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Mohd Salman
Mohd Salman
PhD Research Scholar (ICMR-SRF), L V Prasad Eye Institute
Verified email at lvpei.org
Title
Cited by
Cited by
Year
Delivery strategies for CRISPR/Cas genome editing tool for retinal dystrophies: challenges and opportunities
A Lohia, DK Sahel, M Salman, V Singh, I Mariappan, A Mittal, D Chitkara
Asian journal of pharmaceutical sciences 17 (2), 153-176, 2022
172022
New frontier in the management of corneal dystrophies: basics, development, and challenges in corneal gene therapy and gene editing
M Salman, A Verma, VK Singh, J Jaffet, S Chaurasia, DK Sahel, ...
The Asia-Pacific Journal of Ophthalmology 11 (4), 346-359, 2022
102022
Cationic lipopolymeric nanoplexes containing the CRISPR/Cas9 ribonucleoprotein for genome surgery
DK Sahel, M Salman, M Azhar, SG Goswami, V Singh, M Dalela, ...
Journal of Materials Chemistry B 10 (37), 7634-7649, 2022
52022
A review of rabbit models of meibomian gland dysfunction and scope for translational research
D Prasad, M Salman, AA Reddy, J Jaffet, A Sahoo, S Jakati, KK Bokara, ...
Indian Journal of Ophthalmology 71 (4), 1227-1236, 2023
22023
Identification and in silico analysis of a spectrum of SLC4A11 variations in Indian familial and sporadic cases of congenital hereditary endothelial dystrophy
M Salman, A Verma, S Chaurasia, D Prasad, C Kannabiran, V Singh, ...
Orphanet Journal of Rare Diseases 17 (1), 361, 2022
22022
Assessment of epithelial restoration using limbal allograft transplantation in rabbit model with persistent corneal epithelial defect
VK Singh, AR Kethiri, A Venuganti, A Sahoo, M Salman, K Bokara, S Basu, ...
Investigative Ophthalmology & Visual Science 63 (7), 3231–A0266-3231–A0266, 2022
12022
Development and validation of a reliable rabbit model of limbal stem cell deficiency by mechanical debridement using an ophthalmic burr
VK Singh, AR Kethiri, T Pingali, A Sahoo, M Salman, MA Koduri, D Prasad, ...
Experimental Eye Research 236, 109667, 2023
2023
Correction to: identification and in silico analysis of a spectrum of SLC4A11 variations in indian familial and sporadic cases of congenital hereditary endothelial dystrophy
M Salman, A Verma, S Chaurasia, D Prasad, C Kannabiran, V Singh, ...
Orphanet Journal of Rare Diseases 18 (1), 170, 2023
2023
Understanding the fate of allo-CLET, allo-SLET and CLAL in Alger brush-induced rabbit model of alkali burn
V Singh, VK Singh, A Venuganti, A Sahoo, T Pingali, MA Koduri, ...
Investigative Ophthalmology & Visual Science 64 (8), 3114-3114, 2023
2023
Generation of a novel rabbit model for meibomian gland dysfunction
PR Donthineni, D Prasad, M Salman, S Jakati, S Basu, V Singh
Investigative Ophthalmology & Visual Science 64 (8), 179-179, 2023
2023
Identification and in-silico analysis of SLC4A11 mutations in Indian patients with congenital hereditary endothelial dystrophy (CHED)
M Salman, A Verma, D Prasad, S Chaurasia, M Ramappa, V Singh
Investigative Ophthalmology & Visual Science 63 (7), 2755–A0244-2755–A0244, 2022
2022
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