O
Oddmund Bakke
Researcher at University of Oslo
Publications - 145
Citations - 9249
Oddmund Bakke is an academic researcher from University of Oslo. The author has contributed to research in topics: Endosome & CD74. The author has an hindex of 46, co-authored 143 publications receiving 8638 citations. Previous affiliations of Oddmund Bakke include SINTEF & Haukeland University Hospital.
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Journal ArticleDOI
Towards a systems understanding of MHC class I and MHC class II antigen presentation
TL;DR: A timely evaluation of the biology of antigen presentation and a survey of issues that are considered unresolved are presented.
Journal ArticleDOI
MHC class II-associated invariant chain contains a sorting signal for endosomal compartments.
TL;DR: The invariant chain (Ii) is a transmembrane protein that associates with the MHC class II molecules in the endoplasmic reticulum and it is proposed that Ii determines the intracellular transport route of these molecules.
Journal ArticleDOI
Post-replicative base excision repair in replication foci.
Marit Otterlei,Emma Warbrick,Toril A. Nagelhus,Terje Haug,Geir Slupphaug,Mansour Akbari,Per Arne Aas,Kristin Solum Steinsbekk,Oddmund Bakke,Hans E. Krokan +9 more
TL;DR: This work reports that the major nuclear uraci‐DNA glycosylase (UNG2) increases in S phase, during which it co‐localizes with incorporated BrdUrd in replication foci and demonstrates rapid post‐replicative removal of incorporated uracil by UNG2.
Journal ArticleDOI
Targeting of membrane proteins to endosomes and lysosomes
TL;DR: The pathways involved in targeting membrane proteins to lysosomes are extraordinarily complex and include routes to endosomes specified by sorting motifs in the cytoplasmic tails of the proteins that are recognized at the TGN or plasma membrane.
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Antigen presentation mediated by recycling of surface HLA-DR molecules
TL;DR: It is shown that presentation of immunodominant epitopes in the haemagglutinin protein of influenza virus and in myeiin basic protein correlates with recycling of surface HLA-DR molecules, and Hla-DR cytoplasmic tails are not required for the conventional presentation pathway, but jointly contribute a signal for an alternative pathway involving internalization of HLAs.