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bladder carcinoma cells
The in vitro growth of bladder carcinoma cells was analyzed by MTT colorimetry, and the apoptosis rate was assayed by TUNEL methods.
      
Using this in situ assay method, we detected the reduced permeability to HRP in aortic and brain microvascular endothelial cells after 4-5 days culture with conditioned media of human astrocytes or bladder carcinoma cells.
      
In line with these data, expression of either p63RhoGEF or GEFT in J82 human bladder carcinoma cells induced the formation of actin stress fibres.
      
Nucleic acid metabolism of bladder carcinoma cells in vitro
      
Nucleic acid metabolism was investigated to determine the metabolic activity of bladder carcinoma cells.
      
Activities of bladder carcinoma cells were determined by their incorporation rates.
      
The results were as follows: 14C-Formate incorporation was much higher in grade III bladder carcinoma cells than in the normal epithelium of the bladder; it was highest in stage B2 bladder carcinoma cells.
      
14C-Adenine was found to be incorporated into nucleic acid bases of bladder carcinoma cells.
      
The latter was more active than the former in bladder carcinoma cells.
      
The photodynamic effect of a pulsed dye laser on human bladder carcinoma cells in vitro
      
The photodynamic effect of a pulsed flashlamp pumped dye laser on cultured human bladder carcinoma cells was studied.
      
The uptake of photosan and the intracellular sites of photoradiation-induced damage were investigated in vitro in bladder carcinoma cells and in normal bladder cells.
      
Photodynamic therapy of human bladder carcinoma cells in vitro with pH-sensitive liposomes as carriers for 9-acetoxy-tetra-n-pro
      
In vitro experiments were performed on human bladder carcinoma cells to evaluate the efficiency of the recently synthesized photosensitizer 9-acetoxy-tetra-n-propylporphycene (ATPPn) for photodynamic therapy.
      
After incubation with liposome-bound ATPPn, bladder carcinoma cells were irradiated by a dye laser with increasing light fluence rates from 1 to 48 J/cm2.
      
Uptake and phototoxic effects of aluminum-chlorophthalocyanine (AISPc) in hurnan bladder carcinoma cells
      
In vitro experiments were performed on human bladder carcinoma cells to evaluate the uptake of aluminum-chlorophthalocyanine (AlSPc) and the subcellular target of phototoxicity.
      
TMHP is taken up by human bladder carcinoma cells after an incubation time of only 1 h.
      
Binding activities against the bladder carcinoma cells were detected.
      
Aminolevulinic acid for photodynamic therapy of bladder carcinoma cells
      
 

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