References analysis of the Wikipedia article "XRCC4" in the Galician version

doi.org

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West CE, Waterworth WM, Jiang Q, Bray CM (outubro de 2000). "Arabidopsis DNA ligase IV is induced by gamma-irradiation and interacts with an Arabidopsis homologue of the double strand break repair protein XRCC4". Plant J. 24 (1): 67–78. PMID 11029705. doi:10.1046/j.1365-313x.2000.00856.x.

Oksenych V, Kumar V, Liu X, Guo C, Schwer B, Zha S, Alt FW (febreiro de 2013). "Functional redundancy between the XLF and DNA-PKcs DNA repair factors in V(D)J recombination and nonhomologous DNA end joining". Proc. Natl. Acad. Sci. U.S.A. 110 (6): 2234–9. PMC 3568359. PMID 23345432. doi:10.1073/pnas.1222573110.

Yurchenko V, Xue Z, Sadofsky MJ (marzo de 2006). "SUMO modification of human XRCC4 regulates its localization and function in DNA double-strand break repair". Mol. Cell. Biol. 26 (5): 1786–94. PMC 1430232. PMID 16478998. doi:10.1128/MCB.26.5.1786-1794.2006.

Andres SN, Vergnes A, Ristic D, Wyman C, Modesti M, Junop M (febreiro de 2012). "A human XRCC4-XLF complex bridges DNA". Nucleic Acids Res. 40 (4): 1868–78. PMC 3287209. PMID 22287571. doi:10.1093/nar/gks022.

Shao N, Jiang WY, Qiao D, Zhang SG, Wu Y, Zhang XX, Hua LX, Ding Y, Feng NH (2012). "An updated meta-analysis of XRCC4 polymorphisms and cancer risk based on 31 case-control studies". Cancer Biomark 12 (1): 37–47. PMID 23321468. doi:10.3233/CBM-120292.

De Bont R, van Larebeke N (maio de 2004). "Endogenous DNA damage in humans: a review of quantitative data". Mutagenesis 19 (3): 169–85. PMID 15123782. doi:10.1093/mutage/geh025.

Lieber MR, Lu H, Gu J, Schwarz K (xaneiro de 2008). "Flexibility in the order of action and in the enzymology of the nuclease, polymerases, and ligase of vertebrate non-homologous DNA end joining: relevance to cancer, aging, and the immune system". Cell Res. 18 (1): 125–33. PMID 18087292. doi:10.1038/cr.2007.108.

Reynolds P, Anderson JA, Harper JV, Hill MA, Botchway SW, Parker AW, O'Neill P (novembro de 2012). "The dynamics of Ku70/80 and DNA-PKcs at DSBs induced by ionizing radiation is dependent on the complexity of damage". Nucleic Acids Res. 40 (21): 10821–31. PMC 3510491. PMID 23012265. doi:10.1093/nar/gks879.

Junop MS, Modesti M, Guarné A, Ghirlando R, Gellert M, Yang W (novembro de 2000). "Crystal structure of the Xrcc4 DNA repair protein and implications for end joining". EMBO J. 19 (22): 5962–70. PMC 305814. PMID 11080143. doi:10.1093/emboj/19.22.5962.

Mari PO, Florea BI, Persengiev SP, Verkaik NS, Brüggenwirth HT, Modesti M, Giglia-Mari G, Bezstarosti K, Demmers JA, Luider TM, Houtsmuller AB, van Gent DC (decembro de 2006). "Dynamic assembly of end-joining complexes requires interaction between Ku70/80 and XRCC4". Proc. Natl. Acad. Sci. U.S.A. 103 (49): 18597–602. PMC 1693708. PMID 17124166. doi:10.1073/pnas.0609061103.

Wu PY, Frit P, Meesala S, Dauvillier S, Modesti M, Andres SN, Huang Y, Sekiguchi J, Calsou P, Salles B, Junop MS (xuño de 2009). "Structural and functional interaction between the human DNA repair proteins DNA ligase IV and XRCC4". Mol. Cell. Biol. 29 (11): 3163–72. PMC 2682001. PMID 19332554. doi:10.1128/MCB.01895-08.

