Ming Ying
Bergen, Norway
Last Updated: 09/26/2026
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Found 13 publications
Tyrosine Hydroxylase Deficiency Impairs TH Axonal Transport, Brain Function, and Neuronal Plasticity.
Journal: Journal of inherited metabolic disease
Published: August 26, 2025
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
Blood phenylalanine reduction corrects CNS dopamine and serotonin deficiencies and partially improves behavioral performance in adult phenylketonuric mice.
Journal: Molecular genetics and metabolism
Published: September 01, 2017
Tetrahydrobiopterin treatment reduces brain L-Phe but only partially improves serotonin in hyperphenylalaninemic ENU1/2 mice.
Journal: Journal of inherited metabolic disease
Published: August 09, 2017
Phosphorylation at serine 31 targets tyrosine hydroxylase to vesicles for transport along microtubules.
Journal: The Journal of biological chemistry
Published: October 07, 2016
Erratum to "Discovery of compounds that protect tyrosine hydroxylase activity through different mechanisms" [Biochim. Biophys. Acta 1854/9 (2015) 1078-1089].
Journal: Biochimica et biophysica acta
Published: March 01, 2016
Discovery of compounds that protect tyrosine hydroxylase activity through different mechanisms.
Journal: Biochimica et biophysica acta
Published: February 26, 2015
Brain catecholamine depletion and motor impairment in a Th knock-in mouse with type B tyrosine hydroxylase deficiency.
Journal: Brain : a journal of neurology
Published: February 08, 2015
Avidity of onconeural antibodies is of clinical relevance.
Journal: Cancer immunology, immunotherapy : CII
Published: December 18, 2012
The peripheral binding of 14-3-3γ to membranes involves isoform-specific histidine residues.
Journal: PloS one
Published: June 17, 2012
Last Updated: 09/26/2026