DNA repair protein XRCC4 (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "DNA repair protein XRCC4" in English language version.

refsWebsite

Global rank English rank

46nih.gov

4^th place

29doi.org

2^nd place

8semanticscholar.org

11^th place

8^th place

3harvard.edu

18^th place

17^th place

2ensembl.org

1,626^th place

1,007^th place

1uzh.ch

3,633^rd place

3,091^st place

1abcam.com

low place

1sigmaaldrich.com

924^th place

2,352^nd place

1jstor.org

26^th place

20^th place

abcam.com

"Anti-XRCC4 antibody - ChIP Grade (ab145) | Abcam". Abcam.; "XRCC4 antibody | Western | SAB2102728". Sigma-Aldrich.

doi.org

West CE, Waterworth WM, Jiang Q, Bray CM (October 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. doi:10.1046/j.1365-313x.2000.00856.x. PMID 11029705.
Oksenych V, Kumar V, Liu X, Guo C, Schwer B, Zha S, Alt FW (February 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. Bibcode:2013PNAS..110.2234O. doi:10.1073/pnas.1222573110. PMC 3568359. PMID 23345432.
Yurchenko V, Xue Z, Sadofsky MJ (March 2006). "SUMO modification of human XRCC4 regulates its localization and function in DNA double-strand break repair". Mol. Cell. Biol. 26 (5): 1786–94. doi:10.1128/MCB.26.5.1786-1794.2006. PMC 1430232. PMID 16478998.
Andres SN, Vergnes A, Ristic D, Wyman C, Modesti M, Junop M (February 2012). "A human XRCC4-XLF complex bridges DNA". Nucleic Acids Res. 40 (4): 1868–78. doi:10.1093/nar/gks022. PMC 3287209. PMID 22287571.
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. doi:10.3233/CBM-120292. PMID 23321468.
De Bont R, van Larebeke N (May 2004). "Endogenous DNA damage in humans: a review of quantitative data". Mutagenesis. 19 (3): 169–85. doi:10.1093/mutage/geh025. PMID 15123782.
Lieber MR, Lu H, Gu J, Schwarz K (January 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. doi:10.1038/cr.2007.108. PMID 18087292.
Reynolds P, Anderson JA, Harper JV, Hill MA, Botchway SW, Parker AW, O'Neill P (November 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. doi:10.1093/nar/gks879. PMC 3510491. PMID 23012265.
Junop MS, Modesti M, Guarné A, Ghirlando R, Gellert M, Yang W (November 2000). "Crystal structure of the Xrcc4 DNA repair protein and implications for end joining". EMBO J. 19 (22): 5962–70. doi:10.1093/emboj/19.22.5962. PMC 305814. PMID 11080143.
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 (December 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. Bibcode:2006PNAS..10318597M. doi:10.1073/pnas.0609061103. PMC 1693708. PMID 17124166.
Wu PY, Frit P, Meesala S, Dauvillier S, Modesti M, Andres SN, Huang Y, Sekiguchi J, Calsou P, Salles B, Junop MS (June 2009). "Structural and functional interaction between the human DNA repair proteins DNA ligase IV and XRCC4". Mol. Cell. Biol. 29 (11): 3163–72. doi:10.1128/MCB.01895-08. PMC 2682001. PMID 19332554.
Mittal RD, Gangwar R, Mandal RK, Srivastava P, Ahirwar DK (February 2012). "Gene variants of XRCC4 and XRCC3 and their association with risk for urothelial bladder cancer". Mol. Biol. Rep. 39 (2): 1667–75. doi:10.1007/s11033-011-0906-z. PMID 21617942. S2CID 15164549.
