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In alloys containing 50 at.% or less Ti, where it was possible to synthesize nearly single phase specimens, the calculated heats of formation agree within a few kJ/mol of the calorimetry data, while the calculated isotropic elastic constants agree within 5% of the experimental values.
Additionally, a high concentration of proinflammatory cytokines/chemokines was detected in the convalescent phase specimens.
In each cycle phase, specimens were partitioned into 80% construction and 20% independent validation sets for margin tree based training and testing of classifiers.
The fallopian tube array included one 1.5 mm core from 11 luteal and 16 follicular phase non-malignant specimens from confirmed BRCA1/2 mutation carriers, and 11 luteal and 12 follicular phase specimens from normal control patients.
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After immersion for 4 h, the tensile strengths of all the specimens immersed were decreased with respect to those of the non-immersed specimens, and the tensile strength of the martensite single phase specimen (C) was higher than that of parent single phase specimen (A) and the parent/martensite mixed phase specimen (B).
Despite all required preventive measures during transport phase, specimen 12CT525 presented premature slippage, probably due to riding procedure, invalidating the test.
At San Bassiano hospital, the implementation of advanced information technology and robotics in the pre-analytical phase (specimen collection and pre-analytical sample handling) have improved accuracy, and clinical efficiency of the laboratory process and created a TTP that minimizes errors.
However, in the post collection phase, specimen transferring from syringes to test tubes (15.8%) and mixing specimen with additives (63.4%) involved highest proportions of undesirability among laboratory and non-laboratory professionals respectively.
On exposing β0 single-phase specimens to hydrogen, β hydride (B2) is easily formed.
Of these 69, ELISA WNV IgM testing was performed on both acute- and convalescent-phase specimens for 23 patients, on only acute-phase specimens for 36 patients, and on only convalescent-phase specimens for 10 patients.
However, MAT serology may be insensitive in early acute-phase specimens [ 28].
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