VIAF

Virtual International Authority File

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Leader 00000nz a2200037n 45 0
001 WKP|Q47697002 (VIAF cluster) (Authority/Source Record)
003 WKP
005 20241120235909.0
008 241120nneanz||abbn n and d
035 ‎‡a (WKP)Q47697002‏
024 ‎‡a 0000-0003-0668-9227‏ ‎‡2 orcid‏
024 ‎‡a 25222849800‏ ‎‡2 scopus‏
035 ‎‡a (OCoLC)Q47697002‏
100 0 ‎‡a José Pedro Cerón-Carrasco‏ ‎‡9 ast‏ ‎‡9 sl‏
375 ‎‡a 1‏ ‎‡2 iso5218‏
400 0 ‎‡a José Pedro Cerón-Carrasco‏ ‎‡c Spanish chemist‏ ‎‡9 en‏
400 0 ‎‡a José Pedro Cerón-Carrasco‏ ‎‡c wetenschapper‏ ‎‡9 nl‏
400 0 ‎‡a José Pedro Cerón-Carrasco‏ ‎‡c químico español‏ ‎‡9 es‏
670 ‎‡a Author's A new fluorescence turn-on chemosensor for nanomolar detection of Al3+ constructed from a pyridine–pyrazole system‏
670 ‎‡a Author's A review of ligand-based virtual screening web tools and screening algorithms in large molecular databases in the age of big data‏
670 ‎‡a Author's A theoretical study of the reaction of beta-carotene with the nitrogen dioxide radical in solution.‏
670 ‎‡a Author's Acetylcholinesterase inhibitory assessment of isolated constituents from Salsola grandis Freitag, Vural & Adıgüzel and molecular modeling studies on N -acetyltryptophan‏
670 ‎‡a Author's Antibodies as Carrier Molecules: Encapsulating Anti-Inflammatory Drugs inside Herceptine‏
670 ‎‡a Author's Antioxidant properties of β-carotene isomers and their role in photosystems: insights from Ab initio simulations.‏
670 ‎‡a Author's Assessing the Importance of Proton Transfer Reactions in DNA‏
670 ‎‡a Author's Atomistic Molecular Dynamics Simulations of the Interactions of Oleic and 2-Hydroxyoleic Acids with Phosphatidylcholine Bilayers‏
670 ‎‡a Author's BRUSELAS: HPC Generic and Customizable Software Architecture for 3D Ligand-Based Virtual Screening of Large Molecular Databases‏
670 ‎‡a Author's Cisplatin cytotoxicity: a theoretical study of induced mutations‏
670 ‎‡a Author's Combined effect of stacking and solvation on the spontaneous mutation in DNA‏
670 ‎‡a Author's Conformational changes of β-carotene and zeaxanthin immersed in a model membrane through atomistic molecular dynamics simulations.‏
670 ‎‡a Author's Corrigendum to "Evaluation of estrogenic activity of red clover (Trifolium pratense L.) sprouts cultivated under different conditions by content of isoflavones, calorimetric study and molecular modelling" [Food Chem. 245 (2018) 324-336]‏
670 ‎‡a Author's Cover Feature: Tuning the Optical Properties of Phenanthriplatin: Towards New Photoactivatable Analogues‏
670 ‎‡a Author's Cover Feature: Tuning the Optical Properties of Phenanthriplatin: Towards New Photoactivatable Analogues (ChemPhotoChem 11/2017)‏
670 ‎‡a Author's Density functional theory study of the stability and vibrational spectra of the beta-carotene isomers.‏
670 ‎‡a Author's Determination of a solvent hydrogen-bond acidity scale by means of the solvatochromism of pyridinium-N-phenolate betaine dye 30 and PCM-TD-DFT calculations‏
670 ‎‡a Author's DFT Simulation of Structural and Optical Properties of 9-Aminoacridine Half-Sandwich Ru(II), Rh(III), and Ir(III) Antitumoral Complexes and Their Interaction with DNA.‏
670 ‎‡a Author's DNA spontaneous mutation and its role in the evolution of GC-content: assessing the impact of the genetic sequence.‏
670 ‎‡a Author's Double proton transfer mechanism in the adenine–uracil base pair and spontaneous mutation in RNA duplex‏
670 ‎‡a Author's Electric field induced DNA damage: an open door for selective mutations‏
670 ‎‡a Author's Electric-field induced mutation of DNA: a theoretical investigation of the GC base pair‏
670 ‎‡a Author's Enhanced Zn2+ ion-sensing behavior of a benzothiazole derivative on encapsulation by β-cyclodextrin‏
670 ‎‡a Author's Evaluation of butyrylcholinesterase inhibitory activity by chlorogenic acids and coffee extracts assed in ITC and docking simulation models‏
670 ‎‡a Author's Evaluation of estrogenic activity of red clover (Trifolium pratense L.) sprouts cultivated under different conditions by content of isoflavones, calorimetric study and molecular modelling‏
