[cite web | title = Entrez Gene: XPA xeroderma pigmentosum, complementation group A| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=7507| accessdate = ] ] PBB_Summary
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References
Further reading
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*cite journal | author=Cleaver JE, Thompson LH, Richardson AS, States JC |title=A summary of mutations in the UV-sensitive disorders: xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy. |journal=Hum. Mutat. |volume=14 |issue= 1 |pages= 9–22 |year= 1999 |pmid= 10447254 |doi= 10.1002/(SICI)1098-1004(1999)14:1<9::AID-HUMU2>3.0.CO;2-6 |doilabel=10.1002/(SICI)1098-1004(1999)14:19::AID-HUMU23.0.CO;2-6
*cite journal | author=Morikawa K, Shirakawa M |title=Three-dimensional structural views of damaged-DNA recognition: T4 endonuclease V, E. coli Vsr protein, and human nucleotide excision repair factor XPA. |journal=Mutat. Res. |volume=460 |issue= 3-4 |pages= 257–75 |year= 2000 |pmid= 10946233 |doi=
*cite journal | author=Satokata I, Tanaka K, Okada Y |title=Molecular basis of group A xeroderma pigmentosum: a missense mutation and two deletions located in a zinc finger consensus sequence of the XPAC gene. |journal=Hum. Genet. |volume=88 |issue= 6 |pages= 603–7 |year= 1992 |pmid= 1339397 |doi=
*cite journal | author=Satokata I, Tanaka K, Yuba S, Okada Y |title=Identification of splicing mutations of the last nucleotides of exons, a nonsense mutation, and a missense mutation of the XPAC gene as causes of group A xeroderma pigmentosum. |journal=Mutat. Res. |volume=273 |issue= 2 |pages= 203–12 |year= 1992 |pmid= 1372103 |doi=
*cite journal | author=Miyamoto I, Miura N, Niwa H, "et al." |title=Mutational analysis of the structure and function of the xeroderma pigmentosum group A complementing protein. Identification of essential domains for nuclear localization and DNA excision repair. |journal=J. Biol. Chem. |volume=267 |issue= 17 |pages= 12182–7 |year= 1992 |pmid= 1601884 |doi=
*cite journal | author=Satokata I, Tanaka K, Miura N, "et al." |title=Characterization of a splicing mutation in group A xeroderma pigmentosum. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=87 |issue= 24 |pages= 9908–12 |year= 1991 |pmid= 1702221 |doi=
*cite journal | author=Miura N, Miyamoto I, Asahina H, "et al." |title=Identification and characterization of xpac protein, the gene product of the human XPAC (xeroderma pigmentosum group A complementing) gene. |journal=J. Biol. Chem. |volume=266 |issue= 29 |pages= 19786–9 |year= 1991 |pmid= 1918083 |doi=
*cite journal | author=Tanaka K, Miura N, Satokata I, "et al." |title=Analysis of a human DNA excision repair gene involved in group A xeroderma pigmentosum and containing a zinc-finger domain. |journal=Nature |volume=348 |issue= 6296 |pages= 73–6 |year= 1990 |pmid= 2234061 |doi= 10.1038/348073a0
*cite journal | author=Li L, Lu X, Peterson CA, Legerski RJ |title=An interaction between the DNA repair factor XPA and replication protein A appears essential for nucleotide excision repair. |journal=Mol. Cell. Biol. |volume=15 |issue= 10 |pages= 5396–402 |year= 1995 |pmid= 7565690 |doi=
*cite journal | author=Nagai A, Saijo M, Kuraoka I, "et al." |title=Enhancement of damage-specific DNA binding of XPA by interaction with the ERCC1 DNA repair protein. |journal=Biochem. Biophys. Res. Commun. |volume=211 |issue= 3 |pages= 960–6 |year= 1995 |pmid= 7598728 |doi=
*cite journal | author=Farndon PA, Morris DJ, Hardy C, "et al." |title=Analysis of 133 meioses places the genes for nevoid basal cell carcinoma (Gorlin) syndrome and Fanconi anemia group C in a 2.6-cM interval and contributes to the fine map of 9q22.3. |journal=Genomics |volume=23 |issue= 2 |pages= 486–9 |year= 1995 |pmid= 7835901 |doi= 10.1006/geno.1994.1528
*cite journal | author=Park CH, Mu D, Reardon JT, Sancar A |title=The general transcription-repair factor TFIIH is recruited to the excision repair complex by the XPA protein independent of the TFIIE transcription factor. |journal=J. Biol. Chem. |volume=270 |issue= 9 |pages= 4896–902 |year= 1995 |pmid= 7876263 |doi=
*cite journal | author=Li L, Elledge SJ, Peterson CA, "et al." |title=Specific association between the human DNA repair proteins XPA and ERCC1. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=91 |issue= 11 |pages= 5012–6 |year= 1994 |pmid= 8197174 |doi=
*cite journal | author=Park CH, Sancar A |title=Formation of a ternary complex by human XPA, ERCC1, and ERCC4(XPF) excision repair proteins. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=91 |issue= 11 |pages= 5017–21 |year= 1994 |pmid= 8197175 |doi=
*cite journal | author=Satokata I, Iwai K, Matsuda T, "et al." |title=Genomic characterization of the human DNA excision repair-controlling gene XPAC. |journal=Gene |volume=136 |issue= 1-2 |pages= 345–8 |year= 1994 |pmid= 8294029 |doi=
*cite journal | author=Tanaka K |title=The Japan Society of Human Genetics Award Lecture. Molecular analysis of xeroderma pigmentosum group A gene. |journal=Jpn. J. Hum. Genet. |volume=38 |issue= 1 |pages= 1–14 |year= 1993 |pmid= 8504220 |doi=
*cite journal | author=Topping RS, Myrand SP, Williams BL, "et al." |title=Characterization of the human XPA promoter. |journal=Gene |volume=166 |issue= 2 |pages= 341–2 |year= 1996 |pmid= 8543191 |doi=
*cite journal | author=Lench NJ, Telford EA, Andersen SE, "et al." |title=An EST and STS-based YAC contig map of human chromosome 9q22.3. |journal=Genomics |volume=38 |issue= 2 |pages= 199–205 |year= 1997 |pmid= 8954802 |doi= 10.1006/geno.1996.0616
*cite journal | author=Selby CP, Sancar A |title=Human transcription-repair coupling factor CSB/ERCC6 is a DNA-stimulated ATPase but is not a helicase and does not disrupt the ternary transcription complex of stalled RNA polymerase II. |journal=J. Biol. Chem. |volume=272 |issue= 3 |pages= 1885–90 |year= 1997 |pmid= 8999876 |doi=
*cite journal | author=Hayashi T, Takao M, Tanaka K, Yasui A |title=ERCC1 mutations in UV-sensitive Chinese hamster ovary (CHO) cell lines. |journal=Mutat. Res. |volume=407 |issue= 3 |pages= 269–76 |year= 1998 |pmid= 9653453 |doi=
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