about
Determining the molecular mechanism of inactivation by chemical modification of triosephosphate isomerase from the human parasite Giardia lamblia: a study for antiparasitic drug designStructural and functional perturbation of Giardia lamblia triosephosphate isomerase by modification of a non-catalytic, non-conserved regionStructural effects of protein aging: terminal marking by deamidation in human triosephosphate isomerase.The stability of G6PD is affected by mutations with different clinical phenotypes.Cloning, Expression and Characterization of Recombinant, NADH Oxidase from Giardia lamblia.Novel giardicidal compounds bearing proton pump inhibitor scaffold proceeding through triosephosphate isomerase inactivation.Allosteric Interactions by p53 mRNA Govern HDM2 E3 Ubiquitin Ligase Specificity under Different Conditions.Giardial triosephosphate isomerase as possible target of the cytotoxic effect of omeprazole in Giardia lambliaKinetics of the thermal inactivation and aggregate formation of rabbit muscle pyruvate kinase in the presence of trehalose.Selectivity of pyruvate kinase for Na+ and K+ in water/dimethylsulfoxide mixtures.Disulfiram as a novel inactivator of Giardia lamblia triosephosphate isomerase with antigiardial potential.Species-Specific Inactivation of Triosephosphate Isomerase from Trypanosoma brucei: Kinetic and Molecular Dynamics Studies.Cloning, expression, purification and characterization of his-tagged human glucose-6-phosphate dehydrogenase: a simplified method for protein yield.Pyruvate kinase revisited: the activating effect of K+.RNAi-Mediated Specific Gene Silencing as a Tool for the Discovery of New Drug Targets in Giardia lamblia; Evaluation Using the NADH Oxidase Gene.Biochemical Analysis of Two Single Mutants that Give Rise to a Polymorphic G6PD A-Double Mutant.Proteomics: a tool to develop novel diagnostic methods and unravel molecular mechanisms of pediatric diseases.The E104D mutation increases the susceptibility of human triosephosphate isomerase to proteolysis. Asymmetric cleavage of the two monomers of the homodimeric enzyme.Synthesis of nitro(benzo)thiazole acetamides and in vitro antiprotozoal effect against amitochondriate parasites Giardia intestinalis and Trichomonas vaginalisThe active (ADHa) and inactive (ADHi) forms of the PQQ-alcohol dehydrogenase from Gluconacetobacter diazotrophicus differ in their respective oligomeric structures and redox state of their corresponding prosthetic groupsDichotomic phylogenetic tree of the pyruvate kinase family: K+ -dependent and -independent enzymesStructure-based identification of a potential non-catalytic binding site for rational drug design in the fructose 1,6-biphosphate aldolase from Giardia lamblia
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Jesús Oria-Hernández
@ast
Jesús Oria-Hernández
@en
Jesús Oria-Hernández
@es
Jesús Oria-Hernández
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type
label
Jesús Oria-Hernández
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Jesús Oria-Hernández
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Jesús Oria-Hernández
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Jesús Oria-Hernández
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Jesús Oria-Hernández
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Jesús Oria-Hernández
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Jesús Oria-Hernández
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Jesús Oria-Hernández
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P106
P1153
56000782700
P21
P31
P496
0000-0001-7147-1879