SLCO1B1 genetic variant associated with statin-induced myopathy: a proof-of-concept study using the clinical practice research datalink
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How drugs get into cells: tested and testable predictions to help discriminate between transporter-mediated uptake and lipoidal bilayer diffusionImpact of New Genomic Technologies on Understanding Adverse Drug ReactionsApplication of routine electronic health record databases for pharmacogenetic researchPhenotype standardization for statin-induced myotoxicityAssociation between SLCO1B1 -521T>C and -388A>G polymorphisms and risk of statin-induced adverse drug reactions: A meta-analysisData Resource Profile: Clinical Practice Research Datalink (CPRD)Absence of anti-HMG-CoA reductase autoantibodies in severe self-limited statin-related myopathy.Linking e-health records, patient-reported symptoms and environmental exposure data to characterise and model COPD exacerbations: protocol for the COPE study.Genetic Determinants of the Pharmacokinetic Variability of Rifampin in Malawian Adults with Pulmonary Tuberculosis.Pharmacogenetics of Statin-Induced Myopathy: A Focused Review of the Clinical Translation of Pharmacokinetic Genetic VariantsThe clinical pharmacogenetics implementation consortium guideline for SLCO1B1 and simvastatin-induced myopathy: 2014 update.Mechanisms and assessment of statin-related muscular adverse effects.Predictors and outcomes of increases in creatine phosphokinase concentrations or rhabdomyolysis risk during statin treatment.Pharmacogenetic Foundations of Therapeutic Efficacy and Adverse Events of Statins.Association Between SLCO1B1 Gene T521C Polymorphism and Statin-Related Myopathy Risk: A Meta-Analysis of Case-Control StudiesSLCO1B1 Variants and Angiotensin Converting Enzyme Inhibitor (Enalapril)-Induced Cough: a Pharmacogenetic Study.Genomics and metabolomics of muscular mass in a community-based sample of UK females.What do drug transporters really do?The frequency of SLCO1B1*5 polymorphism genotypes among Russian and Sakha (Yakutia) patients with hypercholesterolemia.Molecular mechanisms of statin intoleranceSLCO1B1 Polymorphisms and Statin-Induced Myopathy.Electronic health records for biological sample collection: feasibility study of statin-induced myopathy using the Clinical Practice Research Datalink.Cardiovascular pharmacogenomics: expectations and practical benefits.How low an LDL-C should we go with statin therapy?Phenotyping Adverse Drug Reactions: Statin-Related Myotoxicity.Evaluating a Web-Based Coaching Program Using Electronic Health Records for Patients With Chronic Obstructive Pulmonary Disease in China: Randomized Controlled Trial.The Application of Genomics in Diabetes: Barriers to Discovery and Implementation.Assessment of pharmacogenetic tests: presenting measures of clinical validity and potential population impact in association studies.GATM locus does not replicate in rhabdomyolysis study.Drugs for rare disorders.Genetic and Clinical Factors Are Associated With Statin-Related Myotoxicity of Moderate Severity: A Case-Control Study.Pharmacogenetics of Lipid-Lowering Agents: an Update Review on Genotype-Dependent Effects of HDL-Targetingand Statin Therapies.Supplementing electronic health records through sample collection and patient diaries: A study set within a primary care research database.Ten-year progress of coronary artery lesions prior to Behçet disease diagnosis: A case report and care-compliant article.Genetic variation in statin intolerance and a possible protective role for UGT1A1.The influences of SLCO1B1 and ABCB1 genotypes on the pharmacokinetics of simvastatin, in relation to CYP3A4 inhibition.SLCO1B1 521T > C polymorphism associated with rosuvastatin-induced myotoxicity in Chinese coronary artery disease patients: a nested case-control study.Recruitment of patients with Chronic Obstructive Pulmonary Disease (COPD) from the Clinical Practice Research Datalink (CPRD) for research.GATM gene variants and statin myopathy riskHLA-B*38:02:01predicts carbimazole/methimazole-induced agranulocytosis
P2860
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P2860
SLCO1B1 genetic variant associated with statin-induced myopathy: a proof-of-concept study using the clinical practice research datalink
description
2013 nî lūn-bûn
@nan
2013 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
SLCO1B1 genetic variant associ ...... cal practice research datalink
@ast
SLCO1B1 genetic variant associ ...... cal practice research datalink
@en
SLCO1B1 genetic variant associ ...... cal practice research datalink
@nl
type
label
SLCO1B1 genetic variant associ ...... cal practice research datalink
@ast
SLCO1B1 genetic variant associ ...... cal practice research datalink
@en
SLCO1B1 genetic variant associ ...... cal practice research datalink
@nl
prefLabel
SLCO1B1 genetic variant associ ...... cal practice research datalink
@ast
SLCO1B1 genetic variant associ ...... cal practice research datalink
@en
SLCO1B1 genetic variant associ ...... cal practice research datalink
@nl
P2093
P2860
P50
P3181
P356
P1476
SLCO1B1 genetic variant associ ...... cal practice research datalink
@en
P2093
P2860
P304
P3181
P356
10.1038/CLPT.2013.161
P407
P577
2013-08-13T00:00:00Z