Xeroderma pigmentosum von Lehmann, Alan R, McGibbon, David, Stefanini, Miria

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Malfunction of Nuclease ERCC1-XPF Results in Diverse Clinical Manifestations and Causes Cockayne Syndrome, Xeroderma Pigmentosum, and Fanconi Anemia von Kashiyama, Kazuya, Nakazawa, Yuka, Pilz, Daniela T., Guo, Chaowan, Shimada, Mayuko, Sasaki, Kensaku, Fawcett, Heather, Wing, Jonathan F., Lewin, Susan O., Carr, Lucinda, Li, Tao-Sheng, Yoshiura, Koh-ichiro, Utani, Atsushi, Hirano, Akiyoshi, Yamashita, Shunichi, Greenblatt, Danielle, Nardo, Tiziana, Stefanini, Miria, McGibbon, David, Sarkany, Robert, Fassihi, Hiva, Takahashi, Yoshito, Nagayama, Yuji, Mitsutake, Norisato, Lehmann, Alan R., Ogi, Tomoo

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Ubiquitin-family modifications in the replication of DNA damage von Lehmann, Alan R.

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Deep phenotyping of 89 xeroderma pigmentosum patients reveals unexpected heterogeneity dependent on the precise molecular defect von Fassihi, Hiva, Sethi, Mieran, Fawcett, Heather, Wing, Jonathan, Chandler, Natalie, Mohammed, Shehla, Craythorne, Emma, S. Morley, Ana M., Lim, Rongxuan, Turner, Sally, Henshaw, Tanya, Garrood, Isabel, Giunti, Paola, Hedderly, Tammy, Abiona, Adesoji, Naik, Harsha, Harrop, Gemma, McGibbon, David, Jaspers, Nicolaas G. J., Botta, Elena, Nardo, Tiziana, Stefanini, Miria, Young, Antony R., Sarkany, Robert P. E., Lehmann, Alan R.

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Xeroderma pigmentosum: overview of pharmacology and novel therapeutic strategies for neurological symptoms von Abeti, Rosella, Zeitlberger, Anna, Peelo, Colm, Fassihi, Hiva, Sarkany, Robert P E, Lehmann, Alan R, Giunti, Paola

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Three DNA Polymerases, Recruited by Different Mechanisms, Carry Out NER Repair Synthesis in Human Cells von Ogi, Tomoo, Limsirichaikul, Siripan, Overmeer, René M., Volker, Marcel, Takenaka, Katsuya, Cloney, Ross, Nakazawa, Yuka, Niimi, Atsuko, Miki, Yoshio, Jaspers, Nicolaas G., Mullenders, Leon H.F., Yamashita, Shunichi, Fousteri, Maria I., Lehmann, Alan R.

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Ubiquitin-Binding Domains in Y-Family Polymerases Regulate Translesion Synthesis von Bienko, Marzena, Green, Catherine M, Crosetto, Nicola, Rudolf, Fabian, Zapart, Grzegorz, Coull, Barry, Kannouche, Patricia, Wider, Gerhard, Peter, Matthias, Lehmann, Alan R, Hofmann, Kay, Dikic, Ivan

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Y-family DNA polymerases and their role in tolerance of cellular DNA damage von Sale, Julian E., Lehmann, Alan R., Woodgate, Roger

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Specialized interfaces of Smc5/6 control hinge stability and DNA association von Alt, Aaron, Dang, Hung Q., Wells, Owen S., Polo, Luis M., Smith, Matt A., McGregor, Grant A., Welte, Thomas, Lehmann, Alan R., Pearl, Laurence H., Murray, Johanne M., Oliver, Antony W.

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Trading Places: How Do DNA Polymerases Switch during Translesion DNA Synthesis? von Friedberg, Errol C., Lehmann, Alan R., Fuchs, Robert P.P.

