid domains conserved with RAD proteins of Saccharomyces cerevisiae and Schizosaccharomyces pombeClinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3Mice with DNA repair gene (ERCC-1) deficiency have elevated levels of p53, liver nuclear abnormalities and die before weaningLoss of heterozygosity and lack of mutations of the XPG/ERCC5 DNA repair gene at 13q33 in prostate cancer.Human nucleotide excision repair protein XPA: extended X-ray absorption fine-structure evidence for a metal-binding domain.Relationship of the xeroderma pigmentosum group E DNA repair defect to the chromatin and DNA binding proteins UV-DDB and replication protein A.The Cockayne syndrome B protein, involved in transcription-coupled DNA repair, resides in an RNA polymerase II-containing complexNon-catalytic Roles for XPG with BRCA1 and BRCA2 in Homologous Recombination and Genome StabilityRodent UV-sensitive mutant cell lines in complementation groups 6-10 have normal general excision repair activity.Transcription and DNA damage: a link to a kink.A 127 kDa component of a UV-damaged DNA-binding complex, which is defective in some xeroderma pigmentosum group E patients, is homologous to a slime mold proteinThe human XPG gene: gene architecture, alternative splicing and single nucleotide polymorphisms.The DNA repair endonuclease XPG interacts directly and functionally with the WRN helicase defective in Werner syndromeMolecular cloning of the human nucleotide-excision-repair gene ERCC4Susceptibility of XPD and RAD51 genetic variants to carcinoma of urinary bladder in North Indian populationXeroderma pigmentosum complementation group G patient with a novel homozygous missense mutation and no neurological abnormalities.Expression of XPG protein in human normal and tumor tissues.An XPG DNA repair defect causing mutagen hypersensitivity in mouse leukemia L1210 cells.Expression and functional analyses of the Dxpa gene, the Drosophila homolog of the human excision repair gene XPA.DNA repair protein XPA binds replication protein A (RPA).Co-correction of the ERCC1, ERCC4 and xeroderma pigmentosum group F DNA repair defects in vitro.DNA damage tolerance and a web of connections with DNA repair at Yale.XPG: its products and biological roles.Mutational analysis of ERCC3, which is involved in DNA repair and transcription initiation: identification of domains essential for the DNA repair function.Yeast nucleotide excision repair proteins Rad2 and Rad4 interact with RNA polymerase II basal transcription factor b (TFIIH)The nature of the 5'-terminus is a major determinant for DNA processing by Schizosaccharomyces pombe Rad2p, a FEN-1 family nuclease.Saccharomyces cerevisiae exonuclease-1 plays a role in UV resistance that is distinct from nucleotide excision repairEffects of genomic context and chromatin structure on transcription-coupled and global genomic repair in mammalian cells.HHR23B, a human Rad23 homolog, stimulates XPC protein in nucleotide excision repair in vitro.Properties of damage-dependent DNA incision by nucleotide excision repair in human cell-free extracts.Studying nucleotide excision repair of mammalian DNA in a cell-free system.Evidence for a repair enzyme complex involving ERCC1 and complementing activities of ERCC4, ERCC11 and xeroderma pigmentosum group F.UVs syndrome, a new general category of photosensitive disorder with defective DNA repair, is distinct from xeroderma pigmentosum variant and rodent complementation group I.Xpg limits the expansion of haematopoietic stem and progenitor cells after ionising radiation.
