| 2010 | A new DNA building block, 4′-selenothymidine: Synthesis and modification to 4′-seleno-AZT as a potential anti-HIV agent | 정낙신; 최원준 | Article |
| 2011 | A3 adenosine receptor agonist reduces brain ischemic injury and inhibits inflammatory cell migration in rats | 정낙신 | Article |
| 2010 | A3 adenosine receptor antagonist, truncated thio-Cl-IB-MECA, induces apoptosis in T24 human bladder cancer cells | 정낙신; 최원준 | Article |
| 2013 | Alternatively driven dual nanowire arrays by ZnO and CuO for selective sensing of gases | 김명화 | Article |
| 2003 | Comment on "Probable Langevin-Like Director Reorientation in an Interface-Induced Disordered SmC*-Like State of Liquid Crystals Characterized by Frustration between Ferro- and Antiferroelectricity" (multiple letters) | 우정원 | Letter |
| 2009 | Design and synthesis of N6-substituted-4′-thioadenosine-5′-uronamides as potent and selective human A3 adenosine receptor agonists | 정낙신; 최원준 | Article |
| 2008 | Design and synthesis of novel 2′,3′-dideoxy-4′-selenonucleosides as potential antiviral agents | 정낙신; 최원준 | Article |
| 2008 | Design and synthesis of truncated 4'-thioadenosine derivatives as potent and selective A3 adenosine receptor antagonists. | 정낙신; 최원준 | Article |
| 2005 | Design, synthesis, and anticancer activity of fluorocyclopentenyl-pyrimidines. | 이강만; 정낙신; 이상국; 최원준 | Article |
| 2010 | Design, synthesis, and binding of homologated truncated 4′-thioadenosine derivatives at the human A3 adenosine receptors | 정낙신; 최선; 최원준 | Article |
| 2003 | Design, synthesis, and biological evaluation of fluoroneplanocin A as the novel mechanism-based inhibitor of S-adenosylhomocysteine hydrolase | 이강만; 정낙신; 이상국 | Article |
| 2009 | Development of next generation 4'-selenonucleosides. | 정낙신 | Article |
| 2019 | Directional Ostwald Ripening for Producing Aligned Arrays of Nanowires | 김명화; 김준수 | Article |
| 2012 | Fluorocyclopentenyl-cytosine with broad spectrum and potent antitumor activity | 정낙신; 최원준 | Article |
| 2002 | Improved and alternative synthesis of D- and L-cyclopentenone derivatives, the versatile intermediates for the synthesis of carbocyclic nucleosides | 정낙신 | Article |
| 2014 | Influence of InAs quantum dots on the transport properties of GaAs-based solar cell devices | 김동욱 | Article |
| 2013 | New RNA purine building blocks, 4'-selenopurine nucleosides: First synthesis and unusual mixture of sugar puckerings | 정낙신; 최원준 | Article |
| 2018 | Optic nerve sheath diameter measured using early unenhanced brain computed tomography shows no correlation with neurological outcomes in patients undergoing targeted temperature management after cardiac arrest | 한철 | Article |
| 2007 | Pentacene and ZnO hybrid channels for complementary thin-film transistor inverters operating at 2 v | 이승준 | Article |
| 2004 | Preparative and Stereoselective Synthesis of the Versatile Intermediate for Carbocyclic Nucleosides: Effects of the Bulky Protecting Groups to Enforce Facial Selectivity | 정낙신 | Article |
| 2004 | Recent advances in 4′-thionucleosides as potential antiviral and antitumor agents | 정낙신 | Review |
| 2011 | Regio- and stereoselective synthesis of truncated 3′- aminocarbanucleosides and their binding affinity at the A 3 adenosine receptor | 정낙신; 최원준 | Article |
| 2011 | Renoprotective antioxidant effect of alagebrium in experimental diabetes | 정낙신; 하헌주; 최원준 | Article |
| 2012 | Stereoselective synthesis and anti-HCV activity of conformationally restricted 2′-C-substituted carbanucleosides | 정낙신; 최원준 | Article |
| 2005 | Stereoselective synthesis of 3-hydroxymethyl-D-cyclopentenone, the versatile intermediate for the synthesis of carbocyclic nucleosides | 이강만; 신윤용; 정낙신 | Conference Paper |
| 2002 | Stereoselective synthesis of amino-substituted apio dideoxynucleosides through a distant neighboring group effect | 정낙신 | Article |
| 2011 | Stereoselective synthesis of MLN4924, an inhibitor of NEDD8-activating enzyme | 정낙신; 최원준 | Article |
| 2004 | Structural determinants of efficacy at A3 adenosine receptors: Modification of the ribose moiety | 정낙신 | Article |
| 2008 | Structure-activity relationships of 2-chloro-N6-substituted-4′-thioadenosine-5′-N,N-dialkyluronamides as human A3 adenosine receptor antagonists | 정낙신; 최원준 | Article |
| 2001 | Structure-activity relationships of apio nucleosides as potential antiviral agents | 정낙신 | Conference Paper |