670 ‎‡a Author's Excited-state nature in benzodifuranone dyes: Insights from ab initio simulations‏
670 ‎‡a Author's Exploiting the cyclodextrins ability for antioxidants encapsulation: A computational approach to carnosol and carnosic acid embedding‏
670 ‎‡a Author's Exposing the G-quadruplex to electric fields: the role played by telomeres in the propagation of DNA errors‏
670 ‎‡a Author's First computational step towards the understanding of the antioxidant activity of the Phycocyanobilin:Ferredoxin Oxidoreductase in complex with biliverdin IXα‏
670 ‎‡a Author's How DNA is damaged by external electric fields: selective mutation vs. random degradation‏
670 ‎‡a Author's Hydrogen Bond-Directed Cruciform and Stacked Packing of a Pyrrole-Based Azaphenacene‏
670 ‎‡a Author's HYDROWEB, an Online Tool for the Calculation of Hydrodynamic Properties of Macromolecules‏
670 ‎‡a Author's Impact of DFT functionals on the predicted magnesium–DNA interaction: an ONIOM study‏
670 ‎‡a Author's Impact of DNA environment on the intrastrand cross-link lesions: hydrogen atom release as the last step of formation of G[8-5m]T.‏
670 ‎‡a Author's In vitro modulatory effects of functionalized pyrimidines and piperidine derivatives on Aryl hydrocarbon receptor‏
670 ‎‡a Author's In vitro modulatory effects of functionalized pyrimidines and piperidine derivatives on Aryl hydrocarbon receptor (AhR) and glucocorticoid receptor (GR) activities‏
670 ‎‡a Author's Influence of Mg2+ on the Guanine-Cytosine Tautomeric Equilibrium: Simulations of the Induced Intermolecular Proton Transfer‏
670 ‎‡a Author's Intermolecular proton transfer in microhydrated guanine-cytosine base pairs: a new mechanism for spontaneous mutation in DNA.‏
670 ‎‡a Author's Interplay between hydroxyl radical attack and H-bond stability in guanine–cytosine‏
670 ‎‡a Author's Interplay between solvent models and predicted optical spectra: A TD-DFT study of 7-OH-coumarin‏
670 ‎‡a Author's Labelling Herceptin with a novel oxaliplatin derivative: a computational approach towards the selective drug delivery.‏
670 ‎‡a Author's Molecular recognition of thiaclopride by Aplysia californica AChBP: new insights from a computational investigation.‏
670 ‎‡a Author's Mutagenic effects induced by the attack of NO2 radical to the guanine-cytosine base pair‏
670 ‎‡a Author's New insights on the molecular features and electrophysiological properties of dinotefuran, imidacloprid and acetamiprid neonicotinoid insecticides‏
670 ‎‡a Author's New insights on the molecular recognition of imidacloprid with Aplysia californica AChBP: a computational study‏
670 ‎‡a Author's Norditerpenoids with Selective Anti-Cholinesterase Activity from the Roots of Perovskia atriplicifolia Benth‏
670 ‎‡a Author's Photoactivatable platinum‏
670 ‎‡a Author's Photoactivatable platinum(II) compounds: in search of novel anticancer drugs‏
670 ‎‡a Author's Photooxidation of DNA as a key step in the cytotoxicity of photochromic diarylethenes‏
670 ‎‡a Author's S-adenosyl- l -methionine analogs as enhanced methyl donors: Towards novel epigenetic regulators‏
670 ‎‡a Author's Sedative and muscle relaxant activities of diterpenoids from Phlomidoschema parviflorum‏
670 ‎‡a Author's Sedative-hypnotic-like effect and molecular docking of di-naphthodiospyrol from Diospyros lotus in an animal model‏
670 ‎‡a Author's Selective in vitro and in silico butyrylcholinesterase inhibitory activity of diterpenes and rosmarinic acid isolated from Perovskia atriplicifolia Benth. and Salvia glutinosa L.‏
670 ‎‡a Author's Size and Flexibility Define the Inhibition of the H3N2 Influenza Endonuclease Enzyme by Calix[n]arenes‏
670 ‎‡a Author's Solvent polarity scales: determination of newET‏
670 ‎‡a Author's Solvent polarity scales: determination of newET(30) values for 84 organic solvents‏
670 ‎‡a Author's Stereoselective Encapsulation for a Triarylmethylium o,o-Dimer by Natural γ-Cyclodextrin: Origin of Chiral Recognition for the Axially Chiral Dicationic Guest‏
