7 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
1 | 34988992 | A new phenotype of syndromic retinitis pigmentosa with myopathy is caused by mutations in retinol dehydrogenase 11. | 2022 Apr | 1 |
2 | 21529959 | Phenotypic variability in RDH5 retinopathy (Fundus Albipunctatus). | 2011 Aug | 1 |
3 | 16837774 | Differences in retinol metabolism and proliferative response between neointimal and medial smooth muscle cells. | 2006 | 1 |
4 | 15190067 | The tumor suppressor adenomatous polyposis coli and caudal related homeodomain protein regulate expression of retinol dehydrogenase L. | 2004 Aug 13 | 2 |
5 | 12536149 | Mapping the ligand binding pocket in the cellular retinaldehyde binding protein. | 2003 Apr 4 | 2 |
6 | 11418621 | Characterization of a dehydrogenase activity responsible for oxidation of 11-cis-retinol in the retinal pigment epithelium of mice with a disrupted RDH5 gene. A model for the human hereditary disease fundus albipunctatus. | 2001 Aug 31 | 1 |
7 | 9931293 | Activity of human 11-cis-retinol dehydrogenase (Rdh5) with steroids and retinoids and expression of its mRNA in extra-ocular human tissue. | 1999 Feb 15 | 4 |