VIAF

Virtual International Authority File

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Leader     00000nz a2200037n 45 0
001     WKP|Q41482449  (VIAF cluster)  (Authority/Source Record)
003     WKP
005     20241020233023.0
008     241020nneanz||abbn n and d
035 ‎‡a  (WKP)Q41482449‏
024 ‎‡a  0000-0003-2400-405X‏ ‎‡2  orcid‏
035 ‎‡a  (OCoLC)Q41482449‏
043 ‎‡c  ES‏
100 0 ‎‡a  Juan Carlos Morales Sánchez‏ ‎‡c  investigador español‏ ‎‡9  es‏
375 ‎‡a  1‏ ‎‡2  iso5218‏
400 0 ‎‡a  Juan Carlos Morales‏ ‎‡c  chercheur espagnol‏ ‎‡9  fr‏
400 0 ‎‡a  Juan Carlos Morales‏ ‎‡c  researcher (ORCID 0000-0003-2400-405X)‏ ‎‡9  en‏
400 0 ‎‡a  Juan Carlos Morales‏ ‎‡c  Spaans onderzoeker‏ ‎‡9  nl‏
400 0 ‎‡a  Juan Carlos Morales Sánchez‏ ‎‡c  investigador espanhol‏ ‎‡9  pt‏
400 0 ‎‡a  Juan Carlos Morales‏ ‎‡c  investigador español‏ ‎‡9  ast‏
400 0 ‎‡a  Juan Carlos Morales Sánchez‏ ‎‡c  investigador espanyol‏ ‎‡9  ca‏
400 0 ‎‡a  Juan Carlos Morales‏ ‎‡c  taighdeoir‏ ‎‡9  ga‏
400 0 ‎‡a  Juan Carlos Morales‏ ‎‡c  hulumtues‏ ‎‡9  sq‏
670 ‎‡a  Author's A concise synthesis of glucuronide metabolites of urolithin-B, resveratrol, and hydroxytyrosol.‏
670 ‎‡a  Author's A highly effective nonpolar isostere of deoxyguanosine: synthesis, structure, stacking, and base pairing‏
670 ‎‡a  Author's A Photoresponsive Stiff-Stilbene Ligand Fuels the Reversible Unfolding of G-Quadruplex DNA.‏
670 ‎‡a  Author's Alkylated resveratrol prodrugs and metabolites as potential therapeutics for neurodegenerative diseases.‏
670 ‎‡a  Author's Antioxidant activity of alkyl gallates and glycosyl alkyl gallates in fish oil in water emulsions: relevance of their surface active properties and of the type of emulsifier‏
670 ‎‡a  Author's Antioxidant activity of resveratrol in several fish lipid matrices: effect of acylation and glucosylation.‏
670 ‎‡a  Author's Apolar carbohydrates as DNA capping agents‏
670 ‎‡a  Author's Binding and Beyond: What Else Can G-Quadruplex Ligands Do?‏
670 ‎‡a  Author's Carbohydrate-DNA interactions at G-quadruplexes: folding and stability changes by attaching sugars at the 5'-end‏
670 ‎‡a  Author's Carbohydrate-naphthalene diimide conjugates as potential antiparasitic drugs: Synthesis, evaluation and structure-activity studies‏
670 ‎‡a  Author's Chemically Tuning Resveratrol for the Effective Killing of Gram-Positive Pathogens‏
670 ‎‡a  Author's Cytotoxic, Antiangiogenic and Antitelomerase Activity of Glucosyl- and Acyl- Resveratrol Prodrugs and Resveratrol Sulfate Metabolites.‏
670 ‎‡a  Author's Divalent Naphthalene Diimide Ligands Display High Selectivity for the Human Telomeric G-quadruplex in K+ Buffer‏
670 ‎‡a  Author's Effect of lipophilization of hydroxytyrosol on its antioxidant activity in fish oils and fish oil-in-water emulsions.‏
670 ‎‡a  Author's Effects of long-term consumption of low doses of resveratrol on diet-induced mild hypercholesterolemia in pigs: a transcriptomic approach to disease prevention.‏
670 ‎‡a  Author's Effects of sugar functional groups, hydrophobicity, and fluorination on carbohydrate-DNA stacking interactions in water.‏
670 ‎‡a  Author's Efficient replication between non-hydrogen-bonded nucleoside shape analogs‏
670 ‎‡a  Author's Enhanced sampling molecular dynamics simulations correctly predict the diverse activities of a series of stiff-stilbene G-quadruplex DNA ligands‏
670 ‎‡a  Author's Enzymatic Synthesis of a Novel Neuroprotective Hydroxytyrosyl Glycoside.‏
670 ‎‡a  Author's Enzymatic Synthesis of a Novel Pterostilbene α-Glucoside by the Combination of Cyclodextrin Glucanotransferase and Amyloglucosidase.‏
670 ‎‡a  Author's Experimental measurement of carbohydrate-aromatic stacking in water by using a dangling-ended DNA model system‏
670 ‎‡a  Author's G-Quadruplex Identification in the Genome of Protozoan Parasites Points to Naphthalene Diimide Ligands as New Antiparasitic Agents.‏
