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RDH5 encodes an enzyme belonging to the short-chain dehydrogenases/reductases (SDR) family. Zusätzlich bieten wir Ihnen Retinol Dehydrogenase 5 (11-Cis/9-Cis) Antikörper (36) und Retinol Dehydrogenase 5 (11-Cis/9-Cis) Kits (3) und viele weitere Produktgruppen zu diesem Protein an.
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zRDHA and zRDHB show strong expression within the gut (zeige GUSB Proteine) of developing zebrafish embryos
A role for G143 in zebrafish 17beta-HSD 1 and M146 and M147 in the two zebrafish paralogs prRDH 1 and prRDH 2, respectively, in substrate specificity.
The role of Rgr (zeige RGR Proteine) using rgr (zeige RGR Proteine)-/- single and rdh5-/-rgr (zeige RGR Proteine)-/- double knockout mice under a number of light conditions was studied; results suggest that RGR (zeige RGR Proteine) and RDH5 are likely to function in the retinoid cycle, although their role is not essential
RDH11 (zeige RDH11 Proteine) has a measurable role in regenerating the visual pigment by complementing RDH5 in retinal pigment epithelium.
We conclude that the expression of Rlbp1 (zeige RLBP1 Proteine) and Rdh5 critically depends on functional Mitf (zeige MITF Proteine) in the RPE (zeige RPE Proteine) and suggest that MITF (zeige MITF Proteine) has an important role in controlling retinoid processing in the RPE (zeige RPE Proteine).
A novel c.832C>T (p.Arg278Ter) nonsense mutation in RDH5 was identified. Preserved rod function was observed in one young subject in this study.
RDH5 sequence analysis revealed a novel five base pair deletion, c.913_917delGTGCT (p.Val305Hisfs*29), in family A, and a novel missense mutation, c.758T>G (p.Met253Arg), in family B with fundus albipunctatus.
Four novel RDH5 gene mutations were identified in fundus albipunctatus Israeli patients. Of them, the null mutations c.343C>T (p.R54X) and c. 242delTGCC were the most prevalent.
The proband had a compound heterozygotic missense mutation of Cys59Ser (TGC (zeige TGM2 Proteine) --> AGC (zeige ACAN Proteine)) and a nonsense mutation of Trp95ter (TGG --> TGA (zeige TBX1 Proteine)) in the RDH5 gene.
The clinical and electrophysiologic phenotype of patients with RDH5 retinopathy is variable.
Mutations in RDH5 associated with fundus albipunctatus seem to prevent normal lipofuscin accumulation.
Macular dystrophy is caused by the RDH5 mutation as a phenotype variation in fundus albipunctus.
Macular dystrophy is caused by the RDH5 gene mutation as a phenotype variation in fundus albipunctatus.
Fundus changes due to Fundus albipunctatus associated with mutations in the RDH5 gene.
This gene encodes an enzyme belonging to the short-chain dehydrogenases/reductases (SDR) family. This retinol dehydrogenase functions to catalyze the final step in the biosynthesis of 11-cis retinaldehyde, which is the universal chromophore of visual pigments. Mutations in this gene cause autosomal recessive fundus albipunctatus, a rare form of night blindness that is characterized by a delay in the regeneration of cone and rod photopigments. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the neighboring upstream BLOC1S1 (biogenesis of lysosomal organelles complex-1, subunit 1) gene.
retinol dehydrogenase 2
, retinol dehydrogenase 5 (11-cis/9-cis)
, 11-cis retinol dehydrogenase
, 11-cis RDH
, 11-cis RoDH
, 9-cis retinol dehydrogenase
, 9-cis-retinol dehydrogenase
, cis-retinol dehydrogenase
, retinol dehydrogenase type 5
, 9-cis-retinol specific dehydrogenase
, retinol dehydrogenase 1
, retinol dehydrogenase 5 (11-cis and 9-cis)
, short chain dehydrogenase/reductase family 9C, member 5