670 ‎‡a Author's Structure-based discovery of clinically approved drugs as Zika virus NS2B-NS3 protease inhibitors that potently inhibit Zika virus infection in vitro and in vivo‏
670 ‎‡a Author's Structure–Property Correlation behind the High Mobility of Carbazolocarbazole‏
670 ‎‡a Author's Synthesis and characterization of carbazolo[2,1-a]carbazole in thin film and single crystal field-effect transistors‏
670 ‎‡a Author's Systematic investigation and molecular modelling of complexation between several groups of flavonoids and HP-β-cyclodextrins‏
670 ‎‡a Author's Theoretical insights on the antioxidant activity of edaravone free radical scavengers derivatives‏
670 ‎‡a Author's Theoretical Prediction of Dual-Potency Anti-Tumor Agents: Combination of Oxoplatin with Other FDA-Approved Oncology Drugs‏
670 ‎‡a Author's Theoretical study of the low-lying excited states of -carotene isomers by a multireference configuration interaction method‏
670 ‎‡a Author's Theoretical study of the tautomerism in the one-electron oxidized guanine-cytosine base pair.‏
670 ‎‡a Author's Tuning the Optical Properties of Novel Antitumoral Drugs Based on Cyclometalated Iridium(III) Complexes‏
670 ‎‡a Author's Tuning the Optical Properties of Phenanthriplatin: Towards New Photoactivatable Analogues‏
670 ‎‡a Author's Using Theory To Reinterpret the Kinetics of Monofunctional Platinum Anticancer Drugs: Stacking Matters‏
670 ‎‡a Author's Visual detection of fluoride ion based on ICT mechanism‏
909 ‎‡a (scopus) 25222849800‏ ‎‡9 1‏
909 ‎‡a (orcid) 0000000306689227‏ ‎‡9 1‏
919 ‎‡a coverfeaturetuningtheopticalpropertiesofphenanthriplatintowardsnewphotoactivatableanalogues‏ ‎‡A Cover Feature: Tuning the Optical Properties of Phenanthriplatin: Towards New Photoactivatable Analogues‏ ‎‡9 1‏
919 ‎‡a corrigendumtoevaluationofestrogenicactivityofredclovertrifoliumpratense50sproutscultivatedunderdifferentconditionsbycontentofisoflavonescalorimetricstudyandmolecularmodelling‏ ‎‡A Corrigendum to "Evaluation of estrogenic activity of red clover (Trifolium pratense L.) sprouts cultivated under different conditions by content of isoflavones, calorimetric study and molecular modelling" [Food Chem. 245 (2018) 324-336]‏ ‎‡9 1‏
919 ‎‡a conformationalchangesofβcaroteneandzeaxanthinimmersedinamodelmembranethroughatomisticmoleculardynamicssimulations‏ ‎‡A Conformational changes of β-carotene and zeaxanthin immersed in a model membrane through atomistic molecular dynamics simulations.‏ ‎‡9 1‏
919 ‎‡a combinedeffectofstackingandsolvationonthespontaneousmutationindna‏ ‎‡A Combined effect of stacking and solvation on the spontaneous mutation in DNA‏ ‎‡9 1‏
919 ‎‡a cisplatincytotoxicityatheoreticalstudyofinducedmutations‏ ‎‡A Cisplatin cytotoxicity: a theoretical study of induced mutations‏ ‎‡9 1‏
919 ‎‡a bruselashpcgenericandcustomizablesoftwarearchitecturefor3dligandbasedvirtualscreeningoflargemoleculardatabases‏ ‎‡A BRUSELAS: HPC Generic and Customizable Software Architecture for 3D Ligand-Based Virtual Screening of Large Molecular Databases‏ ‎‡9 1‏
919 ‎‡a atomisticmoleculardynamicssimulationsoftheinteractionsofoleicand2hydroxyoleicacidswithphosphatidylcholinebilayers‏ ‎‡A Atomistic Molecular Dynamics Simulations of the Interactions of Oleic and 2-Hydroxyoleic Acids with Phosphatidylcholine Bilayers‏ ‎‡9 1‏
919 ‎‡a assessingtheimportanceofprotontransferreactionsindna‏ ‎‡A Assessing the Importance of Proton Transfer Reactions in DNA‏ ‎‡9 1‏
919 ‎‡a antioxidantpropertiesofβcaroteneisomersandtheirroleinphotosystemsinsightsfromabinitiosimulations‏ ‎‡A Antioxidant properties of β-carotene isomers and their role in photosystems: insights from Ab initio simulations.‏ ‎‡9 1‏
919 ‎‡a antibodiesascarriermoleculesencapsulatingantiinflammatorydrugsinsideherceptine‏ ‎‡A Antibodies as Carrier Molecules: Encapsulating Anti-Inflammatory Drugs inside Herceptine‏ ‎‡9 1‏
