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The redshift in our Fe-doped ZnO samples may also due to this reason.
The absence of peak broadening of Ti 2p3/2 signals (FWHM was about 1.4 eV for all samples) may also indicate the presence of Ti4+ species only [32], and good crystallization for all samples [33].
We note, however, that our proposed thermal mechanism for partial TRM of the tree samples may also cause some degree of aliasing on the tree ring scale due to thermal flow inwards that would be competing with natural cooling capacity of the tree to maintain lower temperature than ambient.
Clinical samples may also be biased toward particular antigen haplotypes [30], [31], [32], [33].
The minimal fixation time, depending on the tissue size, should be around 6 h, but samples may also stay in formalin for several days, e.g. if they arrive shortly before the weekend or public holidays.
Sputum samples may also be analysed for disease-related biomarkers.
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Methods combining image-derived IF and later blood sampling may also help minimize spillover effects [26, 27].
It is worth noting that improved nonlinear properties of the CCTO/Au1 sample may also be related to modification of microstructure.
This decrease is more pronounced in septic than in nonseptic patients [4], at least in part because of their inflammatory response; more frequent blood sampling may also contribute.
The timing of the plasma sampling may also falsely underestimate the association between HBP and markers of permeability, as discussed below.
The greater thermal stability of the AgGO sample may also be due to the existence of AgNP. Figure 6 TGA of GO and AgGO.
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