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In vitro cell studies by MC3T3-E1 mouse preosteoblast cells showed that the prepared 3D scaffolds supported cell adhesion, tissue growth and cell differentiation.
Novel platforms combining controlled release, improved adhesion, tissue penetration, and selective intestinal targeting may overcome these issues and potentially diminish the toxicity and high frequency of administration associated with conventional oral delivery.
To determine whether the insulin receptor (IR), insulin-like growth factor-I receptor (IGF-IR), and IGF-I are expressed differentially in fibroblasts isolated from normal peritoneal and adhesion tissue before and after 24-hour treatment with increasing glucose concentrations.
CD146 has important functions in adhesion, tissue invasion and signalling [ 18, 19].
Therefore, the scaffold had both excellent biomechanical properties and enlarged surface area for cells adhesion, tissue ingrowths, and nutrients supply [ 33].
Among the classes of adhesion molecules, desmosomes have been widely recognized and studied for their various roles in cell adhesion, tissue morphogenesis, and cell signaling [ 3].
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To determine whether the COX-2 gene is expressed in human fibroblasts isolated from normal peritoneal and adhesion tissues.
To determine whether α smooth muscle cell actin (αSMCA) is expressed in human fibroblasts isolated from normal peritoneal and adhesion tissues.
To determine the levels of COX-1, COX-2, and prostaglandin (PG) E2 in human fibroblasts isolated from normal peritoneal and adhesion tissues.
To study the modulation of the inducible nitric oxide synthase/nitric oxide (iNOS/NO) expression system in fibroblasts isolated from human peritoneum and adhesion tissues by hypoxia.
To examine the effect of interferon (IFN -γ treatment under normal and hypoxIFN -γditreatmentthe BCL-2/BAX ratio of fibroblasts obtained from normal peritoneal and adhesion tissunderf the same patienormal
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