Sentence examples for mutation derived from from inspiring English sources

HNIL(H143), harboring a type-2 el1 mutation derived from the 'H143' cultivar, shows an early-flowering phenotype only in long days, but not in short days, compared with the HNIL(M23), which has a functional EL1 allele derived from the 'Milyang23 (M23)' cultivar (Kwon et al. 2014).

Receptor occupancy is dramatically reduced in the fasted state and in a receptor carrying a mutation derived from patients with Maturity Onset Diabetes of the Young 1 (MODY1).

One of these clones had one nucleotide polymorphism in the sequence overlapping with one of the primers used for amplification (mutation derived from the primer and not the cloning strategy), one clone had a PCR-induced mutation, and two clones had the correct sequence.

Because only half of the G2 females will carry any mutation derived from a G1 male, a fully penetrant monogenic mutation should affect 12.5%% of the G3 progeny.

iPS cell lines with that particular mutation derived from a severely symptomatic LQT2 patient with recorded TdP have been generated (Itzhaki et al., 2011).

In the case of scFv (single-chain fragment variable), a mutation generating 133 times higher binding affinity and a mutation derived from a different loop region generating 59 times higher affinity to an antigen were integrated into one molecule, resulting in generation of a 1200 times higher affinity mutant in contrast with the wild-type version [ 43].

We successfully applied this method to detect 12 point mutations derived from human p53 gene.

With caveats, computational prediction of stability can be used to guide mutation, and mutations derived from consensus sequence analysis, especially improved by recent co-variation filters, are very likely to stabilize without sacrificing function.

Then, throughout the fifties, a few other movies addressed the problem of nuclear destruction directly while horror films raised similar problems in the themes of alien invasions or human mutations derived from uncontrolled radioactivity.

Most 21OHD patients are carriers of deletions of the gene encoding 21OH, CYP21A2, or of any of the 9 most frequent point mutations derived from the non-functional CYP21A1P pseudogene.

Moreover, the protocol is based on assembly of PCR products rather than of sequenced inserts in plasmids, which means that a portion of the constructs obtained will contain mutations derived from the primers or the PCR amplification.