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Variations of the main scenarios are described through their expected consequence impact, as defined in column two of the table.
where A L, B LL), E k ( L ), a(L), f(L), and E k ( L ) are as defined in column 3 in Table 7.
where A(U), E k ( U ), a(U), f(U) and E k ( U ) are as defined in column 2 of Table 7.
The third column contains the disease abbreviations (as defined in column two) of traits which have an agonistic link to the disorder in column one, followed by the chromosomal location of the agonistically associated variant(s) in parentheses.
The third column contains the abbreviated diseases as defined in column two which have an antagonistic link to the disorder in column one, followed by the chromosomal location of the antagonistically associated variant(s) in parentheses.
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hNumber of patients who met the criteria for substantial weight gain as defined in the first column of this table.
hNumber of patients who met the criteria for substantial BMI change as defined in the first column of this table.
The average dendritic z-profiles of excitatory neurons at a given soma depth were convolved with a neuron density z-profile that represented the number of excitatory neurons at that depth within an average TC projection column as defined in the 2 preceding articles (Meyer et al. 2010; Wimmer et al. 2010).
In this table, we present the size of the subset Y of haplotypes found in the region (column 2), the values PD Y), PDmin(| Y|), PDmax(| Y|) (columns 3-5), and the normalized diversity score PD* Y) (column 6) as defined in the Methods section.
Thus, for instance, the first block, which is the red-colored one, is computed taking the average of the first, the second, the ninth and the tenth columns of Ψ, as defined in (3).
The qualitative values for consequence and likelihood (as defined in Table 1) were inserted in the threat table, columns 3 and 4, for each identified threat.
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