Structure, function, and control of phosphoinositide-specific phospholipase C.
By M. Rebecchi, S. Pentyala. Physiological Reviews, 2000
979 citations recorded by the source corpus.
Subfields: Cell Biology, Genetics, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/f2778210e6a529b73eab29666ee7b3b174c3e88a
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Citations in the corpus
- Plasma membrane phosphoinositide organization by protein electrostatics (2005, background): “Well-characterized phosphoinositide-specific phospholipase Cs (PLCs) hydrolyse PIP 2 into these second messenger”
- Modelling of simple and complex calcium oscillations (2002, background): “Mechanisms for this coupling are the activating effect of Cacyt on the d isoform of PLC [43,63] and on the IP3 3-kinase (EC 2.”
- Distinct coincidence detectors govern the corticostriatal spike timing‐dependent plasticity (2010, background): “…a coincidence detector involve elevation of calcium concentration, which is needed for its catalytic function, and its concomitant activation by Gq/11-coupled receptors, including group-I mGluRs, M1/M3 muscarinic and 5-HT2 serotoninergic receptors (5-HT2Rs) (Rebecchi & Pentyala, 2000; Rhee, 2001).”
- PI(4,5)P2 regulates the activation and desensitization of TRPM8 channels through the TRP domain (2005, background): “Coexpression of PLCδ1, the PLC isoform most sensitive to activation by calciu”
- AKAP signalling complexes: focal points in space and time (2004, background): “, which generates DAG through hydrolysis of PtdIns(4,5)P 2 (Ref”
- The trp ion channel family (2001, background): “Brief review of signal transduction The three classes of phosphatidylinositol-specific PLC (PLC-β 1–4 , PLC-γ 1,2 and PLC-δ 1–4 ) can be distinguished by their primary structure and modes of regulatio”