about
Insights into molecular interactions between CaM and its inhibitors from molecular dynamics simulations and experimental data.A structural model for facultative anion channels in an oligomeric membrane protein: the yeast TRK (K(+)) system.Aqueous extract of Annona macroprophyllata: a potential α-glucosidase inhibitor.Microarray-Based Immunoassay with Synthetic Mimotopes for the Detection of Fumonisin B1.Calmodulin inhibitors from natural sources: an update.(+)-Ascosalitoxin and Vermelhotin, a Calmodulin Inhibitor, from an Endophytic Fungus Isolated from Hintonia latifloraImportance of the interaction protein-protein of the CaM-PDE1A and CaM-MLCK complexes in the development of new anti-CaM drugs.The N-terminal strand modulates immunoglobulin light chain fibrillogenesis.An alternative assay to discover potential calmodulin inhibitors using a human fluorophore-labeled CaM protein.Site-directed fluorescence labeling reveals differences on the R-conformer of glucosamine 6-phosphate deaminase of Escherichia coli induced by active or allosteric site ligands at steady state.(Z)-3-butylidenephthalide from Ligusticum porteri , an α-glucosidase inhibitor.α-Glucosidase Inhibitors from Salvia circinata.Synthesis, biological evaluation, and docking studies of gigantol analogs as calmodulin inhibitors.Correction to α-Glucosidase Inhibitors from Brickellia cavanillesii.Effect of N-Benzylpiperazine, Its Metabolite N-Benzylethylenediamine, and Its Disubstituted Analogue N,N'-Dibenzylpiperazine on the Acquisition, Formation, and Consolidation of Memory in Mice.α-glucosidase inhibitors from Brickellia cavanillesii.Development of new hCaM-Alexa Fluor® biosensors for a wide range of ligands.Saccharomyces cerevisiae Differential Functionalization of Presumed ScALT1 and ScALT2 Alanine Transaminases Has Been Driven by Diversification of Pyridoxal Phosphate Interactions.Gnaphaliin A and B relax smooth muscle of guinea-pig trachea and rat aorta via phosphodiesterase inhibitionBiosensor for on-line fluorescent detection of trifluoroperazine based on genetically modified calmodulinDifferential modulation of human GABA-ρ1 receptor by sulfur-containing compounds structurally related to taurineMutational and genetic determinants of λ6 light chain amyloidogenesisMetabolites from the entophytic fungus Sporormiella minimoides isolated from Hintonia latifloraAdditional α-glucosidase inhibitors from Malbranchea flavorosea (Leotiomycetes, Ascomycota)Development of the fluorescent biosensor hCalmodulin (hCaM)L39C-monobromobimane(mBBr)/V91C-mBBr, a novel tool for discovering new calmodulin inhibitors and detecting calciumFluorescence, circular dichroism, NMR, and docking studies of the interaction of the alkaloid malbrancheamide with calmodulinPostprandial glycaemia and inhibition of α-glucosidase activity by aqueous extract from Coriandrum sativumCorrection: Effect of curcuminoids and curcumin derivate products on thioredoxin-glutathione reductase from Taenia crassiceps cysticerci. Evidence suggesting a curcumin oxidation product as a suitable inhibitorEffect of curcuminoids and curcumin derivate products on thioredoxin-glutathione reductase from Taenia crassiceps cysticerci. Evidence suggesting a curcumin oxidation product as a suitable inhibitorα-Glucosidase and Protein Tyrosine Phosphatase 1B Inhibitors from Malbranchea circinata
P50
Q30897301-2D6B7CA8-F2CD-4DDB-AF84-F6E686778520Q34481883-0811E60D-CF7F-4E18-B273-311E9853CCFBQ34658105-5D4EABCB-C5AF-435A-8148-44265811B673Q36364396-999FDB82-7014-4720-9957-18649BA04503Q38299077-2C307A0B-94E7-498D-827F-7C75FF615D2EQ43756211-93446C8E-0B77-4940-9119-D81F55DCD35BQ44327186-79B3E786-7653-400B-BB60-BCC802525C85Q45265524-E0EA36E8-9C16-4B1D-818E-12EFB893BBF4Q46137400-38D4F2E8-E09B-44EE-A1F1-45BA5E9E7750Q46802077-BEDD2320-63A1-4E22-AD22-31D1F8989B22Q47356688-3E9F672F-8AC0-4D6D-8D9E-4BC9ECE30FD4Q48258726-89756C32-A5CB-4575-85AD-785B2EC65DFAQ48269250-1EFB0C66-4C96-4A6A-BE7E-D817CACD2E45Q48649083-CEDF9338-7E48-44C6-A00B-F7E043AB4377Q50454919-6A95B119-BA2B-4462-95E6-E42C0C9687B5Q51356744-734104AD-71BC-4DBB-96A6-C38109CCF6BDQ51390986-9AF0EBE6-4BE9-44DB-A0EA-9614F060AB03Q55093010-58B76505-B619-41B4-8469-7E90FA6D0FEEQ57099077-A23938F1-E7B6-45EE-B1EA-628274313622Q58479595-830A4178-AFB3-4906-B523-7CC35F23FCA4Q58802293-FEF2E5C9-25FF-40F0-88A8-CAA7ACDC8FCBQ58925865-3A928F24-0532-411D-A094-23BA87DC21FAQ78287310-3A93561A-046B-4410-80A1-767392518D23Q78446181-958BBC26-2EDB-4A11-A32D-70126C7412C4Q83873952-B917EBF1-CA2A-47C2-BDF9-6FFF3EC7784DQ85183155-762620CB-0010-4EBC-9B2E-9AC6782E715DQ87893584-DA036E2A-546E-4FC7-AED7-9A49C025E68AQ90562685-E47038D1-7BF9-49B2-8129-C257BA0E1B2CQ92073381-0118A48B-6A8B-4EA4-A480-208888113B73Q92395688-34D63F6B-1E4C-430B-89C9-8AB916AF0666
P50
description
Forscher
@de
chercheur
@fr
investigador
@es
researcher
@en
ricercatore
@it
研究者
@zh
name
Martín González-Andrade
@ast
Martín González-Andrade
@en
Martín González-Andrade
@es
Martín González-Andrade
@nl
type
label
Martín González-Andrade
@ast
Martín González-Andrade
@en
Martín González-Andrade
@es
Martín González-Andrade
@nl
prefLabel
Martín González-Andrade
@ast
Martín González-Andrade
@en
Martín González-Andrade
@es
Martín González-Andrade
@nl
P31
P496
0000-0002-8910-3035