logo
Insulin-like growth factor-I and complications of prematurity: a focus on bronchopulmonary dysplasia
Highly sensitive thyroglobulin measurements in differentiated thyroid carcinoma management
Proteomic pattern of plasma in off-pump coronary artery bypass surgery
Association of CHRNA2 polymorphisms with overweight/obesity and clinical characteristics in a Korean population
Relevance of glutathione S-transferase M1 and cytochrome P450 1A1 genetic polymorphisms to the development of head and neck cancers
Association of the insertion/deletion gene polymorphism of the apolipoprotein B signal peptide with myocardial infarction in Tunisian patients
The influence of smoking and homocysteine on subclinical atherosclerosis is modified by the connexin37 C1019T polymorphism - The Cardiovascular Risk in Young Finns Study
Tests for the measurement of factor VII-activating protease (FSAP) activity and antigen levels in citrated plasma, their correlation to PCR testing, and utility for the detection of the Marburg I-polymorphism of FSAP
An improved quality control for bisulfite-PCR-based DNA methylation analysis: cycle threshold value
Can E-cadherin and CD34 be used as indicators of prognosis for hepatocellular carcinoma patients?
Determination of serum creatinine by Jaffe method and how to calibrate to eliminate matrix interference problems
Calcium oxalate stone formation risk - a case of disturbed relative concentrations of urinary components
Half-lives of albumin and cholinesterase in critically ill patients
Early detection of an early onset infection in the neonate based on measurements of procalcitonin and C-reactive protein concentrations in cord blood
Serum neopterin, nitric oxide, inducible nitric oxide synthase and tumor necrosis factor-α levels in patients with ischemic heart disease
Estimation of serum M-protein concentration from polyclonal immunoglobulins: an alternative to serum protein electrophoresis and standard immunochemical procedures
Are serum lipids measured on stroke admission prognostic?
Pre-analytical variation of some haematological quantities
Long-term stability of endogenous B-type natriuretic peptide after storage at -20°C or -80°C
Can both EDTA and citrate plasma samples be used in measurements of fibrinogen and C-reactive protein concentrations?
Non-homogeneous separation of triglycerides, γ-glutamyltransferase, C-reactive protein and lactate dehydrogenase after centrifugation of lithium-heparin tubes
Computer-assisted detection of monoclonal components: results from the multicenter study for the evaluation of CASPER (Computer Assisted Serum Protein Electrophoresis Recognizer) algorithm
Quality indicators and specifications for strategic and support processes in laboratory medicine
Evaluation of the DCA Vantage analyzer for HbA1c assay
Optimization of imprecision and cost saving on hemoglobin A1c controls through aliquot freezing
Estimation of glomerular filtration rate by the modification of diet in renal disease (MDRD) equation in patients with sickle cell disease
Antithrombin III as a criteria factor in liver diseases
Development, organisation and content of polyvalent medical biopathology in Slovakia
Evaluation of p53 and cytochrome c as indicators of apoptosis in serum of patients with type II diabetes and subjects with impaired glucose tolerance
Serum selenium reference values in Croatian
First pilot survey to implement an external quality control for CD4+ T cells in 11 developing countries from the African and Asian continent
Serum C-reactive protein and total antioxidant status in serum and platelets of patients with community-acquired pneumonia
Integration of point-of-care tests into laboratory information system
Integrated System UniCel DxC 880i for laboratory consolidation
Atopic dermatitis, laboratory assessment of disease activity before and after treatment
Assay comparison between Kryptor and Roche estradiol
Rational use of multiparametric POCT analyzers
Tetrahydrobiopterin shows chaperone activity for tyrosine hydroxylase
The diagnostic value of indirect immunofluorescence (IFI) in human toxoplasmosis infections: study of 4346 tests
Evaluation of the consolidated Beckman Coulter UniCel® DxC 880i analyser
Prevalence of vitamin B12 deficiency and vitamin B12 depletion: a population based study in a central European country
Training on quality management to support genetic testing laboratories in continuous improvement and progress towards accreditation
Characterization of a 1.7 Mb X-chromosomal deletion in a patient with McLeod syndrome by array CGH
The engraftment in patients with autologous stem cell transplantation at the Kantonsspital Aarau
A new mouse model for BH4 deficiency generated by knocking-in a single codon exchange (R15C) in the BH4 biosynthetic gene 6-pyruvolytetrahydropterin s
Decreasing kidney function predicts vascular events independently from the glomerular filtration rate at baseline