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. doi:10.7314/APJCP.2012.13.7.3431. PMID 22994773.
Cifci S, Yilmaz M, Pehlivan M, Sever T, Okan V, Pehlivan S (November 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. doi:10.1179/102453311X13127324303399. PMID 22183071. S2CID 45344195.
Mandal RK, Singh V, Kapoor R, Mittal RD (May 2011). "Do polymorphisms in XRCC4 influence prostate cancer susceptibility in North Indian population?". Biomarkers. 16 (3): 236–42. doi:10.3109/1354750X.2010.547599. PMID 21506695. S2CID 43551117.
Wang JH, Alt FW, Gostissa M, Datta A, Murphy M, Alimzhanov MB, Coakley KM, Rajewsky K, Manis JP, Yan CT (December 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. doi:10.1084/jem.20082271. PMC 2605230. PMID 19064702.
Wu CN, Liang SY, Tsai CW, Bau DT (November 2008). "The role of XRCC4 in carcinogenesis and anticancer drug discovery". Recent Pat Anti-Cancer Drug Discov. 3 (3): 209–19. doi:10.2174/157489208786242304. PMID 18991789.
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. doi:10.1038/cdd.2016.65. PMC 5071568. PMID 27391797.
Lee KJ, Dong X, Wang J, Takeda Y, Dynan WS (September 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. doi:10.4049/jimmunol.169.6.3413. PMID 12218164.
Takeda Y, Dynan WS (November 2001). "Autoantibodies against DNA double-strand break repair proteins". Front. Biosci. 6: D1412–22. doi:10.2741/Takeda. PMID 11689355. S2CID 21179835.
Hsieh YY, Bau DT, Chang CC, Tsai CH, Chen CP, Tsai FJ (May 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. doi:10.1002/mrd.20829. PMID 18246529. S2CID 11018.
Zheng Z, Ng WL, Zhang X, Olson JJ, Hao C, Curran WJ, Wang Y (March 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. doi:10.1158/0008-5472.CAN-11-2785. PMID 22237628.
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" (PDF). Human Molecular Genetics. 24 (13): 3708–17. doi:10.1093/hmg/ddv115. PMID 25839420.
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. doi:10.1016/j.ajhg.2015.01.013. PMC 4375537. PMID 25728776.
Roy S, Andres SN, Vergnes A, Neal JA, Xu Y, Yu Y, Lees-Miller SP, Junop M, Modesti M, Meek K (February 2012). "XRCC4's interaction with XLF is required for coding (but not signal) end joining". Nucleic Acids Res. 40 (4): 1684–94. doi:10.1093/nar/gkr1315. PMC 3287172. PMID 22228831.
Massip L, Caron P, Iacovoni JS, Trouche D, Legube G (August 2010). "Deciphering the chromatin landscape induced around DNA double strand breaks". Cell Cycle. 9 (15): 2963–72. doi:10.4161/cc.9.15.12412. PMID 20714222. S2CID 24883245.
Giaccia A, Weinstein R, Hu J, Stamato TD (September 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. doi:10.1007/BF01534842. PMID 3862244. S2CID 31533353.
Stamato TD, Dipatri A, Giaccia A (August 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. Bibcode:1988RadR..115..325S. doi:10.2307/3577168. JSTOR 3577168. PMID 3406371.
Giaccia AJ, Richardson E, Denko N, Stamato TD (January 1989). "Genetic analysis of XR-1 mutation in hamster and human hybrids". Somat. Cell Mol. Genet. 15 (1): 71–7. doi:10.1007/BF01534671. PMID 2916163. S2CID 21199573.

