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Diverge tests for the presence of functional divergence of two types, functional divergence type I and type II.
We consider the second-order divergence type elliptic equation (also called -harmonic equation or Leray-Lions equation): (1.1).
This article mainly concerns double obstacle problems for second order divergence type elliptic equation divA x, u, ▽u) = divf(x).
The plate may have both flutter and divergence type instabilities when the force is non-conservative, although it may have only divergence type instabilities when the force is conservative.
In 1999, Chen [19] introduced the concept of semimonotonicity for a single valued mapping, which occurred in the study of nonlinear partial differential equations of divergence type.
Let Ω be a bounded open set of R n, n ≥ 2. We consider the second order divergence type elliptic equation (also called A-harmonic equation or Leray-Lions equation) div A ( x, u ( x ), ∇ u ( x ) ) = div f ( x ).
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In this article, we studied two basic types of functional divergence (type-I and type-II) in depth in order to give an accurate estimation of functional divergence-related sites.
We applied this approach to full length protein sequences to estimate the pairwise coefficient of functional divergence (type-I functional divergence or θI) between all FFRPs.
Two types of functional divergence (Type-I and Type-II) between gene clusters of the caleosin subfamily were estimated using DIVERGE2 [ 38], which evaluates shifts in evolutionary rate and altered amino acid properties after gene duplication.
Two types of functional divergence (Type-I and Type-II) between gene clusters of the NIP subfamily were estimated by posterior analysis using DIVERGE2 that evaluates shifted evolutionary rate and altered amino acid property after gene duplication [ 54, 55].
Two types of functional divergence (type-I and type-II) between gene clusters of the OPR family were estimated by posterior analysis using the DIVERGE v2.0 program [ 36], which evaluates the shifted evolutionary rate and altered amino acid properties after gene duplication [ 37, 38].
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