Literature DB >> 21344187

Adeno-associated virus (AAV) based gene therapy for eye diseases.

Shuang Wang1, Peng Liu, Lei Song, Lei Lu, Wensong Zhang, Yazhen Wu.   

Abstract

Gene therapy emerged as important approach in treatment for many inborn disorders caused by genetic defects, as well as other diseases. This manuscript focused on Adeno-associated virus (AAV) based gene therapy to eye diseases. The paper firstly introduced the AAV vectors and the techniques of eye delivery, then summarized some tested genes that were used in past treatment to retinal degeneration disorders. Finally the paper discussed the updated optogenetics and its roles in AAV based gene therapy for eye diseases.

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Year:  2011        PMID: 21344187     DOI: 10.1007/s10561-011-9243-7

Source DB:  PubMed          Journal:  Cell Tissue Bank        ISSN: 1389-9333            Impact factor:   1.522


  1 in total

1.  Sustained gene expression in the retina by improved episomal vectors.

Authors:  Sofia M Calado; Ana V Oliveira; Susana Machado; Rudolf Haase; Gabriela A Silva
Journal:  Tissue Eng Part A       Date:  2014-05-09       Impact factor: 3.845

  1 in total

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