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GenomicsmiRNA Expression analysis from genomic form of Rhodopsin DNA Nanoparticles treated P23H Knock-in Heterozygous Mouse (P23H+/-)
miRNA Expression analysis from genomic form of Rhodopsin DNA Nanoparticles treated P23H Knock-in Heterozygous Mouse (P23H+/-)
PRJNA641357 | ENA
GenomicsTranscriptomic profiling in juvenile P23H Retinitis Pigmentosa mouse retinas
Transcriptomic profiling in juvenile P23H Retinitis Pigmentosa mouse retinas
PRJNA639510 | ENA
GenomicsmiRNA Expression analysis from genomic form of Rhodopsin DNA Nanoparticles treated P23H Knock-in Heterozygous Mouse (P23H+/-)
Expression of miRNA analysis in mouse retinocytes was analysed using Next-generation sequencing (NGS) method in Rhodopsin DNA Nanoparticles treated P23H Knock-in Heterozygous Mouse (P23H+/-).
ORGANISM(S): Mus musculus 
2020-06-24 | GSE153053 | GEO
GenomicsHalofantrine protects photoreceptors in multiple models of retinal degeneration [P23H]
Halofantrine protects photoreceptors in multiple models of retinal degeneration [P23H]
PRJNA1450704 | ENA
GenomicsTranscriptomic profiling in 3-month-old P23H Retinitis Pigmentosa mouse retinas
Transcriptomic profiling in 3-month-old P23H Retinitis Pigmentosa mouse retinas
PRJNA658272 | ENA
UnknownInherent instability of the retinitis pigmentosa P23H mutant opsin.
Not available
S-EPMC3979360 | biostudies-literature
GenomicsThe outer retina in young P23H retinitis pigmentosa mice overexpresses critical components of synaptic transmission
The outer retina in young P23H retinitis pigmentosa mice overexpresses critical components of synaptic transmission
PRJNA1236275 | ENA
UnknownGenotypic and phenotypic characterization of P23H line 1 rat model.
Not available
S-EPMC4444340 | biostudies-literature
OtherCas9/sgRNA selective targeting of the P23H Rhodopsin mutant allele for treating retinitis pigmentosa by intravitreal AAV9.PHP.B-based delivery
P23H is the most common mutation in the RHODOPSIN (RHO) gene leading to a dominant form of retinitis pigmentosa (RP), a rod photoreceptor degeneration that invariably causes vision loss. Specific disruption of the disease P23H RHO mutant while preserving the wild-type (WT) functional allele would be...
ORGANISM(S): Mus musculus 
2019-03-20 | GSE128579 | GEO
UnknownNetwork biology analysis of P23H rhodopsin interactome identifies protein and mRNA quality control mechanisms.
Not available
S-EPMC9579138 | biostudies-literature
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