Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
First Independent Research Support & Transition (FIRST) Awards (R29)
Project #
1R29GM048457-01
Application #
3468969
Study Section
Cellular Biology and Physiology Subcommittee 1 (CBY)
Project Start
1993-01-01
Project End
1997-12-31
Budget Start
1993-01-01
Budget End
1993-12-31
Support Year
1
Fiscal Year
1993
Total Cost
Indirect Cost
Name
University of Texas MD Anderson Cancer Center
Department
Type
Other Domestic Higher Education
DUNS #
001910777
City
Houston
State
TX
Country
United States
Zip Code
77030
Wu, Y; Pan, S; Che, S et al. (2001) Overexpression of Hp95 induces G1 phase arrest in confluent HeLa cells. Differentiation 67:139-53
Che, S; El-Hodiri, H M; Wu, C F et al. (1999) Identification and cloning of xp95, a putative signal transduction protein in Xenopus oocytes. J Biol Chem 274:5522-31
Che, S; Wu, W; Nelman-Gonzalez, M et al. (1998) A phosphatase activity in Xenopus oocyte extracts preferentially dephosphorylates the MPM-2 epitope. FEBS Lett 424:225-33
Che, S; Weil, M M; Nelman-Gonzalez, M et al. (1997) MPM-2 epitope sequence is not sufficient for recognition and phosphorylation by ME kinase-H. FEBS Lett 413:417-23
Che, S; Weil, M M; Etkin, L D et al. (1997) Molecular cloning of a splice variant of Caenorhabditis elegans YNK1, a putative element in signal transduction. Biochim Biophys Acta 1354:231-40
Kuang, J; Ashorn, C L (1993) At least two kinases phosphorylate the MPM-2 epitope during Xenopus oocyte maturation. J Cell Biol 123:859-68