about
Quantitative characterization of the influence of the nanoscale morphology of nanostructured surfaces on bacterial adhesion and biofilm formationEfficient one-pot synthesis, molecular docking and in silico ADME prediction of bis-(4-hydroxycoumarin-3-yl) methane derivatives as antileishmanial agents.Micro-nanopatterning as tool to study the role of physicochemical properties on cell-surface interactions.Cost effective technologies and renewable substrates for biosurfactants' production.Multiple Roles of Biosurfactants in Biofilms.Antileishmanial evaluation of clubbed bis(indolyl)-pyridine derivatives: One-pot synthesis, in vitro biological evaluations and in silico ADME prediction.Biphenyl tetrazole-thiazolidinediones as novel bacterial peptide deformylase inhibitors: Synthesis, biological evaluations and molecular docking study.Biosurfactant/s from Lactobacilli species: Properties, challenges and potential biomedical applications.Biomineralized anisotropic gold microplate-macrophage interactions reveal frustrated phagocytosis-like phenomenon: a novel paclitaxel drug delivery vehicle.Mur Ligase Inhibitors as Anti-bacterials: A Comprehensive Review.The antibacterial agent, moxifloxacin inhibits virulence factors of Candida albicans through multitargeting.Nanowires of silver-polyaniline nanocomposite synthesized via in situ polymerization and its novel functionality as an antibacterial agent.Hierarchical nanostructures of Au@ZnO: antibacterial and antibiofilm agent.The human muscarinic acetylcholine receptor antagonist, Dicyclomine targets signal transduction genes and inhibits the virulence factors in the human pathogen, Candida albicans.Limonene inhibits Candida albicans growth by inducing apoptosis.Antimicrobial properties of uncapped silver nanoparticles synthesized by DC arc thermal plasma techniqueBiofilm inhibition of linezolid-like Schiff bases: synthesis, biological activity, molecular docking and in silico ADME predictionAntileishmanial activity of novel indolyl-coumarin hybrids: Design, synthesis, biological evaluation, molecular docking study and in silico ADME predictionSynthesis, antileishmanial activity and docking study of N'-substitutedbenzylidene-2-(6,7-dihydrothieno[3,2-c]pyridin-5(4H)-yl)acetohydrazidesBacterial Peptide deformylase inhibition of cyano substituted biaryl analogs: Synthesis, in vitro biological evaluation, molecular docking study and in silico ADME predictionSerum responsive proteome reveals correlation between oxidative phosphorylation and morphogenesis in Candida albicans ATCC10231Molecular targets of biofabricated silver nanoparticles in Candida albicansSynthesis and anti-leishmanial activity of TRIS-glycine-β-alanine dipeptidic triazole dendron coated with nonameric mannoside glycoclusterGelatin interpenetration in poly N-isopropylacrylamide network reduces the compressive modulus of the scaffold: A property employed to mimic hepatic matrix stiffnessHelminthicidal and Larvicidal Potentials of Biogenic Silver Nanoparticles Synthesized from Medicinal Plant Momordica charantia
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Q27319511-1DA1ADFD-3D44-421E-8AE1-92C58EA9191AQ36519306-4CA4503B-45DC-41C8-9BEC-23D10087FC0FQ38096336-E09BE8CC-0D70-47E3-BD95-89ACDD654BCDQ38310210-1C88E02F-E84C-4DB6-BC3F-445366DBA50BQ38703287-D11406C5-2C39-4B73-95C6-BCA5FC206EE3Q38779566-12684E2A-DFB9-41E5-9CC1-E7F6836A2B0AQ38807495-0D8B2171-11F8-486C-B180-42E7086A2EEFQ38902936-04682853-BAD2-4FC8-9F45-E78EB8920D92Q38973251-BB6A2496-4E35-4899-89CD-7D41CAA4B80FQ39137012-82C4A1B9-14A0-4559-AF29-7B6C9AC145F8Q40250981-67990175-CD81-4E36-8131-58BCEFCCCAF7Q43438755-B52D01C4-DB39-4E06-A14F-85B4546C2438Q46583634-6F74C5E4-0F01-4E0D-933C-075FC757CC59Q49951687-29E01181-C8D9-4FD7-9971-58D87C2176C8Q50113612-29214A40-2FF7-4D78-B2D5-22EAC3DCE8B4Q84217694-31568B42-92A5-49FF-A626-8365AF7D4E67Q86542195-2EAE7A82-7120-4980-A2BB-C10303E22591Q87099888-3AEAFAAE-FA39-4E37-B3B3-A02751279203Q87263464-162DB155-EB41-46F3-AC88-FCB2B8606373Q87601961-4938320E-696E-4AB0-902F-F9E4FE852AF1Q89355019-C43CFC9C-01AE-4F46-94DA-75C0AB232463Q90284005-1D5DF315-D1A3-42F2-B736-94CC20BCE9A5Q90773435-5444F9A8-8FDE-4C6B-8189-0A7D8E917C1FQ91136066-CCDB7970-C4B8-47C9-A483-6791D1D76BFBQ92818830-BE74A75C-8A03-4958-BC18-1F9F1893464C
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description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Rajendra H Patil
@en
Rajendra H Patil
@nl
type
label
Rajendra H Patil
@en
Rajendra H Patil
@nl
prefLabel
Rajendra H Patil
@en
Rajendra H Patil
@nl
P31
P496
0000-0003-0534-7356