Mittal RD, Gangwar R, Mandal RK, Srivastava P, Ahirwar DK (febreiro de 2012). "Gene variants of XRCC4 and XRCC3 and their association with risk for urothelial bladder cancer". Mol. Biol. Rep. 39 (2): 1667–75. PMID 21617942. doi:10.1007/s11033-011-0906-z.

Zhou LP, Luan H, Dong XH, Jin GJ, Ma DL, Shang H (2012). "Association of functional polymorphisms of the XRCC4 gene with the risk of breast cancer: a meta-analysis". Asian Pac. J. Cancer Prev. 13 (7): 3431–6. PMID 22994773. doi:10.7314/APJCP.2012.13.7.3431.

Cifci S, Yilmaz M, Pehlivan M, Sever T, Okan V, Pehlivan S (novembro de 2011). "DNA repair genes polymorphisms in multiple myeloma: no association with XRCC1 (Arg399Gln) polymorphism, but the XRCC4 (VNTR in intron 3 and G-1394T) and XPD (Lys751Gln) polymorphisms is associated with the disease in Turkish patients". Hematology 16 (6): 361–7. PMID 22183071. doi:10.1179/102453311X13127324303399.

Mandal RK, Singh V, Kapoor R, Mittal RD (maio de 2011). "Do polymorphisms in XRCC4 influence prostate cancer susceptibility in North Indian population?". Biomarkers 16 (3): 236–42. PMID 21506695. doi:10.3109/1354750X.2010.547599.

Wang JH, Alt FW, Gostissa M, Datta A, Murphy M, Alimzhanov MB, Coakley KM, Rajewsky K, Manis JP, Yan CT (decembro de 2008). "Oncogenic transformation in the absence of Xrcc4 targets peripheral B cells that have undergone editing and switching". J. Exp. Med. 205 (13): 3079–90. PMC 2605230. PMID 19064702. doi:10.1084/jem.20082271.

Wu CN, Liang SY, Tsai CW, Bau DT (novembro de 2008). "The role of XRCC4 in carcinogenesis and anticancer drug discovery". Recent Pat Anticancer Drug Discov 3 (3): 209–19. PMID 18991789. doi:10.2174/157489208786242304.

Li Z, Zhang W, Chen Y, Guo W, Zhang J, Tang H, Xu Z, Zhang H, Tao Y, Wang F, Jiang Y, Sun FL, Mao Z (2016). "Impaired DNA double-strand break repair contributes to the age-associated rise of genomic instability in humans". Cell Death Differ. 23 (11): 1765–1777. PMC 5071568. PMID 27391797. doi:10.1038/cdd.2016.65.

Lee KJ, Dong X, Wang J, Takeda Y, Dynan WS (setembro de 2002). "Identification of human autoantibodies to the DNA ligase IV/XRCC4 complex and mapping of an autoimmune epitope to a potential regulatory region". J. Immunol. 169 (6): 3413–21. PMID 12218164. doi:10.4049/jimmunol.169.6.3413.

Takeda Y, Dynan WS (novembro de 2001). "Autoantibodies against DNA double-strand break repair proteins". Front. Biosci. 6: D1412–22. PMID 11689355. doi:10.2741/Takeda.

Hsieh YY, Bau DT, Chang CC, Tsai CH, Chen CP, Tsai FJ (maio de 2008). "XRCC4 codon 247*A and XRCC4 promoter -1394*T related genotypes but not XRCC4 intron 3 gene polymorphism are associated with higher susceptibility for endometriosis". Mol. Reprod. Dev. 75 (5): 946–51. PMID 18246529. doi:10.1002/mrd.20829.

Zheng Z, Ng WL, Zhang X, Olson JJ, Hao C, Curran WJ, Wang Y (marzo de 2012). "RNAi-mediated targeting of noncoding and coding sequences in DNA repair gene messages efficiently radiosensitizes human tumor cells". Cancer Res. 72 (5): 1221–8. PMID 22237628. doi:10.1158/0008-5472.CAN-11-2785.

