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Our results indicated that the GluR2-containing AMPARs were mainly contributed to the modulation of AMPAR mediated basal synaptic transmission by Tmub1/HOPS (Figures 3C, D).
We also examined whether PARP-1 activation contributed to the modulation of ATP levels and β-Lap could restore ATP levels altered by cisplatin treatment.
To further examine how vestibular inputs contributed to the modulation during head-pursuit, Figure 5 G, H plots phase and sensitivity of discharge modulation of the 32 neurons during head-pursuit against phase and sensitivity during passive whole-body rotation.
We not only confirmed IFN-γ and TNF-α secretion in mice infected with Salmonella, but also observed that many of the genes regulated by cytokine IFN-γ and TNF-α contributed to the modulation of cell proliferation and growth, apoptosis, and developmental disorders.
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It has been suggested that OsGLU3 can contribute to the modulation of root growth in response to phosphate starvation (Zhang et al. [2012a]).
However, how DTCs enter into quiescence and subsequently reactivate, as well as which types of microenvironmental cues contribute to the modulation of tumor dormancy, remains largely unknown.
HOX1 is regulated by auxin and stress related signals, such as jasmonate and nitric oxide (Chen et al. [2012]; Hsu et al. [2012]), which suggests that this pathway can contribute to the modulation of root architecture in response to stress.
We show that both the level of tRNA competition and the type of cognate binding interaction contribute to the modulation of elongation rate, and that optimization of a heterologous transcript for faster elongation rate is achieved by combining the two.
Elements critical for tissue differentiation, like extracellular stimuli, adhesion and cell shape properties, and transcription factors all contribute to the modulation of gene expression and thus, are likely to impinge on the nuclear mechanisms of epigenetic gene expression control.
Post-translational engineering, allosteric engineering, and dynamic pathway analyses and control will also contribute to the modulation and control of the metabolism of engineered B. subtilis, ultimately producing the desired cellular traits.
These results support the notion that OT differentially modulates visual attention toward social signals of positive approach and threat and thereby contributes to the modulation of non-verbal interpersonal communication.
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