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These mutations contain a total of six SNPs and eight deletions within a 25 bp region of the exon 7 as compared to the wild type allele in the tested non-fragrant varieties.
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Because all three analyzed mutations contain an intact C-terminal of PTEN, it is unlikely that the spontaneous DNA DSBs caused by these mutations are due to the loss of binding between the mutant PTEN and CENP-C.
In contrast, both LMNA-mutated samples (E358K and R541P, Lamin A/C mutations) contained a small percentage (up to 0.5%) of myofibers with cytoplasmic NPCs, similar to our three new patient mutations.
In biopsy samples from oesophageal cancer-free individuals, the p53 missense mutations containing a hotspot mutation were found in NDE, which was identified as an LUL.
The p53 missense mutations containing a hotspot mutation were found in LULs-NDE in oesophageal cancer-free individuals without reflux oesophagitis.
To test this, we generated diploid strains heterozygous for pif1Δ, exo1Δ, cdc13Δ and tlc1Δ mutations, containing a plasmid that carried a wild-type copy of CDC13.
The reason for including the first Tudor-like domain resides in the characterization of the tudA36 mutation containing a substitution in this domain [29].
The blue curves correspond to the results obtained for the tyrosinase gene mouse mutation containing a single heterology, and the red curves, the results obtained for a mutation involving three consecutive heterologies.
Therefore, the set of haplotypes that carry the selected mutation contains a subsample of neutral variation in the ancestral population, and can be contrasted with the set carrying the ancestral allele.
The bh23 mutation contains a 364-bp deletion overlapping with the 5′ region of the Cbr-lin-39 coding sequence.
This protein sequence following the frame shift mutation contains a high level of Lys and Gln amino acids, indicating a high potential for interactions with other proteins.
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