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Within the framework of transition state theory, the maximum folding rate for a specific native structure depends simply on the entropic barrier as well as the heat capacity of activation.
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We note that the rate of secretion for a live cell likely fluctuates over time, depending on extrinsic factors, such as the quality of its environment, as well as intrinsic factors, including its secretory capacity, state of activation, and stage in the cell cycle.
Importantly, and in contrast to other NRs, constitutively lymphocyte-expressed NR2F6 is already prebound to its hormone response elements within i.e. the Il17a cytokine promoter loci in a resting state and thereby may simply inhibit the induced DNA binding capacities of activation-dependent TFs (see for our working model cartoon in Figure 3).
Boija, A. et al. Transcription factors activate genes through the phase-separation capacity of their activation domains.
Transcription Factors Activate Genes through the Phase-Separation Capacity of Their Activation Domains.
Of note, the capacity of GPR120 activation to modify intracellular kinases (for example, p38 MAPK) suggests that GPR120 may have additional and direct effects on BAT activity and WAT browning.
In contrast, the capacity of myostatin activation to trigger muscle atrophy is not obvious.
Pretreatment of wild-type and AhR-proficient HaCaT variants with BP did strongly enhance TRAIL-induced apoptosis, indicating that the cytotoxic capacity of AhR activation is not specifically associated with CD95.
This could be an indicator that this group of children quickly developed the capacity of vegetative activation through Qigong practice being able to minimize anxiety-induced cold hands in a short period of time and on demand as a part of the child reactive repertoire.
As shown in Fig. 4, reduction in receptor levels in IGF-1R+/− mutants has limited inhibitory effect on downstream signaling in B6 mice under basal conditions, but we speculated that peak concentrations in IGF-I hormone are able to reveal differences in capacity of pathway activation between IGF-1R+/− and WT mice.
Our data indicate a decreased capacity for activation of helper T lymphocytes in patients with active tuberculosis, represented by the lowest percentage of CD69+ cells.
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