Impact of CYP 2C9 polymorphysm on warfarin dose during initial anticoagulation in patients with deep venous thrombosis
Metrological aspects of chemical activity measurements
Real time quantitative RT-PCR with RNA from reticulocytes purified from peripheral blood of thalassemia patients
Key role of low HDL cholesterol for the association of the metabolic syndrome with inflammation in coronary patients
Prevalence of decreased glomerular filtration rate in patients seeking non-nephrological medical care
Elevated serum concentrations of intercellular adhesion molecule ICAM-1 in pseudoxanthoma elasticum patients
Epigenetic biomarkers as diagnostic tools for human cancers: analytical and biological obstacles to their clinical application
EuroGentest medical genetics quality assurance database
Old suspects and new culprits in 5-fluorouracil pharmacogenetics: novel insights from a haplotype analysis of the dihydropyrimidine dehydrogenase gene
Early recognition and follow-up of dementia - preliminary results of the EAGLE study
Performance evaluation of a new test for clostridium difficile on the VIDAS” instrument
Generation of recombinant antibodies to nitrotyrosine and chlorotyrosine to facilitate the identification of novel protein biomarkers for atherosclerosis
Biochemical study of five cases of xanthomatosis
Validation of the renin assay on the liaison automated analyzer
Adiponectin and leptin serum concentrations in dyslipidemic subjects with small dense LDL particles
Analytical performance of Accu Chek Compact Plus blood glucometer
Team climate
Evaluation of a specific immunological test for 3,4-methylendioxy-N-methylamphetamin (MDMA ecstasy)
Study of the isoforms of peripheral benzodiazepine receptor by RFLP and real-time PCR
Phenotypes of complex combinations of globin gene mutations in hemoglobinopathy patients: implications for genetic counselling
Basophil activation test and allergy: clinical report
DHPLC as a screening tool for human Fas-gene (TNFRSF6) mutations
Clinical significance and prevalence of T315I mutation in Indian CML patients treated with Imatinib mesylate
Transcriptional regulation and polymorphic variants of the chemokine-like 1 receptor
Development of an HPLC-MS method for the differentiated quantification of the 15 major human bile acids in serum
Method development and bioanalysis of 27-hydroxycholesterol as candidate biomarker for atherosclerosis
Diagnosis of tetrahydrobiopterin deficiency using filter paper blood spots: a 3 years experience
The AmpliChip® CYP450 test: cytochrome P450 2D6 genotype assessment and phenotype prediction
Rapid and accurate alpha-thalassemia-screening using light cycler technology
Transcriptional control of the lipoxin receptor ALXR
Comparative study for the detection of norovirus in stools: kit RIDASCREEN® norovirus ELISA, kit AnDiaTec® norovirus RT-PCR, RT-PCR norovirus «homemade»1
Mobile e-health sensor for non-invasive multi parameter diagnostics of blood biochemistry
Mass Spectrometry: a tool for enhanced detection of hemoglobin variants
Identification of novel protein biomarkers of atherosclerotic cardiovascular disease
Automated digital cell morphology: a new approach for microscopy in the daily routine of haematology
Rapid identification of clinical relevant bacterial isolates utilizing MALDI-TOF profiling - the MALDI biotyper workflow
Intraplatform reproducibility and technical precision of gene expression profiling in four laboratories investigating 160 leukemia samples: DACH study
SmileMS: a new mass spectrometry based identification platform for small molecules
The determination of nutritional status of patients with Alzheimer type senile dementia
Evaluation of the Architect i2000SR for single platform analysis of cyclosporine, tacrolimus and sirolimus
Influence of preanalytic on RBCs during storage
Analytical and clinical evaluation of the routine and intraoperative intact parathyroid hormone assay for Beckman Coulter Unicel® DxI 800
The accumulation of two atypical sphingolipids cause hereditary sensory neuropathy type 1 (HSAN1)
SPTLC3 subunit of serine palmitoyltransferase is responsible for the generation of short chain sphingoid bases
Salivary oxidative stress and periodontitis
Portal vein thrombosis in hepatocellular carcinoma: tumor related or a coagulation disorder or both
Thrombin generation capacity in thrombophilic pregnant women
Clinical value of a competitive NT-proBNP assay compared to the Roche NT-proBNP platform
1911_B Liver enzymes, the metabolic syndrome, and angiographically determined coronary atherosclerosis
Methylphenidate as cocain substitute in heroin addicts
Brain cells take up guanidinoacetate and convert it to creatine
Retrospective comparison of human papilloma virus detection in 42 HSIL samples, by using RNA-based NucliSENS EasyQ(TM) HPV assay and DNA genotyping.