919 ‎‡a acetylcholinesteraseinhibitoryassessmentofisolatedconstituentsfromsalsolagrandisfreitagvuralandadiguzelandmolecularmodelingstudiesonnacetyltryptophan‏ ‎‡A Acetylcholinesterase inhibitory assessment of isolated constituents from Salsola grandis Freitag, Vural & Adıgüzel and molecular modeling studies on N -acetyltryptophan‏ ‎‡9 1‏
919 ‎‡a theoreticalstudyofthereactionofbetacarotenewiththenitrogendioxideradicalinsolution‏ ‎‡A A theoretical study of the reaction of beta-carotene with the nitrogen dioxide radical in solution.‏ ‎‡9 1‏
919 ‎‡a reviewofligandbasedvirtualscreeningwebtoolsandscreeningalgorithmsinlargemoleculardatabasesintheageofbigdata‏ ‎‡A A review of ligand-based virtual screening web tools and screening algorithms in large molecular databases in the age of big data‏ ‎‡9 1‏
919 ‎‡a newfluorescenceturnonchemosensorfornanomolardetectionofal3+constructedfromapyridinepyrazolesystem‏ ‎‡A A new fluorescence turn-on chemosensor for nanomolar detection of Al3+ constructed from a pyridine–pyrazole system‏ ‎‡9 1‏
919 ‎‡a visualdetectionoffluorideionbasedonictmechanism‏ ‎‡A Visual detection of fluoride ion based on ICT mechanism‏ ‎‡9 1‏
919 ‎‡a usingtheorytoreinterpretthekineticsofmonofunctionalplatinumanticancerdrugsstackingmatters‏ ‎‡A Using Theory To Reinterpret the Kinetics of Monofunctional Platinum Anticancer Drugs: Stacking Matters‏ ‎‡9 1‏
919 ‎‡a tuningtheopticalpropertiesofphenanthriplatintowardsnewphotoactivatableanalogues‏ ‎‡A Tuning the Optical Properties of Phenanthriplatin: Towards New Photoactivatable Analogues‏ ‎‡9 1‏
919 ‎‡a tuningtheopticalpropertiesofnovelantitumoraldrugsbasedoncyclometalatediridium3complexes‏ ‎‡A Tuning the Optical Properties of Novel Antitumoral Drugs Based on Cyclometalated Iridium(III) Complexes‏ ‎‡9 1‏
919 ‎‡a theoreticalstudyofthetautomerisminthe1electronoxidizedguaninecytosinebasepair‏ ‎‡A Theoretical study of the tautomerism in the one-electron oxidized guanine-cytosine base pair.‏ ‎‡9 1‏
919 ‎‡a theoreticalstudyofthelowlyingexcitedstatesofcaroteneisomersbyamultireferenceconfigurationinteractionmethod‏ ‎‡A Theoretical study of the low-lying excited states of -carotene isomers by a multireference configuration interaction method‏ ‎‡9 1‏
919 ‎‡a theoreticalpredictionofdualpotencyantitumoragentscombinationofoxoplatinwithotherfdaapprovedoncologydrugs‏ ‎‡A Theoretical Prediction of Dual-Potency Anti-Tumor Agents: Combination of Oxoplatin with Other FDA-Approved Oncology Drugs‏ ‎‡9 1‏
919 ‎‡a theoreticalinsightsontheantioxidantactivityofedaravonefreeradicalscavengersderivatives‏ ‎‡A Theoretical insights on the antioxidant activity of edaravone free radical scavengers derivatives‏ ‎‡9 1‏
919 ‎‡a systematicinvestigationandmolecularmodellingofcomplexationbetweenseveralgroupsofflavonoidsandhpβcyclodextrins‏ ‎‡A Systematic investigation and molecular modelling of complexation between several groups of flavonoids and HP-β-cyclodextrins‏ ‎‡9 1‏
919 ‎‡a synthesisandcharacterizationofcarbazolocarbazoleinthinfilmandsinglecrystalfieldeffecttransistors‏ ‎‡A Synthesis and characterization of carbazolo[2,1-a]carbazole in thin film and single crystal field-effect transistors‏ ‎‡9 1‏
919 ‎‡a structurepropertycorrelationbehindthehighmobilityofcarbazolocarbazole‏ ‎‡A Structure–Property Correlation behind the High Mobility of Carbazolocarbazole‏ ‎‡9 1‏
919 ‎‡a structurebaseddiscoveryofclinicallyapproveddrugsaszikavirusns2bns3proteaseinhibitorsthatpotentlyinhibitzikavirusinfectioninvitroandinvivo‏ ‎‡A Structure-based discovery of clinically approved drugs as Zika virus NS2B-NS3 protease inhibitors that potently inhibit Zika virus infection in vitro and in vivo‏ ‎‡9 1‏
919 ‎‡a stereoselectiveencapsulationforatriarylmethyliumoodimerbynaturalγcyclodextrinoriginofchiralrecognitionfortheaxiallychiraldicationicguest‏ ‎‡A Stereoselective Encapsulation for a Triarylmethylium o,o-Dimer by Natural γ-Cyclodextrin: Origin of Chiral Recognition for the Axially Chiral Dicationic Guest‏ ‎‡9 1‏
919 ‎‡a solventpolarityscalesdeterminationofnewet30valuesfor84organicsolvents‏ ‎‡A Solvent polarity scales: determination of newET(30) values for 84 organic solvents‏ ‎‡9 1‏
