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To identify specific cellular processes influenced by miR-215-5p miR-215-5p miR-215-5pxperimentseries been perfofmed.
In vitro experiments have also confirmed that such entities are prone to phagocytosis.
In vivo and in vitro experiments have demonstrated that CS reaches the joint, and distributes into the cartilage and subchondral layers43,44.
In vitro experiments have shown that the application of synthetic scaffolds is a promising alternative to existing therapeutic options.
Prior in vitro experiments have shown that BCP can help differentiate MSCs and substantially improve new matrix deposition.
Most in vitro experiments have used 10 100 ng/ml TNF-α36, and the sensitivity of various cell types to various TNF-α doses has been evaluated under different experimental conditions37,38.
A series of in vitro experiments have been performed using transient transfection of miR-215-5p miR-215-5p miR-215-5pcell lines to identify specific cellular processes affected by mimics5-5p.
In vitro experiments have included different cell lines and preclinical irradiation beams (microbeam radiation therapy, low-energy X-ray).
Previous in vitro experiments have demonstrated that particulate debris from joint implants causes cells in culture to release products that have been implicated in this pathological bone resorption.
In vivo and in vitro experiments have suggested a correlative relationship between elevated TNFα and the severity of demyelinating disease [5].
In vitro experiments have shown that branching enzymes can catalyze the synthesis of amylose branches (Buleon et al. 1998; Takeda and Hizukuri 1987).
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