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期刊名:Pharmacogenomics

缩写:PHARMACOGENOMICS

ISSN:1462-2416

e-ISSN:1744-8042

IF/分区:1.6/Q4

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共收录本刊相关文章索引2820条
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
María Del Carmen Plaza-Serón,Elena García-Martín,Jose Augusto Agúndez et al. María Del Carmen Plaza-Serón et al.
Nonsteroidal anti-inflammatory drugs are the medications most frequently involved in hypersensitivity reactions to drugs. These can be induced by specific immunological and nonimmunological mechanisms, being the latter the most frequent. Th...
Ellie H Jhun,Nilanjana Sadhu,Yingwei Yao et al. Ellie H Jhun et al.
Aim: Pain in sickle cell disease patients is heterogeneous and genetic polymorphisms may predispose an individual to varied vulnerability to painful events. We studied the association of SNPs in the glucocorticoid recepto...
Magnus Ingelman-Sundberg,Volker M Lauschke Magnus Ingelman-Sundberg
Recent phenotypically and functionally relevant human hepatic in vitro systems combine the ability to preserve interindividual molecular differences between patients' livers in culture with the accessibility and high-throughput compatibilit...
Alessandra Raimondi,Federico Nichetti,Giorgia Peverelli et al. Alessandra Raimondi et al.
Gastric cancer is a highly heterogeneous disease, displaying a complex genomic landscape and an unfavorable outcome with standard therapies. Based on distinctive genomic alterations, novel targeted agents have been developed with the aim of...
Wan Zhu,Ling Xue,Hongwei Peng et al. Wan Zhu et al.
Aim: To develop a population pharmacokinetic (PK) model of tacrolimus in Chinese Han renal transplant population and establish the influence of different covariates (especially different CYP3A5/3A4/POR genotype) on PK pro...
Marin M Jukic,Volker M Lauschke,Takahiro Saito et al. Marin M Jukic et al.
The ultrarapid CYP2D6 metabolizer (UM) phenotype is caused by CYP2D6 gene duplications in some, but not all, UM individuals. CYP2D6 and the adjacent pseudogene CYP2D7 are highly homologous; however, CYP2D7 harbors a premature stop codon, wh...
Melissa D Klein,Craig R Lee,George A Stouffer Melissa D Klein
It is well established that the CYP2C19 nonfunctional *2 and *3 polymorphisms impair the bioactivation and antiplatelet effects of clopidogrel, and increase the risk of adverse cardiovascular events following percutaneous coronary intervent...
Na Liu,Guihua Yang,Mei Hu et al. Na Liu et al.
Aim: The clinical benefits of lipid-lowering therapy with statins are widely recognized. However, the lipid-lowering efficacy of statins shows significant differences between individuals. ABCC2 has been demonstrated to co...