Nucleotide excision repair (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Nucleotide excision repair" in English language version.

refsWebsite

Global rank English rank

44nih.gov

4^th place

26doi.org

2^nd place

3harvard.edu

18^th place

17^th place

3semanticscholar.org

11^th place

8^th place

1handle.net

102^nd place

76^th place

doi.org

Fuss JO, Cooper PK (June 2006). "DNA repair: dynamic defenders against cancer and aging". PLOS Biology. 4 (6): e203. doi:10.1371/journal.pbio.0040203. PMC 1475692. PMID 16752948.
Le May N, Egly JM, Coin F (2010). "True lies: the double life of the nucleotide excision repair factors in transcription and DNA repair". Journal of Nucleic Acids. 2010: 1–10. doi:10.4061/2010/616342. PMC 2915888. PMID 20725631.
Morita R, Nakane S, Shimada A, et al. (2010). "Molecular mechanisms of the whole DNA repair system: a comparison of bacterial and eukaryotic systems". Journal of Nucleic Acids. 2010: 1–32. doi:10.4061/2010/179594. PMC 2957137. PMID 20981145.
Truglio JJ, Croteau DL, Van Houten B, Kisker C (February 2006). "Prokaryotic nucleotide excision repair: the UvrABC system". Chemical Reviews. 106 (2): 233–252. doi:10.1021/cr040471u. PMID 16464004.
Zhang Y, Rohde LH, Wu H (June 2009). "Involvement of nucleotide excision and mismatch repair mechanisms in double strand break repair". Current Genomics. 10 (4): 250–258. doi:10.2174/138920209788488544. PMC 2709936. PMID 19949546.
Kwok PY, Gu Z (December 1999). "Single nucleotide polymorphism libraries: why and how are we building them?". Molecular Medicine Today. 5 (12): 538–543. doi:10.1016/S1357-4310(99)01601-9. PMID 10562720.
Karahalil B, Bohr V, Wilson D (October 2012). "Impact of DNA polymorphisms in key DNA base excision repair proteins on cancer risk". Human & Experimental Toxicology. 31 (10): 981–1005. Bibcode:2012HETox..31..981K. doi:10.1177/0960327112444476. PMC 4586256. PMID 23023028.
Hou SM, Fält S, Angelini S, Yang K, Nyberg F, Lambert B, Hemminki K (April 2002). "The XPD variant alleles are associated with increased aromatic DNA adduct level and lung cancer risk". Carcinogenesis. 23 (4): 599–603. doi:10.1093/carcin/23.4.599. PMID 11960912.
Wang M, Gu D, Zhang Z, Zhou J, Zhang Z (2009). "XPD polymorphisms, cigarette smoking, and bladder cancer risk: a meta-analysis". Journal of Toxicology and Environmental Health Part A. 72 (11–12): 698–705. Bibcode:2009JTEHA..72..698W. doi:10.1080/15287390902841029. PMID 19492231. S2CID 22991719.
Mittal RD, Mandal RK (January 2012). "Genetic variation in nucleotide excision repair pathway genes influence prostate and bladder cancer susceptibility in North Indian population". Indian Journal of Human Genetics. 18 (1): 47–55. doi:10.4103/0971-6866.96648. PMC 3385179. PMID 22754221.
Blankenburg S, König IR, Moessner R, Laspe P, Thoms KM, Krueger U, Khan SG, Westphal G, Berking C, Volkenandt M, Reich K, Neumann C, Ziegler A, Kraemer KH, Emmert S (June 2005). "Assessment of 3 xeroderma pigmentosum group C gene polymorphisms and risk of cutaneous melanoma: a case-control study". Carcinogenesis. 26 (6): 1085–1090. doi:10.1093/carcin/bgi055. PMID 15731165.
Shore RE, Zeleniuch-Jacquotte A, Currie D, Mohrenweiser H, Afanasyeva Y, Koenig KL, Arslan AA, Toniolo P, Wirgin I (May 2008). "Polymorphisms in XPC and ERCC2 genes, smoking and breast cancer risk". International Journal of Cancer. 122 (9): 2101–2105. doi:10.1002/ijc.23361. PMID 18196582. S2CID 9456435.
Qiao Y, Spitz MR, Guo Z, Hadeyati M, Grossman L, Kraemer KH, Wei Q (November 2002). "Rapid assessment of repair of ultraviolet DNA damage with a modified host-cell reactivation assay using a luciferase reporter gene and correlation with polymorphisms of DNA repair genes in normal human lymphocytes". Mutation Research. 509 (1–2): 165–174. doi:10.1016/S0027-5107(02)00219-1. PMID 12427537.
