Vitenskapelig artikkel
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Tai, Mary Dayne Sia; Ochoa, Lissette; Flydal, Marte Innselset
et al. (2025). Structural recognition and stabilization of tyrosine hydroxylase by the J-domain protein DNAJC12. (ekstern lenke)
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C, Kunwar Jung K; Tristán-Noguero, Alba; Altankhuyag, Altanchimeg
et al. (2024). Tetrahydrobiopterin (BH<inf>4</inf>) treatment stabilizes tyrosine hydroxylase: Rescue of tyrosine hydroxylase deficiency phenotypes in human neurons and in a knock-in mouse model. (ekstern lenke)
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Catevilla, Oscar Aubi; Prestegård, Karina Skjervheim; C, Kunwar Jung K
et al. (2021). The Pah-R261Q mouse reveals oxidative stress associated with amyloid-like hepatic aggregation of mutant phenylalanine hydroxylase. (ekstern lenke)
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Waløen, Kai; C, Kunwar Jung K; Vecchia, Elisa D.
et al. (2021). Cysteine modification by ebselen reduces the stability and cellular levels of 14-3-3 Proteins. (ekstern lenke)
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C, Kunwar Jung K; Himmelreich, Nastassja; Prestegård, Karina Skjervheim
et al. (2019). Phenylalanine hydroxylase variants interact with the co-chaperone DNAJC12. (ekstern lenke)
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Bezem, Maria Teresa; Johannessen, Fredrik Gullaksen; C, Kunwar Jung K
et al. (2018). Stabilization of Human Tyrosine Hydroxylase in Maltodextrin Nanoparticles for Delivery to Neuronal Cells and Tissue. (ekstern lenke)
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Finnigan, Ana Jorge; Kleppe, Rune; C, Kunwar Jung K
et al. (2017). Phosphorylation at serine 31 targets tyrosine hydroxylase to
vesicles for transport along microtubules. (ekstern lenke)
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Baumann, Anne; Finnigan, Ana Jorge; Kunwar, Jung K. C.
et al. (2016). Tyrosine Hydroxylase Binding to Phospholipid Membranes Prompts Its Amyloid Aggregation and Compromises Bilayer Integrity. (ekstern lenke)
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