Biochemical and molecular analysis in a patient compound heterozygous for p.A467T and a novel splice site mutation in POLG1
Hypermethylation of the dihydropyrimidine dehydrogenase gene promoter region does not predict severe toxicity in 5-fluorouracil based chemotherapy
High triglycerides, low HDL cholesterol, and small LDL particles predict incident type 2 diabetes in non-diabetic coronary patients
Epidemiological typing of MRSA by antibiogram compared with typing by pulsed-field gel electrophoresis (PFGE)
Type 2 diabetes significantly modulates the cardiovascular risk conferred by the PAI-1 -675 5G/4G polymorphism in angiographied coronary patients
First results with a multiplex real-time PCR assay for detection of bacteria and fungi in blood
Birth of new exons in LINE-2 and in antisense AluSq by intronic mutations in the PTS gene leading to tetrahydrobiopterin (BH4)-cofactor deficiency
Prevalence of reduced estimated glomerular filtration rate (eGFR) in the anemic elderly
Lipopolysaccharide binding protein - a novel biomarker for the diagnosis of infectious endocarditis?
Comparison of different methods for the detection of urine cannabinoids after intake of cannabis sativa extracts
Do methylmalonic (MMA) plasma, urine and CSF concentrations reflect MMA cerebral metabolism in MMA-CoA mutase deficient patients?
Long-term correction of hyperphenylalaninemia in a mouse model for PKU by liver or intramuscular delivery of AAV expressing PAH with various serotypes
Endothelial cells transcytose apolipoprotein A-I and high density lipoproteins
Postgraduate training of laboratory specialists: experience and evaluation of a pilot e-training course on the pre-analytical phase
ABCA1 and ABCG1 are specific receptors for lipid-free ApoA-I and lipidated lipoproteins, respectively
The fourth Santorini conference: Systems biology and personalized prevention
The ApoE story continues: a mechanism for Alzheimer’s disease and a new drug target
Protein Networks and Drug Action
Multiscale cardiac models for personalized medicine
Nucleic acid biomarkers for personalized medicine: gene expression, somatic mutations, epigenetics
Role of nuclear receptors RXRs, VDR and RARγ in atopic diseases (dermatitis and asthma)
Control of lipid and glucose homeostasis by the nuclear receptor FXR
The regulation of atherosclerosis: pathways revealed by microarray analysis of gene expression
Beta-carotene and arachidonic acid - induced changes in DNA methylation of human endothelial cells and its progenitors
Transcriptome mapping and ChIP-Seq - comprehensive methods for next generation sequencing data analysis
Proteins, peptides and small molecules analysis in laboratory medicine
From transcriptome to cytome - diagnosis and systemic impact of chronic inflammation
Making it small: protein microarrays for biomarker discovery
Deconvolution of multiprotein complexes and signaling networks in heart disease
Can lipoprotein measurement using nuclear magnetic resonance (NMR) improve clinical decision making for individual patients?
High density lipoprotein subfractionation by microfluidics technology
Tests for the determination of factor VII-activating protease parameters and clinical implications
Proteomics of exhaled breath condensate: perspectives in searching for potential biomarkers of inflammation and other pathological processes in human airways
Resequencing of human genomes using the Genome Sequencer FLX System
A novel, one step sample collection device that simplifies the transfer of buccal cells from an applicator to FTA matrixes
The cardiovascular genomics revolution - where is the benefit in clinical practice?