Huang MY, Fang WY, Lee SC, Cheng TL, Wang JY, Lin SR (2008). "ERCC2 2251A>C genetic polymorphism was highly correlated with early relapse in high-risk stage II and stage III colorectal cancer patients: a preliminary study". BMC Cancer. 8: 50. doi:10.1186/1471-2407-8-50. PMC 2262891. PMID 18267032.
Vermeij WP, Dollé ME, Reiling E, Jaarsma D, Payan-Gomez C, Bombardieri CR, Wu H, Roks AJ, Botter SM, van der Eerden BC, Youssef SA, Kuiper RV, Nagarajah B, van Oostrom CT, Brandt RM, Barnhoorn S, Imholz S, Pennings JL, de Bruin A, Gyenis Á, Pothof J, Vijg J, van Steeg H, Hoeijmakers JH (2016). "Restricted diet delays accelerated ageing and genomic stress in DNA-repair-deficient mice". Nature. 537 (7620): 427–431. Bibcode:2016Natur.537..427V. doi:10.1038/nature19329. PMC 5161687. PMID 27556946.
Andressoo JO, Hoeijmakers JH, Mitchell JR (2006). "Nucleotide excision repair disorders and the balance between cancer and aging". Cell Cycle. 5 (24): 2886–8. doi:10.4161/cc.5.24.3565. PMID 17172862.
Fuss JO, Tainer JA (2011). "XPB and XPD helicases in TFIIH orchestrate DNA duplex opening and damage verification to coordinate repair with transcription and cell cycle via CAK kinase". DNA Repair (Amst.). 10 (7): 697–713. doi:10.1016/j.dnarep.2011.04.028. PMC 3234290. PMID 21571596.
Andressoo JO, Mitchell JR, de Wit J, Hoogstraten D, Volker M, Toussaint W, Speksnijder E, Beems RB, van Steeg H, Jans J, de Zeeuw CI, Jaspers NG, Raams A, Lehmann AR, Vermeulen W, Hoeijmakers JH, van der Horst GT (2006). "An Xpd mouse model for the combined xeroderma pigmentosum/Cockayne syndrome exhibiting both cancer predisposition and segmental progeria". Cancer Cell. 10 (2): 121–32. doi:10.1016/j.ccr.2006.05.027. hdl:10029/5565. PMID 16904611.
Oh KS, Khan SG, Jaspers NG, Raams A, Ueda T, Lehmann A, Friedmann PS, Emmert S, Gratchev A, Lachlan K, Lucassan A, Baker CC, Kraemer KH (2006). "Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome". Hum. Mutat. 27 (11): 1092–103. doi:10.1002/humu.20392. PMID 16947863. S2CID 22852219.
Gregg SQ, Robinson AR, Niedernhofer LJ (2011). "Physiological consequences of defects in ERCC1-XPF DNA repair endonuclease". DNA Repair (Amst.). 10 (7): 781–91. doi:10.1016/j.dnarep.2011.04.026. PMC 3139823. PMID 21612988.
Barnhoorn S, Uittenboogaard LM, Jaarsma D, Vermeij WP, Tresini M, Weymaere M, Menoni H, Brandt RM, de Waard MC, Botter SM, Sarker AH, Jaspers NG, van der Horst GT, Cooper PK, Hoeijmakers JH, van der Pluijm I (2014). "Cell-autonomous progeroid changes in conditional mouse models for repair endonuclease XPG deficiency". PLOS Genet. 10 (10): e1004686. doi:10.1371/journal.pgen.1004686. PMC 4191938. PMID 25299392.
Iyama T, Wilson DM (2016). "Elements That Regulate the DNA Damage Response of Proteins Defective in Cockayne Syndrome". J. Mol. Biol. 428 (1): 62–78. doi:10.1016/j.jmb.2015.11.020. PMC 4738086. PMID 26616585.
Koch S, Garcia Gonzalez O, Assfalg R, Schelling A, Schäfer P, Scharffetter-Kochanek K, Iben S (2014). "Cockayne syndrome protein A is a transcription factor of RNA polymerase I and stimulates ribosomal biogenesis and growth". Cell Cycle. 13 (13): 2029–37. doi:10.4161/cc.29018. PMC 4111694. PMID 24781187.
Edifizi D, Schumacher B (2015). "Genome Instability in Development and Aging: Insights from Nucleotide Excision Repair in Humans, Mice, and Worms". Biomolecules. 5 (3): 1855–69. doi:10.3390/biom5031855. PMC 4598778. PMID 26287260.
Gorbunova V, Seluanov A, Mao Z, Hine C (2007). "Changes in DNA repair during aging". Nucleic Acids Res. 35 (22): 7466–74. doi:10.1093/nar/gkm756. PMC 2190694. PMID 17913742.
Goukassian D, Gad F, Yaar M, Eller MS, Nehal US, Gilchrest BA (2000). "Mechanisms and implications of the age-associated decrease in DNA repair capacity". FASEB J. 14 (10): 1325–34. doi:10.1096/fj.14.10.1325. PMID 10877825.