919 ‎‡a solventpolarityscalesdeterminationofnewet‏ ‎‡A Solvent polarity scales: determination of newET‏ ‎‡9 1‏
919 ‎‡a sizeandflexibilitydefinetheinhibitionoftheh3n2influenzaendonucleaseenzymebycalixarenes‏ ‎‡A Size and Flexibility Define the Inhibition of the H3N2 Influenza Endonuclease Enzyme by Calix[n]arenes‏ ‎‡9 1‏
919 ‎‡a selectiveinvitroandinsilicobutyrylcholinesteraseinhibitoryactivityofditerpenesandrosmarinicacidisolatedfromperovskiaatriplicifoliabenthandsalviaglutinosa50‏ ‎‡A Selective in vitro and in silico butyrylcholinesterase inhibitory activity of diterpenes and rosmarinic acid isolated from Perovskia atriplicifolia Benth. and Salvia glutinosa L.‏ ‎‡9 1‏
919 ‎‡a sedativehypnoticlikeeffectandmoleculardockingof501naphthodiospyrolfromdiospyroslotusinananimalmodel‏ ‎‡A Sedative-hypnotic-like effect and molecular docking of di-naphthodiospyrol from Diospyros lotus in an animal model‏ ‎‡9 1‏
919 ‎‡a sedativeandmusclerelaxantactivitiesofditerpenoidsfromphlomidoschemaparviflorum‏ ‎‡A Sedative and muscle relaxant activities of diterpenoids from Phlomidoschema parviflorum‏ ‎‡9 1‏
919 ‎‡a sadenosyl50methionineanalogsasenhancedmethyldonorstowardsnovelepigeneticregulators‏ ‎‡A S-adenosyl- l -methionine analogs as enhanced methyl donors: Towards novel epigenetic regulators‏ ‎‡9 1‏
919 ‎‡a photooxidationofdnaasakeystepinthecytotoxicityofphotochromicdiarylethenes‏ ‎‡A Photooxidation of DNA as a key step in the cytotoxicity of photochromic diarylethenes‏ ‎‡9 1‏
919 ‎‡a photoactivatableplatinum2compoundsinsearchofnovelanticancerdrugs‏ ‎‡A Photoactivatable platinum(II) compounds: in search of novel anticancer drugs‏ ‎‡9 1‏
919 ‎‡a photoactivatableplatinum‏ ‎‡A Photoactivatable platinum‏ ‎‡9 1‏
919 ‎‡a norditerpenoidswithselectiveanticholinesteraseactivityfromtherootsofperovskiaatriplicifoliabenth‏ ‎‡A Norditerpenoids with Selective Anti-Cholinesterase Activity from the Roots of Perovskia atriplicifolia Benth‏ ‎‡9 1‏
919 ‎‡a newinsightsonthemolecularrecognitionofimidaclopridwithaplysiacalifornicaachbpacomputationalstudy‏ ‎‡A New insights on the molecular recognition of imidacloprid with Aplysia californica AChBP: a computational study‏ ‎‡9 1‏
919 ‎‡a newinsightsonthemolecularfeaturesandelectrophysiologicalpropertiesofdinotefuranimidaclopridandacetamipridneonicotinoidinsecticides‏ ‎‡A New insights on the molecular features and electrophysiological properties of dinotefuran, imidacloprid and acetamiprid neonicotinoid insecticides‏ ‎‡9 1‏
919 ‎‡a mutageniceffectsinducedbytheattackofno2radicaltotheguaninecytosinebasepair‏ ‎‡A Mutagenic effects induced by the attack of NO2 radical to the guanine-cytosine base pair‏ ‎‡9 1‏
919 ‎‡a molecularrecognitionofthiaclopridebyaplysiacalifornicaachbpnewinsightsfromacomputationalinvestigation‏ ‎‡A Molecular recognition of thiaclopride by Aplysia californica AChBP: new insights from a computational investigation.‏ ‎‡9 1‏
919 ‎‡a labellingherceptinwithanoveloxaliplatinderivativeacomputationalapproachtowardstheselectivedrugdelivery‏ ‎‡A Labelling Herceptin with a novel oxaliplatin derivative: a computational approach towards the selective drug delivery.‏ ‎‡9 1‏
919 ‎‡a interplaybetweensolventmodelsandpredictedopticalspectraatddftstudyof75coumarin‏ ‎‡A Interplay between solvent models and predicted optical spectra: A TD-DFT study of 7-OH-coumarin‏ ‎‡9 1‏
919 ‎‡a interplaybetweenhydroxylradicalattackandhbondstabilityinguaninecytosine‏ ‎‡A Interplay between hydroxyl radical attack and H-bond stability in guanine–cytosine‏ ‎‡9 1‏
919 ‎‡a intermolecularprotontransferinmicrohydratedguaninecytosinebasepairsanewmechanismforspontaneousmutationindna‏ ‎‡A Intermolecular proton transfer in microhydrated guanine-cytosine base pairs: a new mechanism for spontaneous mutation in DNA.‏ ‎‡9 1‏
919 ‎‡a influenceofmg2+ontheguaninecytosinetautomericequilibriumsimulationsoftheinducedintermolecularprotontransfer‏ ‎‡A Influence of Mg2+ on the Guanine-Cytosine Tautomeric Equilibrium: Simulations of the Induced Intermolecular Proton Transfer‏ ‎‡9 1‏
