| 2010 | Melphalan inhibits adenoma development through modulating the expression of K-ras-specific markers in K-ras Tg mice | 신윤용 | Article |
| 2010 | Melphalan modulates the expression of E7-specific biomarkers in E7-Tg mice | 신윤용 | Article |
| 2006 | MMTV/c-Neu transgenic mice as a model to study antitumor activity against breast cancer in vivo | 신윤용; 김대기 | Meeting Abstract |
| 2012 | Moesin is a biomarker for the assessment of genotoxic carcinogens in mouse lymphoma | 신윤용 | Article |
| 2000 | Nitric oxide inhibits dioxin action for the stimulation of Cyp1a1 promoter activity | 신윤용 | Article |
| 2010 | Novel ALK5 Inhibitor Inhibits Breast Tumor Metastasis and Increases the Interactions of SnoN and Ski to the Promoters of TGF beta Target Genes. | 신윤용; 김대기 | Meeting Abstract |
| 2011 | Novel ALK5 inhibitor에 의한 유방암 세포의 폐암 전이 억제 작용에서 MMP-9/2 활성에 대한 연구 | 윤은정 | Master's Thesis |
| 2016 | Novel oral transforming growth factor- signaling inhibitor EW-7197 eradicates CML-initiating cells | 신윤용; 김대기 | Article |
| 2005 | NSE-controlled carboxyl-terminus of APP gene over-expressing in transgenic mice induces altered expressions in behavior, Aβ-42, and GSK3β binding proteins | 신윤용 | Article |
| 2003 | PAH regualtion of CYP1 gene in ZR-75-1 human breast cancer cells. | 신윤용 | Meeting Abstract |
| 2006 | PAH regulation of CYP1 genes in Hepa 1, MCF-7 cells and CYP1B1 transgenic mice | 신윤용 | Meeting Abstract |
| 2003 | Peroxisome Proliferator-Activated Receptor-γ Activator 15-Deoxy-Δ 12,14-Prostaglandin J 2 Inhibits Neuroblastoma Cell Growth through Induction of Apoptosis: Association with Extracellular Signal-Regulated Kinase Signal Pathway | 신윤용 | Article |
| 2008 | Pharmacokinetics and tissue distribution of 3-((5-(6-methylpyridin-2-yl)-4- (quinoxalin-6-yl)-1H-imidazol-2-yl)methyl)benzamide; a novel ALK5 inhibitor and a potential anti-fibrosis drug | 신윤용; 이화정; 김대기 | Article |
| 2002 | Phthalate levels in beverages in Japan and Korea | 신윤용 | Article |
| 2006 | Potent in vivo anti-breast cancer activity of IN-2001, a novel inhibitor of histone deacetylase, in MMTV/c-Neu Mice | 신윤용; 김대기 | Article |
| 2010 | Prediction of carcinogenicity in vitro based on genotoxicity and toxicogenomic data | 신윤용 | Meeting Abstract |
| 2007 | Prediction of carcinogenicity in vitro based on genotoxicity, toxicogenomics data and statistical approaches including LogitBoost | 신윤용 | Meeting Abstract |
| 2009 | Profiling of transcripts and proteins modulated by the E7 oncogene in the lung tissue of E7-Tg mice by the omics approach | 신윤용 | Article |
| 2000 | Quantitative assessment of estrogenic activity in the water environment of Korea by the E-SCREEN assay | 신윤용 | Article |
| 2022 | Radiotherapy-induced oxidative stress and fibrosis in breast cancer are suppressed by vactosertib, a novel, orally bioavailable TGF-β/ALK5 inhibitor | 신윤용 | Article |
| 2019 | Simultaneous quantitative determination of 19 new psychoactive substances in human plasma and metabolic profiles of 25N-NBOMe and 25E-NBOMe in human liver microsomes | 홍진 | Doctoral Thesis |
| 2005 | Stereoselective synthesis of 3-hydroxymethyl-D-cyclopentenone, the versatile intermediate for the synthesis of carbocyclic nucleosides | 이강만; 신윤용; 정낙신 | Conference Paper |
| 1997 | Stimulation of trout CYP1A gene expression in mouse HEPA-1 cells by 3-methylcholanthrene | 신윤용 | Article |
| 2011 | Synthesis and biological evaluation of 1-substituted-3(5)-(6-methylpyridin- 2-yl)-4-(quinolin-6-yl)pyrazoles as transforming growth factor-β type 1 receptor kinase inhibitors | 신윤용; 김대기 | Article |
| 2011 | Synthesis and biological evaluation of 1-substituted-3(5)-(6-methylpyridin- 2-yl)-4-(quinoxalin-6-yl)pyrazoles as transforming growth factor-β type 1 receptor kinase inhibitors | 신윤용; 김대기 | Article |
| 2011 | Synthesis and biological evaluation of 1-substituted-3-(6-methylpyridin-2- yl)-4-([1,2,4triazolo[1,5-apyridin-6-yl)pyrazoles as transforming growth factor-β type 1 receptor kinase inhibitors | 신윤용; 김대기 | Article |
| 2012 | Synthesis and biological evaluation of 2-benzylamino-4(5)-(6-methylpyridin- 2-yl)-5(4)-([1,2,4]triazolo[1,5-a]-pyridin-6-yl)thiazoles as transforming growth factor-β type 1 receptor kinase inhibitors | 신윤용; 김대기; 김승원 | Article |
| 2010 | Synthesis and biological evaluation of 4(5)-(6-methylpyridin-2-yl)imidazoles and -pyrazoles as transforming growth factor-β type 1 receptor kinase inhibitors | 신윤용; 김대기 | Article |
| 2015 | Synthesis and biological evaluation of 5-(fluoro-substituted-6-methylpyridin-2-yl)-4-([1,2,4]triazolo[1,5-alpha]pyridin-6-yl)imidazoles as inhibitors of transforming growth factor-beta type I receptor kinase | 신윤용; 김대기 | Article |
| 2013 | Targeting the transforming growth factor-β signaling in cancer therapy | 신윤용 | Review |
