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EC Number
Disease
PubMed ID
Title of Publication
Category
Confidence Level
Blindness
Low prevalence of lecithin retinol acyltransferase mutations in patients with Leber congenital amaurosis and autosomal recessive retinitis pigmentosa.
causal interaction
3
Blindness
Pathophysilogical mechanism and treatment strategies for leber congenital amaurosis.
causal interaction
3
Blindness
Genetic deletion of S-opsin prevents rapid cone degeneration in a mouse model of Leber congenital amaurosis.
causal interaction
1
Blindness
Low prevalence of lecithin retinol acyltransferase mutations in patients with Leber congenital amaurosis and autosomal recessive retinitis pigmentosa.
ongoing research
2
Blindness
Cone opsin determines the time course of cone photoreceptor degeneration in Leber congenital amaurosis.
unassigned
0
Blindness
Chemical chaperone TUDCA preserves cone photoreceptors in a mouse model of Leber congenital amaurosis.
unassigned
0
Blindness
Low prevalence of lecithin retinol acyltransferase mutations in patients with Leber congenital amaurosis and autosomal recessive retinitis pigmentosa.
unassigned
0
Blindness
Pathophysilogical mechanism and treatment strategies for leber congenital amaurosis.
unassigned
0
Blindness
Genetic deletion of S-opsin prevents rapid cone degeneration in a mouse model of Leber congenital amaurosis.
unassigned
0
Carcinoma
Reduced lecithin:retinol acyl transferase activity in cultured squamous cell carcinoma lines results in increased substrate-driven retinoic acid synthesis.
diagnostic usage
1
Results 1 - 10 of 83 > >>