New functions of XPC in the protection of human skin cells from oxidative damage

Genome maintenance mechanisms for preventing cancer

Hoeijmakers, J. H. J. (2001) · Nature · doi:10.1038/35077232 · Cited by 3,939

Oxidative DNA damage and disease: induction, repair and significance

Evans, M. D., Dizdaroglu, M., & Cooke, M. S. (2004) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2003.11.001 · Cited by 1,372

The basal layer in human squamous tumors harbors more UVA than UVB fingerprint mutations: A role for UVA in human skin carcinogenesis

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DNA repair-deficient diseases, xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy

Lehmann, A. (2003) · Biochimie · doi:10.1016/j.biochi.2003.09.010 · Cited by 518

Subpathways of nucleotide excision repair and their regulation

Hanawalt, P. C. (2002) · Oncogene · doi:10.1038/sj.onc.1206096 · Cited by 447

A multistep damage recognition mechanism for global genomic nucleotide excision repair

Sugasawa, K., Okamoto, T., Shimizu, Y., Masutani, C., Iwai, S., & Hanaoka, F. (2001) · Genes & Development · doi:10.1101/gad.866301 · Cited by 435

Stimulation of human 8-oxoguanine-DNA glycosylase by AP-endonuclease: potential coordination of the initial steps in base excision repair

Hill, J. W. (2001) · Nucleic Acids Research · doi:10.1093/nar/29.2.430 · Cited by 416

Opposite base‐dependent reactions of a human base excision repair enzyme on DNA containing 7,8‐dihydro‐8‐oxoguanine and abasic sites

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Removal of oxygen free-radical-induced 5′,8-purine cyclodeoxynucleosides from DNA by the nucleotide excision-repair pathway in human cells

Kuraoka, I., Bender, C., Romieu, A., Cadet, J., Wood, R. D., & Lindahl, T. L. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.070471597 · Cited by 349

Centrosome Protein Centrin 2/Caltractin 1 Is Part of the Xeroderma Pigmentosum Group C Complex That Initiates Global Genome Nucleotide Excision Repair

Araki, M., Masutani, C., Takemura, M., Uchida, A., Sugasawa, K., Kondoh, J., Ohkuma, Y., & Hanaoka, F. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m100855200 · Cited by 335

Measurement of (5′R)- and (5′S)-8,5′-cyclo-2′-deoxyadenosines in DNA in vivo by liquid chromatography/isotope-dilution tandem mass spectrometry

Jaruga, P., Xiao, Y., Nelson, B. C., & Dizdaroğlu, M. (2009) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2009.06.107 · Cited by 38

Catalase overexpression reduces UVB-induced apoptosis in a human xeroderma pigmentosum reconstructed epidermis

Rezvani, H. R., Ged, C., Bouadjar, B., de Verneuil, H., & Taı̈eb, A. (2008) · Cancer Gene Therapy · doi:10.1038/sj.cgt.7701102 · Cited by 37

Telomere Length and Telomerase Activity Impact the UV Sensitivity Syndrome Xeroderma Pigmentosum C

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Cellular response to endogenous DNA damage: DNA base modifications in gene expression regulation

Bordin, D. L., Lirussi, L., & Nilsen, H. L. (2021) · DNA repair · doi:10.1016/j.dnarep.2021.103051 · Cited by 37

Transcription coupled base excision repair in mammalian cells: So little is known and so much to uncover

Chakraborty, A., Tapryal, N., Islam, A., MITRA, S. P., & Hazra, T. K. (2021) · DNA repair · doi:10.1016/j.dnarep.2021.103204 · Cited by 39

Nucleotide excision repair: a versatile and smart toolkit

Zhang, X., Yin, M., & Hu, J. (2022) · Acta Biochimica et Biophysica Sinica · doi:10.3724/abbs.2022054 · Cited by 42

XPC: Its Product and Biological Roles

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Chlamydomonas reinhardtii: a convenient model system for the study of DNA repair in photoautotrophic eukaryotes

Vlček, D., Ševčovičová, A., Sviežená, B., Gálová, E., & Miadoková, E. (2007) · Current Genetics · doi:10.1007/s00294-007-0163-9 · Cited by 35

XPC silencing sensitizes glioma cells to arsenic trioxide via increased oxidative damage.