919 ‎‡a invitromodulatoryeffectsoffunctionalizedpyrimidinesandpiperidinederivativesonarylhydrocarbonreceptorahrandglucocorticoidreceptorgractivities‏ ‎‡A In vitro modulatory effects of functionalized pyrimidines and piperidine derivatives on Aryl hydrocarbon receptor (AhR) and glucocorticoid receptor (GR) activities‏ ‎‡9 1‏
919 ‎‡a invitromodulatoryeffectsoffunctionalizedpyrimidinesandpiperidinederivativesonarylhydrocarbonreceptor‏ ‎‡A In vitro modulatory effects of functionalized pyrimidines and piperidine derivatives on Aryl hydrocarbon receptor‏ ‎‡9 1‏
919 ‎‡a impactofdnaenvironmentontheintrastrandcrosslinklesionshydrogenatomreleaseasthelaststepofformationofgt‏ ‎‡A Impact of DNA environment on the intrastrand cross-link lesions: hydrogen atom release as the last step of formation of G[8-5m]T.‏ ‎‡9 1‏
919 ‎‡a impactofdftfunctionalsonthepredictedmagnesiumdnainteractionanoniomstudy‏ ‎‡A Impact of DFT functionals on the predicted magnesium–DNA interaction: an ONIOM study‏ ‎‡9 1‏
919 ‎‡a hydrowebanonlinetoolforthecalculationofhydrodynamicpropertiesofmacromolecules‏ ‎‡A HYDROWEB, an Online Tool for the Calculation of Hydrodynamic Properties of Macromolecules‏ ‎‡9 1‏
919 ‎‡a hydrogenbonddirectedcruciformandstackedpackingofapyrrolebasedazaphenacene‏ ‎‡A Hydrogen Bond-Directed Cruciform and Stacked Packing of a Pyrrole-Based Azaphenacene‏ ‎‡9 1‏
919 ‎‡a howdnaisdamagedbyexternalelectricfieldsselectivemutationvsrandomdegradation‏ ‎‡A How DNA is damaged by external electric fields: selective mutation vs. random degradation‏ ‎‡9 1‏
919 ‎‡a 1computationalsteptowardstheunderstandingoftheantioxidantactivityofthephycocyanobilinferredoxinoxidoreductaseincomplexwithbiliverdinixα‏ ‎‡A First computational step towards the understanding of the antioxidant activity of the Phycocyanobilin:Ferredoxin Oxidoreductase in complex with biliverdin IXα‏ ‎‡9 1‏
919 ‎‡a exposingthegquadruplextoelectricfieldstheroleplayedbytelomeresinthepropagationofdnaerrors‏ ‎‡A Exposing the G-quadruplex to electric fields: the role played by telomeres in the propagation of DNA errors‏ ‎‡9 1‏
919 ‎‡a exploitingthecyclodextrinsabilityforantioxidantsencapsulationacomputationalapproachtocarnosolandcarnosicacidembedding‏ ‎‡A Exploiting the cyclodextrins ability for antioxidants encapsulation: A computational approach to carnosol and carnosic acid embedding‏ ‎‡9 1‏
919 ‎‡a excitedstatenatureinbenzodifuranonedyesinsightsfromabinitiosimulations‏ ‎‡A Excited-state nature in benzodifuranone dyes: Insights from ab initio simulations‏ ‎‡9 1‏
919 ‎‡a evaluationofestrogenicactivityofredclovertrifoliumpratense50sproutscultivatedunderdifferentconditionsbycontentofisoflavonescalorimetricstudyandmolecularmodelling‏ ‎‡A Evaluation of estrogenic activity of red clover (Trifolium pratense L.) sprouts cultivated under different conditions by content of isoflavones, calorimetric study and molecular modelling‏ ‎‡9 1‏
919 ‎‡a evaluationofbutyrylcholinesteraseinhibitoryactivitybychlorogenicacidsandcoffeeextractsassedinitcanddockingsimulationmodels‏ ‎‡A Evaluation of butyrylcholinesterase inhibitory activity by chlorogenic acids and coffee extracts assed in ITC and docking simulation models‏ ‎‡9 1‏
919 ‎‡a enhancedzn2+ionsensingbehaviorofabenzothiazolederivativeonencapsulationbyβcyclodextrin‏ ‎‡A Enhanced Zn2+ ion-sensing behavior of a benzothiazole derivative on encapsulation by β-cyclodextrin‏ ‎‡9 1‏
919 ‎‡a electricfieldinducedmutationofdnaatheoreticalinvestigationofthegcbasepair‏ ‎‡A Electric-field induced mutation of DNA: a theoretical investigation of the GC base pair‏ ‎‡9 1‏
919 ‎‡a electricfieldinduceddnadamageanopendoorforselectivemutations‏ ‎‡A Electric field induced DNA damage: an open door for selective mutations‏ ‎‡9 1‏
919 ‎‡a doubleprotontransfermechanismintheadenineuracilbasepairandspontaneousmutationinrnaduplex‏ ‎‡A Double proton transfer mechanism in the adenine–uracil base pair and spontaneous mutation in RNA duplex‏ ‎‡9 1‏
