Additionally, through sequencing the mtgenome of A. barbouri JPB34342, unisexual JPB39932 and other specimens we showed that cyt-b gene did not have any duplicated component residing in the mitochondrial genome.
By varying the laser power and thereby the heating and cooling rate of the specimen, we show that the most stable glass-forming composition within the explored range is Cu64.7Zr35.3, in excellent agreement with the previously reported optimum composition of Cu64.5Zr35.5 that was identified by trial and error.
In a previous study we have analyzed the diagnostic yield of panfungal PCR on fresh tissue biopsy specimens; in contrast to FFPE specimens, we could show a high sensitivity of the PCR approach on patient level and a higher positive rate compared to culture and/or histology [ 17].
Using corresponding cryopreserved tissue specimens as controls, we show that formalin fixation and paraffin embedding does not interfere with the formaldehyde based dimethyl labeling.
None of the four specimens we examined showed absence of the cement mantle in any region.
That 60% of the specimens we examined showed mycobacterial DNA agrees with certain previous studies (12, 13), but other studies were negative for mycobacterial DNA (10, 11).
Applying a composite definition for PJI (comprising histological and clinical criteria to fulfil a "gold standard"), and defining positive microbiology as 2 or more similar isolates from multiple specimens, we have shown that the majority of clinically significant organisms are detected by BACTEC™ within 3 days of incubation.
By comparing the theory to a direct numerical simulation (DNS) of the microstructure for a specimen in tension, we show that the model capture the main physics, and at the same time, remains computationally affordable.
By analyzing different ontogenetic stages in five Addax individuals (three captive and two wild specimens) from a museum collection, we show that bone histology may be a reliable tool for determining certain key life history traits.
We show that specimens collected from multiple locations in six tumours revealed very little variation in MDR1 expression suggesting that the levels of MDR1 in these tumours do not vary greatly with location within the tumour mass.
