XPD Mutations Prevent TFIIH-Dependent Transactivation by Nuclear Receptors and Phosphorylation of RARα

A decade of molecular biology of retinoic acid receptors

Chambon, P. (1996) · The FASEB Journal · doi:10.1096/fasebj.10.9.8801176 · Cited by 2,889

The coregulator exchange in transcriptional functions of nuclear receptors

Glass, C. K., & Rosenfeld, M. G. (2000) · Genes & Development · doi:10.1101/gad.14.2.121 · Cited by 2,233

Activation of the estrogen receptor through phosphorylation by mitogen-activated protein kinase

Kato, S., Endoh, H., Masuhiro, Y., Kitamoto, T., Uchiyama, S., Sasaki, H., Masushige, S., Gotoh, Y., Nishida, E., Kawashima, H., et al. (1995) · Science · doi:10.1126/science.270.5241.1491 · Cited by 1,964

Dissecting the regulatory circuitry of a eukaryotic genome

Holstege, F. C. P., Jennings, E. G., Wyrick, J. J., Lee, T. I., Hengartner, C. J., Green, M. R., Golub, T. R., Lander, E. S., & Young, R. A. (1998) · Cell · doi:10.1016/s0092-8674(00)81641-4 · Cited by 1,670

The C-terminal domain of RNA polymerase II couples mRNA processing to transcription

McCracken, S. A., Fong, N., Yankulov, K., Ballantyne, S. M., Pan, G., Greenblatt, J., Patterson, S. D., Wickens, M., & Bentley, D. L. (1997) · Nature · doi:10.1038/385357a0 · Cited by 925

Nucleotide excision repair and human syndromes

de Boer, J., & Hoeijmakers, J. H. J. (2000) · Carcinogenesis · doi:10.1093/carcin/21.3.453 · Cited by 674

Proteasome-dependent degradation of the human estrogen receptor

Nawaz, Z., Lonard, D. M., Dennis, A. P., Smith, C. L., & O’Malley, B. W. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.5.1858 · Cited by 589

Prevention of Skin Cancer in Xeroderma Pigmentosum with the Use of Oral Isotretinoin

Kraemer, K. H., DiGiovanna, J. J., Moshell, A. N., Tarone, R. E., & Peck, G. L. (1988) · New England Journal of Medicine · doi:10.1056/nejm198806233182501 · Cited by 574

The 26S Proteasome Is Required for Estrogen Receptor-α and Coactivator Turnover and for Efficient Estrogen Receptor-α Transactivation

Lonard, D. M., Nawaz, Z., Smith, C. L., & O’Malley, B. W. (2000) · Molecular Cell · doi:10.1016/s1097-2765(00)80259-2 · Cited by 559

Reversible Phosphorylation of the C-terminal Domain of RNA Polymerase II

Dahmus, M. E. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.32.19009 · Cited by 501

Transcription-coupled DNA repair: two decades of progress and surprises

Hanawalt, P. C., & Spivak, G. (2008) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2549 · Cited by 1,081

Sensors and signals: a coactivator/corepressor/epigenetic code for integrating signal-dependent programs of transcriptional response

Rosenfeld, M. G., Lunyak, V. V., & Glass, C. K. (2006) · Genes & Development · doi:10.1101/gad.1424806 · Cited by 952

The General Transcription Machinery and General Cofactors

Thomas, M. C., & Chiang, C. (2006) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.1080/10409230600648736 · Cited by 992

Nuclear retinoid receptors and the transcription of retinoid-target genes

Bastien, J., & Rochette-Egly, C. (2004) · Gene · doi:10.1016/j.gene.2003.12.005 · Cited by 773

Controlling nuclear receptors: the circular logic of cofactor cycles

Perissi, V., & Rosenfeld, M. G. (2005) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1680 · Cited by 507

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

Cancer in xeroderma pigmentosum and related disorders of DNA repair

Cleaver, J. E. (2005) · Nature Reviews Cancer · doi:10.1038/nrc1652 · Cited by 427

