|1.||Henderson, Kimberly: 1 article (01/2009)|
|2.||Eckhert, Curtis D: 1 article (01/2009)|
|3.||Stella, Salvatore L: 1 article (01/2009)|
|4.||Kobylewski, Sarah: 1 article (01/2009)|
|5.||Stamm, C: 1 article (06/2004)|
|6.||del Nido, P J: 1 article (06/2004)|
|7.||Aydin, Jan: 1 article (08/2003)|
|8.||Lännergren, Jan: 1 article (08/2003)|
|9.||Bruton, Joseph: 1 article (08/2003)|
|10.||Tavi, Pasi: 1 article (08/2003)|
06/01/2004 - "We introduced the long-wavelength fluorescent Ca (2+) indicator Rhod-2 for real-time recording of cytosolic Ca (2+) transients in Langendorff-perfused rabbit, rat, and mouse hearts, and utilized it to study the impact of PKC on myocardial Ca (2+) handling during ischemia and reperfusion. "
06/01/2004 - "We first established that the dissociation constant for Rhod-2 and Ca (2+) must be adjusted to account for changes in pH and temperature during ischemia and reperfusion. "
11/09/2001 - "Rhod-2 fluorescence gradually increased during simulated ischemia and rose even further with reperfusion. "
06/01/2004 - "Protein kinase C and myocardial calcium handling during ischemia and reperfusion: lessons learned using Rhod-2 spectrofluorometry."
11/09/2001 - "In contrast, inhibitors of the mitochondrial permeability transition (MPT), cyclosporin A and bongkrekic acid, did not alter [Ca(2+)](m) accumulation during ischemia, but markedly suppressed the surge in rhod-2 fluorescence during reperfusion. "
02/01/1996 - "In another series of experiments, rhod-2 was injected directly into 12 pyramidal cell-like neurons in layer II/III through patch pipettes, and changes in Ca2+ concentration in apical dendritic areas during tetanus were measured simultaneously with recordings of excitatory postsynaptic potentials (EPSPs) evoked by test stimulation of layer IV. It was found that LTP of EPSPs was induced in 4 cells which exhibited a strong rise of dendritic Ca2+ signal (197.1 +/- 18.5%) while LTD was induced in other 5 cells which showed a weak rise of the signal (31.0 +/- 4.1%). "
07/18/2002 - "Labeling endocytosed vesicular structures with a fluorescent styryl dye, FM1-43, and measuring intracellular Ca2+ concentrations with a Ca2+ indicator, rhod-2, we show here that the ECP is replenished by SVs endocytosed during stimulation, and this process depends on external Ca2+. In contrast, the RP is refilled after cessation of tetanus by a process mediated by Ca2+ released from internal stores."
|2.||Protein Kinase C
|6.||Indo-1 pentaacetoxymethyl ester