handle.net

hdl.handle.net

Andressoo JO, Mitchell JR, de Wit J, Hoogstraten D, Volker M, Toussaint W, Speksnijder E, Beems RB, van Steeg H, Jans J, de Zeeuw CI, Jaspers NG, Raams A, Lehmann AR, Vermeulen W, Hoeijmakers JH, van der Horst GT (2006). "An Xpd mouse model for the combined xeroderma pigmentosum/Cockayne syndrome exhibiting both cancer predisposition and segmental progeria". Cancer Cell. 10 (2): 121–32. doi:10.1016/j.ccr.2006.05.027. hdl:10029/5565. PMID 16904611.

harvard.edu

ui.adsabs.harvard.edu

Karahalil B, Bohr V, Wilson D (October 2012). "Impact of DNA polymorphisms in key DNA base excision repair proteins on cancer risk". Human & Experimental Toxicology. 31 (10): 981–1005. Bibcode:2012HETox..31..981K. doi:10.1177/0960327112444476. PMC 4586256. PMID 23023028.
Wang M, Gu D, Zhang Z, Zhou J, Zhang Z (2009). "XPD polymorphisms, cigarette smoking, and bladder cancer risk: a meta-analysis". Journal of Toxicology and Environmental Health Part A. 72 (11–12): 698–705. Bibcode:2009JTEHA..72..698W. doi:10.1080/15287390902841029. PMID 19492231. S2CID 22991719.
Vermeij WP, Dollé ME, Reiling E, Jaarsma D, Payan-Gomez C, Bombardieri CR, Wu H, Roks AJ, Botter SM, van der Eerden BC, Youssef SA, Kuiper RV, Nagarajah B, van Oostrom CT, Brandt RM, Barnhoorn S, Imholz S, Pennings JL, de Bruin A, Gyenis Á, Pothof J, Vijg J, van Steeg H, Hoeijmakers JH (2016). "Restricted diet delays accelerated ageing and genomic stress in DNA-repair-deficient mice". Nature. 537 (7620): 427–431. Bibcode:2016Natur.537..427V. doi:10.1038/nature19329. PMC 5161687. PMID 27556946.