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GTF2E2 Mutations Destabilize the General Transcription Factor Complex TFIIE in Individuals with DNA Repair-Proficient Trichothiodystrophy von Kuschal, Christiane, Botta, Elena, Orioli, Donata, Digiovanna, John J., Seneca, Sara, Keymolen, Kathelijn, Tamura, Deborah, Heller, Elizabeth, Khan, Sikandar G., Caligiuri, Giuseppina, Lanzafame, Manuela, Nardo, Tiziana, Ricotti, Roberta, Peverali, Fiorenzo A., Stephens, Robert, Zhao, Yongmei, Lehmann, Alan R., Baranello, Laura, Levens, David, Kraemer, Kenneth H., Stefanini, Miria

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Replication of damaged DNA by translesion synthesis in human cells von Lehmann, Alan R.

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Regulation of proliferating cell nuclear antigen ubiquitination in mammalian cells von Niimi, Atsuko, Brown, Stephanie, Sabbioneda, Simone, Kannouche, Patricia L, Scott, Andrew, Yasui, Akira, Green, Catherine M, Lehmann, Alan R

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Gaps and forks in DNA replication: Rediscovering old models von Lehmann, Alan R., Fuchs, Robert P.

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Human exonuclease 1 connects nucleotide excision repair (NER) processing with checkpoint activation in response to UV irradiation von Sertic, Sarah, Pizzi, Sara, Cloney, Ross, Lehmann, Alan R, Marini, Federica, Plevani, Paolo, Muzi-Falconi, Marco

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Hypomorphic PCNA mutation underlies a human DNA repair disorder von Baple, Emma L, Chambers, Helen, Cross, Harold E, Fawcett, Heather, Nakazawa, Yuka, Chioza, Barry A, Harlalka, Gaurav V, Mansour, Sahar, Sreekantan-Nair, Ajith, Patton, Michael A, Muggenthaler, Martina, Rich, Phillip, Wagner, Karin, Coblentz, Roselyn, Stein, Constance K, Last, James I, Taylor, A Malcolm R, Jackson, Andrew P, Ogi, Tomoo, Lehmann, Alan R, Green, Catherine M, Crosby, Andrew H

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A semi-automated non-radioactive system for measuring recovery of RNA synthesis and unscheduled DNA synthesis using ethynyluracil derivatives von Nakazawa, Yuka, Yamashita, Shunichi, Lehmann, Alan R., Ogi, Tomoo

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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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XRCC4 deficiency in human subjects causes a marked neurological phenotype but no overt immunodeficiency von Guo, Chaowan, PhD, Nakazawa, Yuka, PhD, Woodbine, Lisa, PhD, Björkman, Andrea, PhD, Shimada, Mayuko, BS, Fawcett, Heather, PhD, Jia, Nan, PhD, Ohyama, Kaname, PhD, Li, Tao-Sheng, MD, PhD, Nagayama, Yuji, MD, PhD, Mitsutake, Norisato, MD, PhD, Pan-Hammarström, Qiang, MD, PhD, Gennery, Andrew R., MD, Lehmann, Alan R., PhD, Jeggo, Penny A., PhD, Ogi, Tomoo, PhD

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Transcription Restores DNA Repair to Heterochromatin, Determining Regional Mutation Rates in Cancer Genomes von Zheng, Christina L., Wang, Nicholas J., Chung, Jongsuk, Moslehi, Homayoun, Sanborn, J. Zachary, Hur, Joseph S., Collisson, Eric A., Vemula, Swapna S., Naujokas, Agne, Chiotti, Kami E., Cheng, Jeffrey B., Fassihi, Hiva, Blumberg, Andrew J., Bailey, Celeste V., Fudem, Gary M., Mihm, Frederick G., Cunningham, Bari B., Neuhaus, Isaac M., Liao, Wilson, Oh, Dennis H., Cleaver, James E., LeBoit, Philip E., Costello, Joseph F., Lehmann, Alan R., Gray, Joe W., Spellman, Paul T., Arron, Sarah T., Huh, Nam, Purdom, Elizabeth, Cho, Raymond J.

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