In 2006, another method for c-MET-targeted molecular imaging based on genetic engineering was developed [72].
Thus, the solution obtained by our method for C = 0 is comparable with that obtained by HAM[10].
A method for C-14 specific activity detection, characterized by simplicity and speed of sampling, was developed by CeSNEF – Department of Nuclear Engineering, Polytechnic of Milan.
However, [38] presents an integrated path and timing analysis method for C programs based on cycle-level symbolic execution using instruction-level simulation techniques.
In 2011, a study by Zhang et al. reported a novel method for c-MET-targeted molecular imaging and therapy monitoring based on gene transfected mice models [71].
In an attempt to overcome this challenge, Yanagawa et al. reported a method for C-teminus specific fluorescence labeling of proteins by using puromycin derivatives [1].
The method for C-labeled D-xylose uptake assay was carried out according to the description by Du et al. [ 29].
Because the traditional cell culture method for C trachomatis detection is no longer readily available, requests for C trachomatis nucleic acid tests in the liquid-based specimens are often for both symptomatic and asymptomatic patients.
