<p>(A) Human platelets were loaded with Fura-2/AM to measure intracellular [Ca<sup>2+</sup>]<sub>i</sub>, in the presence or absence of TRPC6 inhibitor (10 μM), and activated with U46619 (0.5 μM), ADPβS (100 μM) and OAG (150 μM). Each experiment was repeated at least three times, with blood obtained from three separate donors. (B) Human platelets were incubated in the presence or absence of TRPC6 inhibitor (10 μM) for 5 minutes and then stimulated with U46619 (0.5 μM), ADPβS (100 μM) for 3 minutes, and subjected to immunoblotting with ERK, pERK, Akt and pAkt antibodies.</p
<p><b>A</b>) Fura red was used as an inverse intracellular calcium indicator and calcium transients ...
AbstractInhibitors of the endoplasmic reticulum Ca2+-ATPase like thapsigargin (TG) and 2,5-di (tert-...
AbstractIn human platelets, the Ca2+ ionophore A23187 stimulated the phosphorylation of a 40 kDa pro...
<p>PRP was incubated without or with the TRPC6 inhibitor (5 μM and/or 10 μM) for 5 min followed by s...
<p>PRP was incubated without or with TRPC6 inhibitor (10 μM) for 5 min followed by stimulation of PR...
<p>Washed platelets were incubated in the presence or absence of TRPC6 inhibitor (10 μM) for 5 minut...
<p>(A) Human platelets were loaded with Fura-2/AM to measure intracellular [Ca2+]<sub>i</sub>, in th...
<p>Binding displacement of 1 nM [<sup>3</sup>H]SQ29,548 with increasing concentrations of the TRPC6 ...
The canonical transient receptor potential channel 6 (TRPC6) is a Ca2+ permeable cation channel. To ...
<p>Platelets (1.2×10<sup>8</sup> platelets/ml) loaded with Fluorfort (10 µM) were pre-incubated or n...
AbstractCytosolic-free Ca2+ plays a crucial role in blood platelet function and is essential for thr...
<p>Clot retraction of washed platelets was intiated by adding thrombin (0.1 U/ml) in the presence or...
AbstractPhosphatidylinositol 4,5-bisphosphate (PIP2) is a versatile regulator of TRP channels. We re...
AbstractWe have investigated the actions of the PLC inhibitor, U73122, and its close analogue, U7334...
AbstractWe have investigated the regulation of tyrosine proteins phosphorylation by intracellular Ca...
<p><b>A</b>) Fura red was used as an inverse intracellular calcium indicator and calcium transients ...
AbstractInhibitors of the endoplasmic reticulum Ca2+-ATPase like thapsigargin (TG) and 2,5-di (tert-...
AbstractIn human platelets, the Ca2+ ionophore A23187 stimulated the phosphorylation of a 40 kDa pro...
<p>PRP was incubated without or with the TRPC6 inhibitor (5 μM and/or 10 μM) for 5 min followed by s...
<p>PRP was incubated without or with TRPC6 inhibitor (10 μM) for 5 min followed by stimulation of PR...
<p>Washed platelets were incubated in the presence or absence of TRPC6 inhibitor (10 μM) for 5 minut...
<p>(A) Human platelets were loaded with Fura-2/AM to measure intracellular [Ca2+]<sub>i</sub>, in th...
<p>Binding displacement of 1 nM [<sup>3</sup>H]SQ29,548 with increasing concentrations of the TRPC6 ...
The canonical transient receptor potential channel 6 (TRPC6) is a Ca2+ permeable cation channel. To ...
<p>Platelets (1.2×10<sup>8</sup> platelets/ml) loaded with Fluorfort (10 µM) were pre-incubated or n...
AbstractCytosolic-free Ca2+ plays a crucial role in blood platelet function and is essential for thr...
<p>Clot retraction of washed platelets was intiated by adding thrombin (0.1 U/ml) in the presence or...
AbstractPhosphatidylinositol 4,5-bisphosphate (PIP2) is a versatile regulator of TRP channels. We re...
AbstractWe have investigated the actions of the PLC inhibitor, U73122, and its close analogue, U7334...
AbstractWe have investigated the regulation of tyrosine proteins phosphorylation by intracellular Ca...
<p><b>A</b>) Fura red was used as an inverse intracellular calcium indicator and calcium transients ...
AbstractInhibitors of the endoplasmic reticulum Ca2+-ATPase like thapsigargin (TG) and 2,5-di (tert-...
AbstractIn human platelets, the Ca2+ ionophore A23187 stimulated the phosphorylation of a 40 kDa pro...