nih.gov

pubmed.ncbi.nlm.nih.gov

Fuss JO, Cooper PK (June 2006). "DNA repair: dynamic defenders against cancer and aging". PLOS Biology. 4 (6): e203. doi:10.1371/journal.pbio.0040203. PMC 1475692. PMID 16752948.
Le May N, Egly JM, Coin F (2010). "True lies: the double life of the nucleotide excision repair factors in transcription and DNA repair". Journal of Nucleic Acids. 2010: 1–10. doi:10.4061/2010/616342. PMC 2915888. PMID 20725631.
Morita R, Nakane S, Shimada A, et al. (2010). "Molecular mechanisms of the whole DNA repair system: a comparison of bacterial and eukaryotic systems". Journal of Nucleic Acids. 2010: 1–32. doi:10.4061/2010/179594. PMC 2957137. PMID 20981145.
Truglio JJ, Croteau DL, Van Houten B, Kisker C (February 2006). "Prokaryotic nucleotide excision repair: the UvrABC system". Chemical Reviews. 106 (2): 233–252. doi:10.1021/cr040471u. PMID 16464004.
Zhang Y, Rohde LH, Wu H (June 2009). "Involvement of nucleotide excision and mismatch repair mechanisms in double strand break repair". Current Genomics. 10 (4): 250–258. doi:10.2174/138920209788488544. PMC 2709936. PMID 19949546.
Kwok PY, Gu Z (December 1999). "Single nucleotide polymorphism libraries: why and how are we building them?". Molecular Medicine Today. 5 (12): 538–543. doi:10.1016/S1357-4310(99)01601-9. PMID 10562720.
Karahalil B, Bohr V, Wilson D (October 2012). "Impact of DNA polymorphisms in key DNA base excision repair proteins on cancer risk". Human & Experimental Toxicology. 31 (10): 981–1005. Bibcode:2012HETox..31..981K. doi:10.1177/0960327112444476. PMC 4586256. PMID 23023028.
Sakoda LC, Loomis MM, Doherty JA, Julianto L, Barnett MJ, Neuhouser ML, Thornquist MD, Weiss NS, Goodman GE, Chen C (2012). "Germ line variation in nucleotide excision repair genes and lung cancer risk in smokers". International Journal of Molecular Epidemiology and Genetics. 3 (1): 1–17. PMC 3316453. PMID 22493747.
Hou SM, Fält S, Angelini S, Yang K, Nyberg F, Lambert B, Hemminki K (April 2002). "The XPD variant alleles are associated with increased aromatic DNA adduct level and lung cancer risk". Carcinogenesis. 23 (4): 599–603. doi:10.1093/carcin/23.4.599. PMID 11960912.
Wang M, Gu D, Zhang Z, Zhou J, Zhang Z (2009). "XPD polymorphisms, cigarette smoking, and bladder cancer risk: a meta-analysis". Journal of Toxicology and Environmental Health Part A. 72 (11–12): 698–705. Bibcode:2009JTEHA..72..698W. doi:10.1080/15287390902841029. PMID 19492231. S2CID 22991719.
Mittal RD, Mandal RK (January 2012). "Genetic variation in nucleotide excision repair pathway genes influence prostate and bladder cancer susceptibility in North Indian population". Indian Journal of Human Genetics. 18 (1): 47–55. doi:10.4103/0971-6866.96648. PMC 3385179. PMID 22754221.
Blankenburg S, König IR, Moessner R, Laspe P, Thoms KM, Krueger U, Khan SG, Westphal G, Berking C, Volkenandt M, Reich K, Neumann C, Ziegler A, Kraemer KH, Emmert S (June 2005). "Assessment of 3 xeroderma pigmentosum group C gene polymorphisms and risk of cutaneous melanoma: a case-control study". Carcinogenesis. 26 (6): 1085–1090. doi:10.1093/carcin/bgi055. PMID 15731165.
Shore RE, Zeleniuch-Jacquotte A, Currie D, Mohrenweiser H, Afanasyeva Y, Koenig KL, Arslan AA, Toniolo P, Wirgin I (May 2008). "Polymorphisms in XPC and ERCC2 genes, smoking and breast cancer risk". International Journal of Cancer. 122 (9): 2101–2105. doi:10.1002/ijc.23361. PMID 18196582. S2CID 9456435.
Qiao Y, Spitz MR, Guo Z, Hadeyati M, Grossman L, Kraemer KH, Wei Q (November 2002). "Rapid assessment of repair of ultraviolet DNA damage with a modified host-cell reactivation assay using a luciferase reporter gene and correlation with polymorphisms of DNA repair genes in normal human lymphocytes". Mutation Research. 509 (1–2): 165–174. doi:10.1016/S0027-5107(02)00219-1. PMID 12427537.
