1 "and partial least squares comparedwith multiple regression in conventional QSAR studies" 198818-25
2 "Understandingthe Protox inhibition activity of novel 1--(5-methyl-3-phenylisoxazolin-5-structure-activity relationship (HQSAR) methodology" 47 : 351-356, 2004
3 "Understandingthe Protox inhibition activity of novel 1--(5-methyl-3-phenyl-isoxazolin-5-yl)methoxy-2-chloro-4-fluorobenzene derivativesusing comparative molecular similarity indices analysis (CoMSIA)methodology" 47 : 414-421, 2004
4 "Understanding the protox inhibition activity of novel 1--(5-methyl-3-phenylisoxazolin-5-yl)methoxy-2-chloro-4-fluorobenzene derivativesusing comparative molecular field analysis (CoMFA)methodology" 8 : 151-161, 2004
5 "Toward its use with 3D-structuraldatabases" 47-59, 1990
6 "Three dimensional quantitative structure-activity relationshipanalyses on the fungicidal activities of new novel 2-alkoxyphenyl-3-phenylthioisoindoline-1-one derivatives usingthe comparative molecular similarity indices analyses(CoMSIA) methodology based on the different alignmentapproaches" 9 : 26-34, 2005
7 "Three dimensional quantitative structure-activity relationship onthe fungicidal activities of new novel 2-alkoxyphenyl-3-phenylthioisoindoline-1-one derivatives using the compar- ativemolecular field analyses methodology based on thedifferent alignment approaches" 48 : 82-88, 2005
8 "The conformational parameter in drug design" In Computer-assisted drugdesign 205-226, 1979
9 "Quantitative structure-activity relationships and molecular shapesimilarity of the herbicidal N-substituted phenyl-3, 4-dimethylmaleimideDerivatives" 7 : 100-107, 2003
10 "New geration of protox-inhibitingherbicides" 19 : 533-535, 2000
1 "and partial least squares comparedwith multiple regression in conventional QSAR studies" 198818-25
2 "Understandingthe Protox inhibition activity of novel 1--(5-methyl-3-phenylisoxazolin-5-structure-activity relationship (HQSAR) methodology" 47 : 351-356, 2004
3 "Understandingthe Protox inhibition activity of novel 1--(5-methyl-3-phenyl-isoxazolin-5-yl)methoxy-2-chloro-4-fluorobenzene derivativesusing comparative molecular similarity indices analysis (CoMSIA)methodology" 47 : 414-421, 2004
4 "Understanding the protox inhibition activity of novel 1--(5-methyl-3-phenylisoxazolin-5-yl)methoxy-2-chloro-4-fluorobenzene derivativesusing comparative molecular field analysis (CoMFA)methodology" 8 : 151-161, 2004
5 "Toward its use with 3D-structuraldatabases" 47-59, 1990
6 "Three dimensional quantitative structure-activity relationshipanalyses on the fungicidal activities of new novel 2-alkoxyphenyl-3-phenylthioisoindoline-1-one derivatives usingthe comparative molecular similarity indices analyses(CoMSIA) methodology based on the different alignmentapproaches" 9 : 26-34, 2005
7 "Three dimensional quantitative structure-activity relationship onthe fungicidal activities of new novel 2-alkoxyphenyl-3-phenylthioisoindoline-1-one derivatives using the compar- ativemolecular field analyses methodology based on thedifferent alignment approaches" 48 : 82-88, 2005
8 "The conformational parameter in drug design" In Computer-assisted drugdesign 205-226, 1979
9 "Quantitative structure-activity relationships and molecular shapesimilarity of the herbicidal N-substituted phenyl-3, 4-dimethylmaleimideDerivatives" 7 : 100-107, 2003
10 "New geration of protox-inhibitingherbicides" 19 : 533-535, 2000
11 "Molecular shapesimilarity of cyclic imides and protoporphyrinogen IX" 22 : 314-320, 1997
12 "In Rational Approaches to Structure andEcotoxicology of Agrochemicals Application of the Hansch-Fujita Method to the Design of Imide and carbamatefungicides" CRCPress chap : 1992
13 "In PeroxidizingHerbicides" Springer-Verlag Berline Heidelberg 1999
14 "In Chemistry andMode of Action of Crop Protection Agents" 1998
15 "In Agrochemical Discovery, Insect, Weed, andFungal control: Similarities in bioanalogous structuraltransformation patterns" AmericanChemical Society (774) : 2002
16 "Effect ofshape on the binding of steroids to carrier proteins" 5959-5967, 1988
17 "Effect of 3-thioalkoxy groups on herbicidalactivities of 2-(5-alkoxyphenyl)-3-phenylthioisoindoline-1-oneDerivatives" Chung-nam National University 5-, 2002
18 "Comparative molecular field analyses (CoMFA) on the growthinhibition activity of N-phenyl-3,4,5,6-tetra-hydrophtalimide andN-phenyl-3,4-dimethylmaleimide Derivatives" 7 : 75-82, 2003
19 "A brief review and tableof semiempirical parameters used in the Huckel molecularorbital method" 235-246, 1967