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Indeed, the thermal quenching of sensitized Er3+ luminescence is small in both samples, indicating that stable room temperature operation of devices based on Er:SRON is possible.
Importantly, the temperature dependence of the mobility and phase coherence length is almost identical for both samples indicating that neither metallization is limiting the thermal equilibrium of carriers.
The N flux was reduced to half along with the growth rate, and the incorporated N content is virtually the same in both samples, indicating that N incorporation is inversely proportional to the growth rate, as has been reported for GaAsN and InGaAsN [44, 45].
In contrast, the Sox2 promoter was unmethylated in both samples, indicating that Sox2 expression was unaffected by zebularine.
The hybridization showed high concordance of both samples indicating that a large percent of the amplified DNA was barley-derived rather than nonspecific synthesis.
As shown, all but one of the CCs were identified in both samples, indicating that that most common clones persisted in Massachusetts over the examined time span.
Similar(48)
The similar PL spectra observed in both samples indicates that the low substrate temperature process followed to keep the mounding morphology after growing thick cap layers has no influence on the optical properties of the InAs QD. Figure 3 Photoluminescence (PL) intensity spectra for 1.4 ML of InAs deposited into GaAs nanoholes capped by 25 nm (black line) or 100 nm (red line) thick GaAs layers.
The majority of both samples indicated that they used CAM in addition to conventional medicine rather than using CAM alone and in place of conventional medicine.
Almost no signals of Fe were detected in both of the samples, indicating that Fe catalyst particles are fully covered by carbon layers.
Interestingly, 149 miRNAs were the same in both DP and IDL samples, indicating that the effects on leaf senescence of DP and IDL treatment are highly similar, and treatment of the entire plant in darkness also can induce senescence.
However, this high expression of AfCYP6M8 is observed in both resistant and susceptible samples indicating that contrary to its A. gambiae AgCYP6M2 orthologue, AfCYP6M8 is not associated with pyrethroid resistance in this FUMOZ-R strain.
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