E. Compe and J. M. Egly, Nucleotide Excision Repair and Transcriptional Regulation: TFIIH and Beyond, Annu Rev Biochem, vol.85, pp.265-90, 2016.

N. L. May, J. M. Egly, and F. Coin, True lies: the double life of the nucleotide excision repair factors in transcription and DNA repair, J Nucleic Acids, 2010.
URL : https://hal.archives-ouvertes.fr/inserm-02461414

D. Bootsma, K. H. Kraemer, J. E. Cleaver, and J. Hoeijmakers, Nucleotide excision repair syndromes: xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy In: The Genetic Basis of Human Cancer (2 nd Edn) McGraw-Hill, 2002.

W. J. Kleijer, V. Laugel, M. Berneburg, T. Nardo, and H. Fawcett, Incidence of DNA repair deficiency disorders in western Europe: Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy, DNA Repair, vol.7, pp.744-50, 2008.
URL : https://hal.archives-ouvertes.fr/hal-00281488

Y. Hirai, Y. Kodama, S. Moriwaki, A. Noda, and H. M. Cullings, Heterozygous individuals bearing a founder mutation in the XPA DNA repair gene comprise nearly 1% of the Japanese population, Mutat Res, vol.601, pp.171-179, 2006.

N. Soufir, C. Ged, A. Bourillon, F. Austerlitz, and C. Chemin, A prevalent mutation with founder effect in xeroderma pigmentosum group C from north Africa, J Invest Dermatol, vol.130, pp.1537-1579, 2010.
URL : https://hal.archives-ouvertes.fr/hal-00549153

B. Halim, N. , B. A. Bouafif, N. Romdhane, L. et al., Consanguinity, endogamy, and genetic disorders in Tunisia, J Community Genet, vol.4, pp.273-84, 2013.
URL : https://hal.archives-ouvertes.fr/pasteur-00859212

P. C. Hanawalt and G. Spivak, Transcription-coupled DNA repair: two decades of progress and surprises, Nat Rev Mol Cell Biol, vol.9, pp.958-70, 2008.

L. May, N. Fradin, D. Iltis, I. Bougnères, P. Egly et al., XPG and XPF endonucleases trigger chromatin looping and DNA demethylation for accurate expression of activated genes, Mol Cell, vol.47, pp.622-654, 2012.
URL : https://hal.archives-ouvertes.fr/hal-02329959

T. Riedl, F. Hanaoka, and J. M. Egly, The comings and goings of nucleotide excision repair factors on damaged DNA, Embo J, vol.22, pp.5293-303, 2003.

L. May, N. Mota-fernandes, D. Vélez-cruz, R. Iltis, I. Biard et al., NER factors are recruited to active promoters and facilitate chromatin modification for transcription in the absence of exogenous genotoxic attack, Mol Cell, vol.38, pp.54-66, 2010.
URL : https://hal.archives-ouvertes.fr/inserm-02461411

I. Satokata, K. Tanaka, N. Miura, M. Narita, and T. Mimaki, Three nonsense mutations responsible for group A xeroderma pigmentosum, Mutat Res, vol.273, pp.193-202, 1992.

C. Nishigori, M. Zghal, T. Yagi, S. Imamura, and M. R. Komoun, High prevalence of the point mutation in exon 6 of the xeroderma pigmentosum group A-complementing (XPAC) gene in xeroderma pigmentosum group A patients in Tunisia, Am J Hum Genet, vol.53, pp.1001-1007, 1993.

C. M. Kelly and J. J. Latimer, Unscheduled DNA synthesis: a functional assay for global genomic nucleotide excision repair, Methods Mol Biol, vol.291, pp.303-323, 2005.

L. V. Mayne and A. R. Lehmann, Failure of RNA synthesis to recover after UV radiation: an early defect in cells from individuals with Cockayne's syndrome and xeroderma pigmentosum, Cancer Res, vol.42, pp.1473-1481, 1982.

M. Volker, M. J. Moné, P. Karmakar, A. Van-hoffen, and W. Schul, Sequential assembly of the nucleotide excision repair factors in vivo, Mol Cell, vol.8, pp.213-237, 2001.

S. G. Khan, K. S. Oh, T. Shahlavi, T. Ueda, and D. B. Busch, Reduced XPC DNA repair gene mRNA levels in clinically normal parents of xeroderma pigmentosum patients, Carcinogenesis, vol.27, pp.84-93, 2006.

L. Li, E. S. Bales, C. A. Peterson, and R. J. Legerski, Characterization of molecular defects in xeroderma pigmentosum group C, Nat Genet, vol.5, pp.413-420, 1993.

J. E. Cleaver, L. H. Thompson, A. S. Richardson, and J. C. States, A summary of mutations in the UV-sensitive disorders: xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy, Hum Mutat, vol.14, pp.9-22, 1999.

S. Benhamou and A. Sarasin, Variability in nucleotide excision repair and cancer risk: a review, Mutat Res, vol.462, pp.149-58, 2000.

J. Willemsen, O. Wicht, J. C. Wolanski, N. Baur, and S. Bastian, Phosphorylation-Dependent Feedback Inhibition of RIG-I by DAPK1 Identified by Kinome-wide siRNA Screening, Mol Cell, vol.65, pp.403-418, 2017.

J. L. Kissil, E. Feinstein, O. Cohen, P. A. Jones, and Y. C. Tsai, DAP-kinase loss of expression in various carcinoma and B-cell lymphoma cell lines: possible implications for role as tumor suppressor gene, Oncogene, vol.15, pp.403-410, 1997.