P2860
Q22008786-2706219F-1986-4EBB-BCE3-22156D1BE291Q22009967-5ED11D68-C9CE-4B5B-980D-3E13B68322C6Q24311788-D078EA9B-3B67-4633-A1C5-AFCA944EC792Q24313274-DCBA0E78-997A-4880-B740-13334127B827Q24336495-8B464E40-E70D-4990-9C06-B49E0A08F6BDQ24596052-7DA61EFB-8673-41D9-B765-3C75744B2EC0Q24629606-081E85EF-9DDE-45A6-A8F6-38708E52D0B3Q24673129-AB7A0A2B-4768-4CD9-A97F-76E92CDE3C91Q28587990-0A9F54CB-22AA-4828-A068-4EDDA4955533Q30304332-5D92EEBB-6E12-4FC3-B84A-AE30CE6AE0B0Q32006420-CD76AAC8-E6B7-4557-81C3-36FAF7CC3DB9Q32064326-007254A5-C605-4339-9AEE-72C0FB51E236Q33887586-BA8198BD-BE12-4992-A76C-BB1D4DC21D9EQ34511817-BC028341-56F1-4E99-A10C-431199FBBECCQ34626556-D1E903EC-0D54-43D6-BF24-02F44133D15BQ34640431-4A03F963-4B2B-48F9-8204-539E5B378DD5Q34999430-9500F6EE-7C3E-41A9-89CC-F8BD921BEFA6Q35085116-35414EEE-749F-4368-9960-03650FC302B3Q35159006-C30E0662-AE8A-4770-A6EE-BD7259ABC081Q35600010-A52CEB5D-A5BB-4176-BFE7-CBCCB6272CC6Q35737487-A5F2D874-AC48-40AB-AE8D-D62377FC3952Q35834957-5CFBFFAD-19CB-4E94-93E2-68F53E2C18BDQ36529982-70231899-83F0-47E2-929B-51942F70C122Q36566743-DDA0C6B1-1F8D-4E37-9138-0CADABC5DCBEQ36694414-02533824-0AF8-4049-A64A-3776549DF88CQ36718103-5B2E9FB8-6E8C-44A5-B502-9BD0BBEE3D2FQ36757154-FBB4E314-90D8-4D96-B640-BA38765AEAC5Q37358566-F513AD1D-9E84-453A-9249-6B6BA0A62376Q37380912-6FFF2674-FEFD-4101-B885-44FE80719CB3Q38307435-93CAE5AD-EE9D-4DB7-823F-5007B67A9F56Q38307487-88CB2224-2F64-4BF8-A0CB-E5EF2E719F59Q39542967-37D3E4E8-37A5-423C-B773-76184088EBA0Q39724404-145D3B19-F322-4851-B3E6-1305D71EC721Q39982171-19219CFB-6FED-43F8-8C3F-6CCB37FFA5D7Q40019757-302CCB11-C7AE-4AF8-AD9A-1308B4F21EF3Q40231519-4260141A-4A18-41E7-BD41-7C682D1DF6CAQ40707413-67DA9DC4-F545-4D00-93B8-6053DD92C90CQ40873926-E014BDD1-3168-401C-A5F0-F4FBDDA310EEQ41342786-E5B09FED-2533-46FC-BB50-6F1A59CF318CQ42225078-8A6A9FC2-AC5F-46C1-A99F-1B0DA5487D9A
P2860
Identical defects in DNA repair in xeroderma pigmentosum group G and rodent ERCC group 5
description
1993 nî lūn-bûn
@nan
1993 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1993 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
name
Identical defects in DNA repair in xeroderma pigmentosum group G and rodent ERCC group 5
@ast
Identical defects in DNA repair in xeroderma pigmentosum group G and rodent ERCC group 5
@en
Identical defects in DNA repair in xeroderma pigmentosum group G and rodent ERCC group 5
@nl
type
label
Identical defects in DNA repair in xeroderma pigmentosum group G and rodent ERCC group 5
@ast
Identical defects in DNA repair in xeroderma pigmentosum group G and rodent ERCC group 5
@en
Identical defects in DNA repair in xeroderma pigmentosum group G and rodent ERCC group 5
@nl
prefLabel
Identical defects in DNA repair in xeroderma pigmentosum group G and rodent ERCC group 5
@ast
Identical defects in DNA repair in xeroderma pigmentosum group G and rodent ERCC group 5
@en
Identical defects in DNA repair in xeroderma pigmentosum group G and rodent ERCC group 5
@nl
P3181
P356
P1433
P1476
Identical defects in DNA repair in xeroderma pigmentosum group G and rodent ERCC group 5
@en
P2093
P2888
P3181
P356
10.1038/363185A0
P407
P4510
P577
1993-05-13T00:00:00Z
P6179
1022759199