ensembl.org

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000152422 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000021615 – Ensembl, May 2017

harvard.edu

ui.adsabs.harvard.edu

Oksenych V, Kumar V, Liu X, Guo C, Schwer B, Zha S, Alt FW (February 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. Bibcode:2013PNAS..110.2234O. doi:10.1073/pnas.1222573110. PMC 3568359. PMID 23345432.
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 (December 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. Bibcode:2006PNAS..10318597M. doi:10.1073/pnas.0609061103. PMC 1693708. PMID 17124166.
Stamato TD, Dipatri A, Giaccia A (August 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. Bibcode:1988RadR..115..325S. doi:10.2307/3577168. JSTOR 3577168. PMID 3406371.

jstor.org

Stamato TD, Dipatri A, Giaccia A (August 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. Bibcode:1988RadR..115..325S. doi:10.2307/3577168. JSTOR 3577168. PMID 3406371.

nih.gov

pubmed.ncbi.nlm.nih.gov

West CE, Waterworth WM, Jiang Q, Bray CM (October 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. doi:10.1046/j.1365-313x.2000.00856.x. PMID 11029705.
Oksenych V, Kumar V, Liu X, Guo C, Schwer B, Zha S, Alt FW (February 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. Bibcode:2013PNAS..110.2234O. doi:10.1073/pnas.1222573110. PMC 3568359. PMID 23345432.
Yurchenko V, Xue Z, Sadofsky MJ (March 2006). "SUMO modification of human XRCC4 regulates its localization and function in DNA double-strand break repair". Mol. Cell. Biol. 26 (5): 1786–94. doi:10.1128/MCB.26.5.1786-1794.2006. PMC 1430232. PMID 16478998.
Andres SN, Vergnes A, Ristic D, Wyman C, Modesti M, Junop M (February 2012). "A human XRCC4-XLF complex bridges DNA". Nucleic Acids Res. 40 (4): 1868–78. doi:10.1093/nar/gks022. PMC 3287209. PMID 22287571.
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. doi:10.3233/CBM-120292. PMID 23321468.
De Bont R, van Larebeke N (May 2004). "Endogenous DNA damage in humans: a review of quantitative data". Mutagenesis. 19 (3): 169–85. doi:10.1093/mutage/geh025. PMID 15123782.
Lieber MR, Lu H, Gu J, Schwarz K (January 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. doi:10.1038/cr.2007.108. PMID 18087292.
Reynolds P, Anderson JA, Harper JV, Hill MA, Botchway SW, Parker AW, O'Neill P (November 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. doi:10.1093/nar/gks879. PMC 3510491. PMID 23012265.
Junop MS, Modesti M, Guarné A, Ghirlando R, Gellert M, Yang W (November 2000). "Crystal structure of the Xrcc4 DNA repair protein and implications for end joining". EMBO J. 19 (22): 5962–70. doi:10.1093/emboj/19.22.5962. PMC 305814. PMID 11080143.
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 (December 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. Bibcode:2006PNAS..10318597M. doi:10.1073/pnas.0609061103. PMC 1693708. PMID 17124166.
Wu PY, Frit P, Meesala S, Dauvillier S, Modesti M, Andres SN, Huang Y, Sekiguchi J, Calsou P, Salles B, Junop MS (June 2009). "Structural and functional interaction between the human DNA repair proteins DNA ligase IV and XRCC4". Mol. Cell. Biol. 29 (11): 3163–72. doi:10.1128/MCB.01895-08. PMC 2682001. PMID 19332554.
Popławski T, Stoczyńska E, Błasiak J (2009). "[Non-homologous DNA end joining--new proteins, new functions, new mechanisms]". Postepy Biochem. (in Polish). 55 (1): 36–45. PMID 19514464.