Huang MY, Fang WY, Lee SC, Cheng TL, Wang JY, Lin SR (2008). "ERCC2 2251A>C genetic polymorphism was highly correlated with early relapse in high-risk stage II and stage III colorectal cancer patients: a preliminary study". BMC Cancer. 8: 50. doi:10.1186/1471-2407-8-50. PMC 2262891. PMID 18267032.
Spitz MR, Wu X, Wang Y, Wang LE, Shete S, Amos CI, Guo Z, Lei L, Mohrenweiser H, Wei Q (February 2001). "Modulation of nucleotide excision repair capacity by XPD polymorphisms in lung cancer patients". Cancer Research. 61 (4): 1354–1357. PMID 11245433.
Vermeij WP, Dollé ME, Reiling E, Jaarsma D, Payan-Gomez C, Bombardieri CR, Wu H, Roks AJ, Botter SM, van der Eerden BC, Youssef SA, Kuiper RV, Nagarajah B, van Oostrom CT, Brandt RM, Barnhoorn S, Imholz S, Pennings JL, de Bruin A, Gyenis Á, Pothof J, Vijg J, van Steeg H, Hoeijmakers JH (2016). "Restricted diet delays accelerated ageing and genomic stress in DNA-repair-deficient mice". Nature. 537 (7620): 427–431. Bibcode:2016Natur.537..427V. doi:10.1038/nature19329. PMC 5161687. PMID 27556946.
Andressoo JO, Hoeijmakers JH, Mitchell JR (2006). "Nucleotide excision repair disorders and the balance between cancer and aging". Cell Cycle. 5 (24): 2886–8. doi:10.4161/cc.5.24.3565. PMID 17172862.
Fuss JO, Tainer JA (2011). "XPB and XPD helicases in TFIIH orchestrate DNA duplex opening and damage verification to coordinate repair with transcription and cell cycle via CAK kinase". DNA Repair (Amst.). 10 (7): 697–713. doi:10.1016/j.dnarep.2011.04.028. PMC 3234290. PMID 21571596.
Andressoo JO, Mitchell JR, de Wit J, Hoogstraten D, Volker M, Toussaint W, Speksnijder E, Beems RB, van Steeg H, Jans J, de Zeeuw CI, Jaspers NG, Raams A, Lehmann AR, Vermeulen W, Hoeijmakers JH, van der Horst GT (2006). "An Xpd mouse model for the combined xeroderma pigmentosum/Cockayne syndrome exhibiting both cancer predisposition and segmental progeria". Cancer Cell. 10 (2): 121–32. doi:10.1016/j.ccr.2006.05.027. hdl:10029/5565. PMID 16904611.
Oh KS, Khan SG, Jaspers NG, Raams A, Ueda T, Lehmann A, Friedmann PS, Emmert S, Gratchev A, Lachlan K, Lucassan A, Baker CC, Kraemer KH (2006). "Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome". Hum. Mutat. 27 (11): 1092–103. doi:10.1002/humu.20392. PMID 16947863. S2CID 22852219.
Gregg SQ, Robinson AR, Niedernhofer LJ (2011). "Physiological consequences of defects in ERCC1-XPF DNA repair endonuclease". DNA Repair (Amst.). 10 (7): 781–91. doi:10.1016/j.dnarep.2011.04.026. PMC 3139823. PMID 21612988.
Barnhoorn S, Uittenboogaard LM, Jaarsma D, Vermeij WP, Tresini M, Weymaere M, Menoni H, Brandt RM, de Waard MC, Botter SM, Sarker AH, Jaspers NG, van der Horst GT, Cooper PK, Hoeijmakers JH, van der Pluijm I (2014). "Cell-autonomous progeroid changes in conditional mouse models for repair endonuclease XPG deficiency". PLOS Genet. 10 (10): e1004686. doi:10.1371/journal.pgen.1004686. PMC 4191938. PMID 25299392.
Iyama T, Wilson DM (2016). "Elements That Regulate the DNA Damage Response of Proteins Defective in Cockayne Syndrome". J. Mol. Biol. 428 (1): 62–78. doi:10.1016/j.jmb.2015.11.020. PMC 4738086. PMID 26616585.
Koch S, Garcia Gonzalez O, Assfalg R, Schelling A, Schäfer P, Scharffetter-Kochanek K, Iben S (2014). "Cockayne syndrome protein A is a transcription factor of RNA polymerase I and stimulates ribosomal biogenesis and growth". Cell Cycle. 13 (13): 2029–37. doi:10.4161/cc.29018. PMC 4111694. PMID 24781187.
Edifizi D, Schumacher B (2015). "Genome Instability in Development and Aging: Insights from Nucleotide Excision Repair in Humans, Mice, and Worms". Biomolecules. 5 (3): 1855–69. doi:10.3390/biom5031855. PMC 4598778. PMID 26287260.
Gorbunova V, Seluanov A, Mao Z, Hine C (2007). "Changes in DNA repair during aging". Nucleic Acids Res. 35 (22): 7466–74. doi:10.1093/nar/gkm756. PMC 2190694. PMID 17913742.
Goukassian D, Gad F, Yaar M, Eller MS, Nehal US, Gilchrest BA (2000). "Mechanisms and implications of the age-associated decrease in DNA repair capacity". FASEB J. 14 (10): 1325–34. doi:10.1096/fj.14.10.1325. PMID 10877825.

