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Using a layer-by-layer approach, synthetic or natural materials, cells and other molecules are printed and stacked into a scaffold shape that mimics the physiological structure and precisely replaces a defect site in damaged or missing tissue.
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However, they have not succeeded until now in cutting out mutations and precisely replacing them with healthy strands of DNA, said Alexander Marson of the University of California, San Francisco, who led the latest research.
RMCE enables enhanced tag-and-exchange strategies by precisely replacing a genomic target cassette by a compatible donor construct.
Our efforts towards a second vaccine generation based on the rational selection of conserved high activity binding peptides (HABPs) whose critical binding residues have to be precisely replaced by others.
The entire coding region of chlL, an essential chloroplast gene required for chlorophyll biosynthesis in the dark in Chlamydomonas reinhardtii, was precisely replaced by either the Klebsiella pneumoniae nifH (encoding the structural component of nitrogenase Fe protein) or the Escherichia coli uidA reporter gene encoding β-glucuronidase.
This work demonstrated that it was possible to use the 'ends-in' based method of homologous recombination [23] to specifically and precisely replace a target gene sequence with that of a reporter (or other heterologous sequence).
Hydration infusion rate was automatically adjusted to precisely replace the patient's urine output.
These additional images belonged to categories in the same way as the food images in Experiment 2, so that they could precisely replace the food images.
In all 38 flies recovered with this rearrangement, the 3′ P-end has been precisely replaced by the 5′ P-end, a structure consistent with the proposed mechanism of repair.
To precisely replace the entire coding sequence, the approach we developed involved the transgenic Cas9 flies, two sgRNAs, and a plasmid DNA donor with a selective marker (Materials and Methods; Figure 3A).
When the reporter was introduced into the fosmid, precisely replacing the entire ceh-63 coding region (construction fUL HF003.1), and the recombineered fosmid was used to generate the transgenic strain UL3025, GFP expression was observed in DVC from late embryogenesis through to the adult stage (Figs. 3A and C) and in the uterus (Fig. 3B) in young adult animals, as for the promoter fusion.
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