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This model was motivated by friction force microscopy data that suggest that in at least some cases a pressure-independent interfacial shear strength can be used to describe molecular-level friction.
In agreement with our microscopy data that Atg17-induced autophagy requires Atg1, coexpression of kinase-dead Atg1 blocked Atg17-induced Atg13 hyperphosphorylation in fat bodies of well-fed larvae (Fig. 7G; Fig. S4I), suggesting that Atg17 induces autophagy at least in part by activating Atg1.
It was established by scanning electron microscopy data that the structure of the shungite samples is formed by a micron-size agglomeration of carbon and silicon dioxide clusters.
We show, from scanning electron microscopy data, that the microspheres produced from the homopolymers are bulk and homogeneous at both temperatures whereas they are hollow when the triblock copolymers are used.
It was clear from both the proliferative response of the TSQ and the microscopy data that there were no deleterious effects of serum withdrawal on the TSQ.
Similar(55)
A second common feature among the Golgi autoantigens is that biochemical evidence and immunoelectron microscopy data show that they are peripheral or transmembrane (giantin) proteins on the cytoplasmic face of the Golgi complex.
Electron microscopy data showed that the formation of surface blebs along with disruption of E. coli membrane, suggesting that galectin-4 might kill the bacteria through increasing the expression of defensins (Lehrer et al., 1989).
Transmission electron microscopy (TEM) studies reveal that the sterically stabilized PS particles have a core-shell morphology and wet atomic force microscopy data confirm that the pH-responsive PDEA component covers the PS latex core and the thickness of the protonated steric polymer is estimated to be approximately 15 nm.
However, preliminary flow cytometry and confocal microscopy data showed that the SL siRNA formulation increased uptake of siRNA into vesicular compartments of HeLa-cells in a concentration-dependent manner that could be augmented by exogenuos sPLA2.
In our results, the bright-field microscopy data showed that cell growth rate of F3-effluc cells incorporated within the soft GPT 1.8 K was higher than that of the cells within the stiff GPT 5.8 K. Adherent F3-effluc cells in 3D culture condition began to migrate out from the hydrogel boundary around 4 days after mixing the cells with the hydrogel of both types.
TUNEL assay and electron microscopy data showed that spermatocytes of sycp2 −/− underwent apoptosis (Yang et al., 2006).
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