ncbi.nlm.nih.gov

Fuss JO, Cooper PK (June 2006). "DNA repair: dynamic defenders against cancer and aging". PLOS Biology. 4 (6): e203. doi:10.1371/journal.pbio.0040203. PMC 1475692. PMID 16752948.
Le May N, Egly JM, Coin F (2010). "True lies: the double life of the nucleotide excision repair factors in transcription and DNA repair". Journal of Nucleic Acids. 2010: 1–10. doi:10.4061/2010/616342. PMC 2915888. PMID 20725631.
Morita R, Nakane S, Shimada A, et al. (2010). "Molecular mechanisms of the whole DNA repair system: a comparison of bacterial and eukaryotic systems". Journal of Nucleic Acids. 2010: 1–32. doi:10.4061/2010/179594. PMC 2957137. PMID 20981145.
Zhang Y, Rohde LH, Wu H (June 2009). "Involvement of nucleotide excision and mismatch repair mechanisms in double strand break repair". Current Genomics. 10 (4): 250–258. doi:10.2174/138920209788488544. PMC 2709936. PMID 19949546.
Karahalil B, Bohr V, Wilson D (October 2012). "Impact of DNA polymorphisms in key DNA base excision repair proteins on cancer risk". Human & Experimental Toxicology. 31 (10): 981–1005. Bibcode:2012HETox..31..981K. doi:10.1177/0960327112444476. PMC 4586256. PMID 23023028.
Sakoda LC, Loomis MM, Doherty JA, Julianto L, Barnett MJ, Neuhouser ML, Thornquist MD, Weiss NS, Goodman GE, Chen C (2012). "Germ line variation in nucleotide excision repair genes and lung cancer risk in smokers". International Journal of Molecular Epidemiology and Genetics. 3 (1): 1–17. PMC 3316453. PMID 22493747.
Mittal RD, Mandal RK (January 2012). "Genetic variation in nucleotide excision repair pathway genes influence prostate and bladder cancer susceptibility in North Indian population". Indian Journal of Human Genetics. 18 (1): 47–55. doi:10.4103/0971-6866.96648. PMC 3385179. PMID 22754221.
Huang MY, Fang WY, Lee SC, Cheng TL, Wang JY, Lin SR (2008). "ERCC2 2251A>C genetic polymorphism was highly correlated with early relapse in high-risk stage II and stage III colorectal cancer patients: a preliminary study". BMC Cancer. 8: 50. doi:10.1186/1471-2407-8-50. PMC 2262891. PMID 18267032.
Vermeij WP, Dollé ME, Reiling E, Jaarsma D, Payan-Gomez C, Bombardieri CR, Wu H, Roks AJ, Botter SM, van der Eerden BC, Youssef SA, Kuiper RV, Nagarajah B, van Oostrom CT, Brandt RM, Barnhoorn S, Imholz S, Pennings JL, de Bruin A, Gyenis Á, Pothof J, Vijg J, van Steeg H, Hoeijmakers JH (2016). "Restricted diet delays accelerated ageing and genomic stress in DNA-repair-deficient mice". Nature. 537 (7620): 427–431. Bibcode:2016Natur.537..427V. doi:10.1038/nature19329. PMC 5161687. PMID 27556946.
