A carregar...
The CYP2C19 Intron 2 Branch Point SNP is the Ancestral Polymorphism Contributing to the Poor Metabolizer Phenotype in Livers with CYP2C19*35 and CYP2C19*2 Alleles
CYP2C19 rs12769205 alters an intron 2 branch point adenine leading to an alternative mRNA in human liver with complete inclusion of intron 2 (exon 2B). rs12769205 changes the mRNA reading frame, introduces 87 amino acids, and leads to a premature stop codon. The 1000 Genomes project (http://browser....
Na minha lista:
Publicado no: | Drug Metab Dispos |
---|---|
Main Authors: | , , , , , , , , , , , |
Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
The American Society for Pharmacology and Experimental Therapeutics
2015
|
Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4518065/ https://ncbi.nlm.nih.gov/pubmed/26021325 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1124/dmd.115.064428 |
Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|