Structural insight into repair of alkylated DNA by a new superfamily of DNA glycosylases comprising HEAT-like repeats

por Dalhus, Bjørn, Helle, Ina Høydal, Backe, Paul H., Alseth, Ingrun, Rognes, Torbjørn, Bjørås, Magnar, Laerdahl, Jon K.
Publicado 2007

Structures of Endonuclease V with DNA Reveal Initiation of Deaminated Adenine Repair

por Dalhus, Bjorn, Arvai, Andrew S., Rosnes, Ida, Olsen, Oyvind E., Backe, Paul H., Alseth, Ingrun, Gao, Honghai, Cao, Weiguo, Tainer, John A., Bjoras, Magnar
Publicado 2009

Identification and Characterization of Novel Mutations in the Human Gene Encoding the Catalytic Subunit Calpha of Protein Kinase A (PKA)

por Søberg, Kristoffer, Larsen, Anja C. V., Diskar, Mandy, Backe, Paul H., Bjørås, Magnar, Jahnsen, Tore, Laerdahl, Jon K., Rognes, Torbjørn, Herberg, Friedrich W., Skålhegg, Bjørn S.
Publicado 2012

Hallmarks of Processivity in Glycoside Hydrolases from Crystallographic and Computational Studies of the Serratia marcescens Chitinases

por Payne, Christina M., Baban, Jamil, Horn, Svein J., Backe, Paul H., Arvai, Andrew S., Dalhus, Bjørn, Bjørås, Magnar, Eijsink, Vincent G. H., Sørlie, Morten, Beckham, Gregg T., Vaaje-Kolstad, Gustav
Publicado 2012

Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis

por Rydning, Siri L, Koht, Jeanette, Sheng, Ying, Sowa, Piotr, Hjorthaug, Hanne S, Wedding, Iselin M, Erichsen, Anne Kjersti, Hovden, Inger Anette, Backe, Paul H, Tallaksen, Chantal M E, Vigeland, Magnus D, Selmer, Kaja K
Publicado en Brain (2019)

A potential founder variant in CARMIL2/RLTPR in three Norwegian families with warts, molluscum contagiosum, and T‐cell dysfunction

por Sorte, Hanne S., Osnes, Liv T., Fevang, Børre, Aukrust, Pål, Erichsen, Hans C., Backe, Paul H., Abrahamsen, Tore G., Kittang, Ole B., Øverland, Torstein, Jhangiani, Shalini N., Muzny, Donna M., Vigeland, Magnus D., Samarakoon, Pubudu, Gambin, Tomasz, Akdemir, Zeynep H. C., Gibbs, Richard A., Rødningen, Olaug K., Lyle, Robert, Lupski, James R., Stray‐Pedersen, Asbjørg
Publicado en Mol Genet Genomic Med (2016)

PGM3 Mutations Cause a Congenital Disorder of Glycosylation with Severe Immunodeficiency and Skeletal Dysplasia

por Stray-Pedersen, Asbjørg, Backe, Paul H., Sorte, Hanne S., Mørkrid, Lars, Chokshi, Niti Y., Erichsen, Hans Christian, Gambin, Tomasz, Elgstøen, Katja B.P., Bjørås, Magnar, Wlodarski, Marcin W., Krüger, Marcus, Jhangiani, Shalini N., Muzny, Donna M., Patel, Ankita, Raymond, Kimiyo M., Sasa, Ghadir S., Krance, Robert A., Martinez, Caridad A., Abraham, Shirley M., Speckmann, Carsten, Ehl, Stephan, Hall, Patricia, Forbes, Lisa R., Merckoll, Else, Westvik, Jostein, Nishimura, Gen, Rustad, Cecilie F., Abrahamsen, Tore G., Rønnestad, Arild, Osnes, Liv T., Egeland, Torstein, Rødningen, Olaug K., Beck, Christine R., Boerwinkle, Eric A., Gibbs, Richard A., Lupski, James R., Orange, Jordan S., Lausch, Ekkehart, Hanson, I. Celine
Publicado 2014