670 ‎‡a  Author's Glucose conjugation of anti-HIV-1 oligonucleotides containing unmethylated CpG motifs reduces their immunostimulatory activity‏
670 ‎‡a  Author's Glucose-nucleobase pairs within DNA: impact of hydrophobicity, alternative linking unit and DNA polymerase nucleotide insertion studies.‏
670 ‎‡a  Author's Glucose-Nucleobase Pseudo Base Pairs: Biomolecular Interactions within DNA‏
670 ‎‡a  Author's Hemolytic activity and solubilizing capacity of raffinose and melezitose fatty acid monoesters prepared by enzymatic synthesis‏
670 ‎‡a  Author's High-fidelity in vivo replication of DNA base shape mimics without Watson-Crick hydrogen bonds.‏
670 ‎‡a  Author's High-level expression and characterization of Galactomyces geotrichum (BT107) lipase I in Pichia pastoris‏
670 ‎‡a  Author's Highly Polar Carbohydrates Stack onto DNA Duplexes via CH/π Interactions‏
670 ‎‡a  Author's Hydroxytyrosol and tyrosol sulfate metabolites protect against the oxidized cholesterol pro-oxidant effect in Caco-2 human enterocyte-like cells‏
670 ‎‡a  Author's Hydroxytyrosol glucuronides protect renal tubular epithelial cells against H‏
670 ‎‡a  Author's Hydroxytyrosol glucuronides protect renal tubular epithelial cells against H(2)O(2) induced oxidative damage.‏
670 ‎‡a  Author's Imide Condensation as a Strategy for the Synthesis of Core‐Diversified G‐Quadruplex Ligands with Anticancer and Antiparasitic Activity‏
670 ‎‡a  Author's Importance of terminal base pair hydrogen-bonding in 3'-end proofreading by the Klenow fragment of DNA polymerase I‏
670 ‎‡a  Author's Improved sample treatment for the determination of fructooligosaccharides in milk related products by liquid chromatography with electrochemical and refractive index detection‏
670 ‎‡a  Author's Kinetics and binding of the thymine-DNA mismatch glycosylase, Mig-Mth, with mismatch-containing DNA substrates‏
670 ‎‡a  Author's Metabolites and tissue distribution of resveratrol in the pig‏
670 ‎‡a  Author's Minor Groove Interactions between Polymerase and DNA: More Essential to Replication than Watson−Crick Hydrogen Bonds?‏
670 ‎‡a  Author's Neuroprotective and Anti-inflammatory Effects of Pterostilbene Metabolites in Human Neuroblastoma SH-SY5Y and RAW 264.7 Macrophage Cells‏
670 ‎‡a  Author's Non-reducing trisaccharide fatty acid monoesters: Novel detergents in membrane biochemistry‏
670 ‎‡a  Author's Parallel-stranded hairpins containing 8-aminopurines. Novel efficient probes for triple-helix formation.‏
670 ‎‡a  Author's Positive-ion ESI mass spectrometry of regioisomeric nonreducing oligosaccharide fatty acid monoesters: in-source fragmentation of sodium adducts.‏
670 ‎‡a  Author's Properties of Triple Helices Formed by Oligonucleotides Containing 8-Aminopurines‏
670 ‎‡a  Author's Properties of triple helices formed by parallel-stranded hairpins containing 8-aminopurines.‏
670 ‎‡a  Author's Resveratrol and some glucosyl, glucosylacyl, and glucuronide derivatives reduce Escherichia coli O157:H7, Salmonella Typhimurium, and Listeria monocytogenes Scott A adhesion to colonic epithelial cell lines‏
670 ‎‡a  Author's Significance of nucleobase shape complementarity and hydrogen bonding in the formation and stability of the closed polymerase-DNA complex‏
670 ‎‡a  Author's Simultaneous determination of eight water-soluble vitamins in supplemented foods by liquid chromatography‏
670 ‎‡a  Author's Skin delivery of antioxidant surfactants based on gallic acid and hydroxytyrosol‏
670 ‎‡a  Author's Stiff-Stilbene Ligands Target G-Quadruplex DNA and Exhibit Selective Anticancer and Antiparasitic Activity‏
670 ‎‡a  Author's Structure and Base Pairing Properties of a Replicable Nonpolar Isostere for Deoxyadenosine‏
670 ‎‡a  Author's Surface-Active Properties of Lipophilic Antioxidants Tyrosol and Hydroxytyrosol Fatty Acid Esters: A Potential Explanation for the Nonlinear Hypothesis of the Antioxidant Activity in Oil-in-Water Emulsions‏