Vitamin A and retinoid signaling: genomic and nongenomic effects

Al Tanoury, Z., Piskunov, A., & Rochette-Egly, C. (2013) · Journal of Lipid Research · doi:10.1194/jlr.r030833 · Cited by 408

Retinoic acid receptors: From molecular mechanisms to cancer therapy

di Masi, A., Leboffe, L., De Marinis, E., Pagano, F., Cicconi, L., Rochette-Egly, C., Lo-Coco, F., Ascenzi, P., & Nervi, C. (2015) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2014.12.003 · Cited by 403

Disorders of nucleotide excision repair: the genetic and molecular basis of heterogeneity

Cleaver, J. E., Lam, E. T., & Revet, I. (2009) · Nature Reviews Genetics · doi:10.1038/nrg2663 · Cited by 428

Secrets of a double agent: CDK7 in cell-cycle control and transcription

Fisher, R. P. (2005) · Journal of Cell Science · doi:10.1242/jcs.02718 · Cited by 371

TFIIH: when transcription met DNA repair

Compe, E., & Egly, J. (2012) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3350 · Cited by 357

DNA Repair in Mammalian Cells: Nucleotide excision repair: variations on versatility

Nouspikel, T. (2009) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-009-8737-y · Cited by 330

TFIIH Transcription Factor, a Target for the Rift Valley Hemorrhagic Fever Virus

May, N. L., Dubaele, S., Proietti‐De‐Santis, L., Billecocq, A., Bouloy, M., & Egly, J. (2004) · Cell · doi:10.1016/s0092-8674(04)00132-1 · Cited by 314

Distinct Roles for the XPB/p52 and XPD/p44 Subcomplexes of TFIIH in Damaged DNA Opening during Nucleotide Excision Repair

Coin, F., Oksenych, V., & Egly, J. (2007) · Molecular Cell · doi:10.1016/j.molcel.2007.03.009 · Cited by 294

Nuclear receptors: integration of multiple signalling pathways through phosphorylation

Rochette-Egly, C. (2003) · Cellular Signalling · doi:10.1016/s0898-6568(02)00115-8 · Cited by 291

Investigating RNA polymerase II carboxyl‐terminal domain (CTD) phosphorylation

Palancade, B., & Bensaude, O. (2003) · European Journal of Biochemistry · doi:10.1046/j.1432-1033.2003.03794.x · Cited by 250

Dynamic and combinatorial control of gene expression by nuclear retinoic acid receptors (RARs)

Rochette‐Egly, C., & Germain, P. (2009) · Nuclear Receptor Signaling · doi:10.1621/nrs.07005 · Cited by 263

NER factors are recruited to active promoters and facilitate chromatin modification for transcription in the absence of exogenous genotoxic attack

Le May, N., Mota-Fernandes, D., Vélez-Cruz, R., Iltis, I., Biard, D., & Egly, J. M. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.03.004 · Cited by 228

ERCC2/XPD gene polymorphisms and cancer risk

Benhamou, S. (2002) · Mutagenesis · doi:10.1093/mutage/17.6.463 · Cited by 227

CSB Is a Component of RNA Pol I Transcription

Bradsher, J., Auriol, J., Proietti‐De‐Santis, L., Iben, S., Vonesch, J., Grummt, I., & Egly, J. (2002) · Molecular Cell · doi:10.1016/s1097-2765(02)00678-0 · Cited by 221

Basal Transcription Defect Discriminates between Xeroderma Pigmentosum and Trichothiodystrophy in XPD Patients

Dubaele, S., Proietti‐De‐Santis, L., Bienstock, R. J., Keriel, A., Stefanini, M., Houten, B. V., & Egly, J. (2003) · Molecular Cell · doi:10.1016/s1097-2765(03)00182-5 · Cited by 204

CDK7 inhibitors as anticancer drugs

Sava, G. P., Fan, H., Coombes, R. C., Buluwela, L., & Ali, S. (2020) · Cancer and Metastasis Reviews · doi:10.1007/s10555-020-09885-8 · Cited by 200

