Sheng-Xiang Lin

17beta-hydroxysteroid dehydrogenase type 5 is negatively correlated to apoptosis inhibitor GRP78 and tumor-secreted protein PGK1, and modulates breast cancer cell viability and proliferation

Sheng-Xiang Lin, Dan Xu, Juliette A. Aka, 2017, The Journal of Steroid Biochemistry and Molecular Biology.

The Ternary Structure of the Double-headed Arrowhead Protease Inhibitor API-A Complexed with Two Trypsins Reveals a Novel Reactive Site Conformation*

Yuxing Chen, Cong-Zhao Zhou, Sheng-Xiang Lin, 2009, The Journal of Biological Chemistry.

Mapping of steroids binding to 17 beta-hydroxysteroid dehydrogenase type 1 using Monte Carlo energy minimization reveals alternative binding modes.

Sheng-Xiang Lin, Boris S Zhorov, Jonathan Blanchet, 2005, Biochemistry.

Correction: Comparison of Functional Proteomic Analyses of Human Breast Cancer Cell Lines T47D and MCF7

Sheng-Xiang Lin, Juliette A. Aka, Sheng-Xiang Lin, 2012, PLoS ONE.

The key role of 17β-hydroxysteroid dehydrogenases in sex steroid biology

Fernand Labrie, Jacques Simard, J. Simard, 1997, Steroids.

How estrogen‐specific proteins discriminate estrogens from androgens: A common steroid‐binding site architecture

Virginie Nahoum, R. Shi, Sheng-Xiang Lin, 2003, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

17β-Hydroxysteroid Dehydrogenase Type 1 Stimulates Breast Cancer by Dihydrotestosterone Inactivation in addition to Estradiol Production

D. Poirier, Sheng-Xiang Lin, M. Mazumdar, 2010 .