Kunwar Kc-Jung
Bergen, Norway
Last Updated: 09/26/2026
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Found 8 publications
Tyrosine Hydroxylase Deficiency Impairs TH Axonal Transport, Brain Function, and Neuronal Plasticity.
Journal: Journal of inherited metabolic disease
Published: August 26, 2025
Structural recognition and stabilization of tyrosine hydroxylase by the J-domain protein DNAJC12.
Journal: Nature communications
Published: November 22, 2023
Tetrahydrobiopterin (BH4) treatment stabilizes tyrosine hydroxylase: Rescue of tyrosine hydroxylase deficiency phenotypes in human neurons and in a knock-in mouse model.
Journal: Journal of inherited metabolic disease
Published: July 14, 2023
Cysteine Modification by Ebselen Reduces the Stability and Cellular Levels of 14-3-3 Proteins.
Journal: Molecular pharmacology
Published: November 16, 2020
The Pah-R261Q mouse reveals oxidative stress associated with amyloid-like hepatic aggregation of mutant phenylalanine hydroxylase.
Journal: Nature communications
Published: November 15, 2019
Phenylalanine hydroxylase variants interact with the co-chaperone DNAJC12.
Journal: Human mutation
Published: November 07, 2018
Phosphorylation at serine 31 targets tyrosine hydroxylase to vesicles for transport along microtubules.
Journal: The Journal of biological chemistry
Published: October 07, 2016
Showing 1-8 of 8
Last Updated: 09/26/2026