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Although these markers have shown promise in predicting poor outcomes in patients treated with therapeutic hypothermia, their sensitivity and specificity remain suboptimal.
Previous research on salivary and serum cortisol markers have shown consistent reliability, with correlation coefficients ranging from r = 0.71 to 0.96 [82], depending on the population being analyzed.
However, reports on prognostic biological markers have shown little consistency or reproducibility [9], [12], [17] [29].
Several studies, mostly based on uniparentally inherited markers, have shown that Central Asian populations harbor genetic features that are intermediate between Europeans and East-Asians [66] [68].
Previously reported immunostainings for apical polarity markers have shown their concentration at the ventricular side of the VZ [16], [18], [24] [26].
However, genealogy reconstructions using molecular markers have shown that subordinates are often not related to the recipients of the subordinates' helping behaviour [5] [10].
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The statistical analysis of the mean percentage of the expressed CD markers has shown that CD62L, CXCR-2, LPAM-1, CD11a/CD18, CD8+, IL-6R and CD20+ were expressed in significant differences in either type of the infection.
Microsatellite analysis with nearly 150 polymorphic markers had shown that all cell lines are unique and monoclonal [ 28].
The use of electrophysiological markers has shown, however, that erring is not an all-or-none process, but is instead a gradual one.
Indeed, two or more copies of a chromosome have been observed in tumour karyotypes, even though molecular analysis with polymorphic markers had shown that those tumours had loss of heterozygosity for that particular chromosome (Lengauer et al, 1998).
Analysis of a suite of allozyme markers has shown the nuclear gene pools of T. macedonicus and T. karelinii to have remained isolated [ 17, 18], Arntzen et al. submitted].
Related(20)
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