|1.||Ito, Arisa: 2 articles (01/2011 - 02/2010)|
|2.||Arai, Tsunenori: 2 articles (01/2011 - 02/2010)|
|3.||Miyoshi, Shunichiro: 2 articles (01/2011 - 02/2010)|
|4.||Ogawa, Satoshi: 2 articles (01/2011 - 02/2010)|
|5.||Schüttler, J: 1 article (09/2015)|
|6.||Wagner, S: 1 article (09/2015)|
|7.||Hein, S: 1 article (09/2015)|
|8.||Friedrich, O: 1 article (09/2015)|
|9.||Schürmann, S: 1 article (09/2015)|
|10.||Ogawa, E: 1 article (01/2014)|
|1.||Photosensitivity Disorders (Photodermatitis)
02/01/2010 - "To study the mechanism of the acute electrical blockade obtained in the ex vivo study, intracellular Ca2+ concentration changes in rat cardiac myocytes were measured by the intensity of the fluorescent Ca2+ indicator Fluo-4 AM. A rapid increase in fluorescence intensity during the photosensitization reaction and a change in cell morphology after the photosensitization reaction were observed. "
01/01/2014 - "The intracellular Ca(2+) of myocardial cell was observed during and until 10 min after the extracellular photosensitization reaction using fluo-4 AM and a confocal microscope varying the irradiance. "
01/01/2011 - "We measured the intracellular Ca(2+) concentration ([Ca(2+) ](in) ) by using a fluorescent Ca(2+) indicator, Fluo-4 AM, under a high-speed confocal laser microscope to evaluate the acute electrophysiological cell response to the photosensitization reaction. "
01/01/2011 - "The measured temporal change in Fluo-4 fluorescence intensity indicated that the response to the photosensitization reaction might be divided into two phases in both photosensitizers. "
03/01/2012 - "Fluorescence microscopy studies of the neuroblastoma SH-SY5Y cells loaded with Ca2+ indicator Fura-2 or with Ca2+ and Na+ indicators Fluo-4 and SBFI were performed to examine effect of MII modification on its ability to inhibit nicotin-induced increases in intracellular free Ca2+ and Na+ concentrations ([Ca2+] and [Na+]i respectively). "
12/01/2005 - "Here we compare [Ca2+]i-changes induced by trimethyltin chloride in neuroblastoma SY5Y and HeLa S3 cells using calcium-sensitive dyes (fluo-4/AM (fluo-4) and rhod-2/AM (rhod-2)) and laser scanning microscopy (LSM). "
09/01/2015 - "Here, we used an endotoxemic LPS rat model to study mechanisms of sepsis on in vivo hemodynamics, multicellular myofibrillar Ca(2+) sensitivity, in vitro cellular Ca(2+) homeostasis and subcellular actomyosin interaction with intracardiac catheters, force transducers, confocal Fluo-4 Ca(2+) recordings in paced cardiomyocytes, and in vitro motility assay, respectively. "
10/26/2005 - "Ischemia in CSF containing 2 mM Ca2+ caused an approximately 3.5-fold increase in fluo-4 emission after 30 min, indicating a large axonal Ca2+ rise well into the micromolar range. "
12/01/2009 - "Myocytes were exposed to hypoxia, extracellular acidosis (pH(o) 6.8), Na-lactate (10 mM), or to combination of those factors for 25 min. Monitoring of [Ca2+]i using fluo-4 AM fluorescent indicator revealed that [Ca2+]i accumulation increased immediately after exposing the cells to Na-lactate and extracellular acidosis, but not during cell exposure to moderate ischemia. "
01/01/2013 - "The control perfusate was switched to treatment solution for 15 min, followed by reperfusion for 30 min. In a second set of experiments, myocardial excitability and diastolic intracellular calcium ion concentration ([Ca(2+)]i) were measured during a 45-min treatment using a calcium-sensitive fluorescent dye fluo-4 AM. Simulated ischemia/reperfusion under ouabain treatment induced loss of membrane integrity, which was suppressed by hyperkalemia. "
07/01/2010 - "Ca(2+) imaging based on a combination of fluo-4 and fura-red was used to monitor PlnA-induced membrane permeabilization in normal rat cortical neurons and glial cells, PC12 cells (from a rat adrenal chromaffin tumor), and murine N2A cells (from a spinal cord tumor). "
12/01/2010 - "Using high content analysis (HCA), we assessed whether cytotoxicity biomarkers translate from in vitro to in vivo models using four anti-cancer drugs (arabinoside C, arsenic trioxide, doxorubicin, and mitoxantrone) and staining live cells with Hoechst 33342 for DNA (nuclear area, nuclear intensity and cell number), Fluo-4 for ionised calcium, TMRM for mitochondrial membrane potential and TOTO-3 for plasma membrane permeability. "
|1.||Fura-2 (Fura 2)
|3.||sodium-binding benzofuran isophthalate (SBFI)
|8.||Photosensitizing Agents (Photosensitizers)
|10.||Biological Markers (Surrogate Marker)
|3.||Prostheses and Implants (Prosthesis)