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Comparison of the in vitro and in vivo phosphorylation site mapping experiments revealed that kinases other than Pho85 phosphorylate the GTP-binding domain of Shs1.
Multiarray electrode mapping experiments revealed a spreading pattern of excitation from the SAN.
In vitro binding assays and domain mapping experiments revealed the existence of a previously unknown RBR within SCML2.
Quantitative trait mapping experiments revealed the presence of a metastasis efficiency modifier locus linked to the proximal end of mouse chromosome 19 [ 12].
Genome-wide mapping experiments revealed thousands of ER-binding events, but linking them to the target genes has been an ongoing struggle.
Single-color FISH mapping experiments revealed that sequenced Class II BACs (TGAA-157B03, TGAA-351E14, TGAA-323J16 and TGAA-47O03) hybridized to several pairs of microchromosomes each, likely due to the high repeat content in these clones (see below).
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Nuclease mapping and footprinting experiments revealed that the minHOTAIR RNA is highly structured, and that protein binding causes protection from RNase V1 at two separate regions of a predicted minHOTAIR secondary structure.
The retinotopic maps we obtained in our experiments revealed previously unknown details of the organisation of the two brain areas.
Epistatically, Opm function was mapped to the Wnt/Wg-secreting cells as cell-mixing experiments revealed that Opm function is not required for signal transduction in the receiving cell (Fig 2D E).
The three experiments revealed that a successful map representation would have significant benefits for the human operator's awareness of both the task and the work environment.
We first describe the mapping of the largest complementation group to the fat2 gene, as these experiments revealed a surprisingly high incidence of cryptic fat2 mutations in the backgrounds of publicly available stocks.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com