Exon Skipping Through Chimeric Antisense <i>U1</i> snRNAs to Correct Retinitis Pigmentosa GTPase-Regulator (<i>RPGR</i>) Splice Defect-Reference-Cited by-同舟云学术

Exon Skipping Through Chimeric Antisense U1 snRNAs to Correct Retinitis Pigmentosa GTPase-Regulator (RPGR) Splice Defect

Published:2022-08-01 Issue:4 Volume:32 Page:333-349
ISSN:2159-3337
Container-title:Nucleic Acid Therapeutics
language:en
Short-container-title:Nucleic Acid Therapeutics

Author:

Covello Giuseppina¹^ORCID,Ibrahim Gehan H.²^ORCID,Bacchi Niccolò¹,Casarosa Simona³⁴⁵^ORCID,Denti Michela Alessandra¹⁴^ORCID

Affiliation:

1. RNA Biology and Biotechnology Laboratory, Department of Cellular, Computational and Integrative Biology - CIBIO, University of Trento, Trento, Italy.

2. Department of Medical Biochemistry, Faculty of Medicine, Suez Canal University, Ismailia, Egypt.

3. Neural Development and Regeneration Laboratory, Department of Cellular, Computational and Integrative Biology - CIBIO, University of Trento, Trento, Italy.

4. Centre for Medical Science - CIS Med, University of Trento, Trento, Italy.

5. CNR Neuroscience Institute, Pisa, Italy.

Publisher

Mary Ann Liebert Inc

Subject

Drug Discovery,Genetics,Molecular Biology,Molecular Medicine,Biochemistry

Link

https://www.liebertpub.com/doi/pdf/10.1089/nat.2021.0053

Reference91 articles.

1. Retinitis Pigmentosa: Genes and Disease Mechanisms

2. Genes and mutations causing retinitis pigmentosa

3. A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X–linked retinitis pigmentosa (RP3)