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OALib Journal期刊
ISSN: 2333-9721
费用:99美元
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ISSN Print: 1473-1150
ISSN Online:
主页:
https://www.nature.com/tpj
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Is a pharmacogenomic panel useful to estimate the risk of oxaliplatin-related neurotoxicity in colorectal cancer patients?
DPYD*6 plays an important role in fluoropyrimidine toxicity in addition to DPYD*2A and c.2846A>T: a comprehensive analysis in 1254 patients
Candidate gene analyses for acute pain and morphine analgesia after pediatric day surgery: African American versus European Caucasian ancestry and dose prediction limits
A genome-wide association study of tramadol metabolism from post-mortem samples
Predicting antidepressant treatment outcome based on socioeconomic status and citalopram dose
Patient-provider communications about pharmacogenomic results increase patient recall of medication changes
Genetic association between CD96 locus and immunogenicity to anti-TNF therapy in Crohn’s disease
Impact of SLCO1B3 polymorphisms on clinical outcomes in lung allograft recipients receiving mycophenolic acid
An economic model of the cost-utility of pre-emptive genetic testing to support pharmacotherapy in patients with major depression in primary care
Precision dosing of warfarin: open questions and strategies
The effect of vitamin D pathway genes and deferasirox pharmacogenetics on liver iron in thalassaemia major patients
Prognostic role of genetic polymorphisms of the interleukin-6 signaling pathway in patients with severe heart failure
Warfarin loading dose guided by pharmacogenetics is effective and safe in cardioembolic stroke patients – a randomized, prospective study
Variants in vincristine pharmacodynamic genes involved in neurotoxicity at induction phase in the therapy of pediatric acute lymphoblastic leukemia
Identification of SAMD9L as a susceptibility locus for intravenous immunoglobulin resistance in Kawasaki disease by genome-wide association analysis
Prognostic impact of genetic variants of CYP19A1 and UGT2B17 in a randomized trial for endocrine-responsive postmenopausal breast cancer
Cost-effectiveness analysis of pharmacogenomics-guided clopidogrel treatment in Spanish patients undergoing percutaneous coronary intervention
A single nucleotide polymorphism of IL6-receptor is associated with response to tocilizumab in rheumatoid arthritis patients
Early modifications of circulating microRNAs levels in metastatic colorectal cancer patients treated with regorafenib
Genome-wide association study of antidepressant treatment resistance in a population-based cohort using health service prescription data and meta-analysis with GENDEP
Genetic polymorphisms in ABCG2 and CYP1A2 are associated with imatinib dose reduction in patients treated for gastrointestinal stromal tumors
Genetic polymorphisms associated with reactive oxygen species and blood pressure regulation
Genotype, phenotype, and medication recommendation agreement among commercial pharmacogenetic-based decision support tools
UGT1A1 polymorphisms associated with prolactin response in risperidone-treated children and adolescents with autism spectrum disorder
The in vitro functional analysis of single-nucleotide polymorphisms associated with growth hormone (GH) response in children with GH deficiency
Two common mutations within CYP2C19 affected platelet aggregation in Chinese patients undergoing PCI: a one-year follow-up study
HLA-C*12:02 is strongly associated with Xuesaitong-induced cutaneous adverse drug reactions
Frequency of vitamin K oxidoreductase complex subunit-1 (VKORC1) polymorphisms and warfarin dose management in patients with venous thromboembolism
An optimized prediction framework to assess the functional impact of pharmacogenetic variants
Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes
Genome-wide association analysis of common genetic variants of resistant hypertension
Genetic markers in methotrexate treatments
Association between HLA-B*5901 and methazolamide-induced Stevens-Johnson syndrome/toxic epidermal necrolysis: a systematic review and meta-analysis
An African-specific profile of pharmacogene variants for rosuvastatin plasma variability: limited role for SLCO1B1 c.521T>C and ABCG2 c.421A>C
Association between SLCO1B1 T521C polymorphism and risk of statin-induced myopathy: a meta-analysis
Genome-wide enrichment of m6A-associated single-nucleotide polymorphisms in the lipid loci
Replication of the pharmacogenetic effect of rs678849 on buprenorphine efficacy in African–Americans with opioid use disorder
Genome-wide association study of response to tumour necrosis factor inhibitor therapy in rheumatoid arthritis
A genome-wide association and admixture mapping study of bronchodilator drug response in African Americans with asthma
BDNF Val66Met polymorphism and clinical response to antipsychotic treatment in schizophrenia and schizoaffective disorder patients: a meta-analysis
Iatrogenic hypertension: a bioinformatic analysis
Polymorphisms in CEP68 gene associated with risk of immediate selective reactions to non-steroidal anti-inflammatory drugs
A non-functional galanin receptor-2 in a multiple sclerosis patient
Genome-wide meta-analysis of SNP-by9-ACEI/ARB and SNP-by-thiazide diuretic and effect on serum potassium in cohorts of European and African ancestry
Pharmacogenetics of platinum-based chemotherapy: impact of DNA repair and folate metabolism gene polymorphisms on prognosis of non-small cell lung cancer patients
Evaluation of a clinical pharmacogenetics model to predict methotrexate response in patients with rheumatoid arthritis
Gamma-aminobutyric acid (GABA) receptors genes polymorphisms and risk for restless legs syndrome
Polymorphisms in cytochrome P450 are associated with extensive efavirenz pharmacokinetics and CNS toxicities in an HIV cohort in Botswana
Cross-ethnicity tagging SNPs for HLA alleles associated with adverse drug reaction
Variation within voltage-gated calcium channel genes and antipsychotic treatment response in a South African first episode schizophrenia cohort
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