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Flavia A. O'Rourke

Assistant Professor of Cell Biology
orourke@nso1.uchc.edu

  • B.S., Central Connecticut State College
  • M.S., University of Connecticut
  • Ph.D., University of Connecticut
  • Cell Biology Graduate Program
  • Not accepting students for Lab Rotations at this time
Flavia A. O'Rourke
Areas of Interest

Research is focused on signal transduction in human platelets with specific interest in the inositol phosphate signaling pathway and its regulation. The IP3 and IP4 receptor systems are currently being investigated to include characterization and purification using techniques of HPLC and affinity chromatography. A HEL cell cDNA expression library using monoclonal antibodies and oligonucleotide probes is also being used to clone and sequence the gene for the receptors.

Selected Publications

O'Rourke FA, LaPlante JM, Feinstein MB. (2003) Antisense-mediated loss of calcium homoeostasis endoplasmic reticulum protein (CHERP; ERPROT213-21) impairs Ca2+ mobilization, nuclear factor of activated T-cells (NFAT) activation and cell proliferation in Jurkat T-lymphocytes. Biochem J.;373.133-143.

LaPlante, J, O'Rourke F.,.Lu,X. Fein, A., Olsen, A and Feinsterin, MB. (2000) Cloning of human Ca2+ homeostasis endoplasmic reticulum protein (CHERP) inhibits intracellular Ca2+ mobilization and decreases cell proliferation. Biochem. J. 348. 189-199.

Lu,X, Fein, A, Feinstein, M. and Orourke, F. (1999) Antisense knockout of the Inositol 1,3,4,5-tetrakisphosphate receptor GAP1 IP4BP in human erythroleukemia cell line leads to the appearance of intermediate conductance K(Ca) channels that hyperpolarize the membrane and enhance calcium influx.J. Gen. Physiol. 115, 81-95.

  
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