A Glimpse of Matrix Metalloproteinases in Diabetic Nephropathy

Por Xu, X., Xiao, L., Xiao, P., Yang, S., Chen, G., Liu, F., Kanwar, Y.Y., Sun, L.
Publicado no Curr Med Chem (2014)

Microbeads-Guided Reconstruction of 3D Osteocyte Network during Microfluidic Perfusion Culture

Por Gu, Yexin, Zhang, Wenting, Sun, Qiaoling, Hao, Yi, Zilberberg, Jenny, Lee, Woo Y.
Publicado no J Mater Chem B Mater Biol Med (2015)

Synthesis and Structure-Activity Relationships of Linear and Conformationally Constrained Peptide Analogs of CIYKYY as Src Tyrosine Kinase Inhibitors

Por Kumar, Anil, Ye, Guofeng, Wang, Yuehao, Lin, Xiaofeng, Sun, Gongqin, Parang, Keykavous
Publicado em 2006

Cyclic Peptides Containing Tryptophan and Arginine as Src Kinase Inhibitors

Por Shirazi, Amir Nasrolahi, Tiwari, Rakesh Kumar, Brown, Alex, Mandal, Dindyal, Sun, Gongqin, Parang, Keykavous
Publicado em 2013

Synthesis and Comparative Biological Evalution of Bifunctional Ligands for Radiotherapy Applications of (90)Y and (177)Lu

Por Chong, Hyun-Soon, Sun, Xiang, Chen, Yunwei, Sin, Inseok, Kang, Chi Soo, Lewis, Michael R., Liu, Dijie, Ruthengael, Varyanna C., Zhong, Yongliang, Wu, Ningjie, Song, Hyun A
Publicado no Bioorg Med Chem (2014)

Synthesis, in Vitro Covalent Binding Evaluation, and Metabolism of (14)C-Labeled Inhibitors of 11β-HSD1

Por Sun, Daqing, Ye, Qiuping, Yan, Xuelei, Rew, Yosup, Fan, Peter, He, Xiao, Jiang, Min, McMinn, Dustin L., Monshouwer, Mario, Tu, Hua, Powers, Jay P.
Publicado no ACS Med Chem Lett (2014)

2-(3-Fluoro-4-methylsulfonylaminophenyl) Propanamides as Potent Transient Receptor Potential Vanilloid 1 (TRPV1) Antagonists: Structure Activity Relationships of 2-Amino Derivative...

Por Kim, Myeong Seop, Ryu, HyungChul, Kang, Dong Wook, Cho, Seong-Hee, Seo, Sejin, Park, Young Soo, Kim, Mi-Yeon, Kwak, Eun Joo, Kim, Yong Soo, Bhondwe, Rahul S., Kim, Ho Shin, Park, Seul-gi, Son, Karam, Choi, Sun, DeAndrea-Lazarus, Ian, Pearce, Larry V., Blumberg, Peter M., Frank, Robert, Bahrenberg, Gregor, Stockhausen, Hannelore, Kögel, Babette Y., Schiene, Klaus, Christoph, Thomas, Lee, Jeewoo
Publicado em 2012

Discovery of Potent and Simplified Piperidinone-Based Inhibitors of the MDM2–p53 Interaction

Por Yu, Ming, Wang, Yingcai, Zhu, Jiang, Bartberger, Michael D., Canon, Jude, Chen, Ada, Chow, David, Eksterowicz, John, Fox, Brian, Fu, Jiasheng, Gribble, Michael, Huang, Xin, Li, Zhihong, Liu, Jiwen (Jim), Lo, Mei-chu, McMinn, Dustin, Oliner, Jonathan D., Osgood, Tao, Rew, Yosup, Saiki, Anne Y., Shaffer, Paul, Yan, Xuelei, Ye, Qiuping, Yu, Dongyin, Zhao, Xiaoning, Zhou, Jing, Olson, Steven H., Medina, Julio C., Sun, Daqing
Publicado em 2014

Optimization of Imidazo[4,5-b]pyridine-Based Kinase Inhibitors: Identification of a Dual FLT3/Aurora Kinase Inhibitor as an Orally Bioavailable Preclinical Development Candidate fo...

Por Bavetsias, Vassilios, Crumpler, Simon, Sun, Chongbo, Avery, Sian, Atrash, Butrus, Faisal, Amir, Moore, Andrew S., Kosmopoulou, Magda, Brown, Nathan, Sheldrake, Peter W., Bush, Katherine, Henley, Alan, Box, Gary, Valenti, Melanie, de Haven Brandon, Alexis, Raynaud, Florence I., Workman, Paul, Eccles, Suzanne A., Bayliss, Richard, Linardopoulos, Spiros, Blagg, Julian
Publicado em 2012

The Stalk Domain and the Glycosylation Status of the Activating Natural Killer Cell Receptor NKp30 Are Important for Ligand Binding

Por Hartmann, Jessica, Tran, Thuy-Van, Kaudeer, Janina, Oberle, Karin, Herrmann, Julia, Quagliano, Isabell, Abel, Tobias, Cohnen, André, Gatterdam, Volker, Jacobs, Andrea, Wollscheid, Bernd, Tampé, Robert, Watzl, Carsten, Diefenbach, Andreas, Koch, Joachim
Publicado em 2012