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Titles
Quantitation of the active alpha-2-macroglobulin by trypsin protease zymography
[1]
Quantitative analysis of arbutin and hydroquinone in strawberry tree (Arbutus unedo L., Ericaceae) leaves by gas chromatography-mass spectrometry
[1]
Quantitative analysis of sesquiterpene lactone cnicin in seven Centaurea species wild-growing in Serbia and Montenegro using 1H-NMR spectroscopy
[1]
Quantitative and qualitative analysis of concrete elements in wind park
[1]
Quantitative evaluation of sulfur-polymer matrix composite quality
[1]
Quantitative structure retention/activity relationships of biologically relevant 4-amino-7-chloroquinoline based compounds
[1]
Quantitative structure-activity relationship analysis of substituted arylazo pyridone dyes in photocatalytic system: Experimental and theoretical study
[2]
Quantitative structure-retention relationship of new N-substituted 2-alkylidene-4-oxothiazolidines
[1]
Quantitative structure-retention relationship study of steroidal tetraoxanes by thin-layer chromatography and multivariate chemometric methods
[1]
Quantitative structure-toxicity relationship study of some natural and synthetic coumarins using retention parameters
[1]
Quantum chemical insight into excited states of organometallic molecules
[1]
Quantum efficiency and responsivity of InSb photodiodes utilizing the Moss-Burstein effect
[1]
Quantum mechanical and spectroscopic (FT-IR, C-13, H-1 NMR and UV) investigations of potent antiepileptic drug 1-(4-chloro-phenyl)-3-phenyl-succinimide
[2]
Quercetagetin 6,7,3',4'-tetramethyl ether: a new flavonol from Artemisia annua
[1]
Quinoline based mono- and bis-(thio) carbohydrazones: synthesis, anticancer activity in 2D and 3D cancer and cancer stem cell models
[1]
Quinolines and Quinolones as Antibacterial, Antifungal, Antivirulence, Antiviral and Anti-parasitic Agents
[1]
Quinones and non-quinones from the defensive secretion of unciger transsilvanicus (Verhoeff, 1899) (diplopoda, julida, julidae), from Serbia
[1]
Računarski generisani molekulski deskriptori kao proxi-ji za modelovanje materijala i njihovog uticaja
[1]
Radical chemistry, degradation mechanism and toxicity evolution of BPA in the UV/chlorine and UV/H2O2
[1]
Radical reactions of xanthates: Annulation of the cyclopentene ring
[1]
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