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Cross-linguistic patterns in the acquisition of quantifiers.
Katsos N, Cummins C, Ezeizabarrena MJ, Gavarró A, Kuvač Kraljević J, Hrzica G, Grohmann KK, Skordi A, Jensen de López K, Sundahl L, van Hout A, Hollebrandse B, Overweg J, Faber M, van Koert M, Smith N, Vija M, Zupping S, Kunnari S, Morisseau T, Rusieshvili M, Yatsushiro K, Fengler A, Varlokosta S, Konstantzou K, Farby S, Guasti MT, Vernice M, Okabe R, Isobe M, Crosthwaite P, Hong Y, Balčiūnienė I, Ahmad Nizar YM, Grech H, Gatt D, Cheong WN, Asbjørnsen A, Torkildsen Jv, Haman E, Miękisz A, Gagarina N, Puzanova J, Anđelković D, Savić M, Jošić S, Slančová D, Kapalková S, Barberán T, Özge D, Hassan S, Chan CY, Okubo T, van der Lely H, Sauerland U, Noveck I. Katsos N, et al. Proc Natl Acad Sci U S A. 2016 Aug 16;113(33):9244-9. doi: 10.1073/pnas.1601341113. Epub 2016 Aug 1. Proc Natl Acad Sci U S A. 2016. PMID: 27482119 Free PMC article.
Chemometrics of anisotropic lipophilicity of anticancer androstane derivatives determined by reversed-phase ultra high performance liquid chromatography with polar aprotic and protic modifiers.
Kovačević S, Karadžić Banjac M, Anojčić J, Podunavac-Kuzmanović S, Jevrić L, Nikolić A, Savić M, Kuzminac I. Kovačević S, et al. J Chromatogr A. 2022 Jun 21;1673:463197. doi: 10.1016/j.chroma.2022.463197. Epub 2022 Jun 3. J Chromatogr A. 2022. PMID: 35688017
The present study is focused on the characterization of physicochemical properties of a series of previously synthesized new androstane derivatives (16E-hydroxyimino derivatives, D-homo lactones and D-seco dinitriles) with anticancer activity applying reversed-phase …
The present study is focused on the characterization of physicochemical properties of a series of previously synthesized new androstane deri …
Central tolerance shapes the neutralizing B cell repertoire against a persisting virus in its natural host.
Florova M, Abreu-Mota T, Paesen GC, Beetschen AS, Cornille K, Marx AF, Narr K, Sahin M, Dimitrova M, Swarnalekha N, Beil-Wagner J, Savic N, Pelczar P, Buch T, King CG, Bowden TA, Pinschewer DD. Florova M, et al. Proc Natl Acad Sci U S A. 2024 Mar 12;121(11):e2318657121. doi: 10.1073/pnas.2318657121. Epub 2024 Mar 6. Proc Natl Acad Sci U S A. 2024. PMID: 38446855 Free PMC article.
N-methyl-D-aspartate receptor blockade during development lowers long-term potentiation threshold without affecting dynamic range of CA3-CA1 synapses.
Savić N, Lüthi A, Gähwiler BH, McKinney RA. Savić N, et al. Proc Natl Acad Sci U S A. 2003 Apr 29;100(9):5503-8. doi: 10.1073/pnas.0831035100. Epub 2003 Apr 17. Proc Natl Acad Sci U S A. 2003. PMID: 12702771 Free PMC article.
During development, excitatory synapses in the CA1 region of the hippocampus undergo activity-dependent and N-methyl-D-aspartate (NMDA) receptor-dependent long-lasting changes in synaptic efficacy. ...
During development, excitatory synapses in the CA1 region of the hippocampus undergo activity-dependent and N-methyl-D-aspartate (NMD …
An application of second-order UV-derivative spectrophotometry for study of solvolysis of a novel fluocinolone acetonide ester.
Markovic B, Vladimirov S, Cudina O, Savic V, Karljikovic-Rajic K. Markovic B, et al. Spectrochim Acta A Mol Biomol Spectrosc. 2010 Feb;75(2):930-5. doi: 10.1016/j.saa.2009.12.043. Epub 2009 Dec 16. Spectrochim Acta A Mol Biomol Spectrosc. 2010. PMID: 20044302
Fluocinolone acetonide (FA) as a solvolyte was determined in the mixture in the concentration range 0.062-0.312 mM using amplitude (2)D(274.96). Experimentally determined LOD value was 0.0295 mM. The accuracy of proposed DS method was confirmed with HPLC referent method. . …
Fluocinolone acetonide (FA) as a solvolyte was determined in the mixture in the concentration range 0.062-0.312 mM using amplitude (2)D …