Involvement of Proteasome in the Dynamic Assembly of the Androgen Receptor Transcription Complex*

Kang, Z., Pirskanen, A., Jänne, O., & Palvimo, J. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m209074200 · Cited by 204

XPG Stabilizes TFIIH, Allowing Transactivation of Nuclear Receptors: Implications for Cockayne Syndrome in XP-G/CS Patients

Ito, S., Kuraoka, I., Chymkowitch, P., Compe, E., Takedachi, A., Ishigami, C., Coin, F., Egly, J., & Tanaka, K. (2007) · Molecular Cell · doi:10.1016/j.molcel.2007.03.013 · Cited by 194

A history of TFIIH: Two decades of molecular biology on a pivotal transcription/repair factor

Egly, J., & Coin, F. (2011) · DNA repair · doi:10.1016/j.dnarep.2011.04.021 · Cited by 198

Divide and conquer: nucleotide excision repair battles cancer and ageing

Mitchell, J. R., Hoeijmakers, J. H., & Niedernhofer, L. J. (2003) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(03)00018-8 · Cited by 160

Nucleotide Excision Repair and Transcriptional Regulation: TFIIH and Beyond

Compe, E., & Egly, J. (2016) · Annual Review of Biochemistry · doi:10.1146/annurev-biochem-060815-014857 · Cited by 165

Phosphorylation by p38MAPK and recruitment of SUG‐1 are required for RA‐induced RARγ degradation and transactivation

Giannì, M., Bauer, A., Garattini, E., Chambon, P., & Rochette‐Egly, C. (2002) · The EMBO Journal · doi:10.1093/emboj/cdf374 · Cited by 151

A UV-sensitive syndrome patient with a specific CSA mutation reveals separable roles for CSA in response to UV and oxidative DNA damage

Nardò, T., Oneda, R., Spivak, G., Vaz, B., Mortier, L., Thomas, P., Orioli, D., Laugel, V., Stary, A., Hanawalt, P. C., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0902113106 · Cited by 140

Dysregulation of the Peroxisome Proliferator-Activated Receptor Target Genes by XPD Mutations

Compe, E., Drané, P., Laurent, C., Diderich, K. E. M., Braun, C., Hoeijmakers, J. H. J., & Egly, J. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.14.6065-6076.2005 · Cited by 139

The molecular physiology of nuclear retinoic acid receptors. From health to disease

Duong, V., & Rochette‐Egly, C. (2010) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2010.10.007 · Cited by 137

The essential and multifunctional TFIIH complex

Rimel, J. K., & Taatjes, D. J. (2018) · Protein Science · doi:10.1002/pro.3424 · Cited by 143

The transcriptional complexity of the TFIIH complex

Zurita, M., & Merino, C. (2003) · Trends in Genetics · doi:10.1016/j.tig.2003.08.005 · Cited by 138

MED23 Mutation Links Intellectual Disability to Dysregulation of Immediate Early Gene Expression

Hashimoto, S., Boissel, S., Zarhrate, M., Rio, M., Münnich, A., Egly, J., & Colleaux, L. (2011) · Science · doi:10.1126/science.1206638 · Cited by 134

Reduced level of the repair/transcription factor TFIIH in trichothiodystrophy

Botta, E. (2002) · Human Molecular Genetics · doi:10.1093/hmg/11.23.2919 · Cited by 124

The phosphorylation of the androgen receptor by TFIIH directs the ubiquitin/proteasome process

Chymkowitch, P., May, N. L., Charneau, P., Compe, E., & Egly, J. (2010) · The EMBO Journal · doi:10.1038/emboj.2010.337 · Cited by 129

MMXD, a TFIIH-Independent XPD-MMS19 Protein Complex Involved in Chromosome Segregation