Liu, S.-Y., Wen, C.-Y., Lee, Y.-J., & Lee, T.-C. (2010) · Toxicological Sciences · doi:10.1093/toxsci/kfq113 · Cited by 36

XPC beyond nucleotide excision repair and skin cancers

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Xeroderma Pigmentosum C (XPC) Mutations in Primary Fibroblasts Impair Base Excision Repair Pathway and Increase Oxidative DNA Damage

Fayyad, N., Kobaisi, F., Beal, D. M., Mahfouf, W., Ged, C., Morice‐Picard, F., Fayyad‐Kazan, M., Fayyad‐Kazan, H., Badran, B. M., Rezvani, H. R., et al. (2020) · Frontiers in Genetics · doi:10.3389/fgene.2020.561687 · Cited by 34

Role of the Oxidative DNA Damage Repair Gene OGG1 in Colorectal Tumorigenesis

Smith, C. G., West, H., Harris, R., Idziaszczyk, S., Maughan, T., Kaplan, R. S., Richman, S. D., Quirke, P., Seymour, M., Moskvina, V., et al. (2013) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/djt183 · Cited by 34

Increased risk of internal tumors in DNA repair-deficient xeroderma pigmentosum patients: analysis of four international cohorts

Nikolaev, S. I., Yurchenko, A. A., & Sarasin, A. R. (2022) · Orphanet Journal of Rare Diseases · doi:10.1186/s13023-022-02203-1 · Cited by 37

Versatile protection from mutagenic DNA lesions conferred by bipartite recognition in nucleotide excision repair

Maillard, O., Camenisch, U., Blagoev, K. B., & Naegeli, H. (2008) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2008.01.007 · Cited by 36

Tools to study DNA repair: what's in the box?

Feuerhahn, S., & Egly, J. (2008) · Trends in Genetics · doi:10.1016/j.tig.2008.07.003 · Cited by 34

Cisplatin induces cytoplasmic to nuclear translocation of nucleotide excision repair factors among spiral ganglion neurons

Guthrie, O. W., Li‐Korotky, H., Durrant, J. D., & Balaban, C. D. (2008) · Hearing Research · doi:10.1016/j.heares.2008.01.013 · Cited by 34

Stimulation of DNA Glycosylase Activities by XPC Protein Complex: Roles of Protein‐Protein Interactions

Shimizu, Y., Uchimura, Y., Dohmae, N., Saitoh, H., Hanaoka, F., & Sugasawa, K. (2010) · Journal of Nucleic Acids · doi:10.4061/2010/805698 · Cited by 33

Nucleotide excision repair of oxidised genomic DNA is not a source of urinary 8-oxo-7,8-dihydro-2′-deoxyguanosine

Evans, M. D., Mistry, V., Singh, R., Gackowski, D., Różalski, R., Siomek, A., Phillips, D. H., Zuo, J., Mullenders, L. H. F., Pines, A., et al. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.08.018 · Cited by 32

Depletion of poly(ADP-ribose) polymerase-1 reduces host cell reactivation of a UV-damaged adenovirus-encoded reporter gene in human dermal fibroblasts

Ghodgaonkar, M. M., Zacal, N., Kassam, S. N., Rainbow, A. J., & Shah, G. M. (2008) · DNA repair · doi:10.1016/j.dnarep.2008.01.001 · Cited by 30

Role of Base Excision Repair Pathway in the Processing of Complex DNA Damage Generated by Oxidative Stress and Anticancer Drugs

Baiken, Y., Kanayeva, D. A., Taipakova, S., Groisman, R., Ishchenko, A. A., Бегимбетова, Д., Matkarimov, B. T., & Saparbaev, M. K. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.617884 · Cited by 34

XPC inhibits NSCLC cell proliferation and migration by enhancing E-Cadherin expression

Cui, T., Srivastava, A. K., Han, C., Yang, L., Zhao, R., Zou, N., Qu, M., Duan, W., Zhang, X., & Wang, Q. (2015) · Oncotarget · doi:10.18632/oncotarget.3542 · Cited by 31

In vitro radiation‐induced expression of XPC mRNA as a possible biomarker for developing adverse reactions during radiotherapy

Wiebalk, K., Schmezer, P., Kropp, S., Chang-Claude, J. C., Celebi, O., Debus, J., Bartsch, H., & Popanda, O. (2007) · International Journal of Cancer · doi:10.1002/ijc.22981 · Cited by 31

Overexpression of matrix metalloproteinase 1 in dermal fibroblasts from DNA repair-deficient/cancer-prone xeroderma pigmentosum group C patients

