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SLCO1B1: Application and Limitations of Deep Mutational Scanning for Genomic Missense Variant Function
SLCO1B1 (solute carrier organic anion transporter family member 1B1) is an important transmembrane hepatic uptake transporter. Genetic variants in the SLCO1B1 gene have been associated with altered protein folding, resulting in protein degradation and decreased transporter activity. Next-generation...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Pharmacology and Experimental Therapeutics
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8042483/ https://www.ncbi.nlm.nih.gov/pubmed/33658230 http://dx.doi.org/10.1124/dmd.120.000264 |