Fuss JO, Tainer JA (2011). "XPB and XPD helicases in TFIIH orchestrate DNA duplex opening and damage verification to coordinate repair with transcription and cell cycle via CAK kinase". DNA Repair (Amst.). 10 (7): 697–713. doi:10.1016/j.dnarep.2011.04.028. PMC 3234290. PMID 21571596.
Gregg SQ, Robinson AR, Niedernhofer LJ (2011). "Physiological consequences of defects in ERCC1-XPF DNA repair endonuclease". DNA Repair (Amst.). 10 (7): 781–91. doi:10.1016/j.dnarep.2011.04.026. PMC 3139823. PMID 21612988.
Barnhoorn S, Uittenboogaard LM, Jaarsma D, Vermeij WP, Tresini M, Weymaere M, Menoni H, Brandt RM, de Waard MC, Botter SM, Sarker AH, Jaspers NG, van der Horst GT, Cooper PK, Hoeijmakers JH, van der Pluijm I (2014). "Cell-autonomous progeroid changes in conditional mouse models for repair endonuclease XPG deficiency". PLOS Genet. 10 (10): e1004686. doi:10.1371/journal.pgen.1004686. PMC 4191938. PMID 25299392.
Iyama T, Wilson DM (2016). "Elements That Regulate the DNA Damage Response of Proteins Defective in Cockayne Syndrome". J. Mol. Biol. 428 (1): 62–78. doi:10.1016/j.jmb.2015.11.020. PMC 4738086. PMID 26616585.
Koch S, Garcia Gonzalez O, Assfalg R, Schelling A, Schäfer P, Scharffetter-Kochanek K, Iben S (2014). "Cockayne syndrome protein A is a transcription factor of RNA polymerase I and stimulates ribosomal biogenesis and growth". Cell Cycle. 13 (13): 2029–37. doi:10.4161/cc.29018. PMC 4111694. PMID 24781187.
Edifizi D, Schumacher B (2015). "Genome Instability in Development and Aging: Insights from Nucleotide Excision Repair in Humans, Mice, and Worms". Biomolecules. 5 (3): 1855–69. doi:10.3390/biom5031855. PMC 4598778. PMID 26287260.
Gorbunova V, Seluanov A, Mao Z, Hine C (2007). "Changes in DNA repair during aging". Nucleic Acids Res. 35 (22): 7466–74. doi:10.1093/nar/gkm756. PMC 2190694. PMID 17913742.

semanticscholar.org

api.semanticscholar.org

Wang M, Gu D, Zhang Z, Zhou J, Zhang Z (2009). "XPD polymorphisms, cigarette smoking, and bladder cancer risk: a meta-analysis". Journal of Toxicology and Environmental Health Part A. 72 (11–12): 698–705. Bibcode:2009JTEHA..72..698W. doi:10.1080/15287390902841029. PMID 19492231. S2CID 22991719.
Shore RE, Zeleniuch-Jacquotte A, Currie D, Mohrenweiser H, Afanasyeva Y, Koenig KL, Arslan AA, Toniolo P, Wirgin I (May 2008). "Polymorphisms in XPC and ERCC2 genes, smoking and breast cancer risk". International Journal of Cancer. 122 (9): 2101–2105. doi:10.1002/ijc.23361. PMID 18196582. S2CID 9456435.
Oh KS, Khan SG, Jaspers NG, Raams A, Ueda T, Lehmann A, Friedmann PS, Emmert S, Gratchev A, Lachlan K, Lucassan A, Baker CC, Kraemer KH (2006). "Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome". Hum. Mutat. 27 (11): 1092–103. doi:10.1002/humu.20392. PMID 16947863. S2CID 22852219.