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.
第一作者:
Amarjit S,Chaudhry
第一单位:
Department of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, Tennessee (A.S.C., E.G.S.); Department of Pharmaceutics, School of Pharmacy, University of Washington, Seattle, Washington (B.P., Y.S., A.F., K.E.T.); Department of Computational Biology, St. Jude Children's Research Hospital, Memphis, Tennessee (D.F., Y.F., S.W., G.W.); Department of Laboratory Medicine, Division of Clinical Pharmacology, Karolinska Institutet, Stockholm, Sweden (E.A.); and Section of Pharmacogenetics, Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden (S.C.S.).
作者:
主题词
乙酰化作用(Acetylation);成年人(Adult);等位基因(Alleles);DNA, 互补(DNA, Complementary);埃塞俄比亚(Ethiopia);外显子(Exons);女(雌)性(Female);基因频率(Gene Frequency);单倍型(Haplotypes);人类(Humans);同工酶类(Isoenzymes);肝(Liver);男(雄)性(Male);美芬妥英(Mephenytoin);表型(Phenotype);种系发生(Phylogeny);多态性, 单核苷酸(Polymorphism, Single Nucleotide);RNA剪接(RNA Splicing);串联质谱法(Tandem Mass Spectrometry)
DOI
10.1124/dmd.115.064428
PMID
26021325
发布时间
2025-02-12
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