Disease relevance of NSC47732

• The accumulation of rhodamine-6G-labeled leukocytes and the number of nonperfused sinusoids (NPS) were monitored (by intravital microscopy) in mouse liver for 1 hour after a 15-minute period of normothermic intestinal ischemia [1].

High impact information on NSC47732

• In view of the known maternal inheritance of mitochondria we have assessed their involvement in Mta expression using the mitochondria specific poison Rhodamine 6G (R6G) [2].
• The exceptional R6G-treated hybrids that continued to express the BALB/c Mta phenotype likewise contained only BALB/c mtDNA [3].
• Leukocytes were fluorescently labeled with rhodamine-6G so that leukocyte-leukocyte interactions could be studied in whole blood [4].
• Luminescence and photoexcitation spectra show that energy transfer from the metal complex to R6G occurs in the films [5].
• Although the fluorescence spectra in the 330-nm-, 850-nm- and 250-microm-sized channels agreed with one another, the fluorescent decays in the nanometer-sized channels were faster for R6G and SR101 and slower for RB than the respective decays in the 250-microm-sized channels [6].

Biological context of NSC47732

• The fluorescence intensity of Rh6G started to increase at the chemotactic thresholds of the stimuli, indicating that negative chemotaxis of T. pyriformis to the hydrophobic stimuli is induced by depolarization of the cell [7].
• Platelet-endothelial cell interactions were quantitatively analyzed using intravital fluorescence microscopy after lobar hepatic I/R in C57BL/6 wild-type and P-selectin-deficient mice after infusion of ex vivo rhodamine-6G-labeled wild-type and P-selectin-deficient platelets [8].
• Adsorption Characteristics and the Kinetics of the Cation Exchange of Rhodamine-6G with Na(+)-Montmorillonite [9].
• The indicator dye for membrane potential is rhodamine 6G (Rh6G) [10].
• Leukocyte-endothelial cell adhesion was monitored with the use of rhodamine-6G [11].

Anatomical context of NSC47732

• Second, the cationic dye rhodamine 6G (R6G) enters cultured cells by a potential-driven process, and single R6G molecules are observed as intense photon bursts when they move in and out of the intracellular laser beam [12].
• METHODS: Thirty patients with complicated bile duct stones were treated perorally with a flashlamp-pulsed Rhodamine-6G dye laser and an automatic stone-tissue discrimination system [13].
• AO and Rh6G induced leukocyte rolling/sticking in postcapillary venules and arterioles when exposed to high light energy levels [14].
• Eighteen patients with giant or impacted common bile duct stones refractory to standard treatment techniques were treated via the endoscopic retrograde route using a rhodamine-6G dye laser with an integrated stone-tissue detection system [15].
• The R6G efflux from oocytes was accelerated at the MII stage more than at the GV stage [16].

Associations of NSC47732 with other chemical compounds

• When chloramphenicol (CAP) resistant cells were used as the R6G-treated parent, the expression of CAP resistance in hybrids and cybrids was greatly reduced [17].
• Ultrafast fluorescence resonance energy transfer (FRET) from coumarin 153 (C153) to rhodamine 6G (R6G) is studied in a neutral PEO(20)-PPO(70)-PEO(20) triblock copolymer (P123) micelle and an anionic micelle (sodium dodecyl sulfate, SDS) using a femtosecond up-conversion setup [18].

Gene context of NSC47732

• P-gp inhibitors significantly blocked the R6G efflux from the MII oocytes, whereas the reagents were ineffective in the GV oocytes [16].

Analytical, diagnostic and therapeutic context of NSC47732

• Laser lithotripsy using the rhodamine-6G dye laser plus stone-tissue detection system appears safe and effective and allows "blind" fragmentation of difficult common bile duct stones to be performed under radiologic control [15].
• METHODS: Dye penetration depth was assessed histologically after the use of formulations containing rhodamine-6G-loaded microspheres dispersed into two different silicones [19].
• Thus, the adsorbed amount of KWK per unit area at a given total KWK concentration, as determined by the centrifugation method, can be plotted against the fractions of R6G anisotropy decay components at the same KWK concentration to relate the anisotropy components to the absolute surface coverage [20].
• The morphology of these films has been characterized by scanning electron microscopy (SEM), and their performance as surface-enhanced Raman scattering (SERS) substrates has been evaluated by using rhodamine 6G (R6G) as a probe molecule [21].
• Comparisons between far-field Raman images of R6G-covered Ag particle aggregates with topographic images recorded using atomic force microscopy (AFM) indicate saturation effects due to resonance excitation [22].

References