Ito, S., Tan, L. J., Andoh, D., Narita, T., Seki, M., Hirano, Y., Narita, K., Kuraoka, I., Hiraoka, Y., & Tanaka, K. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.07.029 · Cited by 121

Trichothiodystrophy: From basic mechanisms to clinical implications

Stefanini, M., Botta, E., Lanzafame, M., & Orioli, D. (2009) · DNA repair · doi:10.1016/j.dnarep.2009.10.005 · Cited by 120

T:G Mismatch-specific Thymine-DNA Glycosylase Potentiates Transcription of Estrogen-regulated Genes through Direct Interaction with Estrogen Receptor α

Chen, D., Lucey, M. J., Phoenix, F. A., Lopez-Garcia, J., Hart, S., Losson, R., Buluwela, L., Coombes, R. C., Chambon, P., Schär, P., et al. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m304286200 · Cited by 116

Vitamin A regulation of gene expression: molecular mechanism of a prototype gene

McGrane, M. M. (2007) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2006.10.006 · Cited by 115

p8/TTD-A as a Repair-Specific TFIIH Subunit

Coin, F., Proietti‐De‐Santis, L., Nardò, T., Zlobinskaya, O., Stefanini, M., & Egly, J. (2006) · Molecular Cell · doi:10.1016/j.molcel.2005.10.024 · Cited by 109

A coordinated phosphorylation cascade initiated by p38MAPK/MSK1 directs RARα to target promoters

Bruck, N., Vitoux, D., Ferry, C., Duong, V., Bauer, A., de Thé, H., & Rochette‐Egly, C. (2009) · The EMBO Journal · doi:10.1038/emboj.2008.256 · Cited by 108

Retinoic acid signaling and mouse embryonic stem cell differentiation: Cross talk between genomic and non-genomic effects of RA

Rochette‐Egly, C. (2014) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2014.04.003 · Cited by 102

A Small Molecule Screen Identifies an Inhibitor of DNA Repair Inducing the Degradation of TFIIH and the Chemosensitization of Tumor Cells to Platinum

Alekseev, S., Ayadi, M., Brino, L., Egly, J., Larsen, A. K., & Coin, F. (2014) · Chemistry & Biology · doi:10.1016/j.chembiol.2013.12.014 · Cited by 97

Increased apoptosis, p53 up-regulation, and cerebellar neuronal degeneration in repair-deficient Cockayne syndrome mice

Laposa, R. R., Huang, E. J., & Cleaver, J. E. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0610619104 · Cited by 94

Molecular communication between androgen receptor and general transcription machinery

Lee, D. K., & Chang, C. (2003) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/s0960-0760(03)00005-0 · Cited by 91

Neurological defects in trichothiodystrophy reveal a coactivator function of TFIIH

Compe, E., Malerba, M., Soler, L., Marescaux, J., Borrelli, E., & Egly, J. (2007) · Nature Neuroscience · doi:10.1038/nn1990 · Cited by 95

Dynamic Combinatorial Networks in Nuclear Receptor-mediated Transcription

Rochette‐Egly, C. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.r500008200 · Cited by 89

Arabidopsis UVH6, a Homolog of Human XPD and Yeast RAD3 DNA Repair Genes, Functions in DNA Repair and Is Essential for Plant Growth

Liu, Z., Hong, S., Escobar, M. M., Vierling, E., Mitchell, D. L., Mount, D. W., & Hall, J. D. (2003) · PLANT PHYSIOLOGY · doi:10.1104/pp.103.021808 · Cited by 87

ARCH domain of XPD, an anchoring platform for CAK that conditions TFIIH DNA repair and transcription activities

Abdulrahman, W., Iltis, I., Radu, L., Braun, C., Maglott, A., Giraudon, C., Egly, J., & Poterszman, A. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1213981110 · Cited by 89

Xeroderma pigmentosum genes: Functions inside and outside DNA repair

Sugasawa, K. (2007) · Carcinogenesis · doi:10.1093/carcin/bgm282 · Cited by 83

P38MAPK‐dependent phosphorylation and degradation of SRC‐3/AIB1 and RARα‐mediated transcription