919 ‎‡a dnaspontaneousmutationanditsroleintheevolutionofgccontentassessingtheimpactofthegeneticsequence‏ ‎‡A DNA spontaneous mutation and its role in the evolution of GC-content: assessing the impact of the genetic sequence.‏ ‎‡9 1‏
919 ‎‡a dftsimulationofstructuralandopticalpropertiesof9aminoacridinehalfsandwichru2rh3andir3antitumoralcomplexesandtheirinteractionwithdna‏ ‎‡A DFT Simulation of Structural and Optical Properties of 9-Aminoacridine Half-Sandwich Ru(II), Rh(III), and Ir(III) Antitumoral Complexes and Their Interaction with DNA.‏ ‎‡9 1‏
919 ‎‡a determinationofasolventhydrogenbondacidityscalebymeansofthesolvatochromismofpyridiniumnphenolatebetainedye30andpcmtddftcalculations‏ ‎‡A Determination of a solvent hydrogen-bond acidity scale by means of the solvatochromism of pyridinium-N-phenolate betaine dye 30 and PCM-TD-DFT calculations‏ ‎‡9 1‏
919 ‎‡a densityfunctionaltheorystudyofthestabilityandvibrationalspectraofthebetacaroteneisomers‏ ‎‡A Density functional theory study of the stability and vibrational spectra of the beta-carotene isomers.‏ ‎‡9 1‏
919 ‎‡a coverfeaturetuningtheopticalpropertiesofphenanthriplatintowardsnewphotoactivatableanalogueschemphotochem11‏ ‎‡A Cover Feature: Tuning the Optical Properties of Phenanthriplatin: Towards New Photoactivatable Analogues (ChemPhotoChem 11/2017)‏ ‎‡9 1‏
943 ‎‡a 201x‏ ‎‡A 2017‏ ‎‡9 1‏
946 ‎‡a b‏ ‎‡9 1‏
996 ‎‡2 SUDOC|170748391‏
996 ‎‡2 BNCHL|10000000000000000275236‏
996 ‎‡2 ISNI|0000000036197213‏
996 ‎‡2 BAV|495_178493‏
996 ‎‡2 BNE|XX4970110‏
996 ‎‡2 BNCHL|10000000000000000079061‏
996 ‎‡2 DNB|1022924788‏
996 ‎‡2 BNE|XX1678667‏
996 ‎‡2 PTBNP|1745463‏
996 ‎‡2 DNB|1158861702‏
996 ‎‡2 NKC|pna2006322488‏
996 ‎‡2 ISNI|0000000042481739‏
996 ‎‡2 DNB|170756068‏
996 ‎‡2 BNE|XX5394726‏
996 ‎‡2 BNE|XX1491918‏
996 ‎‡2 BNE|XX839822‏
996 ‎‡2 ISNI|0000000115903569‏
996 ‎‡2 LC|no 97039752‏
996 ‎‡2 CAOONL|ncf10471502‏
996 ‎‡2 LC|n 2014019347‏
996 ‎‡2 SUDOC|108385701‏
996 ‎‡2 LC|no2014060482‏
996 ‎‡2 DNB|116236128X‏
996 ‎‡2 RERO|A006472048‏
996 ‎‡2 DNB|1057078409‏
996 ‎‡2 BNE|XX1503618‏
996 ‎‡2 BNC|981061106869206706‏
996 ‎‡2 DNB|1277582017‏
996 ‎‡2 BNC|981058611154006706‏
996 ‎‡2 ISNI|0000000059347720‏
996 ‎‡2 BNE|XX841888‏
996 ‎‡2 BNCHL|10000000000000000168728‏
996 ‎‡2 BNE|XX4731044‏
996 ‎‡2 LC|no 95040773‏
996 ‎‡2 DNB|1125983639‏
996 ‎‡2 BNF|14041892‏
996 ‎‡2 ISNI|0000000084638263‏
996 ‎‡2 BNE|XX1207212‏
996 ‎‡2 BNF|12253170‏
996 ‎‡2 LC|n 94070503‏
996 ‎‡2 LC|n 84168995‏
996 ‎‡2 LC|no2010087283‏
996 ‎‡2 BNC|981058521208306706‏
996 ‎‡2 ISNI|000000006712755X‏
996 ‎‡2 CAOONL|ncf13668933‏
996 ‎‡2 SUDOC|031286682‏
996 ‎‡2 ISNI|0000000060195170‏
996 ‎‡2 BNCHL|10000000000000000837551‏
996 ‎‡2 ISNI|0000000037667168‏
996 ‎‡2 BNE|XX4781863‏
996 ‎‡2 BNE|XX1409003‏
996 ‎‡2 SUDOC|072401354‏
996 ‎‡2 J9U|987007450186705171‏
996 ‎‡2 ISNI|0000000068411798‏
996 ‎‡2 BNE|XX939135‏
996 ‎‡2 ISNI|0000000060740781‏
996 ‎‡2 LC|n 96074242‏
996 ‎‡2 RERO|A027419012‏
996 ‎‡2 ISNI|0000000039746716‏
996 ‎‡2 BLBNB|000391434‏
996 ‎‡2 BIBSYS|4073527‏
996 ‎‡2 ISNI|0000000107815358‏
996 ‎‡2 LC|no2004017282‏
996 ‎‡2 LC|no2019052163‏
996 ‎‡2 BNE|XX1671197‏
996 ‎‡2 BNF|14830802‏
996 ‎‡2 LC|ns2016003147‏
996 ‎‡2 LC|n 96071307‏
996 ‎‡2 LC|no 93017325‏
996 ‎‡2 BNE|XX1051831‏
996 ‎‡2 NTA|095913254‏
996 ‎‡2 LC|no2023110802‏
996 ‎‡2 LC|n 82087895‏
996 ‎‡2 LC|n 93065904‏
996 ‎‡2 BNC|981058522082106706‏
996 ‎‡2 BNE|XX1424795‏
996 ‎‡2 ISNI|0000000059409936‏
996 ‎‡2 BNCHL|10000000000000000212552‏
996 ‎‡2 ISNI|000000006075856X‏
996 ‎‡2 ISNI|0000000109332448‏
996 ‎‡2 ISNI|0000000059601178‏
996 ‎‡2 ISNI|0000000043532964‏
996 ‎‡2 BNC|981058516468506706‏
996 ‎‡2 SUDOC|09740957X‏
996 ‎‡2 BNE|XX1751861‏
996 ‎‡2 BNC|981058521168906706‏
996 ‎‡2 BNC|981058512520906706‏
996 ‎‡2 DNB|1299320856‏
996 ‎‡2 BNE|XX4772398‏
996 ‎‡2 LC|n 93123754‏
996 ‎‡2 ISNI|0000000136881653‏
996 ‎‡2 CAOONL|ncf11496348‏
996 ‎‡2 BNCHL|10000000000000000022351‏
996 ‎‡2 LC|n 85255373‏
996 ‎‡2 DNB|1060680890‏
996 ‎‡2 DNB|1059899698‏
996 ‎‡2 NII|DA15863408‏
996 ‎‡2 NUKAT|n 2016261590‏
996 ‎‡2 PTBNP|224601‏
996 ‎‡2 BNE|XX1141512‏
996 ‎‡2 BNE|XX1589312‏