Fréchet, M., Warrick, E., Vioux, C., Chevallier, O., Spatz, A., Benhamou, S., Sarasin, A. R., Bernerd, F., & Magnaldo, T. (2008) · Oncogene · doi:10.1038/onc.2008.153 · Cited by 34

Role of mitochondrial dysfunction in the pathophysiology of DNA repair disorders

Mori, M. P., & de Souza-Pinto, N. C. (2017) · Cell Biology International · doi:10.1002/cbin.10917 · Cited by 31

miR‐200a Modulates the Expression of the DNA Repair Protein OGG1 Playing a Role in Aging of Primary Human Keratinocytes

Tinaburri, L., D’Errico, M., Sileno, S., Maurelli, R., Degan, P., Magenta, A., & Dellambra, E. (2018) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2018/9147326 · Cited by 31

Exogenous melatonin enhances soybean ( Glycine max (L.) Merr.) seedling tolerance to saline‐alkali stress by regulating antioxidant response and DNA damage repair

Zhao, Q., Chen, S., Wang, G., Du, Y., Zhang, Z., Yu, G., Ren, C., Zhang, Y., & Du, J. (2022) · Physiologia Plantarum · doi:10.1111/ppl.13731 · Cited by 30

Defective DNA repair and increased chromatin binding of DNA repair factors in Down syndrome fibroblasts

Necchi, D., Pinto, A., Tillhon, M., Dutto, I., Serafini, M. M., Lanni, C., Govoni, S. M., Racchi, M., & Prosperi, E. (2015) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2015.07.009 · Cited by 31

Oxidative Stress and DNA Damage at Telomeres

Opresko, P. L., Sanford, S. L., & De Rosa, M. (2025) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a041707 · Cited by 30

Oxidative and Energy Metabolism as Potential Clues for Clinical Heterogeneity in Nucleotide Excision Repair Disorders

Hosseini, M., Ezzedine, K., Taïeb, A., & Rezvani, H. R. (2014) · Journal of Investigative Dermatology · doi:10.1038/jid.2014.365 · Cited by 33

Lack of XPC leads to a shift between respiratory complexes I and II but sensitizes cells to mitochondrial stress

Mori, M. P., Costa, R. A. P. E., Soltys, D. T., Freire, T. D. S., Rossato, F. A., Amigo, I., Kowaltowski, A. J., Vercesi, A. E., & de Souza-Pinto, N. C. (2017) · Scientific Reports · doi:10.1038/s41598-017-00130-x · Cited by 28

Structure and Stability of Duplex DNA Containing (5′S)-5′,8-Cyclo-2′-deoxyadenosine: An Oxidatively Generated Lesion Repaired by NER

Zaliznyak, T., Lukin, M., & Santos, C. D. L. (2012) · Chemical Research in Toxicology · doi:10.1021/tx300193k · Cited by 30

Differential contribution of XPC, RAD23A, RAD23B and CENTRIN 2 to the UV-response in human cells

Renaud, E., Miccoli, L., Zacal, N., Biard, D. S. F., Craescu, C. T., Rainbow, A. J., & Angulo, J. F. (2011) · DNA repair · doi:10.1016/j.dnarep.2011.05.003 · Cited by 31

Photosensitive human syndromes

Spivak, G., & Hanawalt, P. C. (2015) · Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis · doi:10.1016/j.mrfmmm.2014.11.003 · Cited by 27

The DNA damage response - from cell biology to human disease

Lam, F. C. (2022) · Journal of Translational Genetics and Genomics · doi:10.20517/jtgg.2021.61 · Cited by 29

SPR imaging for label-free multiplexed analyses of DNA N-glycosylase interactions with damaged DNA duplexes

Corne, C., Fiche, J.-B., Gasparutto, D., Cunin, V., Suraniti, E., Buhot, A., Fuchs, J., Calemczuk, R., Livache, T., & Favier, A. E. (2008) · The Analyst · doi:10.1039/b801086b · Cited by 32

Signaling Pathways, Chemical and Biological Modulators of Nucleotide Excision Repair: The Faithful Shield against UV Genotoxicity

Kobaisi, F., Fayyad, N., Rezvani, H. R., Fayyad‐Kazan, M., Sulpice, E., Badran, B., Fayyad‐Kazan, H., Gidrol, X., & Rachidi, W. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/4654206 · Cited by 26

