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We have performed a computational analysis of DNA structural features in 18 fully sequenced prokaryotic genomes using models for DNA curvature, DNA flexibility, and DNA stability.
Other possible application of O-ring stanalysisanalysis is elastic models for DNA (Goriely 2006; Benham 1983).
As well as providing suitable preclinical models for DNA vaccines in a "self" model of prostate cancer, these xenoantigens have been used by groups in an effort to increase the immunogenicity of DNA vaccines.
This article aims to provide an overview of the different legislative models for DNA databasing in Europe and ponder if wider inclusion criteria – and, consequently, database size – translates into more matches between profiles of crime scene stains and included individuals (performance ratio).
Substitution models for DNA evolution were selected using AIC in ModelTest3.7/ModelTestJ [69]; GTR+G (for original Alignment 1) and GTR+G+I (and moderately stringent Alignment 2 and the stringent Alignment 3).
Parameters of the evolution models for DNA and protein sequences were automatically estimated on each alignment using TREE-PUZZLE [ 47].
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In mammals, a two-step model for DNA fragmentation in apoptosis has been proposed, where caspases activate CAD to degrade DNA in dying cells, and DNase II finishes the degradation within lysosomes of engulfing cells.
A cryo-electron microscopy structure of the chromatin remodelling factor Chd1 bound to a nucleosome leads to a model for DNA translocation by its ATPase motor.
In a previous study by Viljoen et al. [2005, A macroscopic kinetic model for DNA polymerase elongation and high-fidelity nucleotide selection.
Here we show that a three-state model for DNA escape, involving stochastic binding interactions of DNA with the pore, accurately reproduces the experimental data.
We describe these results and propose a new structural model for DNA binding and homologous pairing.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com