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In 15 RTAs, of different material, a cut was inserted at the incisal edge of tooth 11.
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Finally, it is possible that transcriptional activation of different RTA target genes require different levels of RTA, so that even a small amount of transcriptionally active RTA present in K13-expressing cells may be sufficient to induce vIL6 expression while failing to induce the expression of other lytic genes.
Therefore during the RTA-DNNSpatial training, the normalized input vectors of different feature combinations were added zeros to remove the inconsistency.
K-RTA is a sequence-specific DNA-binding protein that regulates gene expression through K-RTA-responsive elements in the transcriptional regulatory regions of different subsequently expressed viral genes [11] [18].
Real time array PCR (RTA PCR) is a recently developed biochemical technique that measures amplification curves (like with quantitative real time Polymerase Chain Reaction (qRT PCR)) of a multitude of different templates in a sample.
The present study aimed to evaluate the force delivery of removable thermoplastic appliances (RTAs), modified by different sized incisal cuts, during tipping of a maxillary central incisor in palatal and vestibular direction.
Forty-five RTAs from three different materials (Biolon®, Erkodur®, Ideal Clear®) of the same thickness (1 mm) were used.
RTAs modified by different sized incisal cuts show altered biomechanical properties and an inversion of the vertical force component, during tipping of a maxillary central incisor.
Figure 7 shows the contents of oxygen and gold in the subsurface layers of Au/Si structures after 15-s RTA treatments at different temperatures for the Wacker-Chemitronic Si wafers.
After PCR, real-time data were collected and converted into relative telomerase activity (RTA) units performing the calculation: RTA of sample=10 (Ct sample-γint)/slope.
The inset of (c) shows the variation of photosensitivity at different intensity of UV light (wavelength 369 nm) for the ZnO NWs RTA treated at 800°C.
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