Pages that link to "Q40257353"

The following pages link to Impacts of two point mutations of RPE65 from Leber's congenital amaurosis on the stability, subcellular localization and isomerohydrolase activity of RPE65. (Q40257353):

Displaying 18 items.

• Pharmacological Amelioration of Cone Survival and Vision in a Mouse Model for Leber Congenital Amaurosis (Q28833543) (← links)
• Human cone photoreceptor dependence on RPE65 isomerase (Q30480075) (← links)
• FATP1 inhibits 11-cis retinol formation via interaction with the visual cycle retinoid isomerase RPE65 and lecithin:retinol acyltransferase (Q33548218) (← links)
• Negative charge of the glutamic acid 417 residue is crucial for isomerohydrolase activity of RPE65. (Q33615882) (← links)
• RPE65: role in the visual cycle, human retinal disease, and gene therapy (Q33652414) (← links)
• Rescue of enzymatic function for disease-associated RPE65 proteins containing various missense mutations in non-active sites (Q33846472) (← links)
• The Retinal Pigment Epithelium in Health and Disease (Q33998365) (← links)
• Fatty acid transport protein 4 (FATP4) prevents light-induced degeneration of cone and rod photoreceptors by inhibiting RPE65 isomerase (Q34585477) (← links)
• Novel RPE65 mutations associated with Leber congenital amaurosis in Chinese patients. (Q35883304) (← links)
• Temperature-sensitive retinoid isomerase activity of RPE65 mutants associated with Leber Congenital Amaurosis (Q35894908) (← links)
• Therapeutic effects of PPARα agonists on diabetic retinopathy in type 1 diabetes models (Q36477286) (← links)
• Complementation test of Rpe65 knockout and tvrm148. (Q37086396) (← links)
• Identification of a novel palmitylation site essential for membrane association and isomerohydrolase activity of RPE65. (Q37075272) (← links)
• Molecular chaperones and photoreceptor function. (Q37167901) (← links)
• Defining the residual vision in leber congenital amaurosis caused by RPE65 mutations (Q37317693) (← links)
• The Rpe65 rd12 allele exerts a semidominant negative effect on vision in mice (Q37714145) (← links)
• Functional Rescue of Retinal Degeneration-Associated Mutant RPE65 Proteins. (Q38831021) (← links)
• Photoreceptor layer topography in children with leber congenital amaurosis caused by RPE65 mutations (Q42119219) (← links)