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It was noted by researchers that although NT-3 had positive effects on SC migration, activation of SC-TrkC receptors inhibited myelination [ 146, 149, 150].
In fact, S100a8/a9 is involved in several steps of the inflammatory response including leukocyte differentiation and chemoattraction, transendothelial migration, activation of immune and epithelial cells, and the induction of pro-inflammatory mediators [ 7].
Chemokines are classified into C, CC, CXC, and CX3C subclasses based on the conserved cysteine motifs [ 11], and are involved in cellular migration, activation of adhesion molecules, cellular proliferation, cytokine production and regulation of apoptosis [ 12, 13].
Recent evidence suggests that these proteins can also regulate non-leukocyte cell functions such as angiogenesis/angiostasis, cell migration, activation of apoptotic cell death, and proliferation (Wang et al, 1998).
Interestingly, and importantly with regard to the functional role of DDR2 in fibroblast migration, activation of DDR2 and the DDR2-associated kinases JAK2, and ERK1/2 appear to be involved in fibroblast migration through collagen IV even though DDR2 is not able to recognize collagen IV.
Similar(55)
It is found that the elements can decrease the stacking fault energy of Ni and raise the migration activation energy of vacancy.
The migration activation enthalpy of the investigated capillary-driven planar boundary/facet was a factor of two higher than the activation enthalpy for migration of a geometrically similar boundary driven by an applied stress.
The migration activation parameters of all investigated boundaries comply with the compensation law, i.e. there is a linear relationship between the activation enthalpy and the logarithm of the pre-exponential mobility factor.
The results shed a light on the mechanism of these elements suppressing the dislocation motion by connecting the stacking fault energy and the migration activation energy of vacancy with the dislocation climbing velocity.
The results revealed that for mechanically induced grain-boundary motion there is a misorientation dependence of migration activation parameters.
BMP-mediated cell migration requires activation of the small GTPase Cdc42 and LIMK1 activities.
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