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Results 1 - 10 of 165 > >>
EC Number
Disease
PubMed ID
Title of Publication
Category
Confidence Level
Insulin Resistance
Abnormal Expression of Genes Involved in Inflammation, Lipid Metabolism, and Wnt Signaling in the Adipose Tissue of Polycystic Ovary Syndrome.
causal interaction
unassigned
4
0
Retinitis Pigmentosa
Association of a novel mutation in the retinol dehydrogenase 12 (RDH12) gene with autosomal dominant retinitis pigmentosa.
causal interaction
ongoing research
unassigned
2
1
0
Stargardt Disease
ATP-binding cassette transporter ABCA4 and chemical isomerization protect photoreceptor cells from the toxic accumulation of excess 11-cis-retinal.
ongoing research
therapeutic application
unassigned
2
1
0
Burkitt Lymphoma
Biallelic deletion and loss of expression analysis of genes at FRA2G common fragile site in tumor-derived cell lines.
ongoing research
unassigned
4
0
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Biallelic deletion and loss of expression analysis of genes at FRA2G common fragile site in tumor-derived cell lines.
ongoing research
unassigned
4
0
Psoriasis
Biochemical characterization of human epidermal retinol dehydrogenase 2.
causal interaction
unassigned
3
0
Blindness
Biochemical properties of purified human retinol dehydrogenase 12 (RDH12): catalytic efficiency toward retinoids and C9 aldehydes and effects of cellular retinol-binding protein type I (CRBPI) and cellular retinaldehyde-binding protein (CRALBP) on the oxidation and reduction of retinoids.
causal interaction
unassigned
2
0
Blindness
Choroidal neovascularization in an adolescent with RDH12-associated retinal degeneration.
causal interaction
unassigned
4
0
Leber Congenital Amaurosis
Choroidal neovascularization in an adolescent with RDH12-associated retinal degeneration.
causal interaction
unassigned
4
0
Retinal Dystrophies
Choroidal neovascularization in an adolescent with RDH12-associated retinal degeneration.
causal interaction
unassigned
4
0
Results 1 - 10 of 165 > >>