Papers associated with plasma membrane (and pik3ca)

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	ERK and phosphoinositide 3-kinase temporally coordinate different modes of actin-based motility during embryonic wound healing., Li J., J Cell Sci. November 1, 2013; 126 (Pt 21): 5005-17.
	IGF-1 increases invasive potential of MCF 7 breast cancer cells and induces activation of latent TGF-β1 resulting in epithelial to mesenchymal transition., Walsh LA., Cell Commun Signal. May 2, 2011; 9 (1): 10.
	Intein-mediated site-specific conjugation of Quantum Dots to proteins in vivo., Charalambous A., J Nanobiotechnology. December 10, 2009; 7 9.
	Subtype-specific regulation of P2X3 and P2X2/3 receptors by phosphoinositides in peripheral nociceptors., Mo G., Mol Pain. August 11, 2009; 5 47.
	Role of SGK1 kinase in regulating glucose transport via glucose transporter GLUT4., Jeyaraj S., Biochem Biophys Res Commun. May 11, 2007; 356 (3): 629-35.
	Regulation of GluR1 abundance in murine hippocampal neurones by serum- and glucocorticoid-inducible kinase 3., Strutz-Seebohm N., J Physiol. June 1, 2005; 565 (Pt 2): 381-90.
	Assigning functional domains within the p101 regulatory subunit of phosphoinositide 3-kinase gamma., Voigt P., J Biol Chem. February 11, 2005; 280 (6): 5121-7.
	The aminoguanidine carboxylate BVT.12777 activates ATP-sensitive K+ channels in the rat insulinoma cell line, CRI-G1., Kinsella JM., BMC Pharmacol. August 24, 2004; 4 17.
	The classical progesterone receptor associates with p42 MAPK and is involved in phosphatidylinositol 3-kinase signaling in Xenopus oocytes., Bagowski CP., J Biol Chem. October 5, 2001; 276 (40): 37708-14.

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