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Results 1 - 10 of 207 > >>
EC Number Disease PubMed ID Title of Publication Category Confidence Level
Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.105Adenoma 23639973 Retinoid acid receptor expression is helpful to distinguish between adenoma and well-differentiated carcinoma in the thyroid. diagnostic usage
unassigned
1
0
Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.105all-trans-retinol dehydrogenase (nad+) deficiency 23267101 Retinol dehydrogenase 10 is indispensible for spermatogenesis in juvenile males. causal interaction
unassigned
1
0
Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.105all-trans-retinol dehydrogenase (nad+) deficiency 27740873 Retinol Dehydrogenase-10 Regulates Pancreas Organogenesis and Endocrine Cell Differentiation via Paracrine Retinoic Acid Signaling. causal interaction
therapeutic application
unassigned
4
1
0
Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.105all-trans-retinol dehydrogenase (nad+) deficiency 31237438 Development of a Gene Therapy Vector for RDH12-Associated Retinal Dystrophy. causal interaction
therapeutic application
unassigned
3
2
0
Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.105Bacteremia 33204758 Trends in Bacteremia Over 2 Decades in the Top End of the Northern Territory of Australia. causal interaction
unassigned
2
0
Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.105Blindness 15865448 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
Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.105Blindness 16269441 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
Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.105Blindness 17197551 RDH12 and RPE65, visual cycle genes causing leber congenital amaurosis, differ in disease expression. causal interaction
unassigned
3
0
Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.105Blindness 17512723 RDH12, a retinol dehydrogenase causing Leber's congenital amaurosis, is also involved in steroid metabolism. causal interaction
unassigned
3
0
Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.105Blindness 17512964 Novel RDH12 mutations associated with Leber congenital amaurosis and cone-rod dystrophy: biochemical and clinical evaluations. causal interaction
ongoing research
unassigned
3
2
0
Results 1 - 10 of 207 > >>