Giannì, M., Parrella, E., Raska, I., Gaillard, E., Nigro, E. A., Gaudon, C., Garattini, E., & Rochette‐Egly, C. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7600981 · Cited by 81

Transcription without XPB Establishes a Unified Helicase-Independent Mechanism of Promoter Opening in Eukaryotic Gene Expression

Alekseev, S., Nagy, Z., Sandoz, J., Weiss, A., Egly, J., May, N. L., & Coin, F. (2017) · Molecular Cell · doi:10.1016/j.molcel.2017.01.012 · Cited by 81

Transcription activities at 8-oxoG lesions in DNA

Larsen, E., Kwon, K.-R., Coin, F., Egly, J., & Klungland, A. (2004) · DNA repair · doi:10.1016/j.dnarep.2004.06.008 · Cited by 81

An Xpd mouse model for the combined xeroderma pigmentosum/Cockayne syndrome exhibiting both cancer predisposition and segmental progeria

Andressoo, J.-O., Mitchell, J. R., de Wit, J., Hoogstraten, D., Volker, M., Toussaint, W., Speksnijder, E., Beems, R. B., van Steeg, H., Jans, J., et al. (2006) · Cancer Cell · doi:10.1016/j.ccr.2006.05.027 · Cited by 78

True Lies: The Double Life of the Nucleotide Excision Repair Factors in Transcription and DNA Repair

May, N. L., Egly, J., & Coin, F. (2010) · Journal of Nucleic Acids · doi:10.4061/2010/616342 · Cited by 78

Phosphorylation of XPB helicase regulates TFIIH nucleotide excision repair activity

Coin, F., Auriol, J., Tapias, A., Clivio, P., Vermeulen, W., & Egly, J. (2004) · The EMBO Journal · doi:10.1038/sj.emboj.7600480 · Cited by 75

Selective Regulation of Vitamin D Receptor-Responsive Genes by TFIIH

Drané, P., Compe, E., Catez, P., Chymkowitch, P., & Egly, J.-M. (2004) · Molecular Cell · doi:10.1016/j.molcel.2004.10.007 · Cited by 75

Cockayne syndrome group B (CSB) protein: At the crossroads of transcriptional networks

Vélez-Cruz, R., & Egly, J. (2013) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2013.03.004 · Cited by 74

Trichothiodystrophy view from the molecular basis of DNA repair/transcription factor TFIIH

Hashimoto, S., & Egly, J. (2009) · Human Molecular Genetics · doi:10.1093/hmg/ddp390 · Cited by 79

Premature aging and cancer in nucleotide excision repair-disorders

Diderich, K. E. M., Alanazi, M. A., & Hoeijmakers, J. H. J. (2011) · DNA repair · doi:10.1016/j.dnarep.2011.04.025 · Cited by 76

Transcription-coupled repair and premature ageing

Andressoo, J., & Hoeijmakers, J. H. J. (2005) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2005.04.004 · Cited by 70

Protein kinases and the proteasome join in the combinatorial control of transcription by nuclear retinoic acid receptors

Bour, G., Lalevée, S., & Rochette‐Egly, C. (2007) · Trends in Cell Biology · doi:10.1016/j.tcb.2007.04.003 · Cited by 76

New clinico‐genetic classification of trichothiodystrophy

Morice‐Picard, F., Cario, M., Rezvani, H. R., Lacombe, D., Sarasin, A. R., & Taı̈eb, A. (2009) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.32902 · Cited by 69

TFIIH Subunit Alterations Causing Xeroderma Pigmentosum and Trichothiodystrophy Specifically Disturb Several Steps during Transcription

Singh, A., Compe, E., May, N. L., & Egly, J. (2015) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2014.12.012 · Cited by 63

Tissue specific mutagenic and carcinogenic responses in NER defective mouse models

Wijnhoven, S., Hoogervorst, E. M., de Waard, H., van der Horst, G. T. J., & STEEG, H. V. (2006) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2005.12.018 · Cited by 64

