ERCC4

ERCC4

Excision repair cross-complementing rodent repair deficiency, complementation group 4, also known as ERCC4, is a human gene.cite web | title = Entrez Gene: ERCC4 excision repair cross-complementing rodent repair deficiency, complementation group 4| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=2072| accessdate = ]

PBB_Summary
section_title =
summary_text =

References

Further reading

PBB_Further_reading
citations =
*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=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=Liu P, Siciliano J, White B, "et al." |title=Regional mapping of human DNA excision repair gene ERCC4 to chromosome 16p13.13-p13.2. |journal=Mutagenesis |volume=8 |issue= 3 |pages= 199–205 |year= 1993 |pmid= 8332082 |doi=
*cite journal | author=Sijbers AM, de Laat WL, Ariza RR, "et al." |title=Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonuclease. |journal=Cell |volume=86 |issue= 5 |pages= 811–22 |year= 1996 |pmid= 8797827 |doi=
*cite journal | author=Brookman KW, Lamerdin JE, Thelen MP, "et al." |title=ERCC4 (XPF) encodes a human nucleotide excision repair protein with eukaryotic recombination homologs. |journal=Mol. Cell. Biol. |volume=16 |issue= 11 |pages= 6553–62 |year= 1996 |pmid= 8887684 |doi=
*cite journal | author=Shen MR, Jones IM, Mohrenweiser H |title=Nonconservative amino acid substitution variants exist at polymorphic frequency in DNA repair genes in healthy humans. |journal=Cancer Res. |volume=58 |issue= 4 |pages= 604–8 |year= 1998 |pmid= 9485007 |doi=
*cite journal | author=Sijbers AM, van Voorst Vader PC, Snoek JW, "et al." |title=Homozygous R788W point mutation in the XPF gene of a patient with xeroderma pigmentosum and late-onset neurologic disease. |journal=J. Invest. Dermatol. |volume=110 |issue= 5 |pages= 832–6 |year= 1998 |pmid= 9579555 |doi= 10.1046/j.1523-1747.1998.00171.x
*cite journal | author=Matsumura Y, Nishigori C, Yagi T, "et al." |title=Characterization of molecular defects in xeroderma pigmentosum group F in relation to its clinically mild symptoms. |journal=Hum. Mol. Genet. |volume=7 |issue= 6 |pages= 969–74 |year= 1998 |pmid= 9580660 |doi=
*cite journal | author=de Laat WL, Sijbers AM, Odijk H, "et al." |title=Mapping of interaction domains between human repair proteins ERCC1 and XPF. |journal=Nucleic Acids Res. |volume=26 |issue= 18 |pages= 4146–52 |year= 1998 |pmid= 9722633 |doi=
*cite journal | author=Köberle B, Masters JR, Hartley JA, Wood RD |title=Defective repair of cisplatin-induced DNA damage caused by reduced XPA protein in testicular germ cell tumours. |journal=Curr. Biol. |volume=9 |issue= 5 |pages= 273–6 |year= 1999 |pmid= 10074455 |doi=
*cite journal | author=McCutchen-Maloney SL, Giannecchini CA, Hwang MH, Thelen MP |title=Domain mapping of the DNA binding, endonuclease, and ERCC1 binding properties of the human DNA repair protein XPF. |journal=Biochemistry |volume=38 |issue= 29 |pages= 9417–25 |year= 1999 |pmid= 10413517 |doi= 10.1021/bi990591
*cite journal | author=Fan F, Liu C, Tavaré S, Arnheim N |title=Polymorphisms in the human DNA repair gene XPF. |journal=Mutat. Res. |volume=406 |issue= 2-4 |pages= 115–20 |year= 1999 |pmid= 10479728 |doi=
*cite journal | author=Shannon M, Lamerdin JE, Richardson L, "et al." |title=Characterization of the mouse Xpf DNA repair gene and differential expression during spermatogenesis. |journal=Genomics |volume=62 |issue= 3 |pages= 427–35 |year= 2000 |pmid= 10644440 |doi= 10.1006/geno.1999.6016
*cite journal | author=Araújo SJ, Nigg EA, Wood RD |title=Strong functional interactions of TFIIH with XPC and XPG in human DNA nucleotide excision repair, without a preassembled repairosome. |journal=Mol. Cell. Biol. |volume=21 |issue= 7 |pages= 2281–91 |year= 2001 |pmid= 11259578 |doi= 10.1128/MCB.21.7.2281-2291.2001
*cite journal | author=Kumaresan KR, Hwang M, Thelen MP, Lambert MW |title=Contribution of XPF functional domains to the 5' and 3' incisions produced at the site of a psoralen interstrand cross-link. |journal=Biochemistry |volume=41 |issue= 3 |pages= 890–6 |year= 2002 |pmid= 11790111 |doi=
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Sridharan D, Brown M, Lambert WC, "et al." |title=Nonerythroid alphaII spectrin is required for recruitment of FANCA and XPF to nuclear foci induced by DNA interstrand cross-links. |journal=J. Cell. Sci. |volume=116 |issue= Pt 5 |pages= 823–35 |year= 2003 |pmid= 12571280 |doi=
*cite journal | author=Zhu XD, Niedernhofer L, Kuster B, "et al." |title=ERCC1/XPF removes the 3' overhang from uncapped telomeres and represses formation of telomeric DNA-containing double minute chromosomes. |journal=Mol. Cell |volume=12 |issue= 6 |pages= 1489–98 |year= 2004 |pmid= 14690602 |doi=
*cite journal | author=Chen Z, Xu XS, Harrison J, Wang G |title=Defining the function of xeroderma pigmentosum group F protein in psoralen interstrand cross-link-mediated DNA repair and mutagenesis. |journal=Biochem. J. |volume=379 |issue= Pt 1 |pages= 71–8 |year= 2004 |pmid= 14728600 |doi= 10.1042/BJ20031143

