Mackey ZB, Niedergang C, Murcia JM, Leppard J, Au K, Chen J, de Murcia G, Tomkinson AE (July 1999). "DNA ligase III is recruited to DNA strand breaks by a zinc finger motif homologous to that of poly(ADP-ribose) polymerase. Identification of two functionally distinct DNA binding regions within DNA ligase III". J. Biol. Chem.274 (31): 21679–87. PMID10419478. doi:10.1074/jbc.274.31.21679.
Chen L, Trujillo K, Sung P, Tomkinson AE (August 2000). "Interactions of the DNA ligase IV-XRCC4 complex with DNA ends and the DNA-dependent protein kinase". J. Biol. Chem.275 (34): 26196–205. PMID10854421. doi:10.1074/jbc.M000491200.
Nash RA, Caldecott KW, Barnes DE, Lindahl T (April 1997). "XRCC1 protein interacts with one of two distinct forms of DNA ligase III". Biochemistry36 (17): 5207–11. PMID9136882. doi:10.1021/bi962281m.
Parsons JL, Dianova II, Finch D, Tait PS, Ström CE, Helleday T, Dianov GL (July 2010). "XRCC1 phosphorylation by CK2 is required for its stability and efficient DNA repair". DNA Repair (Amst.)9 (7): 835–41. PMID20471329. doi:10.1016/j.dnarep.2010.04.008.
Cappelli E, Taylor R, Cevasco M, Abbondandolo A, Caldecott K, Frosina G (September 1997). "Involvement of XRCC1 and DNA ligase III gene products in DNA base excision repair". J. Biol. Chem.272 (38): 23970–5. PMID9295348. doi:10.1074/jbc.272.38.23970.
Moser J, Kool H, Giakzidis I, Caldecott K, Mullenders LH, Fousteri MI (July 2007). "Sealing of chromosomal DNA nicks during nucleotide excision repair requires XRCC1 and DNA ligase III alpha in a cell-cycle-specific manner". Mol. Cell27 (2): 311–23. PMID17643379. doi:10.1016/j.molcel.2007.06.014.
Wang H, Rosidi B, Perrault R, Wang M, Zhang L, Windhofer F, Iliakis G (May 2005). "DNA ligase III as a candidate component of backup pathways of nonhomologous end joining". Cancer Res.65 (10): 4020–30. PMID15899791. doi:10.1158/0008-5472.CAN-04-3055.
Girard PM, Kysela B, Härer CJ, Doherty AJ, Jeggo PA (October 2004). "Analysis of DNA ligase IV mutations found in LIG4 syndrome patients: the impact of two linked polymorphisms". Hum. Mol. Genet.13 (20): 2369–76. PMID15333585. doi:10.1093/hmg/ddh274.
O'Driscoll M, Cerosaletti KM, Girard PM, Dai Y, Stumm M, Kysela B, Hirsch B, Gennery A, Palmer SE, Seidel J, Gatti RA, Varon R, Oettinger MA, Neitzel H, Jeggo PA, Concannon P (December 2001). "DNA ligase IV mutations identified in patients exhibiting developmental delay and immunodeficiency". Mol. Cell8 (6): 1175–85. PMID11779494. doi:10.1016/S1097-2765(01)00408-7.
Riballo E, Critchlow SE, Teo SH, Doherty AJ, Priestley A, Broughton B, Kysela B, Beamish H, Plowman N, Arlett CF, Lehmann AR, Jackson SP, Jeggo PA (July 1999). "Identification of a defect in DNA ligase IV in a radiosensitive leukaemia patient". Curr. Biol.9 (13): 699–702. PMID10395545. doi:10.1016/S0960-9822(99)80311-X.
Barnes DE, Tomkinson AE, Lehmann AR, Webster AD, Lindahl T (May 1992). "Mutations in the DNA ligase I gene of an individual with immunodeficiencies and cellular hypersensitivity to DNA-damaging agents". Cell69 (3): 495–503. PMID1581963. doi:10.1016/0092-8674(92)90450-Q.
Ahel I, Rass U, El-Khamisy SF, Katyal S, Clements PM, McKinnon PJ, Caldecott KW, West SC (October 2006). "The neurodegenerative disease protein aprataxin resolves abortive DNA ligation intermediates". Nature443 (7112): 713–6. PMID16964241. doi:10.1038/nature05164.
Date H, Onodera O, Tanaka H, Iwabuchi K, Uekawa K, Igarashi S, Koike R, Hiroi T, Yuasa T, Awaya Y, Sakai T, Takahashi T, Nagatomo H, Sekijima Y, Kawachi I, Takiyama Y, Nishizawa M, Fukuhara N, Saito K, Sugano S, Tsuji S (October 2001). "Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene". Nat. Genet.29 (2): 184–8. PMID11586299. doi:10.1038/ng1001-184.
Moreira MC, Barbot C, Tachi N, Kozuka N, Uchida E, Gibson T, Mendonça P, Costa M, Barros J, Yanagisawa T, Watanabe M, Ikeda Y, Aoki M, Nagata T, Coutinho P, Sequeiros J, Koenig M (October 2001). "The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxin". Nat. Genet.29 (2): 189–93. PMID11586300. doi:10.1038/ng1001-189.
El-Khamisy SF, Saifi GM, Weinfeld M, Johansson F, Helleday T, Lupski JR, Caldecott KW (March 2005). "Defective DNA single-strand break repair in spinocerebellar ataxia with axonal neuropathy-1". Nature434 (7029): 108–13. PMID15744309. doi:10.1038/nature03314.
