Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Search results (26)

« Back to Publications

CRISPR targeting of SNPs associated with age-related macular degeneration in ARPE-19 cells: a potential model for manipulating the complement system

Salman A. et al, (2025), Gene Therapy, 32, 132 - 141

Comparison of CRISPR-Cas13b RNA base editing approaches for USH2A-associated inherited retinal degeneration

Fry LE. et al, (2025), Communications Biology, 8

Spontaneously Immortalised Nonhuman Primate Müller Glia Cell Lines as Source to Explore Retinal Reprogramming Mechanisms for Cell Therapies

Salman A. et al, (2025), Journal of Cellular Physiology, 240

CRISPR targeting of SNPs associated with Age-related Macular Degeneration in ARPE-19 cells: a potential model for manipulating the complement system

Salman A. et al, (2024)

Rescue of cone and rod photoreceptor function in a CDHR1-model of age-related retinal degeneration

Yusuf IH. et al, (2024), Molecular Therapy, 32, 1445 - 1460

CRISPR Manipulation of Age-Related Macular Degeneration Haplotypes in the Complement System: Potential Future Therapeutic Applications/Avenues

Salman A. et al, (2024), International Journal of Molecular Sciences, 25, 1697 - 1697

Developmental Expression of the Cell Cycle Regulator p16INK4a in Retinal Glial Cells: A Novel Marker for Immature Ocular Astrocytes?

Martinez-Fernandez de la Camara C. et al, (2023), Journal of Histochemistry & Cytochemistry, 71, 301 - 320

CRISPR approach for allele-specific targeting of SNPs associated with Age-related Macular Degeneration in ARPE19 cells

Salman A. et al, (2023), INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 64

Testing cone targeting with AAV5 and the GRK1 promoter in mice for future CRISPR-based applications

Rhodes E. et al, (2023), INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 64

Minicircle Delivery to the Neural Retina as a Gene Therapy Approach

Staurenghi F. et al, (2022), International Journal of Molecular Sciences, 23, 11673 - 11673

Non-Viral Delivery of CRISPR/Cas Cargo to the Retina Using Nanoparticles: Current Possibilities, Challenges, and Limitations

Salman A. et al, (2022), Pharmaceutics, 14, 1842 - 1842

In vitro characterisation of spontaneously immortalised Non-Human Primate Muller glia cell lines as a potential source for cell replacement therapies for retinal degenerative eye disease

Salman A. et al, (2022), INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 63

CRISPR approach for allele-specific targeting of SNPs associated with Age-related Macular Degeneration in ARPE19 cells

Salman A. et al, (2022), HUMAN GENE THERAPY, 33, A155 - A155

Development of CRISPR-Cas9 repressors for targeted epigenome editing

Kantor A. et al, (2022), INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 63

Development of a minicircle gene therapy system for expanding treatment options of inherited retinal disease

Staurenghi F. et al, (2022), INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 63

Load More