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The critical void volume fraction for coalescence and the distribution of ductile damage below the fracture surface is markedly different between blunt-notched and pre-cracked specimens, with notched specimens exhibiting a significantly lower critical void volume fraction and a more extensive distribution of ductile damage below the fracture surface than is observed in pre-cracked specimens.
MST was successfully applied to 7/10 clinical specimens exhibiting a Cts ≤ 42 cycles in internal transcribed spacer-real time PCR.
In cancer specimens exhibiting a TP53 mutation, cells without a mutation are present as well.
Of the primary tumor specimens exhibiting a loss of DSC3 expression, several were not associated with cytosine methylation of its promoter region.
Of the two specimens exhibiting a discrepancy between the Xpert assay and the phenotypic DST results, one isolate was identified as RIF-resistant by the Xpert assay but was phenotypically susceptible.
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The specimens exhibited a bending strength up to 90 MPa.
The packed specimens exhibited a significant difference from the others.
While the coarse structured specimens exhibited a compressive strength of 80% relative to this.
The specimens exhibited a "strong column weak beam" type of flexural yielding mechanism.
When the bond strength was adequate, the specimens exhibited a ductile behaviour prior to failure (Fig. 12a).
All specimens exhibited a good ductility and still retained the integrity when the displacement reached 30 mm.
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