670 ‎‡a  Author's Synthesis and Biophysical Investigations of Oligonucleotides Containing Galactose-Modified DNA, LNA, and 2'-Amino-LNA Monomers.‏
670 ‎‡a  Author's Synthesis, Binding Properties, and Differences in Cell Uptake of G-Quadruplex Ligands Based on Carbohydrate Naphthalene Diimide Conjugates.‏
670 ‎‡a  Author's Synthesis, cell-surface binding, and cellular uptake of fluorescently labeled glucose-DNA conjugates with different carbohydrate presentation.‏
670 ‎‡a  Author's Synthesis, RNAi activity and nuclease-resistant properties of apolar carbohydrates siRNA conjugates.‏
670 ‎‡a  Author's The effect of l-thymidine, acyclic thymine and 8-bromoguanine on the stability of model G-quadruplex structures‏
670 ‎‡a  Author's The gut microbiota ellagic acid-derived metabolite urolithin A and its sulfate conjugate are substrates for the drug efflux transporter breast cancer resistance protein‏
670 ‎‡a  Author's The gut microbiota ellagic acid-derived metabolite urolithin A and its sulfate conjugate are substrates for the drug efflux transporter breast cancer resistance protein (ABCG2/BCRP).‏
670 ‎‡a  Author's Tyrosol and hydroxytyrosol derivatives as antitrypanosomal and antileishmanial agents‏
670 ‎‡a  Author's Tyrosol and its metabolites as antioxidative and anti-inflammatory molecules in human endothelial cells.‏
670 ‎‡a  Author's Visible-light photoswitching of ligand binding mode suggests G-quadruplex DNA as a target for photopharmacology‏
909 ‎‡a  (orcid) 000000032400405x‏ ‎‡9  1‏
919 ‎‡a  visiblelightphotoswitchingofligandbindingmodesuggestsgquadruplexdnaasatargetforphotopharmacology‏ ‎‡A  Visible-light photoswitching of ligand binding mode suggests G-quadruplex DNA as a target for photopharmacology‏ ‎‡9  1‏
919 ‎‡a  tyrosolanditsmetabolitesasantioxidativeandantiinflammatorymoleculesinhumanendothelialcells‏ ‎‡A  Tyrosol and its metabolites as antioxidative and anti-inflammatory molecules in human endothelial cells.‏ ‎‡9  1‏
919 ‎‡a  tyrosolandhydroxytyrosolderivativesasantitrypanosomalandantileishmanialagents‏ ‎‡A  Tyrosol and hydroxytyrosol derivatives as antitrypanosomal and antileishmanial agents‏ ‎‡9  1‏
919 ‎‡a  gutmicrobiotaellagicacidderivedmetaboliteurolithinaanditssulfateconjugatearesubstratesforthedrugeffluxtransporterbreastcancerresistanceproteinabcg2bcrp‏ ‎‡A  The gut microbiota ellagic acid-derived metabolite urolithin A and its sulfate conjugate are substrates for the drug efflux transporter breast cancer resistance protein (ABCG2/BCRP).‏ ‎‡9  1‏
919 ‎‡a  gutmicrobiotaellagicacidderivedmetaboliteurolithinaanditssulfateconjugatearesubstratesforthedrugeffluxtransporterbreastcancerresistanceprotein‏ ‎‡A  The gut microbiota ellagic acid-derived metabolite urolithin A and its sulfate conjugate are substrates for the drug efflux transporter breast cancer resistance protein‏ ‎‡9  1‏
919 ‎‡a  effectof50thymidineacyclicthymineand8bromoguanineonthestabilityofmodelgquadruplexstructures‏ ‎‡A  The effect of l-thymidine, acyclic thymine and 8-bromoguanine on the stability of model G-quadruplex structures‏ ‎‡9  1‏
919 ‎‡a  synthesisrnaiactivityandnucleaseresistantpropertiesofapolarcarbohydratessirnaconjugates‏ ‎‡A  Synthesis, RNAi activity and nuclease-resistant properties of apolar carbohydrates siRNA conjugates.‏ ‎‡9  1‏
919 ‎‡a  synthesiscellsurfacebindingandcellularuptakeoffluorescentlylabeledglucosednaconjugateswithdifferentcarbohydratepresentation‏ ‎‡A  Synthesis, cell-surface binding, and cellular uptake of fluorescently labeled glucose-DNA conjugates with different carbohydrate presentation.‏ ‎‡9  1‏
919 ‎‡a  synthesisbindingpropertiesanddifferencesincelluptakeofgquadruplexligandsbasedoncarbohydratenaphthalenediimideconjugates‏ ‎‡A  Synthesis, Binding Properties, and Differences in Cell Uptake of G-Quadruplex Ligands Based on Carbohydrate Naphthalene Diimide Conjugates.‏ ‎‡9  1‏
