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The mechanism by which the Y copy of SlWUS1 has disappeared could be deletion of an entire Y region, deleting several or many genes, or by a specific deletion of just this gene, or by loss-of-function mutations followed by sequence divergence, so that no Y-linked copy remains detectable even in our low-stringency Southern blotting experiments, including in S. dioica and S. diclinis (see Results).
The punishment for speaking out is likely to be "deletion" (which sounds like a particularly writerly form of doom).
One possibility for this observation might be deletion of TRP-164 78-specific TRP-164 78-specificor peripheral TRP-164 78-specific
The most likely explanation for the generation mechanism of OwlAlp1 would be deletion of part of the OwlAlp2 sequence.
If n/N was ≥0.8, we postulated that LOH to be deletion mediated; while the remaining ones (n/N <0.8) as copy neutral LOH.
The genetic polymorphisms at the GSTM1 and GSTT1 genes were reported to be deletion of nucleotides (referred to as null GSTM1 and null GSTT1 alleles), which have been associated with susceptibility to cancer [ 37, 38].
Similar(51)
The solution, then, is deletion — like the third-party Twitter tools that nuke your tweets after a set amount of time (a day, a week, a month).
The strongest suppressor of TDP-43 toxicity was deletion of DBR1, which encodes an RNA lariat debranching enzyme.
Alleles that affect both eyecolor and chromosome segregation are deletion mutants that affect both transcripts.
For the seven VOUS, six were duplications and one was deletion.
All other genomic subclones were deletion derivatives of pCZ483.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com