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We analyze a model of repeated encounters in which two agents ask each other queries over time.
In this section, we analyze a model in which the strength of a team is assumed to be a latent variable.
We analyze a model of network formation where the costs of link formation are publicly known but individual benefits are not known to the social planner.
We analyze a model of two-attribute competition for a decision maker who follows a non-compensatory choice procedure that only responds to ordinal rankings along the two dimensions.
We analyze a model for motor-level adaptation in Escherichia coli based upon the premise that clockwise (CW) and counter-clockwise (CCW) states have different preferred numbers of FliM subunits.
We analyze a model of the mosquito population dynamics when genetically modified individuals are introduced into a wild type population so that the effect of their introduction can be assessed.
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We analyzed a model of a coevolving community by focusing on competing consumer species with an evolvable trait and the invasion of an alien predator species and/or resource species into the community.
Finally, we analyzed a model with three levels of resistance: non-ACSSuT, R-type ACSSuT (Nx-sensitive), and R-type ACSSuTNx.
We analyzed a model of delayed CA stem attachment to the aorta, Isl1 heterozygosity (Cai et al., 2008a), which postpones the initiation of blood flow (Chen et al., 2014a).
We analyzed a model explicitly linking the epidemiological and population genetics processes occurring at nested levels of biological organization: (i) within-host population genetics and evolutionary processes and (ii) between-host epidemiological processes.
To understand how competition might influence substrate degradation timing, we analyzed a model with two substrates, C and S, that are based on the yeast substrates Clb5 and securin-2A.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com