Y. Qian

发表

Design of potent, orally available antagonists of the transient receptor potential vanilloid 1. Structure-activity relationships of 2-piperazin-1-yl-1H-benzimidazoles.

J. Treanor, C. Dominguez, C. Fotsch, 2006, Journal of medicinal chemistry.

Biosynthetic Processing of neu Differentiation Factor

D. Brankow, S. Ross, T. Burgess, 1995, The Journal of Biological Chemistry.

The uptake and distribution of phosphorothioate oligonucleotides into vascular smooth muscle cells in vitro and in rabbit arteries.

T. Burgess, J. Bready, C. Farrell, 1995, Antisense research and development.

Activation of mast cell K+ channels through multiple G protein-linked receptors.

M. McCloskey, Y. Qian, 1993, Proceedings of the National Academy of Sciences of the United States of America.

Selective expression of potassium channels during mast cell differentiation.

M. McCloskey, Y. Qian, 1994, The Journal of biological chemistry.

(4-Piperidinylphenyl)aminoethyl amides as a novel class of non-covalent cathepsin K inhibitors.

V. Viswanadhan, J. Cheetham, A. Tasker, 2004, Bioorganic & medicinal chemistry letters.

Osteoclast markers accumulate on cells developing from human peripheral blood mononuclear precursors

D. Lacey, V. Shalhoub, T. Burgess, 1999, Journal of cellular biochemistry.

Osteoprotegerin Ligand Is a Cytokine that Regulates Osteoclast Differentiation and Activation

D. Lacey, I. Sarosi, J. Delaney, 1998, Cell.

The Ligand for Osteoprotegerin (OPGL) Directly Activates Mature Osteoclasts

D. Lacey, M. Kelley, W. J. Boyle, 1999, The Journal of cell biology.

The antiproliferative activity of c-myb and c-myc antisense oligonucleotides in smooth muscle cells is caused by a nonantisense mechanism.

S. Ross, T. Burgess, G. Pierce, 1995, Proceedings of the National Academy of Sciences of the United States of America.

Chemical Constituents of the Endophytic Fungus Pestalotiopsis microspora Derived from Artemisia argyi and their P-Glycoprotein Inhibitory Activity

Jun He, Y. Qian, Jian Kang, 2023, Chemistry of Natural Compounds.

Pharmaceutical Optimization of Peptide Toxins for Ion Channel Targets: Potent, Selective, and Long-Lived Antagonists of Kv1.3.

J. Sullivan, C. Gegg, J. Werner, 2015, Journal of medicinal chemistry.

Identification of a novel SPT inhibitor WXP-003 by docking-based virtual screening and investigation of its anti-fungi effect

Xin Sun, Xin Wang, Xin Yang, 2021, Journal of enzyme inhibition and medicinal chemistry.

Secondary Metabolites from Endophytic Pestalotiopsis uvicola and Their P-Glycoprotein Inhibitory Activity

Ji-Chuan Kang, Y. Qian, Jun He, 2022, Chemistry of Natural Compounds.