PubMed · 3256004
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W Kohler. 1988. [Creative possibilities using multicolored wax].. https://pubmed.ncbi.nlm.nih.gov/3256004/
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The objective of this study was to measure the differences in color and color parameters between dental porcelain and porcelain-repairing resin composites. The colors of three shades (A2, A3, A3.5) of one brand of dental porcelain, three original shades (A2, A3, A3.5), and three combinations (A2/A3, A3/3.5, A2/A3.5) of three brands of porcelain-repairing resin composites (ABT, FSP, TCR) were measured. The specimens were 2 mm thick, and 1 mm of each shade was layered to make combined shades. Differences in color (DeltaE(ab) (*)), lightness (DeltaL*), chroma (DeltaC(ab) (*)), and hue (DeltaH(*)) between porcelain and resin composite were calculated. Color difference was calculated as DeltaE(ab) (*) = (DeltaL*(2) + Deltaa*(2) + Deltab*(2))(1/2), chroma difference was calculated as DeltaC(ab) (*) = (Deltaa*(2) + Deltab*(2))(1/2), and hue difference was calculated as DeltaH(ab) (*) = (DeltaE(ab) (*2) - DeltaL*(2) - DeltaC(ab) (*2))(1/2). The influence of porcelain shade, brand of resin composites, and shade of resin composites were analyzed by three-way analyses of variance, and the differential influence of color parameters on color difference was analyzed with multiple regression analysis (alpha = 0.05). Differences in color and color parameters were influenced by the porcelain shade, brand and shade of resin composites. The DeltaE(ab) (*) value was in the range of 2.2-16.9. The DeltaE(ab) (*) value was correlated with DeltaC(ab) (*) (standardized correlation coefficient, beta = - 0.85), DeltaL* (beta = - 0.52), and DeltaH(ab) (*) (beta = 0.08). Between the same shade designated pairs of porcelain and repairing composite, color difference was perceptible. Therefore, studies to improve the color matching between porcelain and repairing resin are recommended.
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Erythrocyte acid phosphatase (ACP1), also named low molecular weight phosphotyrosine phosphatase (LMW-PTP) is an enzyme involved in signal transduction pathways of tyrosine kinase receptor. The precise physiological role of ACP1 remains to be elucidated, however recent advancements suggest that it may play an important role in the control of cell proliferation. ACP1 is a highly polymorphic enzyme that has been investigated by case-control studies for decades. Initially based on protein electrophoresis, the phenotype of ACP1 is now detected by DNA-based techniques. Here, we report a new rapid single tube genotyping method for ACP1 by FRET based amplification and dual color melting curve analysis. This method does not require a post-procedure amplification process and allows unambiguous genotyping of 30 samples in less than 1 h.