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Telomerase substrate (TS) primer was extended by telomerase to form long elongation products which contain several TTAGGG repeat units.
Long elongation times reduce recombination but do not eliminate the problem (Meyerhans et al, 1990).
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The longest elongation was secured with a viscosity of 80 cP, as expected, while the shortest is for 40 cP.
Based on the results of density function theory (DFT) calculations, it is found that phosphorus incorporated into the graphene matrix exhibit the highest catalytic activity due to its lowest adsorption energy of benzylamine and longest elongation of OO bonds.
In transcriptionally silent oocytes, truncation and elongation events are consistent with relative stabilization of short or long isoforms, respectively.
Although cell maturation occurs normally in the absence of PLCγ2, the null cells appear larger, lack long membrane elongations that DCs form to interact with T cells, and present abnormal podosome structures, characterized by condensed actin dots not surrounded by the typical ring of vinculin.
However, due to its isotropy, Neo-Hookean deformation misses key characteristic deformation modes, mainly long-axis elongation and twist.
In IMR-32 cells, HOXC9 re-expression led to a neuronal-like phenotype with a large network of cells interconnected by long neurite elongations, while similar changes were not observed in the other cell lines.
Depending on the exact composition of both fatty acid residues in the respective lipids, this association could be caused by long-chain elongations (C14 to C16 and C16 to C18 through fatty acid synthase and ELOVL6, respectively), by very-long-chain elongations (C22 4 to C24 4 through ELOVL2 or ELOVL5) and even by peroxisomal β -oxidation of fatty acids (through ACOX1 or ACOX3).
Moreover, we also observed a trend toward higher 5′-codon bias in short versus long genes indicating that elongation dynamics driven by codon bias is unlikely to be the cause of higher ribosomal densities on short genes.
For both models the parameters were obtained fitting the response to 0.5 mm long step-wise elongations, which are reproduced quite well by both models; the QLV model used here is actually an average fit over the length of the muscle, and so it does not fit the step data as well as the AQLV model.
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