1.1.1.105	Retinal Dystrophies	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=7028497&form=6&db=m	Retinal reductase activity in rats with and without inherited retinal dystrophy.	ongoing research,unassigned	2,0	
1.1.1.105	Retinal Dystrophies	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=15258582&form=6&db=m	Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause childhood-onset severe retinal dystrophy.	causal interaction,unassigned	4,0	
1.1.1.105	Retinal Dystrophies	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16269441&form=6&db=m	Retinal degeneration associated with RDH12 mutations results from decreased 11-cis retinal synthesis due to disruption of the visual cycle.	causal interaction,unassigned	4,0	
1.1.1.105	Retinal Dystrophies	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17011878&form=6&db=m	Screening genes of the retinoid metabolism: novel LRAT mutation in leber congenital amaurosis.	ongoing research,therapeutic application,unassigned	2,1,0	
1.1.1.105	Retinal Dystrophies	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17032653&form=6&db=m	Retinol dehydrogenase (RDH12) protects photoreceptors from light-induced degeneration in mice.	causal interaction,unassigned	3,0	
1.1.1.105	Retinal Dystrophies	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17130236&form=6&db=m	Targeted disruption of the murine retinal dehydrogenase gene Rdh12 does not limit visual cycle function.	causal interaction,unassigned	3,0	
1.1.1.105	Retinal Dystrophies	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17389517&form=6&db=m	The phenotype of early-onset retinal degeneration in persons with RDH12 mutations.	causal interaction,diagnostic usage,therapeutic application,unassigned	4,3,1,0	
1.1.1.105	Retinal Dystrophies	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17925390&form=6&db=m	Overproduction of bioactive retinoic acid in cells expressing disease-associated mutants of retinol dehydrogenase 12.	causal interaction,therapeutic application,unassigned	3,1,0	
1.1.1.105	Retinal Dystrophies	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=18048336&form=6&db=m	Redundant and unique roles of retinol dehydrogenases in the mouse retina.	causal interaction,unassigned	1,0	
1.1.1.105	Retinal Dystrophies	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=18326732&form=6&db=m	Retinol dehydrogenases RDH11 and RDH12 in the mouse retina: expression levels during development and regulation by oxidative stress.	causal interaction,unassigned	3,0