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More realistic models were developed by combining RC derived from hot spots in cold background, RC from cold spots in hot background, and RC from hot spots in warm background, allowing both spill out and spill in effects to be accounted for (e.g., [ 15]), but were never applied to real clinical studies.
We developed a method for predicting RC from genotype using support vector machines (SVMs) trained on about 300 genotype-RC pairs.
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If a drug has the number of conformers less than 80 due to limited flexibility, RCDTC showed the least failure in acquiring 10% sized RC from original conformers.
The primary objective of this study was to compare the MH and RC measurements and to develop an equation to predict CH4 measured in RC from measurements taken during group feeding.
The frequency of reporting of 11 basic elements of design and analysis was evaluated in randomized clinical trials (RCT), nonrandomized clinical trials (NRCT), and retrospective cohorts (RC) from JPS by consensus of 2 assessors.
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We investigated 10 cases diagnosed as rapidly progressive glomerulonephritis (RPGN) by randomly selecting 10 RCs from each case.
RCs from 90Y PET imaging were also lower than those from 18F PET imaging, with the exception of the largest sphere size at the highest activity.
The reference RCs could be determined from a specific set of scanner/reconstruction combinations used as part of a clinical trial (i.e. by taking the lowest set of RCs from the scanner/reconstruction combination with the lowest resolution).
For this study, we have used the reference RCs published by Boellaard et al. [4]; although as the phantom was filled according to the NEMA Standards Publication NU 2-2007 [6], we have only used the RCs from the four smallest spheres.
pMT-cindr-V5 was generated by amplifying the longest predicted isoform cindr-RC from S2R+ cell cDNA, adding Not1/Xba1 sites, and ligating into pMT-V5/6xHis (Invitrogen).
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