Mittal RD, Gangwar R, Mandal RK, Srivastava P, Ahirwar DK (February 2012). "Gene variants of XRCC4 and XRCC3 and their association with risk for urothelial bladder cancer". Mol. Biol. Rep. 39 (2): 1667–75. doi:10.1007/s11033-011-0906-z. PMID 21617942. S2CID 15164549.
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. doi:10.7314/APJCP.2012.13.7.3431. PMID 22994773.
Cifci S, Yilmaz M, Pehlivan M, Sever T, Okan V, Pehlivan S (November 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. doi:10.1179/102453311X13127324303399. PMID 22183071. S2CID 45344195.
Mandal RK, Singh V, Kapoor R, Mittal RD (May 2011). "Do polymorphisms in XRCC4 influence prostate cancer susceptibility in North Indian population?". Biomarkers. 16 (3): 236–42. doi:10.3109/1354750X.2010.547599. PMID 21506695. S2CID 43551117.
Wang JH, Alt FW, Gostissa M, Datta A, Murphy M, Alimzhanov MB, Coakley KM, Rajewsky K, Manis JP, Yan CT (December 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. doi:10.1084/jem.20082271. PMC 2605230. PMID 19064702.
Wu CN, Liang SY, Tsai CW, Bau DT (November 2008). "The role of XRCC4 in carcinogenesis and anticancer drug discovery". Recent Pat Anti-Cancer Drug Discov. 3 (3): 209–19. doi:10.2174/157489208786242304. PMID 18991789.
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. doi:10.1038/cdd.2016.65. PMC 5071568. PMID 27391797.
Lee KJ, Dong X, Wang J, Takeda Y, Dynan WS (September 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. doi:10.4049/jimmunol.169.6.3413. PMID 12218164.
Takeda Y, Dynan WS (November 2001). "Autoantibodies against DNA double-strand break repair proteins". Front. Biosci. 6: D1412–22. doi:10.2741/Takeda. PMID 11689355. S2CID 21179835.
Hsieh YY, Bau DT, Chang CC, Tsai CH, Chen CP, Tsai FJ (May 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. doi:10.1002/mrd.20829. PMID 18246529. S2CID 11018.
Zheng Z, Ng WL, Zhang X, Olson JJ, Hao C, Curran WJ, Wang Y (March 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. doi:10.1158/0008-5472.CAN-11-2785. PMID 22237628.
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" (PDF). Human Molecular Genetics. 24 (13): 3708–17. doi:10.1093/hmg/ddv115. PMID 25839420.
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. doi:10.1016/j.ajhg.2015.01.013. PMC 4375537. PMID 25728776.
Roy S, Andres SN, Vergnes A, Neal JA, Xu Y, Yu Y, Lees-Miller SP, Junop M, Modesti M, Meek K (February 2012). "XRCC4's interaction with XLF is required for coding (but not signal) end joining". Nucleic Acids Res. 40 (4): 1684–94. doi:10.1093/nar/gkr1315. PMC 3287172. PMID 22228831.
Massip L, Caron P, Iacovoni JS, Trouche D, Legube G (August 2010). "Deciphering the chromatin landscape induced around DNA double strand breaks". Cell Cycle. 9 (15): 2963–72. doi:10.4161/cc.9.15.12412. PMID 20714222. S2CID 24883245.
Giaccia A, Weinstein R, Hu J, Stamato TD (September 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. doi:10.1007/BF01534842. PMID 3862244. S2CID 31533353.
Stamato TD, Dipatri A, Giaccia A (August 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. Bibcode:1988RadR..115..325S. doi:10.2307/3577168. JSTOR 3577168. PMID 3406371.
Giaccia AJ, Richardson E, Denko N, Stamato TD (January 1989). "Genetic analysis of XR-1 mutation in hamster and human hybrids". Somat. Cell Mol. Genet. 15 (1): 71–7. doi:10.1007/BF01534671. PMID 2916163. S2CID 21199573.
Giaccia AJ, Denko N, MacLaren R, Mirman D, Waldren C, Hart I, Stamato TD (September 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.