PBB_Controls
update_page = yes
require_manual_inspection = no
update_protein_box = yes
update_summary = yes
update_citations = yes


Wikimedia Foundation. 2010.

Игры ⚽ Поможем написать курсовую

Look at other dictionaries:

  • Xeroderma pigmentosum — XP1 redirects here. For the phone, see Sonim XP1 ToughPhone. Xeroderma pigmentosum Classification and external resources ICD 10 Q82.1 ICD 9 …   Wikipedia

  • Excision repair cross-complementing — (ERCC) is a set of proteins which are involved in DNA repair.The genes include: Gene|ERCC1, ERCC2 , Gene|ERCC3, Gene|ERCC4, Gene|ERCC5, Gene|ERCC6, and Gene|ERCC8.Members 6 and 8 are associated with Cockayne syndrome …   Wikipedia

  • ERCC1 — Excision repair cross complementing rodent repair deficiency, complementation group 1 (includes overlapping antisense sequence), also known as ERCC1, is a human gene. PBB Summary section title = summary text = Further readingPBB Further reading… …   Wikipedia

  • XPA — Xeroderma pigmentosum, complementation group A, also known as XPA, is a human gene.cite web | title = Entrez Gene: XPA xeroderma pigmentosum, complementation group A| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView… …   Wikipedia

  • Xeroderma pigmentosum — Référence MIM Voir article Transmission Récessive Chromosome Voir article Gène Voir article Empreinte parentale Non Anticipation Non …   Wikipédia en Français

  • ERCC1 — Saltar a navegación, búsqueda Proteína de reparación por escisión del grupo de complementación cruzada 1 también conocida como ERCC1 Identificadores Símbolo ERCC1 Entrez …   Wikipedia Español

  • ДЕФЕКТЫ РЕПАРАЦИИ ДНК — мед. Репарация клеточный механизм коррекции повреждённой последовательности ДНК (точечные мутации, делеции, структурные нарушения и др.). Системы репарации • Темновая (фотореактивация): удаляются УФ индуцированные ковалентные связи между смежными …   Справочник по болезням

Share the article and excerpts

Direct link
Do a right-click on the link above
and select “Copy Link”