Y F Wang

Overexpression in Escherichia coli and characterization of the chloroplast triosephosphate isomerase from spinach.

G. Tang, Y. F. Wang, G L Tang, 1999, Protein expression and purification.

6-Substituted-4-(3-bromophenylamino)quinazolines as putative irreversible inhibitors of the epidermal growth factor receptor (EGFR) and human epidermal growth factor receptor (HER-2) tyrosine kinases with enhanced antitumor activity.

R. Nilakantan, A. Wissner, C. Discafani, 2001, Journal of medicinal chemistry.

4-Anilino-6,7-dialkoxyquinoline-3-carbonitrile inhibitors of epidermal growth factor receptor kinase and their bioisosteric relationship to the 4-anilino-6,7-dialkoxyquinazoline inhibitors.

D. Boschelli, R. Nilakantan, D. Berger, 2000, Journal of medicinal chemistry.

Structural basis for sugar translocation through maltoporin channels at 3.1 A resolution

J. Rosenbusch, Y. F. Wang, Tilman Schirmer, 1995, Science.

Irreversible inhibition of epidermal growth factor receptor tyrosine kinase with in vivo activity by N-[4-[(3-bromophenyl)amino]-6-quinazolinyl]-2-butynamide (CL-387,785).

D. Kitchen, Z. Husain, R. Nilakantan, 1999, Biochemical pharmacology.