New insights into the structure and function of human phenylalanine hydroxylase : interallelic complementation, protein misfolding and mechanism of catalytic activation [PDF]
Tese de doutoramento, Farmácia (Bioquímica), Universidade de Lisboa, Faculdade de Farmácia, 2011Phenylketonuria (PKU) is an autosomal recessive human inborn error of metabolism caused by dysfunction of the liver homotetrameric/homodimeric enzyme ...
Leandro, João Paulo Travassos, 1981-
core
Insights into Molecular Structure of Pterins Suitable for Biomedical Applications. [PDF]
Buglak AA +3 more
europepmc +1 more source
Tetrahydrobiopterin Deficiency in Autism Spectrum Disorder [PDF]
Tetrahydrobiopterin is an essential cofactor for critical metabolic pathways, including those involved in the production of monoamine neurotransmitters and nitric oxide.
Frye, MD, PhD, Richard E.
core +1 more source
Nitric Oxide Signalling in Vascular Control and Cardiovascular Risk [PDF]
Schmidt, Annette
core +1 more source
Sleeve gastrectomy is feasible in obese patients with phenylketonuria: A case report and literature review. [PDF]
Quarenghi M +3 more
europepmc +1 more source
In Vitro and In Vivo Chaperone Effect of (R)-2-amino-6-(1R, 2S)-1,2-dihydroxypropyl)-5,6,7,8-tetrahydropterin-4(3H)-one on the C1473G Mutant Tryptophan Hydroxylase 2. [PDF]
Arefieva AB +4 more
europepmc +1 more source
Tetrahydrobiopterin as a Trigger for Vitiligo: Phototransformation during UV Irradiation. [PDF]
Telegina TA +3 more
europepmc +1 more source
Tetrahydrobiopterin and endothelial nitric oxide synthase activity [PDF]
Cosentino, Francesco +1 more
core
Neopterin extends <i>C. elegans</i> lifespan in an ATFS-1-dependent manner. [PDF]
Pitkänen M +3 more
europepmc +1 more source