996 ‎‡2 LC|no2002068567‏
996 ‎‡2 ISNI|0000000501382335‏
996 ‎‡2 BNC|981058509903506706‏
996 ‎‡2 PTBNP|1630281‏
996 ‎‡2 ISNI|0000000059421572‏
996 ‎‡2 BNE|XX1584216‏
996 ‎‡2 LC|no2013114760‏
996 ‎‡2 ISNI|0000000081545141‏
996 ‎‡2 BNCHL|10000000000000000128781‏
996 ‎‡2 BNE|XX5001812‏
996 ‎‡2 DNB|118829181‏
996 ‎‡2 BNC|981061105474506706‏
996 ‎‡2 DNB|1032973005‏
996 ‎‡2 JPG|500035965‏
996 ‎‡2 BNE|XX5758762‏
996 ‎‡2 SUDOC|219876584‏
996 ‎‡2 LC|n 80059904‏
996 ‎‡2 LC|no2015148556‏
996 ‎‡2 LC|n 94104831‏
996 ‎‡2 DNB|1229995250‏
996 ‎‡2 BNCHL|10000000000000000238341‏
996 ‎‡2 BNE|XX835811‏
996 ‎‡2 BNE|XX1757993‏
996 ‎‡2 BNC|981061194968006706‏
996 ‎‡2 BNE|XX5850338‏
996 ‎‡2 SUDOC|195241827‏
996 ‎‡2 BNE|XX1089439‏
996 ‎‡2 BNCHL|10000000000000000120146‏
996 ‎‡2 NTA|072639814‏
996 ‎‡2 LC|nr 98015110‏
996 ‎‡2 BNCHL|10000000000000000839033‏
996 ‎‡2 BNC|981058508766106706‏
996 ‎‡2 LC|n 98106323‏
996 ‎‡2 LC|no2022080070‏
996 ‎‡2 LC|n 87913656‏
996 ‎‡2 DNB|1057465887‏
996 ‎‡2 NKC|mzk20211106410‏
996 ‎‡2 DE633|pe50050316‏
996 ‎‡2 ISNI|0000000061136113‏
996 ‎‡2 BNC|981059719196006706‏
996 ‎‡2 LC|n 2003011733‏
996 ‎‡2 LC|no2012099957‏
996 ‎‡2 LC|n 88652383‏
996 ‎‡2 BNE|XX977706‏
996 ‎‡2 BNE|XX5399998‏
996 ‎‡2 ISNI|000000012211906X‏
996 ‎‡2 BNE|XX1511142‏
996 ‎‡2 LC|no2017146166‏
996 ‎‡2 ISNI|0000000033699998‏
996 ‎‡2 BNE|XX1737570‏
996 ‎‡2 LC|n 2006087054‏
996 ‎‡2 ISNI|0000000030463939‏
996 ‎‡2 BNE|XX902240‏
996 ‎‡2 ISNI|0000000059538498‏
996 ‎‡2 BNE|XX985293‏
996 ‎‡2 LC|no2002046435‏
996 ‎‡2 BNE|XX1110421‏
996 ‎‡2 SUDOC|091531446‏
996 ‎‡2 BNF|15511729‏
996 ‎‡2 BNE|XX950862‏
996 ‎‡2 BNC|981058516166006706‏
996 ‎‡2 SUDOC|11297886X‏
996 ‎‡2 LC|n 50001870‏
996 ‎‡2 BNE|XX1120244‏
996 ‎‡2 NYNYRILM|92291‏
996 ‎‡2 BNC|981058513963606706‏
996 ‎‡2 BNE|XX1717097‏
996 ‎‡2 DNB|171155262‏
996 ‎‡2 LC|n 90616287‏
996 ‎‡2 LC|n 88074829‏
996 ‎‡2 BNC|981058508939506706‏
996 ‎‡2 ISNI|0000000059430188‏
996 ‎‡2 BNC|981058510783906706‏
996 ‎‡2 RERO|A003221595‏
996 ‎‡2 BNE|XX1183954‏
996 ‎‡2 ISNI|000000003791152X‏
996 ‎‡2 BNE|XX5721802‏
996 ‎‡2 DNB|129575984‏
996 ‎‡2 ISNI|0000000062124528‏
996 ‎‡2 CAOONL|ncf12003945‏
996 ‎‡2 ISNI|0000000029757403‏
996 ‎‡2 BNCHL|10000000000000000008369‏
996 ‎‡2 BNCHL|10000000000000000128784‏
996 ‎‡2 BNE|XX1080655‏
996 ‎‡2 LC|n 94002384‏
996 ‎‡2 LC|n 97022568‏
996 ‎‡2 LC|n 83136213‏
996 ‎‡2 SUDOC|09587075X‏
996 ‎‡2 LC|no2023059513‏
996 ‎‡2 BNCHL|10000000000000000092070‏
996 ‎‡2 BNCHL|10000000000000000224248‏
996 ‎‡2 BNE|XX1051828‏
996 ‎‡2 N6I|vtls001277920‏
996 ‎‡2 BNE|XX4918882‏
996 ‎‡2 ISNI|0000000123145366‏
996 ‎‡2 LC|no2015109494‏
996 ‎‡2 BNE|XX934930‏
996 ‎‡2 LC|no2017145468‏
996 ‎‡2 LC|nr2001052345‏
996 ‎‡2 BNE|XX835650‏
996 ‎‡2 PTBNP|1720192‏
996 ‎‡2 BNE|XX1724439‏
996 ‎‡2 LC|n 80152753‏
996 ‎‡2 BNE|XX5102478‏
996 ‎‡2 ISNI|000000003178622X‏
996 ‎‡2 LC|no2007101067‏
996 ‎‡2 BNC|981058612561906706‏
996 ‎‡2 ISNI|000000007076340X‏
996 ‎‡2 SUDOC|027426998‏
996 ‎‡2 ISNI|0000000059538324‏
996 ‎‡2 BNCHL|10000000000000000059869‏
996 ‎‡2 LC|nb2003028707‏
996 ‎‡2 J9U|987007318018805171‏
996 ‎‡2 NTA|104708832‏
996 ‎‡2 BNE|XX871668‏
996 ‎‡2 BNF|16597350‏
996 ‎‡2 BNC|981060895163706706‏
996 ‎‡2 BNE|XX894156‏
996 ‎‡2 BNE|XX922456‏
996 ‎‡2 BNE|XX1221019‏
996 ‎‡2 ISNI|0000000059294411‏
996 ‎‡2 ISNI|0000000101126500‏
996 ‎‡2 PTBNP|35381‏
996 ‎‡2 ISNI|0000000059349718‏
996 ‎‡2 ISNI|0000000452132478‏
996 ‎‡2 BNC|981058517738206706‏
996 ‎‡2 BNC|981058522283106706‏
996 ‎‡2 ISNI|0000000059252975‏
996 ‎‡2 BNF|16248281‏
996 ‎‡2 SUDOC|077812603‏
996 ‎‡2 BNE|XX4940557‏
996 ‎‡2 PLWABN|9810555932605606‏
996 ‎‡2 ISNI|0000000097869773‏
996 ‎‡2 BNE|XX5648834‏
996 ‎‡2 ISNI|0000000118525727‏
996 ‎‡2 ISNI|0000000059522728‏
996 ‎‡2 BNE|XX5463993‏
996 ‎‡2 BNE|XX1125738‏
996 ‎‡2 ISNI|0000000069512814‏
996 ‎‡2 BNC|981061006764506706‏
996 ‎‡2 BNE|XX1165366‏
996 ‎‡2 RERO|A018645027‏
996 ‎‡2 LC|no2022122339‏
996 ‎‡2 BNCHL|10000000000000000839229‏
996 ‎‡2 NII|DA15385452‏
996 ‎‡2 ISNI|0000000027109648‏
996 ‎‡2 SUDOC|092422896‏
996 ‎‡2 SUDOC|203587561‏
996 ‎‡2 LC|n 2009050189‏
997 ‎‡a 0 0 lived 0 0‏ ‎‡9 1‏