His main research concerns Molecular biology, Biochemistry, DNA repair, DNA glycosylase and Cell biology. Arne Klungland has researched Molecular biology in several fields, including Gene knockout, Barrier function and Knockout mouse. His study on Transfer RNA, DNA ligase, DNA and Wobble base pair is often connected to Selenocysteine as part of broader study in Biochemistry.
As part of one scientific family, Arne Klungland deals mainly with the area of DNA, narrowing it down to issues related to the Gene, and often Endogeny. His DNA repair study frequently draws connections to other fields, such as DNA damage. His studies deal with areas such as RNA, Messenger RNA and Demethylation as well as Cell biology.
His primary scientific interests are in Cell biology, Molecular biology, DNA, DNA repair and Biochemistry. His Cell biology research is multidisciplinary, incorporating perspectives in RNA, Messenger RNA and Epigenetics. He interconnects RNA methylation and N6-Methyladenosine in the investigation of issues within Messenger RNA.
Arne Klungland combines subjects such as Wild type, DNA glycosylase, DNA-formamidopyrimidine glycosylase and Knockout mouse with his study of Molecular biology. His DNA study combines topics in areas such as 5-Hydroxymethylcytosine, Computational biology and Gene. His DNA repair research includes elements of Polymerase, DNA damage and Mitochondrial DNA.
Arne Klungland mostly deals with Cell biology, DNA, RNA, Epigenetics and DNA glycosylase. His study in the field of Neurogenesis is also linked to topics like Maternal to zygotic transition. DNA is a subfield of Biochemistry that Arne Klungland investigates.
In his study, which falls under the umbrella issue of RNA, DNA methylation and AlkB is strongly linked to Methylation. His research integrates issues of Base excision repair, Thymine, Cytosine and Molecular biology in his study of DNA glycosylase. His studies in Molecular biology integrate themes in fields like Haematopoiesis and Hematopoietic stem cell.
Arne Klungland mostly deals with Cell biology, RNA, Messenger RNA, Biochemistry and Transfer RNA. Many of his research projects under Cell biology are closely connected to Maternal to zygotic transition with Maternal to zygotic transition, tying the diverse disciplines of science together. His study in RNA is interdisciplinary in nature, drawing from both Methylation and DNA.
His Messenger RNA study incorporates themes from RNA methylation, N6-Methyladenosine and Demethylation. His study in DNA repair, DNA demethylation and Base excision repair is carried out as part of his Biochemistry studies. His Base excision repair research incorporates themes from DNA glycosylase, Nucleotide excision repair and Methylated DNA immunoprecipitation.
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ALKBH5 Is a Mammalian RNA Demethylase that Impacts RNA Metabolism and Mouse Fertility
Guanqun Zheng;John Arne Dahl;Yamei Niu;Peter Fedorcsak.
Molecular Cell (2013)
ACCUMULATION OF PREMUTAGENIC DNA LESIONS IN MICE DEFECTIVE IN REMOVAL OF OXIDATIVE BASE DAMAGE
Arne Klungland;Ian Rosewell;Stephan Hollenbach;Elisabeth Larsen.
Proceedings of the National Academy of Sciences of the United States of America (1999)
Second pathway for completion of human DNA base excision‐repair: reconstitution with purified proteins and requirement for DNase IV (FEN1)
Arne Klungland;Tomas Lindahl.
The EMBO Journal (1997)
Reconstitution of DNA base excision-repair with purified human proteins: interaction between DNA polymerase beta and the XRCC1 protein.
Y Kubota;R A Nash;A Klungland;P Schär.
The EMBO Journal (1996)
DNA repair in mammalian cells: Base excision repair: the long and short of it.
A. B. Robertson;A. Klungland;T. Rognes;I. Leiros.
Cellular and Molecular Life Sciences (2009)
Post-translational modification of poly(ADP-ribose) polymerase induced by DNA strand breaks.
Tomas Lindahl;Masahiko S. Satoh;Guy G. Poirier;Arne Klungland.
Trends in Biochemical Sciences (1995)
A majority of m6A residues are in the last exons, allowing the potential for 3′ UTR regulation
Shengdong Ke;Endalkachew A. Alemu;Claudia Mertens;Emily Conn Gantman.
Genes & Development (2015)
OGG1 initiates age-dependent CAG trinucleotide expansion in somatic cells
Irina V. Kovtun;Yuan Liu;Magnar Bjoras;Arne Klungland.
Nature (2007)
Molecular cloning and functional expression of a human cDNA encoding the antimutator enzyme 8-hydroxyguanine-DNA glycosylase
Teresa Roldán-Arjona;Ying-Fei Wei;Kenneth C. Carter;Arne Klungland.
Proceedings of the National Academy of Sciences of the United States of America (1997)
Repair of 8-Oxodeoxyguanosine Lesions in Mitochondrial DNA Depends on the Oxoguanine DNA Glycosylase (OGG1) Gene and 8-Oxoguanine Accumulates in the Mitochondrial DNA of OGG1-defective Mice
Nadja C. de Souza-Pinto;Lars Eide;Barbara A. Hogue;Tanja Thybo.
Cancer Research (2001)
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