Aud Øvervatn

发表

p62/SQSTM1 forms protein aggregates degraded by autophagy and has a protective effect on huntingtin-induced cell death

Terje Johansen, Harald Stenmark, G. Bjørkøy, 2005, The Journal of cell biology.

p62/SQSTM1 Binds Directly to Atg8/LC3 to Facilitate Degradation of Ubiquitinated Protein Aggregates by Autophagy*

G. Bjørkøy, T. Lamark, A. Brech, 2007, Journal of Biological Chemistry.

A reporter cell system to monitor autophagy based on p62/SQSTM1

G. Bjørkøy, T. Lamark, Aud Øvervatn, 2010, Autophagy.

p62/SQSTM1 and ALFY interact to facilitate the formation of p62 bodies/ALIS and their degradation by autophagy

G. Bjørkøy, T. Lamark, A. Brech, 2010, Autophagy.

TRIM32, but not its muscular dystrophy-associated mutant, positively regulates and is targeted to autophagic degradation by p62/SQSTM1

V. Deretic, T. Lamark, Aud Øvervatn, 2019, Journal of Cell Science.

TRIM32, but not its muscular dystrophy-associated mutant, positively regulates and is targeted to autophagic degradation by p62/SQSTM1

V. Deretic, T. Lamark, Aud Øvervatn, 2019, Journal of Cell Science.

The FMRpolyGlycine Protein Mediates Aggregate Formation and Toxicity Independent of the CGG mRNA Hairpin in a Cellular Model for FXTAS

T. Lamark, A. Brech, Aud Øvervatn, 2019, Front. Genet..

FYCO1 is a Rab7 effector that binds to LC3 and PI3P to mediate microtubule plus end–directed vesicle transport

G. Bjørkøy, T. Lamark, A. Brech, 2010, The Journal of cell biology.

p62/SQSTM1 Is a Target Gene for Transcription Factor NRF2 and Creates a Positive Feedback Loop by Inducing Antioxidant Response Element-driven Gene Transcription*

M. McMahon, J. Hayes, T. Lamark, 2010, The Journal of Biological Chemistry.

Nucleocytoplasmic Shuttling of p62/SQSTM1 and Its Role in Recruitment of Nuclear Polyubiquitinated Proteins to Promyelocytic Leukemia Bodies*

G. Bjørkøy, T. Lamark, Aud Øvervatn, 2009, The Journal of Biological Chemistry.

ATG8 Family Proteins Act as Scaffolds for Assembly of the ULK Complex

K. Torgersen, T. Lamark, Aud Øvervatn, 2012, The Journal of Biological Chemistry.

A role for NBR1 in autophagosomal degradation of ubiquitinated substrates.

M. Komatsu, G. Bjørkøy, T. Lamark, 2009, Molecular cell.

Monitoring autophagic degradation of p62/SQSTM1.

G. Bjørkøy, T. Lamark, A. Brech, 2009, Methods in enzymology.

FYCO1 Contains a C-terminally Extended, LC3A/B-preferring LC3-interacting Region (LIR) Motif Required for Efficient Maturation of Autophagosomes during Basal Autophagy*

T. Mizushima, G. Evjen, K. Takagi, 2015, The Journal of Biological Chemistry.

Reversion of Ras- and Phosphatidylcholine-hydrolyzing Phospholipase C-mediated Transformation of NIH 3T3 Cells by a Dominant Interfering Mutant of Protein Kinase C λ Is Accompanied by the Loss of Constitutive Nuclear Mitogen-activated Protein Kinase/Extracellular Signal-regulated Kinase Activity*

G. Bjørkøy, Aud Øvervatn, T. Johansen, 1997, The Journal of Biological Chemistry.

FKBP8 recruits LC3A to mediate Parkin‐independent mitophagy

T. Lamark, Aud Øvervatn, T. Johansen, 2017, EMBO reports.

p 62 / SQSTM 1 forms protein aggregates degraded by autophagy and has a protective effect on huntingtin-induced cell death

G. Bjørkøy, T. Lamark, A. Brech, 2005 .

Interaction Codes within the Family of Mammalian Phox and Bem1p Domain-containing Proteins*

G. Bjørkøy, T. Lamark, H. Outzen, 2003, Journal of Biological Chemistry.

p62/SQSTM1 forms protein aggregates degraded by autophagy and has a protective effect on huntingtin-induced cell death

G. Bjørkøy, T. Lamark, A. Brech, 2005, The Journal of cell biology.

NIH 3T3 cells stably transfected with the gene encoding phosphatidylcholine-hydrolyzing phospholipase C from Bacillus cereus acquire a transformed phenotype

M. Diaz-Meco, J. Moscat, G. Bjørkøy, 1994, Molecular and cellular biology.

p62/SQSTM1 Is a Target Gene for Transcription Factor NRF2 and Creates a Positive Feedback Loop by Inducing Antioxidant Response Element-driven Gene Transcription*

M. McMahon, J. Hayes, T. Lamark, 2010, The Journal of Biological Chemistry.

FYCO1 Contains a C-terminally Extended, LC3A/B-preferring LC3-interacting Region (LIR) Motif Required for Efficient Maturation of Autophagosomes during Basal Autophagy*

T. Mizushima, G. Evjen, K. Takagi, 2015, The Journal of Biological Chemistry.