Rosin N, Elcioglu NH, Beleggia F, Isgüven P, Altmüller J, Thiele H, Steindl K, Joset P, Rauch A, Nürnberg P, Wollnik B, Yigit G (Apr 2015). "Mutations in XRCC4 cause primary microcephaly, short stature and increased genomic instability". Human Molecular Genetics 24: 3708–17. PMID 25839420. doi:10.1093/hmg/ddv115.

Murray JE, van der Burg M, IJspeert H, Carroll P, Wu Q, Ochi T, Leitch A, Miller ES, Kysela B, Jawad A, Bottani A, Brancati F, Cappa M, Cormier-Daire V, Deshpande C, Faqeih EA, Graham GE, Ranza E, Blundell TL, Jackson AP, Stewart GS, Bicknell LS (Mar 2015). "Mutations in the NHEJ component XRCC4 cause primordial dwarfism". American Journal of Human Genetics 96 (3): 412–24. PMC 4375537. PMID 25728776. doi:10.1016/j.ajhg.2015.01.013.

Roy S, Andres SN, Vergnes A, Neal JA, Xu Y, Yu Y, Lees-Miller SP, Junop M, Modesti M, Meek K (febreiro de 2012). "XRCC4's interaction with XLF is required for coding (but not signal) end joining". Nucleic Acids Res. 40 (4): 1684–94. PMC 3287172. PMID 22228831. doi:10.1093/nar/gkr1315.

Massip L, Caron P, Iacovoni JS, Trouche D, Legube G (agosto de 2010). "Deciphering the chromatin landscape induced around DNA double strand breaks". Cell Cycle 9 (15): 2963–72. PMID 20714222. doi:10.4161/cc.9.15.12412.

Giaccia A, Weinstein R, Hu J, Stamato TD (setembro de 1985). "Cell cycle-dependent repair of double-strand DNA breaks in a gamma-ray-sensitive Chinese hamster cell". Somat. Cell Mol. Genet. 11 (5): 485–91. PMID 3862244. doi:10.1007/BF01534842.

Stamato TD, Dipatri A, Giaccia A (agosto de 1988). "Cell-cycle-dependent repair of potentially lethal damage in the XR-1 gamma-ray-sensitive Chinese hamster ovary cell". Radiat. Res. 115 (2): 325–33. PMID 3406371. doi:10.2307/3577168.

Giaccia AJ, Richardson E, Denko N, Stamato TD (xaneiro de 1989). "Genetic analysis of XR-1 mutation in hamster and human hybrids". Somat. Cell Mol. Genet. 15 (1): 71–7. PMID 2916163. doi:10.1007/BF01534671.

nih.gov

ncbi.nlm.nih.gov

De Bont R, van Larebeke N (maio de 2004). "Endogenous DNA damage in humans: a review of quantitative data". Mutagenesis 19 (3): 169–85. PMID 15123782. doi:10.1093/mutage/geh025.

"Entrez Gene: XRCC4 X-ray repair complementing defective repair in Chinese hamster cells 4".

Popławski T, Stoczyńska E, Błasiak J (2009). "[Non-homologous DNA end joining--new proteins, new functions, new mechanisms]". Postepy Biochem. (en Polish) 55 (1): 36–45. PMID 19514464.

Takeda Y, Dynan WS (novembro de 2001). "Autoantibodies against DNA double-strand break repair proteins". Front. Biosci. 6: D1412–22. PMID 11689355. doi:10.2741/Takeda.

Giaccia AJ, Denko N, MacLaren R, Mirman D, Waldren C, Hart I, Stamato TD (setembro de 1990). "Human chromosome 5 complements the DNA double-strand break-repair deficiency and gamma-ray sensitivity of the XR-1 hamster variant". Am. J. Hum. Genet. 47 (3): 459–69. PMC 1683886. PMID 1697445.

XRCC4 (Galician Wikipedia)

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