Exact(43)
To test this hypothesis, we generated in silico mutants of these basic residues in Bad peptide and Mcl-1/A1 proteins.
This is because the stochastic signals we generated in the present study only trigger spike trains with ISIs that are long as compared to the intrinsic IRP.
Since we do not aim at observing variations of model structure, we consider the 31 models that we generated in the second experiment, with 30 branches, 15 joins, 1 loop and maximum depth 25.
We are now analyzing the results from the third and final phase of the initiative, our quantitative survey to put data behind the theories we generated in the qualitative phases.
We generated in silico reads from Saccharomyces cerevisiae (yeast), Drosophila melanogaster (fly), Arabidoposis thaliana, and Homo sapiens (human) transcripts.
In addition, there are discrepancies of phenotypes between Cthrc1 transgenic mice which we generated in this study and the transgenic mice overexpressing Cthrc1 previously reported [14].
Similar(16)
Given the large confidence intervals generated by BayesAss+ with the laboratory-cultured data sets, we generated in-silico simulated data sets both under conditions similar to our in-vitro experimental design (see Methods) and with an increasing number of sampled individuals and/or number of loci.
In order to gain even more insight into the mechanism by which MafB-induced reprogramming of stem cells into tumour plasma cells, we generated in-vivo genome-scale maps of DNA methylation in both stem cells and mature B cells.
To map the interacting domains, we generated in-frame One-STrEP and HA-tagged truncation mutants of the key domains of IRF5 and FLAG-tagged truncation mutants of the key domains of RelA.
For finding conserved positions in alignments among organisms sharing a particular niche preference, we generated in-house R scripts for counting shared positions between them which differ in the rest and created a null distribution counting the same for all possible random groups of genomes.
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