Your English writing platform
Discover LudwigSuggestions(5)
Exact(1)
A clone with a single mutation (the deletion) was selected for error correction.
Similar(59)
The detected sequence variations are likely due to strain-specific and/or allelic differences resulting in three silent mutations, the deletion of one proline within a proline-rich region, and one amino acid substitution (glycine/arginine).
Of all these types of mutations, the deletion mutation is believed to be the main cause of this phenotype.
The mutation involves the deletion of part of a gene on the surface of cells.
One of the best described examples of a transport-defective mutation is the deletion of Phe508 in the cystic fibrosis transmembrane conductance regulator (Δ F508 CFTR).
The mutation determines the deletion of the entire exon (131 bp) in the RNA processing, causing a severe alteration of the protein structure and thus the disease.
It was assumed that point mutations preceded the deletion of RDs.
As all three sets of Nnd-1 lines share the DSE mutation but only two share the deletion mutation, the parsimonious conclusion is that the DSE mutation is the ancestral mutation.
SNM identified the mutation and determined the deletion endpoints.
The second most frequently found mutation is the nonsense mutation in LoF; for GoF, it was the deletion mutation.
In contrast, the Spi- mutation (deletion mutations) frequencies from the outer medulla were significantly greater (about three fold) than the controls.
Write better and faster with AI suggestions while staying true to your unique style.
Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com