XPC deficiency increases risk of hematologic malignancies through mutator phenotype and characteristic mutational signature von Yurchenko, Andrey A., Padioleau, Ismael, Matkarimov, Bakhyt T., Soulier, Jean, Sarasin, Alain, Nikolaev, Sergey

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UVSSA and USP7: new players regulating transcription-coupled nucleotide excision repair in human cells von Sarasin, Alain

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Increased risk of internal tumors in DNA repair-deficient xeroderma pigmentosum patients: analysis of four international cohorts von Nikolaev, Sergey, Yurchenko, Andrey A, Sarasin, Alain

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Defective transcription of ATF3 responsive genes, a marker for Cockayne Syndrome von Epanchintsev, Alexey, Rauschendorf, Marc-Alexander, Costanzo, Federico, Calmels, Nadege, Obringer, Cathy, Sarasin, Alain, Coin, Frederic, Laugel, Vincent, Egly, Jean-Marc

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BRN2 is a non-canonical melanoma tumor-suppressor von Hamm, Michael, Sohier, Pierre, Petit, Valérie, Raymond, Jérémy H., Delmas, Véronique, Le Coz, Madeleine, Gesbert, Franck, Kenny, Colin, Aktary, Zackie, Pouteaux, Marie, Rambow, Florian, Sarasin, Alain, Charoenchon, Nisamanee, Bellacosa, Alfonso, Sanchez-del-Campo, Luis, Mosteo, Laura, Lauss, Martin, Meijer, Dies, Steingrimsson, Eirikur, Jönsson, Göran B., Cornell, Robert A., Davidson, Irwin, Goding, Colin R., Larue, Lionel

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Reversal of mitochondrial defects with CSB-dependent serine protease inhibitors in patient cells of the progeroid Cockayne syndrome von Chatre, Laurent, Biard, Denis S. F., Sarasin, Alain, Ricchetti, Miria

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How history and geography may explain the distribution in the Comorian archipelago of a novel mutation in DNA repair-deficient xeroderma pigmentosum patients von Sarasin, Alain, Munier, Patrick, Cartault, Francois

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An overview of the mechanisms of mutagenesis and carcinogenesis von Sarasin, Alain

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Genomic mutation landscape of skin cancers from DNA repair-deficient xeroderma pigmentosum patients von Yurchenko, Andrey A., Rajabi, Fatemeh, Braz-Petta, Tirzah, Fassihi, Hiva, Lehmann, Alan, Nishigori, Chikako, Wang, Jinxin, Padioleau, Ismael, Gunbin, Konstantin, Panunzi, Leonardo, Morice-Picard, Fanny, Laplante, Pierre, Robert, Caroline, Kannouche, Patricia L., Menck, Carlos F. M., Sarasin, Alain, Nikolaev, Sergey I.

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Corrigendum: Expression of constitutive fusion of ubiquitin to PCNA restores the level of immunoglobulin A/T mutations during somatic hypermutation in the Ramos cell line von Lerner, Leticia K, Bonte, Dorine, Le Guillou, Morwenna, Mohammad, Mahwish Mian, Kasraian, Zeinab, Sarasin, Alain, Despras, Emmanuelle, Aoufouchi, Said

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Translesion synthesis mechanisms depend on the nature of DNA damage in UV-irradiated human cells von Quinet, Annabel, Martins, Davi Jardim, Vessoni, Alexandre Teixeira, Biard, Denis, Sarasin, Alain, Stary, Anne, Menck, Carlos Frederico Martins

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Skin Tumors Induced by Sorafenib; Paradoxic RAS―RAF Pathway Activation and Oncogenic Mutations of HRAS, TP53, and TGFBR1 von ARNAULT, Jean Philippe, MATEUS, Christine, ANDRE, Jocelyne, KAMSU-KOM, Nyam, BOUSSEMART, Lise, LACROIX, Ludovic, SPATZ, Alain, EGGERMONT, Alexander M, DRUILLENNEC, Sabine, VAGNER, Stephan, EYCHENE, Alain, DUMAZ, Nicolas, ESCUDIER, Bernard, ROBERT, Caroline, TOMASIC, Gorana, WECHSLER, Janine, HOLLVILLE, Emilie, SORIA, Jean-Charles, MALKA, David, SARASIN, Alain, LARCHER, Magalie

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Gene Expression Profiling of Primary Cutaneous Melanoma and Clinical Outcome von Winnepenninckx, Véronique, Lazar, Vladimir, Michiels, Stefan, Dessen, Philippe, Stas, Marguerite, Alonso, Soledad R., Avril, Marie-Françoise, Ortiz Romero, Pablo L., Robert, Thomas, Balacescu, Ovidiu, Eggermont, Alexander M. M., Lenoir, Gilbert, Sarasin, Alain, Tursz, Thomas, van den Oord, Joost J., Spatz, Alain

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New Functional Signatures for Understanding Melanoma Biology from Tumor Cell Lineage-Specific Analysis von Rambow, Florian, Job, Bastien, Petit, Valérie, Gesbert, Franck, Delmas, Véronique, Seberg, Hannah, Meurice, Guillaume, Van Otterloo, Eric, Dessen, Philippe, Robert, Caroline, Gautheret, Daniel, Cornell, Robert A., Sarasin, Alain, Larue, Lionel

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The French Cohort of DNA Repair-Deficient Xeroderma Pigmentosum Patients: Risk of Hematological Malignancies von Sarasin, Alain

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Targeted gene therapy of xeroderma pigmentosum cells using meganuclease and TALEN von Dupuy, Aurélie, Valton, Julien, Leduc, Sophie, Armier, Jacques, Galetto, Roman, Gouble, Agnès, Lebuhotel, Céline, Stary, Anne, Pâques, Frédéric, Duchateau, Philippe, Sarasin, Alain, Daboussi, Fayza

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Transcriptional mutagenesis induced by 8-oxoguanine in mammalian cells von Brégeon, Damien, Peignon, Paul-Antoine, Sarasin, Alain

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ERCC1 Codon 118 Polymorphism Is a Predictive Factor for the Tumor Response to Oxaliplatin/5-Fluorouracil Combination Chemotherapy in Patients with Advanced Colorectal Cancer von VIGUIER, Jérome, BOIGE, Valérie, MIQUEL, Catherine, POCARD, Marc, GIRAUDEAU, Bruno, SABOUNN, Jean-Christophe, DUCREUX, Michel, SARASIN, Alain, PRAZ, Francoise

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Incidence of DNA repair deficiency disorders in western Europe: Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy von Kleijer, Wim J., Laugel, Vincent, Berneburg, Mark, Nardo, Tiziana, Fawcett, Heather, Gratchev, Alexei, Jaspers, Nicolaas G.J., Sarasin, Alain, Stefanini, Miria, Lehmann, Alan R.

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Large deletions in immunoglobulin genes are associated with a sustained absence of DNA Polymerase η von Lerner, Leticia K., Nguyen, Thuy V., Castro, Ligia P., Vilar, Juliana B., Munford, Veridiana, Le Guillou, Morwenna, Mohammad, Mahwish Mian, Vergé, Véronique, Rosselli, Filippo, Menck, Carlos F. M., Sarasin, Alain, Aoufouchi, Said

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