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GenomicsPrecision Medicine for Inherited Retinal Degenerations
Precision Medicine for Inherited Retinal Degenerations
PRJNA736120 | ENA
GenomicsPrecision Medicine for Inherited Retinal Degenerations
Precision Medicine for Inherited Retinal Degenerations
PRJNA736121 | ENA
ProteomicsRetinal proteome profiling of inherited retinal degeneration across three different mouse models suggests common drug targets in retinitis pigmentosa
Inherited retinal degenerations (IRDs) are a leading cause of blindness among the young population in the developed world. Approximately half of IRDs initially manifest as gradual loss of night vision and visual fields, characteristic of retinitis pigmentosa (RP). Due to challenges in genetic testi...
ORGANISM(S): Mus musculus (Mouse) 
2024-10-10 | PXD052547 | Pride
Retinal degeneration Retinal proteome : inherited retinal degenerations Rd10 Retinitis pigmentosa 
ProteomicsCFAP418 participates in membrane-associated cellular processes through binding lipids during ciliogenesis
iliopathies and retinal degenerative diseases are heterogeneous groups of genetic diseases. CFAP418 is a causative gene of both diseases, and its sequence is evolutionarily conserved. Here, we employ affinity purification coupled with mass spectrometry and quantitative lipidomic, proteomic, and phos...
ORGANISM(S): Mus Musculus (ncbitaxon:10090) 
2022-05-05 | MSV000089424 | MassIVE
ProteomicsRetinal proteome profiling of inherited retinal degeneration across three different mouse models suggests common drug targets in retinitis pigmentosa
Inherited retinal degenerations (IRDs) are a leading cause of blindness among the young population in the developed world. Approximately half of IRDs initially manifest as gradual loss of night vision and visual fields, characteristic of retinitis pigmentosa (RP). Due to challenges in genetic testi...
ORGANISM(S): Mus musculus (Mouse) 
2024-10-10 | PXD052549 | Pride
Retinal degeneration Retinal proteome Rpe65-/- Inherited retinal degenerations Rd10 Retinitis pigmentosa P23h 
ProteomicsRetinal proteome profiling of inherited retinal degeneration across three different mouse models suggests common drug targets in retinitis pigmentosa
Inherited retinal degenerations (IRDs) are a leading cause of blindness among the young population in the developed world. Approximately half of IRDs initially manifest as gradual loss of night vision and visual fields, characteristic of retinitis pigmentosa (RP). Due to challenges in genetic testi...
ORGANISM(S): Mus musculus (Mouse) 
2024-10-10 | PXD052554 | Pride
Retinal degeneration Retinal proteome Rpe65-/- Inherited retinal degenerations Rd10 Retinitis pigmentosa P23h 
UnknownGene-agnostic approaches to treating inherited retinal degenerations.
Not available
S-EPMC10133473 | biostudies-literature
UnknownPhotoreceptor Disease at Ambiguous Transition Zones in Inherited Retinal Degenerations.
Not available
S-EPMC12338365 | biostudies-literature
ProteomicsRetinal proteome profiling of inherited retinal degeneration across three different mouse models suggests common drug targets in retinitis pigmentosa
Inherited retinal degenerations (IRDs) are a leading cause of blindness among the young population in the developed world. Approximately half of IRDs initially manifest as gradual loss of night vision and visual fields, characteristic of retinitis pigmentosa (RP). Due to challenges in genetic testi...
ORGANISM(S): Mus musculus (Mouse) 
2024-10-10 | PXD052555 | Pride
Retinal degeneration Retinal proteome Rpe65-/- Inherited retinal degenerations Rd10 Retinitis pigmentosa P23h 
UnknownRetinal prolactin isoform PRLΔE1 sustains rod disease in inherited retinal degenerations.
Not available
S-EPMC11410941 | biostudies-literature
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