Protein kinase C isozymes and the regulation of diverse cell responses.
By E. Dempsey, A. Newton, D. Mochly‐Rosen, A. Fields, M. Reyland, P. Insel, R. Messing. American Journal of Physiology - Lung cellular and Molecular Physiology, 2000
744 citations recorded by the source corpus.
Subfields: Cell Biology, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/a3462dbe91cf84370fc806e04f19fd0c765865d7
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Citations in the corpus
- A PKCε–ENH–channel complex specifically modulates N-type Ca2+ channels (2003, background): “gif" NDATA ITEM> ]> Protein kinase C (PKC) represents a family of lipid-dependent serine/threonine kinases that are responsible for the rapid regulation of a variety of neuronal functions, such as membrane excitability, neurotransmitter release and gene expressio”
- Free radicals and antioxidants in normal physiological functions and human disease. (2007, background): “It appears certain that oxidant-induced PKC activation plays a critical role in cancer proliferation and clearly this has important functional consequences on downstream signalling pathways; i.e. activation of MAPKs, defined transcription factors and proto-oncogenes (Dempsey et al., 2000).”
- Structural Basis of Protein Kinase C Isoform Function (2008, background): “Protein kinase C (PKC) comprises a multigene family of related serine/threonine kinases that sit at the crossroads of many signal transduction pathways and are implicated in a wide range of G protein-coupled receptor and other growth factor-dependent cellular responses (41, 176).”