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https://bme.duke.edu/research/drug-gene-delivery
Research Interests: Drug and gene delivery, mechanisms of molecular transport in cells and tissues, and tumor pathophysiology.
https://history.as.uky.edu/research/gene-delivery
Gene Delivery Share this page: ... Research Interests A&S Affiliations External Affiliations ; Jason DeRouchey : Biophysical Chemistry, Supramolecular Self-Assembly, DNA condensation and damage, Environmental Impacts of Nanomaterials, Amyloid Proteins, Nanomaterial Transport in Complex Media, Gene Delivery: Analytical, Biological, ...
https://pharmacy.unc.edu/research-interest/gene-delivery/
Home / Faculty Members. Research Interest: Gene Delivery
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5449975/
Apr 28, 2017 · Gene therapy refers collectively to methods aimed at influencing gene expression in living organisms through delivery of integrating or non-integrating exogenous DNA or RNA to treat or prevent diseases.Author: Michael K. Riley, Wilfred Vermerris
https://www.kingston.ac.uk/research/research-interests-and-expertise/research-interests-directory/topic/1139/gene-delivery/
Find out more about gene delivery. Kingston University London has a large variety of academics who are regarded as experts in their fields and who are willing to speak to the media about their work.
https://www.sciencedirect.com/science/article/pii/S0378595519305179
Gene delivery could be paired with cochlear implantation by injecting gene vectors through the electrode array port, or by insertion of an array wrapped in a porous medium impregnated with the vector. Both methods could provide access to the perilymph in the basal and middle turns of the cochlea.Author: Sungsu Lee, Anna Dondzillo, Samuel P. Gubbels, Yehoash Raphael
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6266271/
Nov 07, 2018 · Interests include both delivery to respiratory epithelia, and systemic delivery strategies that might correct CF defects in multiple affected organs. Whether the goal is gene addition or gene repair, for gene therapy to be successful, the vector selected must either integrate into a basal cell or other progenitor cell types or be readministered.Author: Ashley L. Cooney, Paul B. McCray, Patrick L. Sinn
http://visionresearch.ufl.edu/research/
Research Interests: Delivery and testing of potentially therapeutic genes using AAV viral vectors for Retinitis Pigmentosa, Achromatopsia, Blue Cone Monochromacy, Macular Degeneration, Diabetic Retinopathy, Glaucoma and Optic Neuropathies in natural and transgenic animal models of …
https://www.researchgate.net/publication/235727655_Non-Viral_Gene_Delivery_Methods
Gene delivery has attracted increasing interest as a highly promising therapeutic method to treat various diseases, including both genetic and acquired disorders.
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