919 ‎‡a  synthesisandbiophysicalinvestigationsofoligonucleotidescontaininggalactosemodifieddnalnaand2aminolnamonomers‏ ‎‡A  Synthesis and Biophysical Investigations of Oligonucleotides Containing Galactose-Modified DNA, LNA, and 2'-Amino-LNA Monomers.‏ ‎‡9  1‏
919 ‎‡a  surfaceactivepropertiesoflipophilicantioxidantstyrosolandhydroxytyrosolfattyacidestersapotentialexplanationforthenonlinearhypothesisoftheantioxidantactivityinoilinwateremulsions‏ ‎‡A  Surface-Active Properties of Lipophilic Antioxidants Tyrosol and Hydroxytyrosol Fatty Acid Esters: A Potential Explanation for the Nonlinear Hypothesis of the Antioxidant Activity in Oil-in-Water Emulsions‏ ‎‡9  1‏
919 ‎‡a  structureandbasepairingpropertiesofareplicablenonpolarisosterefordeoxyadenosine‏ ‎‡A  Structure and Base Pairing Properties of a Replicable Nonpolar Isostere for Deoxyadenosine‏ ‎‡9  1‏
919 ‎‡a  stiffstilbeneligandstargetgquadruplexdnaandexhibitselectiveanticancerandantiparasiticactivity‏ ‎‡A  Stiff-Stilbene Ligands Target G-Quadruplex DNA and Exhibit Selective Anticancer and Antiparasitic Activity‏ ‎‡9  1‏
919 ‎‡a  skindeliveryofantioxidantsurfactantsbasedongallicacidandhydroxytyrosol‏ ‎‡A  Skin delivery of antioxidant surfactants based on gallic acid and hydroxytyrosol‏ ‎‡9  1‏
919 ‎‡a  simultaneousdeterminationof8watersolublevitaminsinsupplementedfoodsbyliquidchromatography‏ ‎‡A  Simultaneous determination of eight water-soluble vitamins in supplemented foods by liquid chromatography‏ ‎‡9  1‏
919 ‎‡a  significanceofnucleobaseshapecomplementarityandhydrogenbondingintheformationandstabilityoftheclosedpolymerasednacomplex‏ ‎‡A  Significance of nucleobase shape complementarity and hydrogen bonding in the formation and stability of the closed polymerase-DNA complex‏ ‎‡9  1‏
919 ‎‡a  resveratrolandsomeglucosylglucosylacylandglucuronidederivativesreduceescherichiacolio157h7salmonellatyphimuriumandlisteriamonocytogenesscottaadhesiontocolonicepithelialcelllines‏ ‎‡A  Resveratrol and some glucosyl, glucosylacyl, and glucuronide derivatives reduce Escherichia coli O157:H7, Salmonella Typhimurium, and Listeria monocytogenes Scott A adhesion to colonic epithelial cell lines‏ ‎‡9  1‏
919 ‎‡a  propertiesoftriplehelicesformedbyparallelstrandedhairpinscontaining8aminopurines‏ ‎‡A  Properties of triple helices formed by parallel-stranded hairpins containing 8-aminopurines.‏ ‎‡9  1‏
919 ‎‡a  propertiesoftriplehelicesformedbyoligonucleotidescontaining8aminopurines‏ ‎‡A  Properties of Triple Helices Formed by Oligonucleotides Containing 8-Aminopurines‏ ‎‡9  1‏
919 ‎‡a  positiveionesimassspectrometryofregioisomericnonreducingoligosaccharidefattyacidmonoestersinsourcefragmentationofsodiumadducts‏ ‎‡A  Positive-ion ESI mass spectrometry of regioisomeric nonreducing oligosaccharide fatty acid monoesters: in-source fragmentation of sodium adducts.‏ ‎‡9  1‏
919 ‎‡a  parallelstrandedhairpinscontaining8aminopurinesnovelefficientprobesfortriplehelixformation‏ ‎‡A  Parallel-stranded hairpins containing 8-aminopurines. Novel efficient probes for triple-helix formation.‏ ‎‡9  1‏
919 ‎‡a  nonreducingtrisaccharidefattyacidmonoestersnoveldetergentsinmembranebiochemistry‏ ‎‡A  Non-reducing trisaccharide fatty acid monoesters: Novel detergents in membrane biochemistry‏ ‎‡9  1‏
919 ‎‡a  neuroprotectiveandantiinflammatoryeffectsofpterostilbenemetabolitesinhumanneuroblastomashsy5yandraw2647macrophagecells‏ ‎‡A  Neuroprotective and Anti-inflammatory Effects of Pterostilbene Metabolites in Human Neuroblastoma SH-SY5Y and RAW 264.7 Macrophage Cells‏ ‎‡9  1‏
919 ‎‡a  minorgrooveinteractionsbetweenpolymeraseanddnamoreessentialtoreplicationthanwatsoncrickhydrogenbonds‏ ‎‡A  Minor Groove Interactions between Polymerase and DNA: More Essential to Replication than Watson−Crick Hydrogen Bonds?‏ ‎‡9  1‏
