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University of Belgrade, Faculty of Pharmacy
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Titles
3d printed buccal films for prolonged-release of propranolol hydrochloride: Development, characterization and bioavailability prediction
[1]
3D printing of carvedilol oral dosage forms using selective laser sintering technique
[1]
3D printing of tablets by photopolymerization and selective laser sintering: development and process optimisation
[1]
3D štampa i karakterizacija nosača za dostavu ibuprofena u koštanom tkivu
[1]
3D štampanje tableta postupcima fotopolimerizacije i selektivnog laserskog sinterovanja: razvoj i optimizacija procesa
[1]
3D tehnika digitalne obrade svetlosti (DLP) primenjena u izradi dvoslojnih tableta: koncept kombinovane polipilule
[1]
3D-QSAR modeling and pharmacophore study of serotonin 5HT-₂A receptors antagonists
[1]
3D-QSAR modelovanje i analiza farmakofore antagonista serotoninskih 5-HT2A receptora
[1]
3D-QSAR studies and design of selective PI3K-α kinase inhibitors as potential antineoplastics
[1]
3D-QSAR studies and pharmacophore identification of AT(1) receptor antagonists
[1]
3D-QSAR studija i razvoj farmakofore agonista serotoninskih 5-HT2A receptora
[1]
3D-QSAR studija i razvoj farmakofore za dizajn novih antidepresiva sa dejstvom na transportere serotonina i histaminske H3 receptore
[1]
3D-QSAR study and design of antidepresives targeting SERT and histamine H3 receptor
[1]
3D-QSAR study and development of pharmacophore for serotonin 5-HT2A receptors agonists
[1]
3D-QSAR study and pharmacophore development of novel antidepressants affecting serotonine transporters and histamine H3 receptors
[1]
3D-QSAR study of adenosine 5'-phosphosulfate (APS) analouges as ligands for APS reductase
[1]
3D-QSAR study of pyrazolo[3,4-d]pyrimidines and 1,3,4-thiadiazoles as BCR-ABL1 inhibitors
[1]
3D-QSAR студија аналога аденозин 5'-фосфосулфата (APS) као лиганда за APS редуктазу
[1]
3D-QSAR, Virtual Screening, Docking and Design of Dual PI3K/mTOR Inhibitors with Enhanced Antiproliferative Activity
[1]
3D-Quantitative Structure-Activity Relationship and design of novel Rho- associated protein kinases-1 (ROCK1) inhibitors
[1]
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