Xeroderma pigmentosum, trichothiodystrophy and Cockayne syndrome: A complex genotype???phenotype relationship, Neuroscience, vol.145, issue.4, pp.1388-1396, 2007. ,
DOI : 10.1016/j.neuroscience.2006.12.020
Molecular genetics of Xeroderma pigmentosum variant, Experimental Dermatology, vol.14, issue.5, pp.529-536, 2003. ,
DOI : 10.1038/sj.neo.7900156
Xeroderma Pigmentosum-Variant Patients from America, Europe, and Asia, Journal of Investigative Dermatology, vol.128, issue.8, pp.2055-2068, 2008. ,
DOI : 10.1038/jid.2008.48
A novel POLH gene mutation in a xeroderma pigmentosum-V Tunisian patient: phenotype???genotype correlation, Journal of Genetics, vol.10, issue.3, pp.483-487, 2011. ,
DOI : 10.1007/s12041-011-0101-y
URL : https://hal.archives-ouvertes.fr/hal-01358550
Xeroderma pigmentosum - bridging a gap between clinic and laboratory, Photodermatology, Photoimmunology & Photomedicine, vol.17, issue.2, pp.47-54, 2001. ,
DOI : 10.1034/j.1600-0781.2001.017002047.x
Xeroderma pigmentosum variant and error-prone DNA polymerases, Biochimie, vol.85, issue.11, pp.1123-1132, 2003. ,
DOI : 10.1016/j.biochi.2003.10.009
Role of DNA Polymerase ?? in the UV Mutation Spectrum in Human Cells, Journal of Biological Chemistry, vol.278, issue.21, pp.18767-18775, 2003. ,
DOI : 10.1074/jbc.M211838200
Xeroderma pigmentosum variant (XP-V) correcting protein from HeLa cells has a thymine dimer bypass DNA polymerase activity, The EMBO Journal, vol.18, issue.12, pp.3491-3501, 1999. ,
DOI : 10.1093/emboj/18.12.3491
The XPV (Xeroderma pigmentosum variant) gene encodes human DNA polymerase í µí¼, Nature, vol.399, issue.6737, pp.700-704, 1999. ,
Participation of mouse DNA polymerase ?? in strand-biased mutagenic bypass of UV photoproducts and suppression of skin cancer, Proceedings of the National Academy of Sciences, vol.103, issue.48, pp.18083-18088, 2006. ,
DOI : 10.1073/pnas.0605247103
Role of DNA polymerases ??, ?? and ?? in UV resistance and UV-induced mutagenesis in a human cell line, DNA Repair, vol.7, issue.9, pp.1551-1562, 2008. ,
DOI : 10.1016/j.dnarep.2008.05.012
URL : https://hal.archives-ouvertes.fr/inserm-00320655
DNA Polymerase ??, a Key Protein in Translesion Synthesis in Human Cells, Sub-Cellular Biochemistry, vol.50, pp.189-209, 2010. ,
DOI : 10.1007/978-90-481-3471-7_10
Structural basis of human DNA polymerase ??-mediated chemoresistance to cisplatin, Proceedings of the National Academy of Sciences, vol.109, issue.19, pp.7269-7274, 2012. ,
DOI : 10.1073/pnas.1202681109
XP43TO, Previously Classified as Xeroderma Pigmentosum Group E, Should be Reclassified as Xeroderma Pigmentosum Variant, hRAD30 mutations in the variant form of Xeroderma pigmentosum, pp.1672-1674, 1999. ,
DOI : 10.1046/j.0022-202x.2001.01619.x
URL : http://doi.org/10.1046/j.0022-202x.2001.01619.x
Molecular analysis of mutations in DNA polymerase ?? in xeroderma pigmentosum-variant patients, Proceedings of the National Academy of Sciences, vol.99, issue.2, pp.815-820, 2002. ,
DOI : 10.1073/pnas.022473899
Molecular Analysis of DNA Polymerase Eta Gene in Japanese Patients Diagnosed as Xeroderma Pigmentosum Variant Type, Journal of Investigative Dermatology, vol.127, issue.7, pp.1745-1751, 2007. ,
DOI : 10.1038/sj.jid.5700759
Four types of possible founder mutations are responsible for 87% of Japanese patients with Xeroderma pigmentosum variant type, Journal of Dermatological Science, vol.52, issue.2, pp.144-148, 2008. ,
DOI : 10.1016/j.jdermsci.2008.07.001
in a Chinese Pedigree with Xeroderma Pigmentosum, Variant Type, International Journal of Medical Sciences, vol.10, issue.6, pp.766-770, 2013. ,
DOI : 10.7150/ijms.6095
Novel mutation in POLH gene responsible of severe phenotype of XP-V, Clinical Dermatology, vol.1, pp.125-129, 2013. ,
Three school-age cases of xeroderma pigmentosum variant type, Photodermatology, Photoimmunology & Photomedicine, vol.128, issue.3, pp.132-139, 2013. ,
DOI : 10.1111/phpp.12038
Mutations, Human Mutation, vol.106, issue.1, pp.117-128, 2014. ,
DOI : 10.1002/humu.22462
Wholeexome sequencing enables rapid determination of Xeroderma pigmentosum molecular etiology, PLoS ONE, vol.8, issue.6, 2013. ,
A simple salting out procedure for extracting DNA from human nucleated cells, Nucleic Acids Research, vol.16, issue.3, p.1215, 1988. ,
DOI : 10.1093/nar/16.3.1215
Fanconi anemia in Tunisia: high prevalence of group???A and identification of new FANCA mutations, Journal of Human Genetics, vol.48, issue.7, pp.352-361, 2003. ,
DOI : 10.1007/s10038-003-0037-z
Homologous recombination mediates S-phase-dependent radioresistance in cells deficient in DNA polymerase eta, Carcinogenesis, vol.33, issue.11, pp.2026-2034, 2012. ,
DOI : 10.1093/carcin/bgs239
A Novel Role of DNA Polymerase ?? in Modulating Cellular Sensitivity to Chemotherapeutic Agents, Molecular Cancer Research, vol.4, issue.4, pp.257-265, 2006. ,
DOI : 10.1158/1541-7786.MCR-05-0118
Homologous and Nonhomologous Recombination Resulting in Deletion: Effects of p53 Status, Microhomology, and Repetitive DNA Length and Orientation, Molecular and Cellular Biology, vol.20, issue.11, pp.4028-4035, 2000. ,
DOI : 10.1128/MCB.20.11.4028-4035.2000
Alu Repeats and Human Disease, Molecular Genetics and Metabolism, vol.67, issue.3, pp.183-193, 1999. ,
DOI : 10.1006/mgme.1999.2864