919 ‎‡a  metabolitesandtissuedistributionofresveratrolinthepig‏ ‎‡A  Metabolites and tissue distribution of resveratrol in the pig‏ ‎‡9  1‏
919 ‎‡a  kineticsandbindingofthethyminednamismatchglycosylasemigmthwithmismatchcontainingdnasubstrates‏ ‎‡A  Kinetics and binding of the thymine-DNA mismatch glycosylase, Mig-Mth, with mismatch-containing DNA substrates‏ ‎‡9  1‏
919 ‎‡a  improvedsampletreatmentforthedeterminationoffructooligosaccharidesinmilkrelatedproductsbyliquidchromatographywithelectrochemicalandrefractiveindexdetection‏ ‎‡A  Improved sample treatment for the determination of fructooligosaccharides in milk related products by liquid chromatography with electrochemical and refractive index detection‏ ‎‡9  1‏
919 ‎‡a  importanceofterminalbasepairhydrogenbondingin3endproofreadingbytheklenowfragmentofdnapolymerase1‏ ‎‡A  Importance of terminal base pair hydrogen-bonding in 3'-end proofreading by the Klenow fragment of DNA polymerase I‏ ‎‡9  1‏
919 ‎‡a  imidecondensationasastrategyforthesynthesisofcorediversifiedgquadruplexligandswithanticancerandantiparasiticactivity‏ ‎‡A  Imide Condensation as a Strategy for the Synthesis of Core‐Diversified G‐Quadruplex Ligands with Anticancer and Antiparasitic Activity‏ ‎‡9  1‏
919 ‎‡a  hydroxytyrosolglucuronidesprotectrenaltubularepithelialcellsagainsth2o2inducedoxidativedamage‏ ‎‡A  Hydroxytyrosol glucuronides protect renal tubular epithelial cells against H(2)O(2) induced oxidative damage.‏ ‎‡9  1‏
919 ‎‡a  hydroxytyrosolglucuronidesprotectrenaltubularepithelialcellsagainsth‏ ‎‡A  Hydroxytyrosol glucuronides protect renal tubular epithelial cells against H‏ ‎‡9  1‏
919 ‎‡a  hydroxytyrosolandtyrosolsulfatemetabolitesprotectagainsttheoxidizedcholesterolprooxidanteffectincaco2humanenterocytelikecells‏ ‎‡A  Hydroxytyrosol and tyrosol sulfate metabolites protect against the oxidized cholesterol pro-oxidant effect in Caco-2 human enterocyte-like cells‏ ‎‡9  1‏
919 ‎‡a  highlypolarcarbohydratesstackontodnaduplexesviachπinteractions‏ ‎‡A  Highly Polar Carbohydrates Stack onto DNA Duplexes via CH/π Interactions‏ ‎‡9  1‏
919 ‎‡a  highlevelexpressionandcharacterizationofgalactomycesgeotrichumbt107lipase1inpichiapastoris‏ ‎‡A  High-level expression and characterization of Galactomyces geotrichum (BT107) lipase I in Pichia pastoris‏ ‎‡9  1‏
919 ‎‡a  highfidelityinvivoreplicationofdnabaseshapemimicswithoutwatsoncrickhydrogenbonds‏ ‎‡A  High-fidelity in vivo replication of DNA base shape mimics without Watson-Crick hydrogen bonds.‏ ‎‡9  1‏
919 ‎‡a  hemolyticactivityandsolubilizingcapacityofraffinoseandmelezitosefattyacidmonoesterspreparedbyenzymaticsynthesis‏ ‎‡A  Hemolytic activity and solubilizing capacity of raffinose and melezitose fatty acid monoesters prepared by enzymatic synthesis‏ ‎‡9  1‏
919 ‎‡a  glucosenucleobasepseudobasepairsbiomolecularinteractionswithindna‏ ‎‡A  Glucose-Nucleobase Pseudo Base Pairs: Biomolecular Interactions within DNA‏ ‎‡9  1‏
919 ‎‡a  glucosenucleobasepairswithindnaimpactofhydrophobicityalternativelinkingunitanddnapolymerasenucleotideinsertionstudies‏ ‎‡A  Glucose-nucleobase pairs within DNA: impact of hydrophobicity, alternative linking unit and DNA polymerase nucleotide insertion studies.‏ ‎‡9  1‏
919 ‎‡a  glucoseconjugationofantihiv1oligonucleotidescontainingunmethylatedcpgmotifsreducestheirimmunostimulatoryactivity‏ ‎‡A  Glucose conjugation of anti-HIV-1 oligonucleotides containing unmethylated CpG motifs reduces their immunostimulatory activity‏ ‎‡9  1‏
919 ‎‡a  gquadruplexidentificationinthegenomeofprotozoanparasitespointstonaphthalenediimideligandsasnewantiparasiticagents‏ ‎‡A  G-Quadruplex Identification in the Genome of Protozoan Parasites Points to Naphthalene Diimide Ligands as New Antiparasitic Agents.‏ ‎‡9  1‏
