A novel polymorphism in the 17beta-hydroxysteroid dehydrogenase type 5 (aldo-keto reductase 1C3) gene is associated with lower serum testosterone levels in caucasian menInvolvement of the atrial natriuretic peptide transcription factor GATA4 in alcohol dependence, relapse risk and treatment response to acamprosateGene expression analysis in RA: towards personalized medicineCommon variations in ERCC2 are associated with response to cisplatin chemotherapy and clinical outcome in osteosarcoma patients.Pharmacogenetic profiling in patients with advanced colorectal cancer treated with first-line FOLFIRI chemotherapy.COMT val158met moderation of dopaminergic drug effects on cognitive function: a critical reviewThiopurine S-methyltransferase testing for averting drug toxicity: a meta-analysis of diagnostic test accuracyInvestigation of 7-dehydrocholesterol reductase pathway to elucidate off-target prenatal effects of pharmaceuticals: a systematic reviewGenes that co-cluster with estrogen receptor alpha in microarray analysis of breast biopsiesExploratory aspirin resistance trial in healthy Japanese volunteers (J-ART) using platelet aggregation as a measure of thrombogenicityBerberine and evodiamine influence serotonin transporter (5-HTT) expression via the 5-HTT-linked polymorphic regionEndothelial nitric oxide synthase genotypes and haplotypes modify the responses to sildenafil in patients with erectile dysfunctionGenetic modulation of the Let-7 microRNA binding to KRAS 3'-untranslated region and survival of metastatic colorectal cancer patients treated with salvage cetuximab-irinotecanSequence diversity and haplotype structure at the human CYP3A clusterGeneration and analysis of mice with a targeted disruption of the arylamine N-acetyltransferase type 2 genecDNA array reveals increased expression of glucose-dependent insulinotropic polypeptide following chronic clozapine treatment: role in atypical antipsychotic drug-induced adverse metabolic effectsChronic fluoxetine upregulates activity, protein and mRNA levels of cytosolic phospholipase A2 in rat frontal cortexIntegrating genotype and phenotype information: an overview of the PharmGKB project. Pharmacogenetics Research Network and Knowledge BaseAnalysis of nucleotide diversity of NAT2 coding region reveals homogeneity across Native American populations and high intra-population diversityA comparison of batch effect removal methods for enhancement of prediction performance using MAQC-II microarray gene expression dataGenome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritisA genome-wide association study of bronchodilator response in asthmaticsA genome-wide association study for irinotecan-related severe toxicities in patients with advanced non-small-cell lung cancerPharmacogenomics in type 2 diabetes: oral antidiabetic drugs.Meta-analysis reveals significant association of 3'-UTR VNTR in SLC6A3 with smoking cessation in Caucasian populations.Common variants of the G protein-coupled receptor type 4 are associated with human essential hypertension and predict the blood pressure response to angiotensin receptor blockade.Time flies like an arrow. Fruit flies like crack?Global perspectives on proteins: comparing genomes in terms of folds, pathways and beyond.Critically assessing the state-of-the-art in protein structure prediction.Site-specific molecular design and its relevance to pharmacogenomics and chemical biology.Efficient discovery of single-nucleotide polymorphisms in coding regions of human genes.Genetic diversity and function in the human cytosolic sulfotransferases.Impact of germline and somatic missense variations on drug binding sitesDetecting signals in pharmacogenomic genome-wide association studiesA new mouse mutant of the Cdh23 gene with early-onset hearing loss facilitates evaluation of otoprotection drugs.Functional analysis of multiple genomic signatures demonstrates that classification algorithms choose phenotype-related genes.Antipsychotic-induced vacuous chewing movements and extrapyramidal side effects are highly heritable in mice.A genetic basis for the variable effect of smoking/nicotine on Parkinson's disease.Database designs for microarray data.Pharmacogenomic analysis: correlating molecular substructure classes with microarray gene expression data.
P1433
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P1433
description
Peer-reviewed Scientific Journal
@en
Wissenschaftliche Fachzeitschrift
@de
revista científica
@es
rivista scientifica
@it
vědecký časopis
@cs
wetenschappelijk tijdschrift van Nature Publishing Group
@nl
वैज्ञानिक पत्रिका
@hi
英语期刊
@zh
name
The Pharmacogenomics Journal
@ast
The Pharmacogenomics Journal
@da
The Pharmacogenomics Journal
@de
The Pharmacogenomics Journal
@en
The Pharmacogenomics Journal
@es
The Pharmacogenomics Journal
@fi
The Pharmacogenomics Journal
@fr
The Pharmacogenomics Journal
@it
The Pharmacogenomics Journal
@nb
The Pharmacogenomics Journal
@nl
type
label
The Pharmacogenomics Journal
@ast
The Pharmacogenomics Journal
@da
The Pharmacogenomics Journal
@de
The Pharmacogenomics Journal
@en
The Pharmacogenomics Journal
@es
The Pharmacogenomics Journal
@fi
The Pharmacogenomics Journal
@fr
The Pharmacogenomics Journal
@it
The Pharmacogenomics Journal
@nb
The Pharmacogenomics Journal
@nl
altLabel
Pharmacogenomics Journal
@en
prefLabel
The Pharmacogenomics Journal
@ast
The Pharmacogenomics Journal
@da
The Pharmacogenomics Journal
@de
The Pharmacogenomics Journal
@en
The Pharmacogenomics Journal
@es
The Pharmacogenomics Journal
@fi
The Pharmacogenomics Journal
@fr
The Pharmacogenomics Journal
@it
The Pharmacogenomics Journal
@nb
The Pharmacogenomics Journal
@nl
P243
P3181
P4616
P101
P1055
P1058
P1156
P1159
P1160
Pharmacogenomics J.
P1476
The Pharmacogenomics Journal
@en
P236
P243
P3181
P407
P571
2001-01-01T00:00:00Z