Oxidative DNA Damage in Neurons: Implication of Ku in Neuronal Homeostasis and Survival

Zio, D. D., Bordi, M., & Cecconi, F. (2012) · International Journal of Cell Biology · doi:10.1155/2012/752420 · Cited by 25

Oxidative DNA Damage in XPC-Knockout and Its Wild Mice Treated with Equine Estrogen

Okamoto, Y., Chou, P., Kim, S. Y., Suzuki, N., Laxmi, Y. R. S., Okamoto, K., Liu, X., Matsuda, T., & Shibutani, S. (2008) · Chemical Research in Toxicology · doi:10.1021/tx700428m · Cited by 26

SIRT2 promotes base excision repair by transcriptionally activating OGG1 in an ATM/ATR-dependent manner

Geng, A., Sun, J., Tang, H., Yu, Y., Wang, X., Zhang, J., Wang, X., Sun, X., Zhou, X., Gao, N., et al. (2024) · Nucleic Acids Research · doi:10.1093/nar/gkae190 · Cited by 25

Xeroderma Pigmentosum Group C Deficiency Alters Cigarette Smoke DNA Damage Cell Fate and Accelerates Emphysema Development

Sears, C. R., Zhou, H., Justice, M. J., Fisher, A. J., Saliba, J., Lamb, I. W., Wicker, J., Schweitzer, K. S., & Petrache, I. (2017) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2017-0251oc · Cited by 24

Role of DNA repair in the protection against genotoxic stress

Camenisch, U., & Naegeli, H. (2009) · Proceedings of the Fourth International Symposium on Polarization Phenomena in Nuclear Reactions · doi:10.1007/978-3-7643-8336-7_5 · Cited by 24

Phosphorylation of xeroderma pigmentosum group C regulates ultraviolet-induced DNA damage repair

Shah, P., Zhao, B., Qiang, L., & He, Y. (2018) · Nucleic Acids Research · doi:10.1093/nar/gky239 · Cited by 24

Impaired spermatogenesis and elevated spontaneous tumorigenesis in xeroderma pigmentosum group A gene (Xpa)-deficient mice

Nakane, H., Hirota, S., Brooks, P. J., Nakabeppu, Y., Nakatsu, Y., Nishimune, Y., Iino, A., & Tanaka, K. (2008) · DNA repair · doi:10.1016/j.dnarep.2008.08.003 · Cited by 22

XPC deficiency is related to APE1 and OGG1 expression and function

de Melo, J. T. A., de Souza Timoteo, A. R., Lajus, T. B. P., Brandão, J. A., de Souza-Pinto, N. C., Menck, C. F. M., Campalans, A., Radicella, J. P., Vessoni, A. T., Muotri, A. R., et al. (2016) · Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis · doi:10.1016/j.mrfmmm.2016.01.004 · Cited by 21

XPC protects against smoking- and carcinogen-induced lung adenocarcinoma

Zhou, H., Saliba, J., Sandusky, G. E., & Sears, C. R. (2019) · Carcinogenesis · doi:10.1093/carcin/bgz003 · Cited by 21

The impact of single-nucleotide polymorphisms (SNPs) in OGG1 and XPC on the age at onset of Huntington disease

Berger, F., Vaslin, L., Belin, L., Asselain, B. J. R., Forlani, S., Humbert, S., Dürr, A., & Hall, J. A. (2013) · Mutation Research/Genetic Toxicology and Environmental Mutagenesis · doi:10.1016/j.mrgentox.2013.04.020 · Cited by 22

The endoperoxide ascaridol shows strong differential cytotoxicity in nucleotide excision repair-deficient cells

Abbasi, R., Efferth, T., Kuhmann, C., Opatz, T., Hao, X., Popanda, O., & Schmezer, P. (2012) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2012.01.006 · Cited by 22

Base Excision Repair and Nucleotide Excision Repair

Izumi, T., & Mellon, I. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-803309-8.00017-3 · Cited by 22

Effect of the multifunctional proteins RPA, YB‐1, and XPC repair factor on AP site cleavage by DNA glycosylase NEIL1

Pestryakov, P. E., Zharkov, D. O., Грин, И. Р., Fomina, E. E., Kim, E. R., Hamon, L., Eliseeva, I. A., Petruseva, I. O., Curmi, P. A., Ovchinnikov, L. P., et al. (2012) · Journal of Molecular Recognition · doi:10.1002/jmr.2182 · Cited by 21

