Retinoids

retinol dehydrogenase 5 ; Homo sapiens







7 Article(s)
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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