DNA Repair in Mammalian Cells von Robertson, A. B, Klungland, A, Rognes, T, Leiros, I

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Second pathway for completion of human DNA base excision-repair: reconstitution with purified proteins and requirement for DNase IV (FEN1) von Klungland, Arne, Lindahl, Tomas

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Repair of methyl lesions in DNA and RNA by oxidative demethylation von Falnes, P.Ø, Klungland, A, Alseth, I

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Deficiency of the Cockayne syndrome B (CSB) gene aggravates the genomic instability caused by endogenous oxidative DNA base damage in mice von TRAPP, C, REITE, K, KLUNGLAND, A, EPE, B

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Repair and mutagenesis at oxidized DNA lesions in the developing brain of wild-type and Ogg1-/- mice von LARSEN, E, REITE, K, NESSE, G, GRAN, C, SEEBERG, E, KLUNGLAND, A

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Reconstitution of DNA base excision‐repair with purified human proteins: interaction between DNA polymerase beta and the XRCC1 protein von Kubota, Y., Nash, R. A., Klungland, A., Schär, P., Barnes, D. E., Lindahl, T.

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Tolerated wobble mutations in siRNAs decrease specificity, but can enhance activity in vivo von Holen, Torgeir, Moe, Svein Erik, Sørbø, Jan Gunnar, Meza, Trine J., Ottersen, Ole Petter, Klungland, Arne

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DNA Repair in Mammalian Cells: Base excision repair: the long and short of it von Robertson, A. B., Klungland, A., Rognes, T., Leiros, I.

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Genome instability and DNA damage accumulation in gene-targeted mice von Nordstrand, L.M, Ringvoll, J, Larsen, E, Klungland, A

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Oxidative damage to purines in DNA: Role of mammalian Ogg1 von Klungland, Arne, Bjelland, Svein

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A novel splice site mutation in the Cockayne syndrome group A gene in two siblings with Cockayne syndrome von Kleppa, L, Kanavin, Ø.J, Klungland, A, Strømme, P

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Epitranscriptomic regulation in bladder cancer von Ougland, R., Monshaugen, I., Su, Z., Dutta, A., Klungland, A.

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P10.12.A CDK12/CDK13 inhibition disrupts a transcriptional program critical for glioblastoma survival von Lier, S, Rein, I, Lund, S, Lång, A, Lång, E, Meyer, N, Dutta, A, Anand, S, Nesse, G, Johansen, R, Klungland, A, Rinholm, J, Bøe, S, Anand, A, Pollard, S, Lerdrup, M, Pandey, D

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Accumulation of Premutagenic DNA Lesions in Mice Defective in Removal of Oxidative Base Damage von Klungland, Arne, Rosewell, Ian, Hollenbach, Stephan, Larsen, Elisabeth, Daly, Graham, Epe, Bernd, Seeberg, Erling, Lindahl, Tomas, Barnes, Deborah E.

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5-Formyluracil and its nucleoside derivatives confer toxicity and mutagenicity to mammalian cells by interfering with normal RNA and DNA metabolism von Klungland, A, Paulsen, R, Rolseth, V, Yamada, Y, Ueno, Y, Wiik, P, Matsuda, A, Seeberg, E, Bjelland, S

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Neil1 is a genetic modifier of somatic and germline CAG trinucleotide repeat instability in R6/1 mice von MØLLERSEN, Linda, ROWE, Alexander D, ILLUZZI, Jennifer L, HILDRESTRAND, Gunn A, GERHOLD, Katharina J, TVETERAS, Linda, BJØLGERUD, Anja, WILSON, David M, BJØRAS, Magnar, KLUNGLAND, Arne

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STIM1 R304W causes muscle degeneration and impaired platelet activation in mice von Gamage, Thilini H., Gunnes, Gjermund, Lee, Robert Hugh, Louch, William Edward, Holmgren, Asbjørn, Bruton, Joseph D., Lengle, Emma, Kolstad, Terje R. Selnes, Revold, Tobias, Amundsen, Silja Svanstrøm, Dalen, Knut Tomas, Holme, Pål Andre, Tjønnfjord, Geir Erland, Christensen, Geir, Westerblad, Håkan, Klungland, Arne, Bergmeier, Wolfgang, Misceo, Doriana, Frengen, Eirik

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Proliferation Failure and Gamma Radiation Sensitivity of Fen1 Null Mutant Mice at the Blastocyst Stage von Larsen, Elisabeth, Gran, Christine, Saether, Barbro Elisabet, Seeberg, Erling, Klungland, Arne

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Spectrum of mutations induced by methyl and ethyl methanesulfonate at the hprt locus of normal and tag expressing Chinese hamster fibroblasts von Klungland, A., Laake, K., Hoff, E., Seeberg, E.

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Deletion of mouse Alkbh7 leads to obesity von Solberg, Anja, Robertson, Adam B, Aronsen, Jan Magnus, Rognmo, Øivind, Sjaastad, Ivar, Wisløff, Ulrik, Klungland, Arne

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