Mackey ZB, Niedergang C, Murcia JM, Leppard J, Au K, Chen J, de Murcia G, Tomkinson AE (July 1999). "DNA ligase III is recruited to DNA strand breaks by a zinc finger motif homologous to that of poly(ADP-ribose) polymerase. Identification of two functionally distinct DNA binding regions within DNA ligase III". J. Biol. Chem.274 (31): 21679–87. PMID10419478. doi:10.1074/jbc.274.31.21679.
Chen L, Trujillo K, Sung P, Tomkinson AE (August 2000). "Interactions of the DNA ligase IV-XRCC4 complex with DNA ends and the DNA-dependent protein kinase". J. Biol. Chem.275 (34): 26196–205. PMID10854421. doi:10.1074/jbc.M000491200.
Nash RA, Caldecott KW, Barnes DE, Lindahl T (April 1997). "XRCC1 protein interacts with one of two distinct forms of DNA ligase III". Biochemistry36 (17): 5207–11. PMID9136882. doi:10.1021/bi962281m.
Parsons JL, Dianova II, Finch D, Tait PS, Ström CE, Helleday T, Dianov GL (July 2010). "XRCC1 phosphorylation by CK2 is required for its stability and efficient DNA repair". DNA Repair (Amst.)9 (7): 835–41. PMID20471329. doi:10.1016/j.dnarep.2010.04.008.
Cappelli E, Taylor R, Cevasco M, Abbondandolo A, Caldecott K, Frosina G (September 1997). "Involvement of XRCC1 and DNA ligase III gene products in DNA base excision repair". J. Biol. Chem.272 (38): 23970–5. PMID9295348. doi:10.1074/jbc.272.38.23970.
Moser J, Kool H, Giakzidis I, Caldecott K, Mullenders LH, Fousteri MI (July 2007). "Sealing of chromosomal DNA nicks during nucleotide excision repair requires XRCC1 and DNA ligase III alpha in a cell-cycle-specific manner". Mol. Cell27 (2): 311–23. PMID17643379. doi:10.1016/j.molcel.2007.06.014.
Wang H, Rosidi B, Perrault R, Wang M, Zhang L, Windhofer F, Iliakis G (May 2005). "DNA ligase III as a candidate component of backup pathways of nonhomologous end joining". Cancer Res.65 (10): 4020–30. PMID15899791. doi:10.1158/0008-5472.CAN-04-3055.
Girard PM, Kysela B, Härer CJ, Doherty AJ, Jeggo PA (October 2004). "Analysis of DNA ligase IV mutations found in LIG4 syndrome patients: the impact of two linked polymorphisms". Hum. Mol. Genet.13 (20): 2369–76. PMID15333585. doi:10.1093/hmg/ddh274.
O'Driscoll M, Cerosaletti KM, Girard PM, Dai Y, Stumm M, Kysela B, Hirsch B, Gennery A, Palmer SE, Seidel J, Gatti RA, Varon R, Oettinger MA, Neitzel H, Jeggo PA, Concannon P (December 2001). "DNA ligase IV mutations identified in patients exhibiting developmental delay and immunodeficiency". Mol. Cell8 (6): 1175–85. PMID11779494. doi:10.1016/S1097-2765(01)00408-7.
Riballo E, Critchlow SE, Teo SH, Doherty AJ, Priestley A, Broughton B, Kysela B, Beamish H, Plowman N, Arlett CF, Lehmann AR, Jackson SP, Jeggo PA (July 1999). "Identification of a defect in DNA ligase IV in a radiosensitive leukaemia patient". Curr. Biol.9 (13): 699–702. PMID10395545. doi:10.1016/S0960-9822(99)80311-X.
Barnes DE, Tomkinson AE, Lehmann AR, Webster AD, Lindahl T (May 1992). "Mutations in the DNA ligase I gene of an individual with immunodeficiencies and cellular hypersensitivity to DNA-damaging agents". Cell69 (3): 495–503. PMID1581963. doi:10.1016/0092-8674(92)90450-Q.
Ahel I, Rass U, El-Khamisy SF, Katyal S, Clements PM, McKinnon PJ, Caldecott KW, West SC (October 2006). "The neurodegenerative disease protein aprataxin resolves abortive DNA ligation intermediates". Nature443 (7112): 713–6. PMID16964241. doi:10.1038/nature05164.
Date H, Onodera O, Tanaka H, Iwabuchi K, Uekawa K, Igarashi S, Koike R, Hiroi T, Yuasa T, Awaya Y, Sakai T, Takahashi T, Nagatomo H, Sekijima Y, Kawachi I, Takiyama Y, Nishizawa M, Fukuhara N, Saito K, Sugano S, Tsuji S (October 2001). "Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene". Nat. Genet.29 (2): 184–8. PMID11586299. doi:10.1038/ng1001-184.
Moreira MC, Barbot C, Tachi N, Kozuka N, Uchida E, Gibson T, Mendonça P, Costa M, Barros J, Yanagisawa T, Watanabe M, Ikeda Y, Aoki M, Nagata T, Coutinho P, Sequeiros J, Koenig M (October 2001). "The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxin". Nat. Genet.29 (2): 189–93. PMID11586300. doi:10.1038/ng1001-189.
El-Khamisy SF, Saifi GM, Weinfeld M, Johansson F, Helleday T, Lupski JR, Caldecott KW (March 2005). "Defective DNA single-strand break repair in spinocerebellar ataxia with axonal neuropathy-1". Nature434 (7029): 108–13. PMID15744309. doi:10.1038/nature03314.