Disease on EC 2.3.1.135 - phosphatidylcholine-retinol O-acyltransferase
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Blindness
Chemical chaperone TUDCA preserves cone photoreceptors in a mouse model of Leber congenital amaurosis.
Blindness
Cone opsin determines the time course of cone photoreceptor degeneration in Leber congenital amaurosis.
Blindness
Deletion of M-opsin prevents "M cone" degeneration in a mouse model of Leber congenital amaurosis.
Blindness
Genetic deletion of S-opsin prevents rapid cone degeneration in a mouse model of Leber congenital amaurosis.
Blindness
Low prevalence of lecithin retinol acyltransferase mutations in patients with Leber congenital amaurosis and autosomal recessive retinitis pigmentosa.
Blindness
Pathophysilogical mechanism and treatment strategies for leber congenital amaurosis.
Carcinoma
Reduced lecithin:retinol acyl transferase activity in cultured squamous cell carcinoma lines results in increased substrate-driven retinoic acid synthesis.
Carcinoma, Squamous Cell
Reduced lecithin:retinol acyl transferase activity in cultured squamous cell carcinoma lines results in increased substrate-driven retinoic acid synthesis.
Leber Congenital Amaurosis
Chemical chaperone TUDCA preserves cone photoreceptors in a mouse model of Leber congenital amaurosis.
Leber Congenital Amaurosis
Cone opsin determines the time course of cone photoreceptor degeneration in Leber congenital amaurosis.
Leber Congenital Amaurosis
Deletion of M-opsin prevents "M cone" degeneration in a mouse model of Leber congenital amaurosis.
Leber Congenital Amaurosis
Genetic deletion of S-opsin prevents rapid cone degeneration in a mouse model of Leber congenital amaurosis.
Leber Congenital Amaurosis
Low prevalence of lecithin retinol acyltransferase mutations in patients with Leber congenital amaurosis and autosomal recessive retinitis pigmentosa.
Leber Congenital Amaurosis
Pathophysilogical mechanism and treatment strategies for leber congenital amaurosis.
Melanoma
Knockdown of lecithin retinol acyltransferase increases all-trans retinoic acid levels and restores retinoid sensitivity in malignant melanoma cells.
Melanoma
Lecithin retinol acyltransferase as a potential prognostic marker for malignant melanoma.
Neoplasm Metastasis
Lecithin retinol acyltransferase as a potential prognostic marker for malignant melanoma.
Neoplasms
Evolutionary history, structural features and biochemical diversity of the NlpC/P60 superfamily of enzymes.
Neoplasms
Expression of the interleukin-4 receptor alpha in human conjunctival epithelial cells.
Neoplasms
Platelet-derived growth factor receptor ? in hepatocellular carcinoma is a prognostic marker independent of underlying liver cirrhosis.
Neoplasms
Reduced lecithin: retinol acyltransferase expression correlates with increased pathologic tumor stage in bladder cancer.
Nevus, Pigmented
Lecithin retinol acyltransferase as a potential prognostic marker for malignant melanoma.
Obesity
The association of lecithin retinol acyltransferase and the 25(OH)D receptor with pediatric overweight and obesity.
Overweight
The association of lecithin retinol acyltransferase and the 25(OH)D receptor with pediatric overweight and obesity.
Pediatric Obesity
The association of lecithin retinol acyltransferase and the 25(OH)D receptor with pediatric overweight and obesity.
Retinal Degeneration
Genomic organization and mutation analysis of the gene encoding lecithin retinol acyltransferase in human retinal pigment epithelium.
Retinal Dystrophies
Cone opsin determines the time course of cone photoreceptor degeneration in Leber congenital amaurosis.
Retinal Dystrophies
Early onset retinal dystrophy due to mutations in LRAT: molecular analysis and detailed phenotypic study.
Retinal Dystrophies
Mutations in the gene encoding lecithin retinol acyltransferase are associated with early-onset severe retinal dystrophy.
Retinal Dystrophies
Pathophysilogical mechanism and treatment strategies for leber congenital amaurosis.
Retinitis Pigmentosa
A novel LRAT mutation affecting splicing in a family with early onset retinitis pigmentosa.
Retinitis Pigmentosa
Low prevalence of lecithin retinol acyltransferase mutations in patients with Leber congenital amaurosis and autosomal recessive retinitis pigmentosa.
Urinary Bladder Neoplasms
Reduced lecithin: retinol acyltransferase expression correlates with increased pathologic tumor stage in bladder cancer.
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