Prasad R, Çağlayan M, Dai DP, Nadalutti CA, Zhao ML, Gassman NR, Jánosházi AK, Stefanick DF, Horton JK, Krasich R, Longley MJ, Copeland WC, Griffith JD, Wilson SH (2017. december 1.). „DNA polymerase β: A missing link of the base excision repair machinery in mammalian mitochondria”. DNA Repair60, 77–88. o. DOI:10.1016/j.dnarep.2017.10.011. PMID29100041. PMC5919216.
Subba Rao K, Martin GM, Loeb LA (1985. október 1.). „Fidelity of DNA polymerase-beta in neurons from young and very aged mice”. Journal of Neurochemistry45 (4), 1273–8. o. DOI:10.1111/j.1471-4159.1985.tb05553.x. PMID3161998.
Orgel LE (1973. június 1.). „Ageing of clones of mammalian cells”. Nature243 (5408), 441–5. o. DOI:10.1038/243441a0. PMID4591306.
Cabelof DC, Raffoul JJ, Yanamadala S, Ganir C, Guo Z, Heydari AR (2002. március 1.). „Attenuation of DNA polymerase beta-dependent base excision repair and increased DMS-induced mutagenicity in aged mice”. Mutation Research500 (1–2), 135–45. o. DOI:10.1016/s0027-5107(02)00003-9. PMID11890943. PMC3339152.
Gao S, Oden PN, Ryan BJ, Yang H, Freudenthal BD, Greenberg MM (2024. április 18.). „Biochemical and structural characterization of Fapy•dG replication by Human DNA polymerase β”. Nucleic Acids Res, gkae277. o. DOI:10.1093/nar/gkae277. PMID38634780.
Canitrot Y, Cazaux C, Fréchet M, Bouayadi K, Lesca C, Salles B, Hoffmann JS (1998. október 1.). „Overexpression of DNA polymerase beta in cell results in a mutator phenotype and a decreased sensitivity to anticancer drugs”. Proceedings of the National Academy of Sciences of the United States of America95 (21), 12586–90. o. DOI:10.1073/pnas.95.21.12586. PMID9770529. PMC22874.
Bergoglio V, Canitrot Y, Hogarth L, Minto L, Howell SB, Cazaux C, Hoffmann JS (2001. szeptember 1.). „Enhanced expression and activity of DNA polymerase beta in human ovarian tumor cells: impact on sensitivity towards antitumor agents”. Oncogene20 (43), 6181–7. o. DOI:10.1038/sj.onc.1204743. PMID11593426.
Narayan S, He F, Wilson SH (1996. augusztus 1.). „Activation of the human DNA polymerase beta promoter by a DNA-alkylating agent through induced phosphorylation of cAMP response element-binding protein-1”. The Journal of Biological Chemistry271 (31), 18508–13. o. DOI:10.1074/jbc.271.31.18508. PMID8702497.
Sarnowska E, Grzybowska EA, Sobczak K, Konopinski R, Wilczynska A, Szwarc M, Sarnowski TJ, Krzyzosiak WJ, Siedlecki JA (2007). „Hairpin structure within the 3'UTR of DNA polymerase beta mRNA acts as a post-transcriptional regulatory element and interacts with Hax-1”. Nucleic Acids Research35 (16), 5499–510. o. DOI:10.1093/nar/gkm502. PMID17704138. PMC2018635.
Date T, Tanihara K, Yamamoto S, Nomura N, Matsukage A (1992. szeptember 1.). „Two regions in human DNA polymerase beta mRNA suppress translation in Escherichia coli”. Nucleic Acids Research20 (18), 4859–64. o. DOI:10.1093/nar/20.18.4859. PMID1408801. PMC334243.
Whitehouse CJ, Taylor RM, Thistlethwaite A, Zhang H, Karimi-Busheri F, Lasko DD, Weinfeld M, Caldecott KW (2001. január 1.). „XRCC1 stimulates human polynucleotide kinase activity at damaged DNA termini and accelerates DNA single-strand break repair”. Cell104 (1), 107–17. o. DOI:10.1016/S0092-8674(01)00195-7. PMID11163244.
Wang L, Bhattacharyya N, Chelsea DM, Escobar PF, Banerjee S (2004. november 1.). „A novel nuclear protein, MGC5306 interacts with DNA polymerase beta and has a potential role in cellular phenotype”. Cancer Research64 (21), 7673–7. o. DOI:10.1158/0008-5472.CAN-04-2801. PMID15520167.
Fan J, Otterlei M, Wong HK, Tomkinson AE, Wilson DM (2004). „XRCC1 co-localizes and physically interacts with PCNA”. Nucleic Acids Research32 (7), 2193–201. o. DOI:10.1093/nar/gkh556. PMID15107487. PMC407833.