Hydroxyl radical is predominantly involved in oxidatively generated base damage to cellular DNA exposed to ionizing radiation

Cadet, J., Angelov, D., & Wagner, J. R. (2022) · International Journal of Radiation Biology · doi:10.1080/09553002.2022.2067363 · Cited by 22

Impact of Age-Associated Cyclopurine Lesions on DNA Repair Helicases

Khan, I., Suhasini, A. N., Banerjee, T., Sommers, J. A., Kaplan, D. L., Kuper, J., Kisker, C., & Brosh, R. M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0113293 · Cited by 21

Generation of guanine–amino acid cross-links by a free radical combination mechanism

Uvaydov, Y., Geacintov, N. E., & Shafirovich, V. (2014) · Physical Chemistry Chemical Physics · doi:10.1039/c4cp00675e · Cited by 21

Rad4 Regulates Protein Turnover at a Postubiquitylation Step

Li, Y., Yan, J. Y., Kim, I., Liu, C., Huo, K., & Rao, H. (2009) · Molecular Biology of the Cell · doi:10.1091/mbc.e09-04-0305 · Cited by 21

Understanding photodermatoses associated with defective DNA repair

Giordano, C. N., Yew, Y. W., Spivak, G., & Lim, H. W. (2016) · Journal of the American Academy of Dermatology · doi:10.1016/j.jaad.2016.03.045 · Cited by 22

XPD/ERCC2 mutations interfere in cellular responses to oxidative stress

Lerner, L. K., Moreno, N. C., Rocha, C. R. R., Munford, V., dos Santos, V. T., Soltys, D. T., Garcia, C. C. M., Sarasin, A. R., & Menck, C. F. M. (2019) · Mutagenesis · doi:10.1093/mutage/gez020 · Cited by 20

Expression of xeroderma pigmentosum complementation group C protein predicts cisplatin resistance in lung adenocarcinoma patients

Ho, S.-P. (2011) · Oncology Reports · doi:10.3892/or.2011.1184 · Cited by 21

Base Excision Repair, the Redox Environment and Therapeutic Implications

Storr, S. J., Woolston, C. M., & Martin, S. G. (2011) · Current Molecular Pharmacology · doi:10.2174/1874-470211205010088 · Cited by 26

Requirement of transcription-coupled nucleotide excision repair for the removal of a specific type of oxidatively induced DNA damage

Sarmini, L., Meabed, M., Emmanouil, E., Atsaves, G., Robeska, E., Karwowski, B. T., Campalans, A., Gimisis, T., & Khobta, A. (2023) · Nucleic Acids Research · doi:10.1093/nar/gkad256 · Cited by 20

8-Oxoadenine: A «New» Player of the Oxidative Stress in Mammals?

Kruchinin, A. A., Kamzeeva, P. N., Zharkov, D. O., Aralov, A. V., & Makarova, А. V. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25021342 · Cited by 24

Purine DNA Lesions at Different Oxygen Concentration in DNA Repair-Impaired Human Cells (EUE-siXPA)

Krokidis, M. G., Parlanti, E., D’Errico, M., Pascucci, B., Pino, A., Alimonti, A., Pietraforte, D., Masi, A., Ferreri, C., & Chatgilialoglu, C. (2019) · Cells · doi:10.3390/cells8111377 · Cited by 19

The Combined Effects of Xeroderma Pigmentosum C Deficiency and Mutagens on Mutation Rates in the Mouse Germ Line

Miccoli, L., Burr, K., Hickenbotham, P. T., Friedberg, E. C., Angulo, J. F., & Dubrova, Y. E. (2007) · Cancer Research · doi:10.1158/0008-5472.can-06-3844 · Cited by 24

Differential DNA damage response to UV and hydrogen peroxide depending of differentiation stage in a neuroblastoma model.

