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Publications by Chulbul M. Ahmed
SRD005825 Acts as a Pharmacologic Chaperone of Opsin and Promotes Survival of Photoreceptors in an Animal Model of Autosomal Dominant Retinitis Pigmentosa
Translational Vision Science and Technology
Ophthalmology
Biomedical Engineering
Related publications
Abnormal Dark Adaptation Kinetics in Autosomal Dominant Sector Retinitis Pigmentosa Due to Rod Opsin Mutation.
British Journal of Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Genomic Rearrangements of thePRPF31Gene Account for 2.5% of Autosomal Dominant Retinitis Pigmentosa
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
AAV Delivery of Wild-Type Rhodopsin Preserves Retinal Function in a Mouse Model of Autosomal Dominant Retinitis Pigmentosa
Human Gene Therapy
Molecular Medicine
Genetics
Molecular Biology
Linkage Analysis of Five Pedigrees Affected With Typical Autosomal Dominant Retinitis Pigmentosa.
Journal of Medical Genetics
Genetics
De Novo Occurrence of a Variant in ARL3 and Apparent Autosomal Dominant Transmission of Retinitis Pigmentosa
PLoS ONE
Multidisciplinary
Mutations in Known Genes Account for 58% of Autosomal Dominant Retinitis Pigmentosa (adRP)
Advances in Experimental Medicine and Biology
Biochemistry
Medicine
Genetics
Molecular Biology
Phenotype-Genotype Correlations in Autosomal Dominant Retinitis Pigmentosa Caused by RHO, D190N
Current Eye Research
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Inherent Instability of the Retinitis Pigmentosa P23H Mutant Opsin
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Presence of a Triple Concentric Autofluorescence Ring inNR2E3-p.G56R–Linked Autosomal Dominant Retinitis Pigmentosa (ADRP)
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