Kubota Y, Nash RA, Klungland A, Schär P, Barnes DE, Lindahl T (1996. december 1.). „Reconstitution of DNA base excision-repair with purified human proteins: interaction between DNA polymerase beta and the XRCC1 protein”. The EMBO Journal15 (23), 6662–70. o. DOI:10.1002/j.1460-2075.1996.tb01056.x. PMID8978692. PMC452490.
Bhattacharyya N, Banerjee S (2001. július 1.). „A novel role of XRCC1 in the functions of a DNA polymerase beta variant”. Biochemistry40 (30), 9005–13. o. DOI:10.1021/bi0028789. PMID11467963.
nih.gov
pubmed.ncbi.nlm.nih.gov
Prasad R, Çağlayan M, Dai DP, Nadalutti CA, Zhao ML, Gassman NR, Jánosházi AK, Stefanick DF, Horton JK, Krasich R, Longley MJ, Copeland WC, Griffith JD, Wilson SH (2017. december 1.). „DNA polymerase β: A missing link of the base excision repair machinery in mammalian mitochondria”. DNA Repair60, 77–88. o. DOI:10.1016/j.dnarep.2017.10.011. PMID29100041. PMC5919216.
Subba Rao K, Martin GM, Loeb LA (1985. október 1.). „Fidelity of DNA polymerase-beta in neurons from young and very aged mice”. Journal of Neurochemistry45 (4), 1273–8. o. DOI:10.1111/j.1471-4159.1985.tb05553.x. PMID3161998.
Orgel LE (1973. június 1.). „Ageing of clones of mammalian cells”. Nature243 (5408), 441–5. o. DOI:10.1038/243441a0. PMID4591306.
Cabelof DC, Raffoul JJ, Yanamadala S, Ganir C, Guo Z, Heydari AR (2002. március 1.). „Attenuation of DNA polymerase beta-dependent base excision repair and increased DMS-induced mutagenicity in aged mice”. Mutation Research500 (1–2), 135–45. o. DOI:10.1016/s0027-5107(02)00003-9. PMID11890943. PMC3339152.
Gao S, Oden PN, Ryan BJ, Yang H, Freudenthal BD, Greenberg MM (2024. április 18.). „Biochemical and structural characterization of Fapy•dG replication by Human DNA polymerase β”. Nucleic Acids Res, gkae277. o. DOI:10.1093/nar/gkae277. PMID38634780.
Canitrot Y, Cazaux C, Fréchet M, Bouayadi K, Lesca C, Salles B, Hoffmann JS (1998. október 1.). „Overexpression of DNA polymerase beta in cell results in a mutator phenotype and a decreased sensitivity to anticancer drugs”. Proceedings of the National Academy of Sciences of the United States of America95 (21), 12586–90. o. DOI:10.1073/pnas.95.21.12586. PMID9770529. PMC22874.
Bergoglio V, Pillaire MJ, Lacroix-Triki M, Raynaud-Messina B, Canitrot Y, Bieth A, Garès M, Wright M, Delsol G, Loeb LA, Cazaux C, Hoffmann JS (2002. június 1.). „Deregulated DNA polymerase beta induces chromosome instability and tumorigenesis”. Cancer Research62 (12), 3511–4. o. PMID12067997.
Bergoglio V, Canitrot Y, Hogarth L, Minto L, Howell SB, Cazaux C, Hoffmann JS (2001. szeptember 1.). „Enhanced expression and activity of DNA polymerase beta in human ovarian tumor cells: impact on sensitivity towards antitumor agents”. Oncogene20 (43), 6181–7. o. DOI:10.1038/sj.onc.1204743. PMID11593426.
Narayan S, He F, Wilson SH (1996. augusztus 1.). „Activation of the human DNA polymerase beta promoter by a DNA-alkylating agent through induced phosphorylation of cAMP response element-binding protein-1”. The Journal of Biological Chemistry271 (31), 18508–13. o. DOI:10.1074/jbc.271.31.18508. PMID8702497.
Sarnowska E, Grzybowska EA, Sobczak K, Konopinski R, Wilczynska A, Szwarc M, Sarnowski TJ, Krzyzosiak WJ, Siedlecki JA (2007). „Hairpin structure within the 3'UTR of DNA polymerase beta mRNA acts as a post-transcriptional regulatory element and interacts with Hax-1”. Nucleic Acids Research35 (16), 5499–510. o. DOI:10.1093/nar/gkm502. PMID17704138. PMC2018635.
Date T, Tanihara K, Yamamoto S, Nomura N, Matsukage A (1992. szeptember 1.). „Two regions in human DNA polymerase beta mRNA suppress translation in Escherichia coli”. Nucleic Acids Research20 (18), 4859–64. o. DOI:10.1093/nar/20.18.4859. PMID1408801. PMC334243.
