Titlebook: Bio-Carrier Vectors; Methods and Protocol Kumaran Narayanan Book 2021 Springer Science+Business Media, LLC, part of Springer Nature 2021 Ba

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https://doi.org/10.1007/978-1-0716-0943-9Bacterial vectors; Natural and artificial vector systems; Drug delivery; Peptide vehicles; Nanoparticles

CANON

978-1-0716-0945-3Springer Science+Business Media, LLC, part of Springer Nature 2021

Engaged

https://doi.org/10.1007/978-3-030-19726-1 provides a simple one-step genetic correction of . mutation in the patient-derived iPSCs. Further differentiation of the corrected iPSCs into hematopoietic stem/progenitor cells will provide an alternative renewable source of cells for the application in autologous transplantation in the future.

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Correction of Hemoglobin E /Beta-Thalassemia Patient-Derived iPSCs Using CRISPR/Cas9 provides a simple one-step genetic correction of . mutation in the patient-derived iPSCs. Further differentiation of the corrected iPSCs into hematopoietic stem/progenitor cells will provide an alternative renewable source of cells for the application in autologous transplantation in the future.

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Jacques Rancière: P?dagogische Lektürentate tracking of the immune cell killing assay, which avoids the need for multiple cell labeling with fluorescent dyes. Our approach is also applicable to the genome editing of other target cell types for functional analysis of effector cells.

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Cell-Derived Nanovesicles as Exosome-Mimetics for Drug Delivery Purposes: Uses and Recommendationsge) and spin cups. Through a series of extrusion and size exclusion steps, CDNs are produced from in vitro cell culture and are found to highly resemble the endogenous exosomes. Thus, we envision that this strategy holds great potential as a viable alternative to exosomes in the development of ideal DDS.

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