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It is found that the AC losses rapidly decrease with increasing twist pitch.
Denser carbon nanotube yarns with smaller diameters were produced either through solvent densification or with increasing twist densities from 5 to ∼15 turns/mm, but led to only minor improvement in yarn tenacity.
The tensile modulus and Poisson's ratio of the yarns decreased with increasing twist angle, whereas the tensile strength of the yarn showed a maximum at the twist angle of 25°.
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The larger the aspect ratio of graphene units and CNTs, the higher the tensile strength of the CF. In the case of fiber geometries, both the σ and E would reduce with increasing twisting MWNT fibers to a larger extent [77].
Our data show that IL-6 increases Twist expression via a transcription-independent mechanism in many SCCHN cell lines.
Our study shows Twist expression can be regulated at the post-translational level through phosphorylation by CK2, which increases Twist stability in response to IL-6 stimulation.
Although it has been reported that IL-6 and its downstream signal mediator, STAT3, can increase Twist expression through transcription in breast cancer cell lines [20], [35], [36], this does not exclude the mechanism of post-translational modification of Twist expression.
CD133pos (Supplementary Figure S7B) and ALDHhigh (Supplementary Figure S7C) cells had increased Twist and Snail expressions compared with CD133neg and ALDHlow cells, respectively.
The Active subtype has high expression of genes involved in activation of fibrosis, cellular movement, increased TWIST expression, and positive expression of TGF-b signatures.
The base stacking interactions were comparable to those observed for the unmodified duplex, although base pair A·T exhibited an increased twist.
The effects of TGFβ1 on both EMT (increased Twist and decreased N-Cadherin expression) and Cai2+ were antagonized by S100A9, which formed heterodimers with TGFβ1 (MALDI-TOF/MS and co-immuno-precipitation).
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