ncbi.nlm.nih.gov

"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
Oksenych V, Kumar V, Liu X, Guo C, Schwer B, Zha S, Alt FW (February 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. Bibcode:2013PNAS..110.2234O. doi:10.1073/pnas.1222573110. PMC 3568359. PMID 23345432.
Yurchenko V, Xue Z, Sadofsky MJ (March 2006). "SUMO modification of human XRCC4 regulates its localization and function in DNA double-strand break repair". Mol. Cell. Biol. 26 (5): 1786–94. doi:10.1128/MCB.26.5.1786-1794.2006. PMC 1430232. PMID 16478998.
Andres SN, Vergnes A, Ristic D, Wyman C, Modesti M, Junop M (February 2012). "A human XRCC4-XLF complex bridges DNA". Nucleic Acids Res. 40 (4): 1868–78. doi:10.1093/nar/gks022. PMC 3287209. PMID 22287571.
Reynolds P, Anderson JA, Harper JV, Hill MA, Botchway SW, Parker AW, O'Neill P (November 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. doi:10.1093/nar/gks879. PMC 3510491. PMID 23012265.
"Entrez Gene: XRCC4 X-ray repair complementing defective repair in Chinese hamster cells 4".
Junop MS, Modesti M, Guarné A, Ghirlando R, Gellert M, Yang W (November 2000). "Crystal structure of the Xrcc4 DNA repair protein and implications for end joining". EMBO J. 19 (22): 5962–70. doi:10.1093/emboj/19.22.5962. PMC 305814. PMID 11080143.
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 (December 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. Bibcode:2006PNAS..10318597M. doi:10.1073/pnas.0609061103. PMC 1693708. PMID 17124166.
Wu PY, Frit P, Meesala S, Dauvillier S, Modesti M, Andres SN, Huang Y, Sekiguchi J, Calsou P, Salles B, Junop MS (June 2009). "Structural and functional interaction between the human DNA repair proteins DNA ligase IV and XRCC4". Mol. Cell. Biol. 29 (11): 3163–72. doi:10.1128/MCB.01895-08. PMC 2682001. PMID 19332554.
Wang JH, Alt FW, Gostissa M, Datta A, Murphy M, Alimzhanov MB, Coakley KM, Rajewsky K, Manis JP, Yan CT (December 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. doi:10.1084/jem.20082271. PMC 2605230. PMID 19064702.
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. doi:10.1038/cdd.2016.65. PMC 5071568. PMID 27391797.
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. doi:10.1016/j.ajhg.2015.01.013. PMC 4375537. PMID 25728776.
Roy S, Andres SN, Vergnes A, Neal JA, Xu Y, Yu Y, Lees-Miller SP, Junop M, Modesti M, Meek K (February 2012). "XRCC4's interaction with XLF is required for coding (but not signal) end joining". Nucleic Acids Res. 40 (4): 1684–94. doi:10.1093/nar/gkr1315. PMC 3287172. PMID 22228831.
Giaccia AJ, Denko N, MacLaren R, Mirman D, Waldren C, Hart I, Stamato TD (September 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.

semanticscholar.org

api.semanticscholar.org

Mittal RD, Gangwar R, Mandal RK, Srivastava P, Ahirwar DK (February 2012). "Gene variants of XRCC4 and XRCC3 and their association with risk for urothelial bladder cancer". Mol. Biol. Rep. 39 (2): 1667–75. doi:10.1007/s11033-011-0906-z. PMID 21617942. S2CID 15164549.
Cifci S, Yilmaz M, Pehlivan M, Sever T, Okan V, Pehlivan S (November 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. doi:10.1179/102453311X13127324303399. PMID 22183071. S2CID 45344195.
Mandal RK, Singh V, Kapoor R, Mittal RD (May 2011). "Do polymorphisms in XRCC4 influence prostate cancer susceptibility in North Indian population?". Biomarkers. 16 (3): 236–42. doi:10.3109/1354750X.2010.547599. PMID 21506695. S2CID 43551117.
Takeda Y, Dynan WS (November 2001). "Autoantibodies against DNA double-strand break repair proteins". Front. Biosci. 6: D1412–22. doi:10.2741/Takeda. PMID 11689355. S2CID 21179835.
Hsieh YY, Bau DT, Chang CC, Tsai CH, Chen CP, Tsai FJ (May 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. doi:10.1002/mrd.20829. PMID 18246529. S2CID 11018.
Massip L, Caron P, Iacovoni JS, Trouche D, Legube G (August 2010). "Deciphering the chromatin landscape induced around DNA double strand breaks". Cell Cycle. 9 (15): 2963–72. doi:10.4161/cc.9.15.12412. PMID 20714222. S2CID 24883245.
Giaccia A, Weinstein R, Hu J, Stamato TD (September 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. doi:10.1007/BF01534842. PMID 3862244. S2CID 31533353.
Giaccia AJ, Richardson E, Denko N, Stamato TD (January 1989). "Genetic analysis of XR-1 mutation in hamster and human hybrids". Somat. Cell Mol. Genet. 15 (1): 71–7. doi:10.1007/BF01534671. PMID 2916163. S2CID 21199573.

sigmaaldrich.com

"Anti-XRCC4 antibody - ChIP Grade (ab145) | Abcam". Abcam.; "XRCC4 antibody | Western | SAB2102728". Sigma-Aldrich.

uzh.ch

zora.uzh.ch

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" (PDF). Human Molecular Genetics. 24 (13): 3708–17. doi:10.1093/hmg/ddv115. PMID 25839420.