Ménage-à-Trois 1 Is Critical for the Transcriptional Function of PPARγ Coactivator 1

Sano, M., Izumi, Y., Helenius, K., Asakura, M., Rossi, D. J., Xie, M., Taffet, G. E., Hu, L., Pautler, R. G., Wilson, C. R., et al. (2007) · Cell Metabolism · doi:10.1016/j.cmet.2007.01.003 · Cited by 71

Bi-allelic TARS Mutations Are Associated with Brittle Hair Phenotype

Theil, A. F., Botta, E., Raams, A., Smith, D. E. C., Mendes, M. I. S., Caligiuri, G., Giachetti, S., Bione, S., Carriero, R., Liberi, G., et al. (2019) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2019.06.017 · Cited by 56

HES1 is a novel interactor of the Fanconi anemia core complex

Tremblay, C. S., Huang, F. F., Habi, O., Huard, C., Godin, C., Lévesque, G., & Carreau, M. (2008) · Blood · doi:10.1182/blood-2008-04-152710 · Cited by 59

Interaction of p21 CDKN1A with PCNA regulates the histone acetyltransferase activity of p300 in nucleotide excision repair

Cazzalini, O., Perucca, P., Savio, M., Necchi, D., Bianchi, L. C., Stivala, L. A., Ducommun, B., Scovassi, A. I., & Prosperi, E. (2008) · Nucleic Acids Research · doi:10.1093/nar/gkn014 · Cited by 62

TFIIH Operates through an Expanded Proximal Promoter To Fine-Tune c -myc Expression

Weber, A., Liu, J., Collins, I. J., & Levens, D. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.25.1.147-161.2005 · Cited by 60

p52 Mediates XPB Function within the Transcription/Repair Factor TFIIH

Jawhari, A., Lainé, J., Dubaele, S., Lamour, V., Poterszman, A., Coin, F., Moras, D., & Egly, J. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m203792200 · Cited by 56

An Xpb Mouse Model for Combined Xeroderma Pigmentosum and Cockayne Syndrome Reveals Progeroid Features upon Further Attenuation of DNA Repair

Andressoo, J., Weeda, G., de Wit, J., Mitchell, J. R., Beems, R. B., STEEG, H. V., van der Horst, G. T. J., & Hoeijmakers, J. H. J. (2008) · Molecular and Cellular Biology · doi:10.1128/mcb.01229-08 · Cited by 57

Nuclear receptor superfamily: Principles of signaling

Germain, P., Altucci, L., Bourguet, W., Rochette-Egly, C., & Gronemeyer, H. (2003) · Pure and Applied Chemistry · doi:10.1351/pac200375111619 · Cited by 53

Phosphorylation of the Retinoid X Receptor at the Omega loop, modulates the expression of retinoic-acid-target genes with a promoter context specificity

Bruck, N., Bastien, J., Bour, G., Tarrade, A., Plassat, J.-L., Bauer, A., Adam-Stitah, S., & Rochette-Egly, C. (2005) · Cellular Signalling · doi:10.1016/j.cellsig.2004.12.006 · Cited by 52

Poly (ADP-ribose) glycohydrolase regulates retinoic acid receptor-mediated gene expression.

May, N. L., Iltis, I., Amé, J., Zhovmer, A., Biard, D., Egly, J., Schreiber, V., & Coin, F. (2012) · Molecules and Cells · doi:10.1016/j.molcel.2012.09.021 · Cited by 48

T:G mismatch-specific thymine-DNA glycosylase (TDG) as a coregulator of transcription interacts with SRC1 family members through a novel tyrosine repeat motif

Lucey, M. J. (2005) · Nucleic Acids Research · doi:10.1093/nar/gki940 · Cited by 49

Both XPD alleles contribute to the phenotype of compound heterozygote xeroderma pigmentosum patients