Ramos-Espinosa, P., Rojas, E., & Valverde, M. (2012) · Neurotoxicology · doi:10.1016/j.neuro.2012.05.017 · Cited by 19

UV-inducible base excision repair of oxidative damaged DNA in human cells

Kassam, S. N., & Rainbow, A. J. (2008) · Mutagenesis · doi:10.1093/mutage/gen054 · Cited by 19

Induction of 8,5′-Cyclo-2′-deoxyadenosine and 8,5′-Cyclo-2′-deoxyguanosine in Isolated DNA by Fenton-Type Reagents

Guerrero, C. R., Wang, J., & Wang, Y. (2013) · Chemical Research in Toxicology · doi:10.1021/tx400221w · Cited by 19

Searching for DNA Damage: Insights From Single Molecule Analysis

Schaich, M. A., & Houten, B. V. (2021) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2021.772877 · Cited by 17

Degradation of p21CDKN1A after DNA damage is independent of type of lesion, and is not required for DNA repair

Savio, M., Coppa, T., Cazzalini, O., Perucca, P., Necchi, D., Nardò, T., Stivala, L. A., & Prosperi, E. (2009) · DNA repair · doi:10.1016/j.dnarep.2009.02.005 · Cited by 18

Transient protein–protein complexes in base excision repair

Endutkin, A. V., Yudkina, A. V., Sidorenko, V. S., & Zharkov, D. O. (2018) · Journal of Biomolecular Structure and Dynamics · doi:10.1080/07391102.2018.1553741 · Cited by 19

Repair of DNA damage induced by anthanthrene, a polycyclic aromatic hydrocarbon (PAH) without bay or fjord regions

Desler, C., Johannessen, C., & Rasmussen, L. J. (2008) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2008.10.056 · Cited by 18

Combination of Aβ Secretion and Oxidative Stress in an Alzheimer-Like Cell Line Leads to the Over-Expression of the Nucleotide Excision Repair Proteins DDB2 and XPC

Forestier, A., Douki, T., Rosa, V. D., Beal, D. M., & Rachidi, W. (2015) · International Journal of Molecular Sciences · doi:10.3390/ijms160817422 · Cited by 17

Radiation-induced damage to cellular DNA: Chemical nature and mechanisms of lesion formation

Cadet, J., & Wagner, J. R. (2016) · Radiation Physics and Chemistry · doi:10.1016/j.radphyschem.2016.04.018 · Cited by 17

Xeroderma pigmentosum group A suppresses mutagenesis caused by clustered oxidative DNA adducts in the human genome

Sassa, A., Kamoshita, N., Kanemaru, Y., Honma, M., & Yasui, M. (2015) · PLOS ONE · doi:10.1371/journal.pone.0142218 · Cited by 13

Candidate gene biodosimeters of mice and human exposure to ionizing radiation by quantitative reverse transcription polymerase chain reaction

Rezaeejam, H., Shirazi, A., Valizadeh, M., & Izadi, P. (2015) · Journal of Cancer Research and Therapeutics · doi:10.4103/0973-1482.160912 · Cited by 15

Chromium III Histidinate Exposure Modulates Gene Expression in HaCaT Human Keratinocytes Exposed to Oxidative Stress

Hazane‐Puch, F., Benaraba, R., Valenti, K., Osman, M., Laporte, F., Favier, A. E., Anderson, R. A., Roussel, A., & Hininger‐Favier, I. (2009) · Biological Trace Element Research · doi:10.1007/s12011-009-8557-9 · Cited by 13

Papel das proteínas XPD e DNA polimerase eta nas respostas de células humanas a danos no genoma

Lerner, L. K. (2014) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.5.2014.tde-20102014-103732 · Cited by 13

Novo papel da proteína XPC na regulação dos complexos da cadeia de transporte de elétrons e desequilíbrio redox

Mori, M. P. (2015) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.46.2015.tde-20072015-105008 · Cited by 13

Divergent effects of oxidatively induced modification to the C8 of 2′‐deoxyadenosine on transcription factor binding: 8,5′(S)‐cyclo‐2′‐deoxyadenosine inhibits the binding of multiple sequence specific transcription factors, while 8‐oxo‐2′‐deoxyadenosine increases binding of CREB and NF‐kappa B to DNA

Abraham, J., & Brooks, P. J. (2010) · Environmental and Molecular Mutagenesis · doi:10.1002/em.20619 · Cited by 12

Genetic Evidence for XPC-KRAS Interactions During Lung Cancer Development

Zhang, X., He, N., Gu, D., Wickliffe, J. K., Salazar, J. J., Boldogh, I., & Xie, J. (2015) · Journal of genetics and genomics/Journal of Genetics and Genomics · doi:10.1016/j.jgg.2015.09.006 · Cited by 12

Radiation-induced (5′R)-and (5′S)-purine 5′,8-cyclo-2′-deoxyribonucleosides in human cells: a revisited analysis of HPLC-MS/MS measurements

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Nucleotide excision repair: DNA damage recognition and preincision complex assembly

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