Literature DB >> 32661283

Large gene delivery to the retina with AAV vectors: are we there yet?

Ivana Trapani1,2, Patrizia Tornabene1,2, Alberto Auricchio3,4.   

Abstract

Year:  2020        PMID： 32661283     DOI： 10.1038/s41434-020-0174-4

Source DB:  PubMed          Journal:  Gene Ther        ISSN： 0969-7128            Impact factor:   5.250


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  1 in total

Review 1.  Adeno-associated Virus (AAV) Dual Vector Strategies for Gene Therapy Encoding Large Transgenes.

Authors:  Michelle E McClements; Robert E MacLaren
Journal:  Yale J Biol Med       Date:  2017-12-19
  1 in total
  4 in total

Review 1.  Gene therapy in color vision deficiency: a review.

Authors:  Zeinab El Moussawi; Marguerita Boueiri; Christiane Al-Haddad
Journal:  Int Ophthalmol       Date:  2021-02-02       Impact factor: 2.031

Review 2.  New Editing Tools for Gene Therapy in Inherited Retinal Dystrophies.

Authors:  Juliette Pulman; José-Alain Sahel; Deniz Dalkara
Journal:  CRISPR J       Date:  2022-05-03

3.  Combinatorial Polycation Synthesis and Causal Machine Learning Reveal Divergent Polymer Design Rules for Effective pDNA and Ribonucleoprotein Delivery.

Authors:  Ramya Kumar; Ngoc Le; Felipe Oviedo; Mary E Brown; Theresa M Reineke
Journal:  JACS Au       Date:  2022-02-07

Review 4.  Maybe you can turn me on: CRISPRa-based strategies for therapeutic applications.

Authors:  Elvir Becirovic
Journal:  Cell Mol Life Sci       Date:  2022-02-12       Impact factor: 9.261
  4 in total

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