Oxidative DNA base damage and cancer susceptibility
- Prosjektnummer
- 2012083
- Ansvarlig person
- Magnar Bjørås
- Institusjon
- Oslo universitetssykehus HF
- Prosjektkategori
- Postdoktorstipend
- Helsekategori
- Cancer
- Forskningsaktivitet
- 1. Underpinning
Cockayne Syndrome group B protein stimulates NEIL2 DNA glycosylase activity.
Mech Ageing Dev 2014 Jan;135():1-14. Epub 2014 jan 7
PMID: 24406253
Fumarylacetoacetate inhibits the initial step of the base excision repair pathway: implication for the pathogenesis of tyrosinemia type I.
J Inherit Metab Dis 2013 Sep;36(5):773-8. Epub 2012 nov 9
PMID: 23138988
Human NEIL3 is mainly a monofunctional DNA glycosylase removing spiroimindiohydantoin and guanidinohydantoin.
DNA Repair (Amst) 2013 Dec;12(12):1159-64. Epub 2013 jun 5
PMID: 23755964
The human homolog of Escherichia coli endonuclease V is a nucleolar protein with affinity for branched DNA structures.
PLoS One 2012;7(11):e47466. Epub 2012 nov 5
PMID: 23139746
Oxygenation of the newborn: a molecular approach.
Neonatology 2012;101(4):315-25. Epub 2012 jun 1
PMID: 22940621
Biochemical mapping of human NEIL1 DNA glycosylase and AP lyase activities.
DNA Repair (Amst) 2012 Sep;11(9):766-73. Epub 2012 aug 1
PMID: 22858590
Release from quiescence stimulates the expression of human NEIL3 under the control of the Ras dependent ERK-MAP kinase pathway.
DNA Repair (Amst) 2012 Apr;11(4):401-9. Epub 2012 feb 23
PMID: 22365498
Hereditary tyrosinaemia type I. Studies on the molecular genetics and DNA repair enzymes
- Disputert:
- november 2012
- Hovedveileder:
- Magnar Bjørås
- Veslemøy Rolseth Postdoktorstipendiat
- Christine Gran Neurauter Prosjektdeltaker
eRapport er utarbeidet av Sølvi Lerfald og Reidar Thorstensen, Regionalt kompetansesenter for klinisk forskning, Helse Vest RHF, og videreutvikles av de fire RHF-ene i fellesskap, med støtte fra Helse Vest IKT
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