Lista de obras - Aurelio A Moya García - Dominio Público Uruguay

AMMO-Prot: amine system project 3D-model finder.

artículo científico publicado en 2008

Aminooxy analog of histamine is an efficient inhibitor of mammalian L-histidine decarboxylase: combined in silico and experimental evidence.

artículo científico publicado en 2013

Analysis of Mammalian Histidine Decarboxylase Dimerization Interface Reveals an Electrostatic Hotspot Important for Catalytic Site Topology and Function

scientific article published on 13 May 2011

Analysis of the decarboxylation step in mammalian histidine decarboxylase. A computational study

artículo científico publicado en 2008

Bicyclic derivatives of L-idonojirimycin as pharmacological chaperones for neuronopathic forms of Gaucher disease.

artículo científico publicado en 2013

Biocomputational resources useful for drug discovery against compartmentalized targets.

artículo científico

Digitalis purpurea P5 beta R2, encoding steroid 5 beta-reductase, is a novel defense-related gene involved in cardenolide biosynthesis

artículo científico publicado en 2009

Insights into polypharmacology from drug-domain associations.

artículo científico publicado en 2013

Local changes in the catalytic site of mammalian histidine decarboxylase can affect its global conformation and stability

scientific journal article

Mapping of catalytically important residues in the rat L-histidine decarboxylase enzyme using bioinformatic and site-directed mutagenesis approaches.

artículo científico publicado en 2004

Molecular characterization of five patients with homocystinuria due to severe methylenetetrahydrofolate reductase deficiency.

artículo científico publicado en 2010

Molecular modeling and site-directed mutagenesis reveal essential residues for catalysis in a prokaryote-type aspartate aminotransferase.

artículo científico publicado en 2009

New structural insights to help in the search for selective inhibitors of mammalian pyridoxal 5'-phosphate-dependent histidine decarboxylase . 4. Synthesis, metabolism and release of histamine

artículo científico publicado en 2006

Structural and Functional View of Polypharmacology.

artículo científico publicado en 2017

Structural features of mammalian histidine decarboxylase reveal the basis for specific inhibition.

artículo científico publicado en 2009

Study by optical spectroscopy and molecular dynamics of the interaction of acridine-spermine conjugate with DNA.

artículo científico publicado en 2007

The function of histamine receptor H4R in the brain revealed by interaction partners

artículo científico publicado en 2011

Lista de obras de Aurelio A Moya García

AMMO-Prot: amine system project 3D-model finder.

Aminooxy analog of histamine is an efficient inhibitor of mammalian L-histidine decarboxylase: combined in silico and experimental evidence.

Analysis of Mammalian Histidine Decarboxylase Dimerization Interface Reveals an Electrostatic Hotspot Important for Catalytic Site Topology and Function

Analysis of the decarboxylation step in mammalian histidine decarboxylase. A computational study

Bicyclic derivatives of L-idonojirimycin as pharmacological chaperones for neuronopathic forms of Gaucher disease.

Biocomputational resources useful for drug discovery against compartmentalized targets.

Digitalis purpurea P5 beta R2, encoding steroid 5 beta-reductase, is a novel defense-related gene involved in cardenolide biosynthesis

Insights into polypharmacology from drug-domain associations.

Local changes in the catalytic site of mammalian histidine decarboxylase can affect its global conformation and stability

Mapping of catalytically important residues in the rat L-histidine decarboxylase enzyme using bioinformatic and site-directed mutagenesis approaches.

Molecular characterization of five patients with homocystinuria due to severe methylenetetrahydrofolate reductase deficiency.

Molecular modeling and site-directed mutagenesis reveal essential residues for catalysis in a prokaryote-type aspartate aminotransferase.

New structural insights to help in the search for selective inhibitors of mammalian pyridoxal 5'-phosphate-dependent histidine decarboxylase . 4. Synthesis, metabolism and release of histamine

Structural and Functional View of Polypharmacology.

Structural features of mammalian histidine decarboxylase reveal the basis for specific inhibition.

Study by optical spectroscopy and molecular dynamics of the interaction of acridine-spermine conjugate with DNA.

The function of histamine receptor H4R in the brain revealed by interaction partners