Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Christine G. Neurauter"'
Autor:
Veslemøy Rolseth, Luisa Luna, Ann Karin Olsen, Rajikala Suganthan, Katja Scheffler, Christine G. Neurauter, Ying Esbensen, Anna Kuśnierczyk, Gunn A. Hildrestrand, Anne Graupner, Jill M. Andersen, Geir Slupphaug, Arne Klungland, Hilde Nilsen, Magnar Bjørås
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-12 (2017)
Abstract Base excision repair (BER) is a major pathway for removal of DNA base lesions and maintenance of genomic stability, which is essential in cancer prevention. DNA glycosylases recognize and remove specific lesions in the first step of BER. The
Externí odkaz:
https://doaj.org/article/5c917068e02c43e0970c726380db6068
Autor:
Christine G. Neurauter, Vuk Palibrk, Lili Zhang, Pål Sætrom, William E. Louch, Ingunn Østlie, Sverre-Henning Brorson, Lars Gullestad, Junbai Wang, Ivar Sjaastad, Ingrid Kristine Ohm, Katrine Alfsnes, Magnar Bjørås, Jonas Øgaard, Geir Christensen, Arne Yndestad, Per Ole Iversen, Arnt E. Fiane, Maria Belland Olsen, Geir Slupphaug, Gunn A. Hildrestrand, Pål Aukrust, Jostein Johansen, Arne Klungland, Anna Kuśnierczyk, Leif Erik Vinge, Luisa Luna, Alexandra Vanessa Finsen, Katja Scheffler
Publikováno v:
Cell reports
Myocardial infarction (MI) triggers a reparative response involving fibroblast proliferation and differentiation driving extracellular matrix modulation necessary to form a stabilizing scar. Recently, it was shown that a genetic variant of the base e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::398a3496b35088cd0c3b7fe83fe856d7
https://hdl.handle.net/11250/2478007
https://hdl.handle.net/11250/2478007
Autor:
Lars Eide, Magnar Bjørås, Kirsten Krohg-Sørensen, Göran K. Hansson, Lasse Folkersen, Daniel F. J. Ketelhuth, Rolf K. Berge, Ingunn Østlie, Bodil Bjørndal, Ulf Hedin, Jeroen J. T. Otten, Tuva B. Dahl, Erik A.L. Biessen, Rajikala Suganthan, Gunn A. Hildrestrand, Per Ole Iversen, Geir Slupphaug, Thor Ueland, Katja Scheffler, Sverre Holm, Asbjørn Svardal, Tonje Skarpengland, Anna Kuśnierczyk, Pål Aukrust, Ole Kristoffer Olstad, Anna M. Lundberg, Christine G. Neurauter, Ståle Nygård, Mona Skjelland, Ida Gregersen, Luisa Luna, Bente Halvorsen, Filip M. Segers
Publikováno v:
Scientific Reports
Skarpengland, T, Holm, S, Scheffler, K, Gregersen, I, Dahl, T B, Suganthan, R, Segers, F M, Østlie, I, Otten, J J T, Luna, L, Ketelhuth, D F J, Lundberg, A M, Neurauter, C G, Hildrestrand, G, Skjelland, M, Bjørndal, B, Svardal, A M, Iversen, P O, Hedin, U, Nygård, S, Olstad, O K, Krohg-Sorensen, K, Slupphaug, G, Eide, L, Kusnierczyk, A, Folkersen, L, Ueland, T, Berge, R K, Hansson, G K, Biessen, E A L, Halvorsen, B, Bjørås, M & Aukrust, P 2016, ' Neil3-dependent base excision repair regulates lipid metabolism and prevents atherosclerosis in Apoe-deficient mice ', Scientific Reports, vol. 6, 28337 . https://doi.org/10.1038/srep28337
Scientific Reports, 6:28337. Nature Publishing Group
6:28337
Skarpengland, T, Holm, S, Scheffler, K, Gregersen, I, Dahl, T B, Suganthan, R, Segers, F M, Østlie, I, Otten, J J T, Luna, L, Ketelhuth, D F J, Lundberg, A M, Neurauter, C G, Hildrestrand, G, Skjelland, M, Bjørndal, B, Svardal, A M, Iversen, P O, Hedin, U, Nygård, S, Olstad, O K, Krohg-Sorensen, K, Slupphaug, G, Eide, L, Kusnierczyk, A, Folkersen, L, Ueland, T, Berge, R K, Hansson, G K, Biessen, E A L, Halvorsen, B, Bjørås, M & Aukrust, P 2016, ' Neil3-dependent base excision repair regulates lipid metabolism and prevents atherosclerosis in Apoe-deficient mice ', Scientific Reports, vol. 6, 28337 . https://doi.org/10.1038/srep28337
Scientific Reports, 6:28337. Nature Publishing Group
6:28337
Increasing evidence suggests that oxidative DNA damage accumulates in atherosclerosis. Recently, we showed that a genetic variant in the human DNA repair enzyme NEIL3 was associated with increased risk of myocardial infarction. Here, we explored the
Autor:
Luisa Luna, Gunn A. Hildrestrand, Yngve Sejersted, Rajikala Suganthan, Christine G. Neurauter, Magnar Bjørås, Silje Zandstra Krokeide, David Kunke, Veslemøy Rolseth
Publikováno v:
Biochimica et biophysica acta. 1833(5)
7,8-Dihydro-8-oxoguanine (8-oxoG) is one of the most common oxidative base lesions in normal tissues induced by a variety of endogenous and exogenous agents. Hydantoins are products of 8-oxoG oxidation and as 8-oxoG, they have been shown to be mutage
Autor:
Veslemøy Rolseth, Cynthia J. Burrows, Rajikala Suganthan, David Kunke, Ola Didrik Saugstad, Gunn A. Hildrestrand, Christine G. Neurauter, Aaron M. Fleming, Luisa Luna, Yngve Sejersted, Monica Atneosen-Åsegg, Silje Zandstra Krokeide, Magnar Bjørås
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 108(46)
Neural stem/progenitor cell proliferation and differentiation are required to replace damaged neurons and regain brain function after hypoxic-ischemic events. DNA base lesions accumulating during hypoxic-ischemic stress are removed by DNA glycosylase
Autor:
Christine G. Neurauter, Stefan Krauss, Gunn A. Hildrestrand, Dzung B. Diep, Luisa Luna, Cesilie Granum Castellanos, Magnar Bjørås
Publikováno v:
BMC Neuroscience
BMC Neuroscience, Vol 10, Iss 1, p 45 (2009)
BMC Neuroscience, Vol 10, Iss 1, p 45 (2009)
Background The base excision repair pathway is responsible for repairing small DNA base lesions caused by endogenous and exogenous damaging agents. Repair is initiated by DNA glycosylases that recognize and remove the lesions. NEIL3 is one of 11 mamm
Autor:
Christine G. Neurauter, Arne Yndestad, Luisa Luna, Lars Eide, Rune Johansen Forstrøm, Magnar Bjørås, Pål Aukrust, Erik Øie, Leif Erik Vinge
Publikováno v:
Mutation research. 666(1-2)
Base excision repair (BER) is the major pathway to counteract the genotoxic effect of endogenous DNA damaging agents. The present study investigated the enzymatic activities and gene transcription of DNA glycosylases initiating BER in an experimental
Publikováno v:
DNA Repair. (4):401-409
Base excision repair (BER) is believed to be the predominant pathway for the repair of oxidative DNA damage. BER is initiated by lesion-specific DNA glycosylases that recognize and remove the damaged base. NEIL1, NEIL2 and NEIL3 are three mammalian m