Many genes from retinoid metabolism cause retinitis pigmentosa. Peropsin, an opsin-like protein with unknown function, is specifically expressed in apical retinal pigment epithelium microvilli. Since rhodopsin and RGR, another opsin-like protein, cause retinitis pigmentosa, we used D-HPLC to screen for the peropsin gene RRH in 331 patients (288 with retinitis pigmentosa and 82 with other retinal dystrophies). We found 13 nonpathogenic variants only, among which a c.730_731delATinsG that truncates the last two transmembrane-spanning fragments and the Lys284 required for retinol binding, but does not segregate with the disease phenotype. We conclude that RRH is not a frequent gene in retinitis pigmentosa
Pericentral retinitis pigmentosa (RP) is an atypical form of RP that affects the near-peripheral ret...
Retinitis pigmentosa (RP) is an inherited retinal dystrophy caused by the loss of photoreceptors and...
The purpose of this dissertation research was to investigate potential mechanisms through which muta...
Many genes from retinoid metabolism cause retinitis pigmentosa. Peropsin, an opsin-like protein with...
PURPOSE: To investigate the peropsin gene (RRH), encoding a retinal pigment epithelium homolog of th...
Retinitis pigmentosa (RP) is a name given to a group of inherited retinal dystrophies that lead to p...
Retinitis pigmentosa (RP) is a name given to a group of inherited retinal dystrophies that lead to p...
To examine the role of R0M1, a homologue of peripherin/ftDS, in autosomal dominant retinitis pigment...
Peropsin is a non-visual opsin in both vertebrate and invertebrate species. In mammals, peropsin is ...
DNA for this study was collected from a sample of 133 retinitis pigmentosa (RP) patients and the rho...
Retinitis pigmentosa (RP) is a group of inherited disorders affecting 1 in 3000-7000 people and char...
Background: Besides the three known genes (RHO, RDS/Peripherin, NRL) involved in autosomal dominant ...
Retinitis pigmentosa (RP) comprises a clinically and genetically heterogeneous group of diseases tha...
Background: Retinitis pigmentosa (RP) is a clinically and genetically heterogeneous group of inherit...
Contains fulltext : 70666.pdf (publisher's version ) (Closed access)Peripherin/rds...
Pericentral retinitis pigmentosa (RP) is an atypical form of RP that affects the near-peripheral ret...
Retinitis pigmentosa (RP) is an inherited retinal dystrophy caused by the loss of photoreceptors and...
The purpose of this dissertation research was to investigate potential mechanisms through which muta...
Many genes from retinoid metabolism cause retinitis pigmentosa. Peropsin, an opsin-like protein with...
PURPOSE: To investigate the peropsin gene (RRH), encoding a retinal pigment epithelium homolog of th...
Retinitis pigmentosa (RP) is a name given to a group of inherited retinal dystrophies that lead to p...
Retinitis pigmentosa (RP) is a name given to a group of inherited retinal dystrophies that lead to p...
To examine the role of R0M1, a homologue of peripherin/ftDS, in autosomal dominant retinitis pigment...
Peropsin is a non-visual opsin in both vertebrate and invertebrate species. In mammals, peropsin is ...
DNA for this study was collected from a sample of 133 retinitis pigmentosa (RP) patients and the rho...
Retinitis pigmentosa (RP) is a group of inherited disorders affecting 1 in 3000-7000 people and char...
Background: Besides the three known genes (RHO, RDS/Peripherin, NRL) involved in autosomal dominant ...
Retinitis pigmentosa (RP) comprises a clinically and genetically heterogeneous group of diseases tha...
Background: Retinitis pigmentosa (RP) is a clinically and genetically heterogeneous group of inherit...
Contains fulltext : 70666.pdf (publisher's version ) (Closed access)Peripherin/rds...
Pericentral retinitis pigmentosa (RP) is an atypical form of RP that affects the near-peripheral ret...
Retinitis pigmentosa (RP) is an inherited retinal dystrophy caused by the loss of photoreceptors and...
The purpose of this dissertation research was to investigate potential mechanisms through which muta...