Ueda, T., Compe, E., Catez, P., Kraemer, K. H., & Egly, J. (2009) · The Journal of Experimental Medicine · doi:10.1084/jem.20091892 · Cited by 50

TFIIH: A multi-subunit complex at the cross-roads of transcription and DNA repair

Kolesnikova, O., Radu, L., & Poterszman, A. (2019) · Advances in protein chemistry and structural biology · doi:10.1016/bs.apcsb.2019.01.003 · Cited by 50

Vinexin β Interacts with the Non-phosphorylated AF-1 Domain of Retinoid Receptor γ (RARγ) and Represses RARγ-mediated Transcription

Bour, G., Plassat, J., Bauer, A., Lalevée, S., & Rochette‐Egly, C. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m501344200 · Cited by 50

Making Myc

Liu, J., & Levens, D. (2006) · Current topics in microbiology and immunology · doi:10.1007/3-540-32952-8_1 · Cited by 50

The core component of the mammalian SWI/SNF complex SMARCD3/BAF60c is a coactivator for the nuclear retinoic acid receptor

Flajollet, S., Lefebvre, B., Cudejko, C., Staels, B., & Lefèbvre, P. (2007) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2007.02.004 · Cited by 47

In TFIIH the Arch domain of XPD is mechanistically essential for transcription and DNA repair

Peissert, S., Sauer, F., Grabarczyk, D. B., Braun, C., Sander, G., Poterszman, A., Egly, J., Kuper, J., & Kisker, C. (2020) · Nature Communications · doi:10.1038/s41467-020-15241-9 · Cited by 47

Cyclin H binding to the RARα activation function (AF)-2 domain directs phosphorylation of the AF-1 domain by cyclin-dependent kinase 7

Bour, G., Gaillard, E., Bruck, N., Lalevée, S., Plassat, J.-L., Busso, D., Samama, J.-P., & Rochette-Egly, C. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0505556102 · Cited by 45

The molecular basis for different disease states caused by mutations in TFIIH and XPG

Schärer, O. D. (2008) · DNA repair · doi:10.1016/j.dnarep.2007.10.007 · Cited by 45

CaMKII regulates retinoic acid receptor transcriptional activity and the differentiation of myeloid leukemia cells

Si, J., Mueller, L., & Collins, S. J. (2007) · Journal of Clinical Investigation · doi:10.1172/jci30779 · Cited by 45

Nuclear and extranuclear effects of vitamin A

Iskakova, M., Karbyshev, M. S., Piskunov, A., & Rochette‐Egly, C. (2015) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/cjpp-2014-0522 · Cited by 47

Mat1 Inhibits Peroxisome Proliferator-Activated Receptor γ-Mediated Adipocyte Differentiation

Helenius, K., Ying, Y., Alasaari, J., & Mäkelä, T. P. (2008) · Molecular and Cellular Biology · doi:10.1128/mcb.00347-08 · Cited by 47

Phosphorylation of Steroidogenic Factor 1 Is Mediated by Cyclin-Dependent Kinase 7

Lewis, A. E., Rusten, M., Høivik, E. A., Vikse, E. L., Hansson, M. L., Wallberg, A. E., & Bakke, M. (2007) · Molecular Endocrinology · doi:10.1210/me.2006-0478 · Cited by 44

Transcription-Associated Breaks in Xeroderma Pigmentosum Group D Cells from Patients with Combined Features of Xeroderma Pigmentosum and Cockayne Syndrome

Theron, T., Fousteri, M. I., Volker, M., Harries, L. W., Botta, E., Stefanini, M., Fujimoto, M., Andressoo, J., Mitchell, J., Jaspers, N. G. J., et al. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.18.8368-8378.2005 · Cited by 46

The DNA mismatch repair gene hMSH2 is a potent coactivator of oestrogen receptor α

Wada‐Hiraike, O., Yano, T., Nei, T., Matsumoto, Y., Nagasaka, K., Takizawa, S., Oishi, H., Arimoto, T., Nakagawa, S., Yasugi, T., et al. (2005) · British Journal of Cancer · doi:10.1038/sj.bjc.6602614 · Cited by 39