919 ‎‡a  experimentalmeasurementofcarbohydratearomaticstackinginwaterbyusingadanglingendeddnamodelsystem‏ ‎‡A  Experimental measurement of carbohydrate-aromatic stacking in water by using a dangling-ended DNA model system‏ ‎‡9  1‏
919 ‎‡a  enzymaticsynthesisofanovelpterostilbeneαglucosidebythecombinationofcyclodextringlucanotransferaseandamyloglucosidase‏ ‎‡A  Enzymatic Synthesis of a Novel Pterostilbene α-Glucoside by the Combination of Cyclodextrin Glucanotransferase and Amyloglucosidase.‏ ‎‡9  1‏
919 ‎‡a  enzymaticsynthesisofanovelneuroprotectivehydroxytyrosylglycoside‏ ‎‡A  Enzymatic Synthesis of a Novel Neuroprotective Hydroxytyrosyl Glycoside.‏ ‎‡9  1‏
919 ‎‡a  enhancedsamplingmoleculardynamicssimulationscorrectlypredictthediverseactivitiesofaseriesofstiffstilbenegquadruplexdnaligands‏ ‎‡A  Enhanced sampling molecular dynamics simulations correctly predict the diverse activities of a series of stiff-stilbene G-quadruplex DNA ligands‏ ‎‡9  1‏
919 ‎‡a  efficientreplicationbetweennonhydrogenbondednucleosideshapeanalogs‏ ‎‡A  Efficient replication between non-hydrogen-bonded nucleoside shape analogs‏ ‎‡9  1‏
919 ‎‡a  effectsofsugarfunctionalgroupshydrophobicityandfluorinationoncarbohydratednastackinginteractionsinwater‏ ‎‡A  Effects of sugar functional groups, hydrophobicity, and fluorination on carbohydrate-DNA stacking interactions in water.‏ ‎‡9  1‏
919 ‎‡a  effectsoflongtermconsumptionoflowdosesofresveratrolondietinducedmildhypercholesterolemiainpigsatranscriptomicapproachtodiseaseprevention‏ ‎‡A  Effects of long-term consumption of low doses of resveratrol on diet-induced mild hypercholesterolemia in pigs: a transcriptomic approach to disease prevention.‏ ‎‡9  1‏
919 ‎‡a  effectoflipophilizationofhydroxytyrosolonitsantioxidantactivityinfishoilsandfishoilinwateremulsions‏ ‎‡A  Effect of lipophilization of hydroxytyrosol on its antioxidant activity in fish oils and fish oil-in-water emulsions.‏ ‎‡9  1‏
919 ‎‡a  divalentnaphthalenediimideligandsdisplayhighselectivityforthehumantelomericgquadruplexink+buffer‏ ‎‡A  Divalent Naphthalene Diimide Ligands Display High Selectivity for the Human Telomeric G-quadruplex in K+ Buffer‏ ‎‡9  1‏
919 ‎‡a  cytotoxicantiangiogenicandantitelomeraseactivityofglucosylandacylresveratrolprodrugsandresveratrolsulfatemetabolites‏ ‎‡A  Cytotoxic, Antiangiogenic and Antitelomerase Activity of Glucosyl- and Acyl- Resveratrol Prodrugs and Resveratrol Sulfate Metabolites.‏ ‎‡9  1‏
919 ‎‡a  chemicallytuningresveratrolfortheeffectivekillingofgrampositivepathogens‏ ‎‡A  Chemically Tuning Resveratrol for the Effective Killing of Gram-Positive Pathogens‏ ‎‡9  1‏
919 ‎‡a  carbohydratenaphthalenediimideconjugatesaspotentialantiparasiticdrugssynthesisevaluationandstructureactivitystudies‏ ‎‡A  Carbohydrate-naphthalene diimide conjugates as potential antiparasitic drugs: Synthesis, evaluation and structure-activity studies‏ ‎‡9  1‏
919 ‎‡a  carbohydratednainteractionsatgquadruplexesfoldingandstabilitychangesbyattachingsugarsatthe5end‏ ‎‡A  Carbohydrate-DNA interactions at G-quadruplexes: folding and stability changes by attaching sugars at the 5'-end‏ ‎‡9  1‏
919 ‎‡a  bindingandbeyondwhatelsecangquadruplexligandsdo‏ ‎‡A  Binding and Beyond: What Else Can G-Quadruplex Ligands Do?‏ ‎‡9  1‏
919 ‎‡a  apolarcarbohydratesasdnacappingagents‏ ‎‡A  Apolar carbohydrates as DNA capping agents‏ ‎‡9  1‏
919 ‎‡a  antioxidantactivityofresveratrolinseveralfishlipidmatriceseffectofacylationandglucosylation‏ ‎‡A  Antioxidant activity of resveratrol in several fish lipid matrices: effect of acylation and glucosylation.‏ ‎‡9  1‏
919 ‎‡a  antioxidantactivityofalkylgallatesandglycosylalkylgallatesinfishoilinwateremulsionsrelevanceoftheirsurfaceactivepropertiesandofthetypeofemulsifier‏ ‎‡A  Antioxidant activity of alkyl gallates and glycosyl alkyl gallates in fish oil in water emulsions: relevance of their surface active properties and of the type of emulsifier‏ ‎‡9  1‏
