Genetic Research of Retinal Diseases
A special issue of Genes (ISSN 2073-4425). This special issue belongs to the section "Human Genomics and Genetic Diseases".
Deadline for manuscript submissions: closed (10 October 2023) | Viewed by 286
Special Issue Editor
Special Issue Information
Dear Colleagues,
Gene-based therapeutics have shown enormous potential for the treatment of inherited and acquired retinal diseases; however, there are some important limitations that need to be acknowledged and addressed in future research. For example, genes implicated in retinal diseases and their related pathophysiologic pathways still need to be elucidated.
The objective of this Special Issue is to provide prospects of currently used and novel genetic testing and diagnoses, gene-based therapeutic strategies, and their applications for retinal diseases.
Genome-editing techniques have shown their potential in the treatment of inherited retinal diseases, which still relies on the identification of appropriate therapeutic targets in disease pathophysiology. Microorganisms have also been shown to play a significant role in retinal diseases. The gut–retina axis may contribute to elucidating previously unknown pathways involved in retinal diseases, presenting a potential therapeutic avenue.
The research areas of this Special Issue may cover functional studies looking at the pathogenicity of disease-related genes rather than only bioinformatic approaches; retinal diseases’ molecular diagnoses and phenotype–genotype correlations; and more sophisticated knowledge of retinal biology and pathophysiology that contributes to the application of gene therapy.
Dr. Ling Zhu
Guest Editor
Manuscript Submission Information
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Keywords
- genetic testing
- gene therapy
- diagnosis
- pathophysiology
