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Since chloroplasts can be considered a population within the cell, major-allelic variations that change amino acid sequences and translation efficiencies may affect or regulate gene functions.
Similarly, temperature variations that change the TFT characteristics directly lead to changes in the displayed image.
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This peroxidase gene in PI407162 also had a non-synonymous SNP variation that changed an amino acid from serine to alanine.
Detailed molecular analyses of this QTL interval have shown that it harbors 17 genes that exhibit genotype-dependent transcript expression between chromosome 1 congenic and C57BL/6J background strain mice and/or nonsynonymous sequence variation that changes the structure of the protein coded for by the gene, either one or both of which may underlie the QTL's influence (Denmark and Buck 2008).
In general, our results show strong lateral velocity variations that can change between −8.5% and up to +4.2%, which is consistent with the magnitude of velocity perturbations from both global (e.g., Sylvander et al. 1997) and regional studies (e.g., Xu and Koper 2009).
Many variants exist including variations that merely change the order of the letters; LGBT or GLBT are the most common terms and the ones most frequently seen in current usage.
While it's not as simple as having a single "addiction gene," years of research shows children of addicts like me are predisposed to the same path, thanks to a spiderweb of genes and polymorphisms, or genetic variations, that can change how we react to substances, how likely we are to become dependent, how vulnerable we are to relapse.
This conclusion is based on the assumption that currently available bioinformatic tools can accurately distinguish variations that will change the protein function and ultimately result in a behavioral phenotype.
Second, for a subset of our model species we considered life history variations that can change both Nb and Ne (and hence the Nb/ Ne ratio) in ways not accounted for in most standard models.
In total, 142,297 indels (36.4%) were in genic regions, of which 2,163 indels were identified as variations that may change amino acid sequences such as frameshift, nonsense, and splice-site SNPs, which may have the potential to cause functional differences.
As for more complicated gene structure variations that cause change of protein translation, such as gene fusion, alternative splicing, it is even more difficult to identify and validate from proteomics level.
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