FANCI functions as a repair/apoptosis switch in response to DNA crosslinks von Shah, Richa B., Kernan, Jennifer L., van Hoogstraten, Anya, Ando, Kiyohiro, Li, Yuanyuan, Belcher, Alicia L., Mininger, Ivy, Bussenault, Andrei M., Raman, Renuka, Ramanagoudr-Bhojappa, Ramanagouda, Huang, Tony T., D’Andrea, Alan D., Chandrasekharappa, Settara C., Aggarwal, Aneel K., Thompson, Ruth, Sidi, Samuel

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Rescue of progeria in trichothiodystrophy by homozygous lethal Xpd alleles von Andressoo, Jaan-Olle, Jans, Judith, de Wit, Jan, Coin, Frederic, Hoogstraten, Deborah, van de Ven, Marieke, Toussaint, Wendy, Huijmans, Jan, Thio, H Bing, van Leeuwen, Wibeke J, de Boer, Jan, Egly, Jean-Marc, Hoeijmakers, Jan H J, van der Horst, Gijsbertus T J, Mitchell, James R

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First Reported Patient with Human ERCC1 Deficiency Has Cerebro-Oculo-Facio-Skeletal Syndrome with a Mild Defect in Nucleotide Excision Repair and Severe Developmental Failure von Jaspers, Nicolaas G.J., Raams, Anja, Silengo, Margherita Cirillo, Wijgers, Nils, Niedernhofer, Laura J., Robinson, Andria Rasile, Giglia-Mari, Giuseppina, Hoogstraten, Deborah, Kleijer, Wim J., Hoeijmakers, Jan H.J., Vermeulen, Wim

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Therapeutic approaches to gastroesophageal junction adenocarcinomas von Blom, Rachel L.G.M., Bogush, Tatiana, Brücher, Björn L.D.M., Chang, Andrew C., Davydov, Mikhail, Dudko, Evgeny, Leong, Trevor, Polotsky, Boris, Swanson, Paul E., van Rossum, Peter S.N., Ruurda, Jelle P., Sagaert, Xavier, Tjulandin, Sergei, Schraepen, Marie-Celine, Sosef, Meindert N., van Hillegersberg, Richard

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Development of ipilimumab: a novel immunotherapeutic approach for the treatment of advanced melanoma von Wolchok, Jedd D., Hodi, F. Stephen, Weber, Jeffrey S., Allison, James P., Urba, Walter J., Robert, Caroline, O'Day, Steven J., Hoos, Axel, Humphrey, Rachel, Berman, David M., Lonberg, Nils, Korman, Alan J.

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DNA repair-deficient diseases, xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy von Lehmann, Alan R.

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Using digital notifications to improve attendance in clinic: systematic review and meta-analysis von Robotham, Dan, Satkunanathan, Safarina, Reynolds, John, Stahl, Daniel, Wykes, Til

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The Epigenetic Role of Vitamin C in Neurodevelopment von Coker, Sharna J, Smith-Díaz, Carlos C, Dyson, Rebecca M, Vissers, Margreet C M, Berry, Mary J

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Biofilm formation: mechanistic insights and therapeutic targets von Wang, Xinyu, Liu, Ming, Yu, Chuanjiang, Li, Jing, Zhou, Xikun

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Genome instability syndromes caused by impaired DNA repair and aberrant DNA damage responses von Terabayashi, Takeshi, Hanada, Katsuhiro

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Synaptic Plasticity Dysfunctions in the Pathophysiology of 22q11 Deletion Syndrome: Is There a Role for Astrocytes? von de Oliveira Figueiredo, Eva Cristina, Bondiolotti, Bianca Maria, Laugeray, Anthony, Bezzi, Paola

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Uncommon nucleotide excision repair phenotypes revealed by targeted high-throughput sequencing von Calmels, Nadège, Greff, Géraldine, Obringer, Cathy, Kempf, Nadine, Gasnier, Claire, Tarabeux, Julien, Miguet, Marguerite, Baujat, Geneviève, Bessis, Didier, Bretones, Patricia, Cavau, Anne, Digeon, Béatrice, Doco-Fenzy, Martine, Doray, Bérénice, Feillet, François, Gardeazabal, Jesus, Gener, Blanca, Julia, Sophie, Llano-Rivas, Isabel, Mazur, Artur, Michot, Caroline, Renaldo-Robin, Florence, Rossi, Massimiliano, Sabouraud, Pascal, Keren, Boris, Depienne, Christel, Muller, Jean, Mandel, Jean-Louis, Laugel, Vincent

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TBX1 Is Responsible for Cardiovascular Defects in Velo-Cardio-Facial/DiGeorge Syndrome von Merscher, Sandra, Funke, Birgit, Epstein, Jonathan A., Heyer, Joerg, Puech, Anne, Lu, Min Min, Xavier, Ramnik J., Demay, Marie B., Russell, Robert G., Factor, Stephen, Tokooya, Kazuhito, Jore, Bruno St, Lopez, Melissa, Pandita, Raj K., Lia, Marie, Carrion, Danaise, Xu, Hui, Schorle, Hubert, Kobler, James B., Scambler, Peter, Wynshaw-Boris, Anthony, Skoultchi, Arthur I., Morrow, Bernice E., Kucherlapati, Raju

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A comprehensive description of the severity groups in Cockayne syndrome von Natale, Valerie

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Persistence of repair proteins at unrepaired DNA damage distinguishes diseases with ERCC2 (XPD) mutations: cancer‐prone xeroderma pigmentosum vs. non‐cancer‐prone trichothiodystrop... von Boyle, Jennifer, Ueda, Takahiro, Oh, Kyu‐Seon, Imoto, Kyoko, Tamura, Deborah, Jagdeo, Jared, Khan, Sikandar G., Nadem, Carine, DiGiovanna, John J., Kraemer, Kenneth H.

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TFIIH Transcription Factor, a Target for the Rift Valley Hemorrhagic Fever Virus von Le May, Nicolas, Dubaele, Sandy, De Santis, Luca Proietti, Billecocq, Agnès, Bouloy, Michèle, Egly, Jean-Marc

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Cerebro-oculo-facio-skeletal syndrome: three additional cases with CSB mutations, new diagnostic criteria and an approach to investigation von Laugel, V, Dalloz, C, Tobias, E S, Tolmie, J L, Martin-Coignard, D, Drouin-Garraud, V, Valayannopoulos, V, Sarasin, A, Dollfus, H

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Multiple roles of ubiquitination in the control of nucleotide excision repair von Nouspikel, Thierry

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Nucleotide excision repair and cancer von Leibeling, Diana, Laspe, Petra, Emmert, Steffen

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Constructive rescue of TFIIH instability by an alternative isoform of XPD derived from a mutated XPD allele in mild but not severe XP-D/CS von Horibata, Katsuyoshi, Kono, Sayaka, Ishigami, Chie, Zhang, Xue, Aizawa, Madoka, Kako, Yuko, Ishii, Takuma, Kosaki, Rika, Saijo, Masafumi, Tanaka, Kiyoji

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