919 ‎‡a  alkylatedresveratrolprodrugsandmetabolitesaspotentialtherapeuticsforneurodegenerativediseases‏ ‎‡A  Alkylated resveratrol prodrugs and metabolites as potential therapeutics for neurodegenerative diseases.‏ ‎‡9  1‏
919 ‎‡a  photoresponsivestiffstilbeneligandfuelsthereversibleunfoldingofgquadruplexdna‏ ‎‡A  A Photoresponsive Stiff-Stilbene Ligand Fuels the Reversible Unfolding of G-Quadruplex DNA.‏ ‎‡9  1‏
919 ‎‡a  highlyeffectivenonpolarisostereofdeoxyguanosinesynthesisstructurestackingandbasepairing‏ ‎‡A  A highly effective nonpolar isostere of deoxyguanosine: synthesis, structure, stacking, and base pairing‏ ‎‡9  1‏
919 ‎‡a  concisesynthesisofglucuronidemetabolitesofurolithinbresveratrolandhydroxytyrosol‏ ‎‡A  A concise synthesis of glucuronide metabolites of urolithin-B, resveratrol, and hydroxytyrosol.‏ ‎‡9  1‏
946 ‎‡a  b‏ ‎‡9  1‏
947 ‎‡a  ES‏ ‎‡9  1‏
996 ‎‡2  ISNI|0000000045129458‏
996 ‎‡2  LC|ns2012002593‏
996 ‎‡2  LC|no 98111003‏
996 ‎‡2  LC|no2014120511‏
996 ‎‡2  BNC|981061132544406706‏
996 ‎‡2  ISNI|0000000458440340‏
996 ‎‡2  BNE|XX5777041‏
996 ‎‡2  LC|no 95040146‏
996 ‎‡2  BNE|XX6386081‏
996 ‎‡2  BNE|XX6311558‏
996 ‎‡2  LC|no2008045545‏
996 ‎‡2  LC|ns2021002212‏
996 ‎‡2  BNE|XX5372207‏
996 ‎‡2  DNB|1337239720‏
996 ‎‡2  SUDOC|110829115‏
996 ‎‡2  LC|n 82093737‏
996 ‎‡2  SUDOC|164452923‏
996 ‎‡2  BNF|16422255‏
996 ‎‡2  LC|no2022010177‏
996 ‎‡2  LC|n 2024007061‏
996 ‎‡2  DNB|1076681123‏
996 ‎‡2  ISNI|0000000040018310‏
996 ‎‡2  BNE|XX1247450‏
996 ‎‡2  DNB|1057474878‏
996 ‎‡2  CAOONL|ncf11456096‏
996 ‎‡2  LC|n 99043166‏
996 ‎‡2  ISNI|0000000083385276‏
996 ‎‡2  RERO|A016578215‏
996 ‎‡2  SZ|1052300758‏
996 ‎‡2  LC|n 2023048665‏
996 ‎‡2  PLWABN|9810689021705606‏
996 ‎‡2  SUDOC|035020830‏
996 ‎‡2  BNF|13532617‏
996 ‎‡2  BNE|XX6136684‏
996 ‎‡2  DNB|1251805426‏
996 ‎‡2  BIBSYS|10080631‏
996 ‎‡2  DNB|1280969830‏
996 ‎‡2  ISNI|0000000035579009‏
996 ‎‡2  BNE|XX904318‏
996 ‎‡2  LC|no2009017922‏
996 ‎‡2  NTA|338928545‏
996 ‎‡2  ISNI|0000000362489641‏
996 ‎‡2  RERO|A000115799‏
996 ‎‡2  ISNI|000000011620265X‏
996 ‎‡2  BNE|XX4786828‏
996 ‎‡2  LC|no2022029574‏
996 ‎‡2  LC|no2012125487‏
996 ‎‡2  ISNI|0000000501149736‏
996 ‎‡2  BNE|XX824524‏
996 ‎‡2  LC|no2007022982‏
996 ‎‡2  NUKAT|nx2024007077‏
996 ‎‡2  SUDOC|201864053‏
996 ‎‡2  LC|no2016035305‏
996 ‎‡2  LC|no2015021542‏
996 ‎‡2  LC|n 2020005980‏
996 ‎‡2  DNB|1158366744‏
996 ‎‡2  ISNI|0000000070622885‏
996 ‎‡2  NKC|jx20080602027‏
996 ‎‡2  LC|no2021106966‏
996 ‎‡2  BNE|XX942858‏
996 ‎‡2  BNE|XX1756034‏
996 ‎‡2  LC|n 2015068623‏
996 ‎‡2  DNB|14072804X‏
996 ‎‡2  LC|ns2020000921‏
996 ‎‡2  BNC|981058517935106706‏
996 ‎‡2  LC|n 2012008313‏
996 ‎‡2  SUDOC|184293669‏
996 ‎‡2  DNB|188356460‏
996 ‎‡2  BNC|981059272201406706‏
996 ‎‡2  BNE|XX1434239‏
996 ‎‡2  DNB|1212959906‏
996 ‎‡2  LC|n 2007026314‏
996 ‎‡2  SUDOC|200484524‏
996 ‎‡2  NTA|183178491‏
996 ‎‡2  SUDOC|111287669‏
996 ‎‡2  ISNI|0000000389121492‏
996 ‎‡2  BNE|XX5392344‏
996 ‎‡2  DNB|1053087039‏
996 ‎‡2  BNC|981058512484206706‏
996 ‎‡2  LC|n 2014029553‏
996 ‎‡2  RERO|A009041453‏
996 ‎‡2  ISNI|0000000071400790‏
996 ‎‡2  SUDOC|270112545‏
996 ‎‡2  NDL|032608519‏
996 ‎‡2  BNE|XX891421‏
996 ‎‡2  ISNI|0000000033002863‏
996 ‎‡2  BNC|981061121376906706‏
996 ‎‡2  BNE|XX1430956‏
996 ‎‡2  BNE|XX1090474‏
996 ‎‡2  ISNI|0000000039944915‏
996 ‎‡2  ISNI|0000000053404990‏
996 ‎‡2  ISNI|0000000046247309‏
996 ‎‡2  J9U|987007357768605171‏
996 ‎‡2  BNF|13738230‏
996 ‎‡2  BNF|15896890‏
996 ‎‡2  BNE|XX1029984‏
996 ‎‡2  DNB|1202732615‏
996 ‎‡2  BNE|XX831092‏
996 ‎‡2  J9U|987007265679005171‏
996 ‎‡2  BNE|XX5462680‏
996 ‎‡2  RERO|A027095628‏
996 ‎‡2  DNB|1056765410‏
996 ‎‡2  DNB|1252689101‏
996 ‎‡2  LC|n 2011006577‏
996 ‎‡2  ISNI|0000000117535886‏
996 ‎‡2  DNB|1056478411‏
996 ‎‡2  BNE|XX1796104‏
996 ‎‡2  BNF|16920453‏
996 ‎‡2  DNB|1057044296‏
996 ‎‡2  RERO|A016530631‏
996 ‎‡2  NTA|078285070‏
