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The construction of tissue engineering chamber model.
Of these, the nerve chamber model has clearly dominated.
The setup for the chamber model is presented in detail.
Selection of biomaterials for peripheral nerve regeneration using data from the nerve chamber model.
Here we verified the pro-angiogenic role of FG-4592 in tube formation model in vitro and subcutaneous tissue engineering chamber model in vivo.
Here we reported for the first time that FG-4592 proangiogenicgiogenic ability both in vitro and in vivo based on a subcutaneous chamber model.
The murine dorsal skinfold window chamber model was used to evaluate the structural remodeling response of the microvasculature.
This LPC spheroid/vascularized chamber model has clinical potential to generate three-dimensional vascularized liver tissue for liver replacement.
Similar to the other solvent chamber models, the parabolic solvent chamber model can adequately predict the cumulative heavy oil production.
Here we reported for the first time that fibrin gel could act as a small molecule drug delivery system to facilitate the local administration of FG-4592 and promote angiogenesis in subcutaneous chamber model.
To determine the immunogenic potential of FG-4592 using our in vivo tissue engineering chamber model, we performed MAC2 IHC staining to evaluate the inflammatory response based on macrophages (Fig. 10A).
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com