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In vivo studies of ADSCs/cryogel constructs implanted in nude mice and pigs demonstrated adipose tissue and new capillary formation, the expression of PPARγ, leptin and CD31 in immunostained explants, and the continued expression of adipocyte-specific genes.
Finally, we assayed the effects of the mutated N-terminus on cell growth and demonstrated that while the deletion of the amino-terminal portion of ERK1 results in the loss of its inhibitory properties on Ras-dependent colony formation, the expression of ERK2 fused with the N-terminus of ERK1 leads to the acquisition of an ERK1-like phenotype.
To further understand the role of VE-cad on the self-assembled network formation, the expression of VE-cad in HBMSC, HUVEC, co-HBMSC and co-HUVEC at different time points was detected after the co-cultured cells were separated (Fig. 2).
We found that, during EB formation, the expression of Dppa3 and Stra8 was decreased dramatically.
To identify possible molecular mechanisms for the action of HBO on the initial stages of monocyte differentiation and multinuclear osteoclast formation, the expression of RANK mRNA, Dc-STAMP mRNA, and NFATc1 mRNA was examined (Table).
In conclusion, both SOX2- and SOX9-positive cells from the adult pituitary have sphere-forming ability, but during their initial formation the expression of the two proteins appears to recapitulate their embryonic pattern.
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These results indicate that ethylene is capable of inducing zygote formation through the expression of zyg1.
Autophagosome formation requires the expression of ATG genes which control levels of Atg proteins [ 101].
In normal secondary lymphoid tissue, germinal center formation requires the expression of numerous cytokines and chemokines.
Therefore, we analyzed the effect of SCD1 downregulation during spheroid formation on the expression of these markers.
As a consequence, VEGF-A induced NRP1/GIPC1 and GIPC1/Syx complex formation without the expression of VEGFR1 or VEGFR2.
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