Super-enhancer in prostate cancer: transcriptional disorders and therapeutic targets

Chen, X., Ma, Q., Shang, Z., & Niu, Y. (2020) · npj Precision Oncology · doi:10.1038/s41698-020-00137-0 · Cited by 37

Transcriptional cyclin-dependent kinases: Potential drug targets in cancer therapy

Liu, Y., Fu, L., Wu, J., Liu, M., Wang, G., Liu, B., & Zhang, L. (2021) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2021.114056 · Cited by 38

Nuclear and Extra-Nuclear Effects of Retinoid Acid Receptors: How They Are Interconnected

Piskunov, A., Tanoury, Z. A., & Rochette‐Egly, C. (2014) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-94-017-9050-5_6 · Cited by 38

Disruption of TTDA Results in Complete Nucleotide Excision Repair Deficiency and Embryonic Lethality

Theil, A. F., Nonnekens, J., Steurer, B., Mari, P., de Wit, J., Boumendil, C., Marteijn, J. A. F., Raams, A., Maas, A., Vermeij, M., et al. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003431 · Cited by 36

Retinoid Signaling in Cancer and Its Promise for Therapy

Coyle, K. M. (2013) · Journal of Carcinogenesis & Mutagenesis · doi:10.4172/2157-2518.s7-006 · Cited by 32

Dissociation of CAK from Core TFIIH Reveals a Functional Link between XP-G/CS and the TFIIH Disassembly State

Arab, H. H., Wani, G., Ray, A., Shah, Z. I., Zhu, Q., & Wani, A. A. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011007 · Cited by 33

Retinoic acid induces leukemia cell G 1 arrest and transition into differentiation by inhibiting cyclin‐dependent kinase‐activating kinase binding and phosphorylation of PML/RAR

Wang, J., Barsky, L. W., Davicioni, E., Weinberg, K. I., Triche, T. J., Zhang, X., & Wu, L. (2006) · The FASEB Journal · doi:10.1096/fj.06-5900fje · Cited by 32

Regulation of UV-induced DNA damage response by ubiquitylation

Bergink, S., Jaspers, N. G. J., & Vermeulen, W. (2007) · DNA repair · doi:10.1016/j.dnarep.2007.01.012 · Cited by 33

XPD mutations prevent TFIIH-dependent transactivation by nuclear receptors and phosphorylation of RARalpha.

Keriel, A., Stary, A., Sarasin, A. R., Rochette‐Egly, C., & Egly, J. (2002) · HAL · Cited by 8

Abnormal XPD-induced nuclear receptor transactivation in DNA repair disorders: trichothiodystrophy and xeroderma pigmentosum

Zhou, X. A., Khan, S. G., Tamura, D., Ueda, T., Boyle, J., Compe, E., Egly, J., DiGiovanna, J. J., & Kraemer, K. H. (2012) · European Journal of Human Genetics · doi:10.1038/ejhg.2012.246 · Cited by 31

Dysregulation of the Peroxisome Proliferator-Activated Receptor Target Genes by XPD Mutations

Compe, E., Drané, P., Laurent, C., Diderich, K. E. M., Braun, C., Hoeijmakers, J. H. J., & Egly, J. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.14.6065-6076.2005 · Cited by 139

Both XPD alleles contribute to the phenotype of compound heterozygote xeroderma pigmentosum patients

Ueda, T., Compe, E., Catez, P., Kraemer, K. H., & Egly, J. (2009) · The Journal of Experimental Medicine · doi:10.1084/jem.20091892 · Cited by 50

Mutations in the XPD helicase gene result in XP and TTD phenotypes, preventing interaction between XPD and the p44 subunit of TFIIH

Coin, F., Marinoni, J., Rodolfo, C., Fribourg, S., Pedrini, A. M., & Egly, J. (1998) · Nature Genetics · doi:10.1038/2491 · Cited by 350