| 2017 | Delayed treatment with fenofibrate protects against high-fat diet-induced kidney injury in mice: the possible role of AMPK autophagy | 하헌주 | Article |
| 2012 | Delayed treatment with human umbilical cord blood-derived stem cells attenuates diabetic renal injury | 하헌주 | Conference Paper |
| 2019 | deMix: Decoding Deuterated Distributions from Heterogeneous Protein States via HDX-MS | 이공주 | Article |
| 2015 | Dendrimeric siRNA for Efficient Gene Silencing | 이혁진 | Article |
| 2022 | Deoxyvasicinone with Anti-Melanogenic Activity from Marine-Derived Streptomyces sp. CNQ-617 | 임경민; 남상집 | Article |
| 1985 | Der Nachweis von nahrungsmittel-hygienisch toxischen Thujon und Caranon - Farbreaktionsmechanismus auf Thujon und Caranon | 유충규 | Article |
| 2011 | Design and evaluation of levodopa methyl ester intranasal delivery systems | 곽혜선 | Article |
| 2011 | Design and evaluation of variants of the protein transduction domain originated from translationally controlled tumor protein | 김화정; 이경림; 권영주; 맹지혜 | Article |
| 2000 | Design and syntheses of 2-oxiranecarboxylate derivatives and their hypoglycemic activities | 김화정 | Article |
| 2004 | Design and synthesis of 3′-ureidoadenosine-5′-uronamides: Effects of the 3′-ureido group on binding to the A 3 adenosine receptor | 정낙신 | Article |
| 2011 | Design and synthesis of 4-amino-2-phenylquinazolines as novel topoisomerase i inhibitors with molecular modeling | 권영주 | Article |
| 2011 | Design and synthesis of 5 '-homo-4 '-fluoro-aristeromycin derivatives as potent antiviral agents | 정낙신; 최원준 | Meeting Abstract |
| 2008 | Design and synthesis of 5''-iodoneplanocin a and its analogues as potential S-adenosylhomocysteine hydrolase inhibitor | 정낙신 | Article |
| 2003 | Design and synthesis of A3 adenosine receptor ligands, 2′-fluoro analogues of Cl-IB-MECA | 정낙신 | Conference Paper |
| 2003 | Design and synthesis of A3 adenosine receptor ligands, 3′-fluoro analogues of Cl-IB-MECA | 정낙신 | Conference Paper |
| 2015 | Design and synthesis of conformationally constrained hydroxylated 4-phenyl-2-aryl chromenopyridines as novel and selective topoisomerase II-targeted antiproliferative agents | 권영주; 전규연 | Article |
| 2009 | Design and synthesis of N6-substituted-4′-thioadenosine-5′-uronamides as potent and selective human A3 adenosine receptor agonists | 정낙신; 최원준 | Article |
| 2015 | Design and synthesis of novel 2,4-diaryl-5H-indeno[1,2-b]pyridine derivatives, and their evaluation of topoisomerase inhibitory activity and cytotoxicity | 권영주 | Article |
| 2008 | Design and synthesis of novel 2′,3′-dideoxy-4′-selenonucleosides as potential antiviral agents | 정낙신; 최원준 | Article |
| 2001 | Design and synthesis of novel fluorocyclopropanoid nucleosides | 정낙신 | Article; Proceedings Paper |
