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A convenient test system for the identification of CYP4V2 inhibitors
PURPOSE: Polymorphisms in the gene that codes for the human cytochrome P450 enzyme CYP4V2 are a cause of Bietti crystalline dystrophy (BCD). Therefore, inhibition of CYP4V2 activity may well be a cause of visual disability. However, monitoring the fatty acid hydroxylation reactions catalyzed by this...
Autores principales: | Sharma, Shishir, Liu, Sijie, Durairaj, Pradeepraj, Machalz, David, Wolber, Gerhard, Bureik, Matthias |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Vision
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8598247/ https://www.ncbi.nlm.nih.gov/pubmed/34880593 |
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