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The reactor model selection and mathematical modeling are demonstrated for interaction of toluene with H-ZSM-5 catalyst measured in both types of setups.
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Such combinatorial high- and low-affinity asymmetric interactions have been demonstrated for 14-3-3 14-3-3 14-3-3interactionsphorylated V3 domain of PKCε (Kostelecky et al., 2009).
The proof-of-concept is demonstrated for the interaction between CD4, a major coreceptor in T-cell signaling, and Lck, a protein tyrosine kinase essential for early T-cell signaling.
Likewise, positive co-operativity has been demonstrated for the interaction of the activation domain of pKID (the phosphorylated kinase inducible domain of CREB, which binds to KIX through the c-Myb interaction site) with KIX in complex with MLL.
However, the effect of ω-conotoxin was reversible, unlike what has been demonstrated for its interaction with N-type Ca2+-channels, suggesting that the effect of ω-conotoxin in α-cells may be unspecific [56].
A similar spectral consistency is demonstrated for enhancing interactions from pairs spanning multiple pathways.
This form of coevolution has been shown in mathematical models to be feasible, and it has been suggested as an explanation for the dynamics of some coevolving interactions, but it has not yet been fully demonstrated for any coevolving interaction (Davies and Brooke 1989; Thompson 2005; Nuismer and Thompson 2006).
This potential use is encouraged by the fact that the TNK2 EGFR interaction is most probably amenable to small peptide interference, as has been previously demonstrated for the Cdc42 TNK2 interaction [ 30, 31].
Activation of lacZ expression, driven by the GAL4 promoter, has been demonstrated for precedented compound protein interactions between FK506 and FK506 binding protein 12 (FKBP12) and also between methotrexate (MTX) and dihydrofolate reductase (DHFR).
Thus, our model can resolve the seemingly contradicting experimental outcomes demonstrated for T cell interactions in those experiments, by providing a mathematical description for the complex relationship between relative TCR activation strength of the interacting cells and outcome of the interaction.
Table III presents lead SNPs at each pair of loci demonstrating strong evidence for interaction (P<10−10) in the second-stage GLM, together with P-values from the first stage rapid test.
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