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Journal of Medicinal Chemistry|August 6, 2008
Inhibitors of Src homology-2 domain containing protein tyrosine phosphatase-2 (Shp2) based on oxindole scaffoldsHarshani R Lawrence, Roberta Pireddu, Liwei Chen, et al.Medchemcomm|January 1, 2013
Pyridylthiazole-based ureas as inhibitors of Rho associated protein kinases (ROCK1 and 2)Roberta Pireddu, Kara D Forinash, Nan N Sun, et al.Proceedings of the National Academy of Sciences of the United States of America|May 28, 2009
A critical role for phosphatase haplodeficiency in the selective suppression of deletion 5q MDS by lenalidomideSheng Wei, Xianghong Chen, Kathy Rocha, et al.Journal of Medicinal Chemistry|July 19, 2012
Development of o-chlorophenyl substituted pyrimidines as exceptionally potent aurora kinase inhibitorsHarshani R Lawrence, Matthew P Martin, Yunting Luo, et al.Journal of Medicinal Chemistry|January 26, 2012
Fragment-based and structure-guided discovery and optimization of Rho kinase inhibitorsRongshi Li, Mathew P Martin, Yan Liu, et al.Pageof 2