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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Nagendra Prasad

Assistant Research Professor

Indiana University School of Medicine

IU Simon Cancer Center

980 W. Walnut Street



Name/email consistency: high



  • Department of Cancer Molecular Sciences, Pfizer Global R&D (formerly Parke-davis Research labs), Ann Arbor, Michigan 48105 USA. 1999-2003
  • Department of Basic Medical Sciences and Purdue Cancer Center, Purdue University, West Lafayette, Indiana 47907, USA. 2003 - 2010
  • Department of Medicine, Indiana University Simon Cancer Center, Indiana University School of Medicine, Indianapolis, Indiana 46202, USA. 2010-current    
  • [1] [2] [7] [8]   [9] [10] [11]


  1. Network Analysis of the Focal Adhesion to Invadopodia Transition Identifies a PI3K-PKCα Invasive Signaling Axis. Hoshino, D., Jourquin, J., Emmons, S.W., Miller, T., Goldgof, M., Costello, K., Tyson, D.R., Brown, B., Lu, Y., Prasad, N.K., Zhang, B., Mills, G.B., Yarbrough, W.G., Quaranta, V., Seiki, M., Weaver, A.M. Sci. Signal. (2012) [Pubmed]
  2. A systems biology approach to the global analysis of transcription factors in colorectal cancer. Pradhan, M.P., Prasad, N.K., Palakal, M.J. BMC. Cancer. (2012) [Pubmed]
  3. SHIP2 phosphoinositol phosphatase positively regulates EGFR-Akt pathway, CXCR4 expression, and cell migration in MDA-MB-231 breast cancer cells. Prasad, N.K. Int. J. Oncol. (2009) [Pubmed]
  4. Specific tyrosine phosphorylations mediate signal-dependent stimulation of SHIP2 inositol phosphatase activity, while the SH2 domain confers an inhibitory effect to maintain the basal activity. Prasad, N.K., Werner, M.E., Decker, S.J. Biochemistry (2009) [Pubmed]
  5. High expression of obesity-linked phosphatase SHIP2 in invasive breast cancer correlates with reduced disease-free survival. Prasad, N.K., Tandon, M., Handa, A., Moore, G.E., Babbs, C.F., Snyder, P.W., Bose, S. Tumour Biol. (2008) [Pubmed]
  6. SH2-containing 5'-inositol phosphatase, SHIP2, regulates cytoskeleton organization and ligand-dependent down-regulation of the epidermal growth factor receptor. Prasad, N.K., Decker, S.J. J. Biol. Chem. (2005) [Pubmed]
  7. Src family tyrosine kinases regulate adhesion-dependent tyrosine phosphorylation of 5'-inositol phosphatase SHIP2 during cell attachment and spreading on collagen I. Prasad, N., Topping, R.S., Decker, S.J. J. Cell. Sci. (2002) [Pubmed]
  8. Phosphoinositol phosphatase SHIP2 promotes cancer development and metastasis coupled with alterations in EGF receptor turnover. Prasad, N.K., Tandon, M., Badve, S., Snyder, P.W., Nakshatri, H. Carcinogenesis. (2008) [Pubmed]
  9. SH2-containing inositol 5'-phosphatase SHIP2 associates with the p130(Cas) adapter protein and regulates cellular adhesion and spreading. Prasad, N., Topping, R.S., Decker, S.J. Mol. Cell. Biol. (2001) [Pubmed]
  10. Oxidative stress and vanadate induce tyrosine phosphorylation of phosphoinositide-dependent kinase 1 (PDK1). Prasad, N., Topping, R.S., Zhou, D., Decker, S.J. Biochemistry. (2000) [Pubmed]
  11. Therapeutic preparations of normal polyspecific IgG (IVIg) induce apoptosis in human lymphocytes and monocytes: a novel mechanism of action of IVIg involving the Fas apoptotic pathway. Prasad, N.K., Papoff, G., Zeuner, A., Bonnin, E., Kazatchkine, M.D., Ruberti, G., Kaveri, S.V. J. Immunol. (1998) [Pubmed]
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