Member of the Norwegian Academy of Science and Letters Biochemistry, Biophysics, and Molecular Biology
His primary areas of investigation include Biochemistry, DNA repair, DNA glycosylase, Molecular biology and DNA. His study in Active site, Mutagenesis, Binding site, Excitatory Amino Acid Transporter 3 and SLC1A1 are all subfields of Biochemistry. His work carried out in the field of DNA repair brings together such families of science as Protein subunit, DNA damage and Cell biology.
Magnar Bjørås has researched DNA glycosylase in several fields, including Base excision repair, AP site, Nucleotide excision repair, Cell cycle and Transcription. His work investigates the relationship between Molecular biology and topics such as Chromatin that intersect with problems in Phosphoserine. His DNA study combines topics in areas such as RNA, Gene and Nucleic acid.
His primary areas of study are DNA repair, DNA glycosylase, Biochemistry, DNA and Molecular biology. His DNA repair research integrates issues from Gene expression, DNA damage, Mitochondrial DNA, DNA ligase and Cell biology. He interconnects Oxidative stress, Internal medicine and Endocrinology in the investigation of issues within DNA damage.
The study incorporates disciplines such as Base excision repair, Nucleotide excision repair and Transcription in addition to DNA glycosylase. His Base excision repair study deals with AP site intersecting with Schizosaccharomyces pombe. His DNA study also includes
Magnar Bjørås focuses on Cell biology, Gene, DNA, Virology and DNA damage. His Cell biology research is multidisciplinary, incorporating perspectives in Base excision repair, DNA repair, Gene expression and RNA. His studies examine the connections between Base excision repair and genetics, as well as such issues in DNA glycosylase, with regards to Transcription.
His DNA repair research is multidisciplinary, incorporating elements of Mutation and Ku80. The various areas that Magnar Bjørås examines in his Gene study include Phosphoglucomutase and Genome instability. His DNA study is related to the wider topic of Biochemistry.
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Cloning and expression of a rat brain L-glutamate transporter.
Gilia Pines;Niels C. Danbolt;Magnar Bjørås;Magnar Bjørås;Yumin Zhang.
Nature (1992)
Base Excision Repair
Hans E. Krokan;Magnar Bjørås.
Cold Spring Harbor Perspectives in Biology (2013)
The base excision repair pathway.
Erling Seeberg;Erling Seeberg;Lars Eide;Magnar Bjørås.
Trends in Biochemical Sciences (1995)
Human and bacterial oxidative demethylases repair alkylation damage in both RNA and DNA
Per Arne Aas;Marit Otterlei;Pål Ø. Falnes;Cathrine B. Vågbø.
Nature (2003)
OGG1 initiates age-dependent CAG trinucleotide expansion in somatic cells
Irina V. Kovtun;Yuan Liu;Magnar Bjoras;Arne Klungland.
Nature (2007)
Opposite base‐dependent reactions of a human base excision repair enzyme on DNA containing 7,8‐dihydro‐8‐oxoguanine and abasic sites
Magnar Bjørås;Luisa Luna;Barbro Johnsen;Elsebeth Hoff.
The EMBO Journal (1997)
Synergistic Actions of Ogg1 and Mutyh DNA Glycosylases Modulate Anxiety-like Behavior in Mice
Monica D. Bjørge;Gunn A. Hildrestrand;Katja Scheffler;Katja Scheffler;Rajikala Suganthan.
Cell Reports (2015)
Human DNA glycosylases of the bacterial Fpg/MutM superfamily: an alternative pathway for the repair of 8‐oxoguanine and other oxidation products in DNA
Ingrid Morland;Veslemøy Rolseth;Luisa Luna;Torbjørn Rognes.
Nucleic Acids Research (2002)
Broad histone H3K4me3 domains in mouse oocytes modulate maternal-to-zygotic transition
John Arne Dahl;Inkyung Jung;Håvard Aanes;Gareth D. Greggains.
Nature (2016)
New functions of XPC in the protection of human skin cells from oxidative damage
Mariarosaria D'Errico;Eleonora Parlanti;Massimo Teson;Bruno M Bernardes De Jesus.
The EMBO Journal (2006)
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