Browsing "약학대학" byAuthorChoi S.

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Showing results 35 to 64 of 74

Issue DateTitleAuthor(s)Type
2011Link between allosteric signal transduction and functional dynamics in a multisubunit enzyme: S-adenosylhomocysteine hydrolase정낙신; 최선Article
2013Mapping the intramolecular signal transduction of G-protein coupled receptors최선Article in Press
2017MLACP: Machine-learning-based prediction of anticancer peptides최선Article
2006Molecular mechanism of cofilin dephosphorylation by ouabain이경림Article
2013Molecular Modeling Studies of the Novel Inhibitors of DNA Methyltransferases SGI-1027 and CBC12: Implications for the Mechanism of Inhibition of DNMTs최선; 유자경Article
2012N-4-t-Butylbenzyl 2-(4-methylsulfonylaminophenyl) propanamide TRPV1 antagonists: Structure-activity relationships in the A-region최선Article
2017N6-Substituted 5′-N-Methylcarbamoyl-4′-selenoadenosines as Potent and Selective A3 Adenosine Receptor Agonists with Unusual Sugar Puckering and Nucleobase Orientation최선Article
2019Network-based integrated analysis of omics data reveal novel players of TGF-β1-induced EMT in human peritoneal mesothelial cells이공주; 하헌주Article
2010New algorithm for the identification of intact disulfide linkages based on fragmentation characteristics in tandem mass spectra이공주Article
2011Novel oxidative modifications in redox-active cysteine residues이공주; 최선; 신동해Article
2006Nuclear factor-κB activated by capacitative Ca2+ entry enhances muscarinic receptor-mediated soluble amyloid precursor protein (sAPPα) release in SH-SY5Y cells김화정; 최신규Article
2009Oxidative modifications of glyceraldehyde-3-phosphate dehydrogenase play a key role in its multiple cellular functions이공주; 김영미; 최선Article
2006Phospholipase A2 is involved in muscarinic receptor-mediated sAPPα release independently of cyclooxygenase or lypoxygenase activity in SH-SY5Y cells김화정; 최신규Article
2014Promiscuous gating modifiers target the voltage sensor of Kv7.2, TRPV1, and Hv1 cation channels최선Article
2009Proton pump inhibitors exert anti-allergic effects by reducing TCTP secretion이경림; 황은숙Article
2017Pyrazole C-region analogues of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides as potent TRPV1 antagonists최선Article
2003QSAR study of quinolinediones with inhibitory activity of endothelium-dependent vasorelaxation by CoMSIA유충규; 박혜영; 김화정Article
2021Recent applications of deep learning methods on evolutionand contact-based protein structure prediction최선Review
2011Receptor activity and conformational analysis of 5′-halogenated resiniferatoxin analogs as TRPV1 ligands최선Article
2012Selectivity Enhancement Arising from Interactions at the PI3K Unique Pocket최선; 이정현Article
2006Stereoselective functionalization of the 1′-position of 4′-thionucleosides정낙신; 최선; 류재상Article
2008Stereoselective synthesis and conformational study of novel 2′,3′-didehydro-2′,3′-dideoxy-4′-selenonucleosides정낙신; 최선; 최원준Article
2014Structural basis of the phosphorylation dependent complex formation of neurodegenerative disease protein Ataxin-1 and RBM17최선Article
2011Structural insights into transient receptor potential vanilloid type 1 (TRPV1) from homology modeling, flexible docking, and mutational studies최선Article
2012Structural origins for the loss of catalytic activities of bifunctional human LTA4H revealed through molecular dynamics simulations최선Article
2018Structure-activity relationship investigation of Phe-Arg mimetic region of human glutaminyl cyclase inhibitors최선Article
2012Structure-activity relationships and molecular modeling of the N-(3-pivaloyloxy-2-benzylpropyl)-N′-[4-(methylsulfonylamino)benzyl] thiourea template for TRPV1 antagonism최선Article
2023Structure-Activity Relationships of Truncated 1′-Homologated Carbaadenosine Derivatives as New PPARγ/δ Ligands: A Study on Sugar Puckering Affecting Binding to PPARs최선Article
2012Structure-activity relationships of truncated C2- or C8-substituted adenosine derivatives as dual acting A 2A and A 3 adenosine receptor ligands정낙신; 최선; 최원준Article
2014Synthesis and anti-renal fibrosis activity of conformationally locked truncated 2-hexynyl-N6-substituted-(N)-methanocarba-nucleosides as A3 adenosine receptor antagonists and partial agonists정낙신; 하헌주; 최선Article

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