Results 91 to 100 of about 1,582 (168)

New insights into the structure and function of human phenylalanine hydroxylase : interallelic complementation, protein misfolding and mechanism of catalytic activation [PDF]

open access: yes, 2011
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]

open access: yesInt J Mol Sci, 2022
Buglak AA   +3 more
europepmc   +1 more source

Tetrahydrobiopterin Deficiency in Autism Spectrum Disorder [PDF]

open access: yes, 2014
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

Sleeve gastrectomy is feasible in obese patients with phenylketonuria: A case report and literature review. [PDF]

open access: yesInt J Surg Case Rep, 2023
Quarenghi M   +3 more
europepmc   +1 more source

Tetrahydrobiopterin and endothelial nitric oxide synthase activity [PDF]

open access: yes, 2017
Cosentino, Francesco   +1 more
core  

Neopterin extends <i>C. elegans</i> lifespan in an ATFS-1-dependent manner. [PDF]

open access: yesMicroPubl Biol
Pitkänen M   +3 more
europepmc   +1 more source

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