996 ‎‡2  ISNI|0000000042782857‏
996 ‎‡2  BNE|XX1371300‏
996 ‎‡2  J9U|987010649072305171‏
996 ‎‡2  SUDOC|199574014‏
996 ‎‡2  LC|no 99054616‏
996 ‎‡2  ISNI|0000000042784473‏
996 ‎‡2  PTBNP|191488‏
996 ‎‡2  BNE|XX835795‏
996 ‎‡2  ISNI|0000000068998138‏
996 ‎‡2  BNF|12286709‏
996 ‎‡2  LC|no2007064526‏
996 ‎‡2  SUDOC|163921067‏
996 ‎‡2  BNE|XX942481‏
996 ‎‡2  ISNI|0000000059599100‏
996 ‎‡2  LC|no 98117626‏
996 ‎‡2  SUDOC|202888347‏
996 ‎‡2  LC|n 2017054174‏
996 ‎‡2  SUDOC|26181012X‏
996 ‎‡2  BNE|XX1023706‏
996 ‎‡2  BNF|16506785‏
996 ‎‡2  ISNI|0000000059933789‏
996 ‎‡2  LC|n 2010014948‏
996 ‎‡2  LC|no2009166970‏
996 ‎‡2  J9U|987009541283305171‏
996 ‎‡2  BNE|XX5080669‏
996 ‎‡2  SUDOC|169741737‏
996 ‎‡2  ISNI|0000000505023460‏
996 ‎‡2  DNB|118600150X‏
996 ‎‡2  ISNI|0000000060338178‏
996 ‎‡2  J9U|987007301462905171‏
996 ‎‡2  DNB|1056204834‏
996 ‎‡2  BNC|981058530186206706‏
996 ‎‡2  LC|no2011087899‏
996 ‎‡2  ISNI|000000007033922X‏
996 ‎‡2  BNE|XX888430‏
996 ‎‡2  BNE|XX6182798‏
996 ‎‡2  BNE|XX1652318‏
996 ‎‡2  ISNI|0000000081991686‏
996 ‎‡2  BNC|981058522065206706‏
996 ‎‡2  NTA|068425759‏
996 ‎‡2  LC|no2006133467‏
996 ‎‡2  DNB|142462284‏
996 ‎‡2  DNB|1055979336‏
996 ‎‡2  ISNI|0000000059687258‏
996 ‎‡2  ISNI|0000000059942845‏
996 ‎‡2  ISNI|0000000427600153‏
996 ‎‡2  LC|no2013026652‏
996 ‎‡2  NUKAT|n 2020216016‏
996 ‎‡2  DNB|1122070373‏
996 ‎‡2  LC|no 97038896‏
996 ‎‡2  SUDOC|230307914‏
996 ‎‡2  LC|no2011074340‏
996 ‎‡2  BNE|XX944478‏
996 ‎‡2  NSK|000280507‏
996 ‎‡2  BNCHL|10000000000000000817317‏
996 ‎‡2  BNE|XX879638‏
996 ‎‡2  LC|nb2015004800‏
996 ‎‡2  LC|no2024108728‏
996 ‎‡2  J9U|987007396002905171‏
996 ‎‡2  BNE|XX5116628‏
996 ‎‡2  BNE|XX1297519‏
996 ‎‡2  LC|no2009170604‏
996 ‎‡2  SUDOC|118941690‏
996 ‎‡2  ARBABN|000052962‏
996 ‎‡2  SUDOC|22834560X‏
996 ‎‡2  BNE|XX994607‏
996 ‎‡2  SUDOC|273266233‏
996 ‎‡2  LC|no2016086468‏
996 ‎‡2  PLWABN|9813297393305606‏
996 ‎‡2  LC|no2010167183‏
996 ‎‡2  SUDOC|145764354‏
996 ‎‡2  BNC|981058525080106706‏
996 ‎‡2  NYNYRILM|278862‏
996 ‎‡2  NSK|000722688‏
996 ‎‡2  ISNI|0000000509842391‏
996 ‎‡2  BNC|981061132418806706‏
996 ‎‡2  DNB|1115274937‏
996 ‎‡2  SUDOC|184140463‏
996 ‎‡2  BNCHL|10000000000000000810717‏
996 ‎‡2  LC|n 78009448‏
996 ‎‡2  LC|no2009113199‏
996 ‎‡2  ISNI|0000000023029528‏
996 ‎‡2  NTA|075270870‏
996 ‎‡2  NTA|111881765‏
996 ‎‡2  LC|n 94091489‏
996 ‎‡2  BNC|981058617959806706‏
996 ‎‡2  SUDOC|189013028‏
996 ‎‡2  DNB|1193271126‏
996 ‎‡2  LC|no2015031962‏
996 ‎‡2  SUDOC|069885192‏
996 ‎‡2  BNE|XX1108441‏
996 ‎‡2  DNB|1213300908‏
996 ‎‡2  BIBSYS|90896140‏
996 ‎‡2  ISNI|000000004422607X‏
996 ‎‡2  ISNI|0000000358266453‏
996 ‎‡2  ISNI|000000011891102X‏
996 ‎‡2  BNF|12389187‏
996 ‎‡2  BNC|981058610760106706‏
996 ‎‡2  BNCHL|10000000000000000835916‏
996 ‎‡2  DNB|1201206553‏
996 ‎‡2  BNE|XX5139222‏
996 ‎‡2  BNCHL|10000000000000000074453‏
996 ‎‡2  BNE|XX1177365‏
996 ‎‡2  SUDOC|272332623‏
996 ‎‡2  DNB|170411389‏
996 ‎‡2  DNB|1117047458‏
996 ‎‡2  ISNI|0000000060649574‏
996 ‎‡2  BNE|XX901209‏
996 ‎‡2  LC|n 86052768‏
996 ‎‡2  ISNI|0000000060061850‏
996 ‎‡2  LC|no2023038295‏
996 ‎‡2  ISNI|0000000059303672‏
996 ‎‡2  BNE|XX4866243‏
996 ‎‡2  ISNI|0000000033214559‏
996 ‎‡2  BNE|XX967761‏
996 ‎‡2  LC|no2009019123‏
996 ‎‡2  SUDOC|034158782‏
996 ‎‡2  PLWABN|9810540887905606‏
996 ‎‡2  NII|DA14264248‏
996 ‎‡2  DNB|1056672366‏
996 ‎‡2  ISNI|0000000059574069‏
996 ‎‡2  ISNI|0000000514293278‏
996 ‎‡2  JPG|500039258‏
996 ‎‡2  LC|no2023110810‏
996 ‎‡2  BNC|981058614219206706‏
996 ‎‡2  BNE|XX1119299‏
996 ‎‡2  BNE|XX1732716‏
996 ‎‡2  ISNI|0000000080908721‏
996 ‎‡2  BNC|981058581295906706‏
996 ‎‡2  LC|no2008185630‏
996 ‎‡2  ISNI|0000000105881378‏
996 ‎‡2  B2Q|0000347010‏
996 ‎‡2  KRNLK|KAC2020S6568‏
996 ‎‡2  ISNI|000000004757212X‏
996 ‎‡2  BNF|14044044‏
996 ‎‡2  BNE|XX1333480‏
996 ‎‡2  RERO|A013210817‏
996 ‎‡2  ISNI|0000000068120106‏
996 ‎‡2  BNF|15053075‏
997 ‎‡a  0 0 lived 0 0‏ ‎‡9  1‏