Whitehouse CJ, Taylor RM, Thistlethwaite A, Zhang H, Karimi-Busheri F, Lasko DD, Weinfeld M, Caldecott KW (2001. január 1.). „XRCC1 stimulates human polynucleotide kinase activity at damaged DNA termini and accelerates DNA single-strand break repair”. Cell104 (1), 107–17. o. DOI:10.1016/S0092-8674(01)00195-7. PMID11163244.
Wang L, Bhattacharyya N, Chelsea DM, Escobar PF, Banerjee S (2004. november 1.). „A novel nuclear protein, MGC5306 interacts with DNA polymerase beta and has a potential role in cellular phenotype”. Cancer Research64 (21), 7673–7. o. DOI:10.1158/0008-5472.CAN-04-2801. PMID15520167.
Fan J, Otterlei M, Wong HK, Tomkinson AE, Wilson DM (2004). „XRCC1 co-localizes and physically interacts with PCNA”. Nucleic Acids Research32 (7), 2193–201. o. DOI:10.1093/nar/gkh556. PMID15107487. PMC407833.
Kubota Y, Nash RA, Klungland A, Schär P, Barnes DE, Lindahl T (1996. december 1.). „Reconstitution of DNA base excision-repair with purified human proteins: interaction between DNA polymerase beta and the XRCC1 protein”. The EMBO Journal15 (23), 6662–70. o. DOI:10.1002/j.1460-2075.1996.tb01056.x. PMID8978692. PMC452490.
Bhattacharyya N, Banerjee S (2001. július 1.). „A novel role of XRCC1 in the functions of a DNA polymerase beta variant”. Biochemistry40 (30), 9005–13. o. DOI:10.1021/bi0028789. PMID11467963.
Prasad R, Çağlayan M, Dai DP, Nadalutti CA, Zhao ML, Gassman NR, Jánosházi AK, Stefanick DF, Horton JK, Krasich R, Longley MJ, Copeland WC, Griffith JD, Wilson SH (2017. december 1.). „DNA polymerase β: A missing link of the base excision repair machinery in mammalian mitochondria”. DNA Repair60, 77–88. o. DOI:10.1016/j.dnarep.2017.10.011. PMID29100041. PMC5919216.
Cabelof DC, Raffoul JJ, Yanamadala S, Ganir C, Guo Z, Heydari AR (2002. március 1.). „Attenuation of DNA polymerase beta-dependent base excision repair and increased DMS-induced mutagenicity in aged mice”. Mutation Research500 (1–2), 135–45. o. DOI:10.1016/s0027-5107(02)00003-9. PMID11890943. PMC3339152.
Canitrot Y, Cazaux C, Fréchet M, Bouayadi K, Lesca C, Salles B, Hoffmann JS (1998. október 1.). „Overexpression of DNA polymerase beta in cell results in a mutator phenotype and a decreased sensitivity to anticancer drugs”. Proceedings of the National Academy of Sciences of the United States of America95 (21), 12586–90. o. DOI:10.1073/pnas.95.21.12586. PMID9770529. PMC22874.
Sarnowska E, Grzybowska EA, Sobczak K, Konopinski R, Wilczynska A, Szwarc M, Sarnowski TJ, Krzyzosiak WJ, Siedlecki JA (2007). „Hairpin structure within the 3'UTR of DNA polymerase beta mRNA acts as a post-transcriptional regulatory element and interacts with Hax-1”. Nucleic Acids Research35 (16), 5499–510. o. DOI:10.1093/nar/gkm502. PMID17704138. PMC2018635.
Date T, Tanihara K, Yamamoto S, Nomura N, Matsukage A (1992. szeptember 1.). „Two regions in human DNA polymerase beta mRNA suppress translation in Escherichia coli”. Nucleic Acids Research20 (18), 4859–64. o. DOI:10.1093/nar/20.18.4859. PMID1408801. PMC334243.
Fan J, Otterlei M, Wong HK, Tomkinson AE, Wilson DM (2004). „XRCC1 co-localizes and physically interacts with PCNA”. Nucleic Acids Research32 (7), 2193–201. o. DOI:10.1093/nar/gkh556. PMID15107487. PMC407833.
Kubota Y, Nash RA, Klungland A, Schär P, Barnes DE, Lindahl T (1996. december 1.). „Reconstitution of DNA base excision-repair with purified human proteins: interaction between DNA polymerase beta and the XRCC1 protein”. The EMBO Journal15 (23), 6662–70. o. DOI:10.1002/j.1460-2075.1996.tb01056.x. PMID8978692. PMC452490.