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As in the rat study, the number of A, B, C and D component trials was not equal between groups (see Table 2) in order to keep outcome frequency at 50%% overall and for presentations of components (19 reinforced, 19 unreinforced) and compounds (3 reinforced, 3 unreinforced).
The number of A, B, C and D component trials was not equal between groups (see Table 1) in order to keep outcome frequency at 50%% overall as well as for presentations of components (20 reinforced, 20 unreinforced) and compounds (4 reinforced, 4 unreinforced).
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In the first part of Phase 1, participants received four presentations each of components A, B, C and D, and eight presentations each of compounds AB and CD.
From days 1 27, rats received six presentations each of components A, B, C and D and twelve presentations each of compounds AB and CD (see Table 1).
During the actual test (Phase 3, parts 2 and 3), the EF compound was presented twice, unreinforced, followed by four unreinforced presentations of the components E and F, intermixed with four unreinforced presentations of the compound EF.
During the last part of Phase 1, participants received nine presentations each of the components and eighteen presentations each of the compounds, while the ratio schedule was increased to a VR 7. In total, participants received sixteen presentations of each component and thirty-two presentations of each compound in the first phase.
Very exciting presentation of Web Components, which let you create standalone, encapsulated, importable components for the web, bundling an HTML template, scoped CSS (and from quick research, scoped JS).
From days 28 36, rats continued to be trained on the negative and positive patterning problems, but additionally received eight presentations each of the generalization stimuli E and F. For the PP transfer group, lever pressing during presentation of the components E and F was not reinforced, while pressing to those components was reinforced for the NP transfer group.
This presentation of the components of value assessment is a prerequisite for the following necessary step of finding a consensus in which these components are summarised into a value judgment for an indication and a treatment method.
The mean number of responses made during presentations of the reinforced components A and B, the unreinforced components C and D, the unreinforced compound AB and the reinforced compound CD are shown in Fig. 4.
The capacity to degrade large quantities of cytoplasm provides cells with a powerful means of killing intracellular pathogens and increasing presentation of microbial components to the immune system.
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