Genome-wide association meets systems biology; discovery of genes implicated in myocardial infarction
The monocyte/macrophage compartment in human omental and subcutaneous adipose tissue relates to BMI
Using the Illumina 50K cardio-metabolic CHIP to explore the genetic architecture of CVD risk traits
Proprotein Convertase Subtilisin Kexin 9: from gene and variants to protein and phenotype
New forms of autosomal dominant hypercholesterolemia
Gene-environment interactions in the STANISLAS Cohort
What did bring phase 1 and 2 wide genome associations in type 2 diabetes and obesity: a global overview
Soluble epoxide hydrolase and CYP450-derived eicosanoids in cardiovascular disease
A direct assessment of genetic contribution to the incidence of coronary infarct in the general population Greek EPIC cohort
Evaluate the utility of adiponectin as a biomarker predictive of glycemic efficacy by pooling existing clinical trial data from previously conducted studies
OMICS-driven biomarkers for personalised nutrition
Gene regulation by fatty acids and the role of PPARs in fatty acid sensing: a systems biology approach
The effect of the plasma n-3/n-6 PUFA ratio on the post-dietary LDL phenotype transformation in patients with metabolic syndrome. The LIPGENE study
TNF-α -308G>A polymorphism predisposes to obesity in children. A gene- nutrient interaction
Old suspects and new culprits in 5-fluorouracil pharmacogenetics: novel insights from a haplotype-based analysis of the dihydropyrimidine dehydrogenase gene
Impact of apolipoprotein A5 gene variants on statin treatment efficacy
High-dose atorvastatin lowers blood pressure in a CXCL5 genotype-dependent manner
The effect of the factor II (F2) G20210A, factor V (F5) R506Q and factor VII (F7) R353Q polymorphism on the effectiveness of statins: the GenHAT study
Polymorphic CYP2C19 but not CYP3A5 genotype affects pharmacokinetics and pharmacodynamics of clopidogrel: a possible mechanism for clopidogrel resistance
Development of a multiplex SNP detection assay for warfarin dosing
Teststrip-based genotyping to assist in the prediction of anticoagulant dose requirement
Pharmacogenetic and individual sensibility in response to warfarin
Pharmacogenomics and systems biology
Epigenetic and posttranscriptional control of cytochrome P450 expression
Genetic variations in regulatory factors affecting drug metabolizing enzymes
Multiplexed genotyping of pharmacogenetic biomarkers using VeraCode Technology
Sex differences in side effect of psychotropic drugs - genes, gender or hormones?
Ethnic variations in pharmacogenomics: relevance for hispanic populations
Here are my genes - now what? How real-life clinical trials will help integrate pharmacogenetics into every day patient care
Personalized medicine enabling personalized justice: methadone pharmacogenomics as an adjunct for molecular autopsy and for addiction and driving under the influence of drugs (DUID)
Pharmacogenomics and adverse reactions (San Feliu Report)
Issues in translating pharmacogenomics to clinical practice
Promoting the use of pharmacogenomics testing by multicentre demonstration projects in teaching hospitals
Biobanking and biomolecular resources research infrastructure European network of biobanks
High impact opportunities within the Biomarkers Consortium
Update on the innovative medicines initiative (IMI)
The industry pharmacogenomics working group: current activities
The biomarker revolution: a step toward personalised medicine
A new prognostic test for primary node-negative breast cancer
H-prune, a target for therapeutic intervention to fight cancer metastases
Theranostics - future or reality?
Use of candidate gene SNPs in combination to present an individual with risk stratification information: moving from population data to the personal consultation
Towards personalized cell replacement therapies for neurodegenerative or demyelinating diseases of the central nervous system
Prospects and challenges in psychiatric drug treatment: the emerging role of pharmacogenetics
Old suspects and new culprits in 5-fluorouracil pharmacogenetics: novel insights from a haplotype-based analysis of the dihydropyrimidine dehydrogenase gene
Alcohol-induced overexpression of coxackie adenovirus receptor and IFN-beta in the myocardium of HIV-1 transgenic and wild type rats
Pancreatic cancer biomarkers discovery by SELDI-TOF-MS
Influence of UCP2 -866G>A polymorphism on circulating coenzyme Q10 (CoQ10) concentrations
A buccal swab DNA isolation method for pharmacogenetic testing
Human formyl peptide receptor 1 c.32C>T mutation is associated with inflammatory indices in healthy subjects selected from the STANISLAS Cohort
B2B2 genotype in cholesterol ester transfer protein gene predicts future cardiovascular death in patients experienced an acute coronary syndrome
Cytogenetic effects of resveratrol extracted from red wine on cell cultures from gastric tumors
Proteomics-derived protein maker is correlated with Western blot for the functionality of Toona Sinensis
Designer aminoglycosides for the treatment of genetic diseases caused by nonsense mutations: diverse drugs for diverse mutations
ATP-binding cassette cholesterol transporter A1 mRNA expression, paraoxonase 1 polymorphism Q191R and atherosclerosis
Increased C-reactive protein, plasminogen activator inhibitor and microalbuminuria, and reduced antioxidant status - in children, adolescents and youth with metabolic and pre-metabolic syndromes
CYP2A6 and NAT2 activities in Serbs: correlation with genotype and cigarette smoking
A new biomarker in molecular medicine for the early detection of prostate cancer
Prognostic role and clinical significance of minimal residual disease in acute lymphoblastic leukemia of childhood
The transcription factor 7-like 2 (TCF7L2) gene is associated with type 2 diabetes in the Moroccan general population
Genetic and molecular treatment approach in the study of a major cardiovascular risk factor: familial hypercholesterolemia
Pharmacogenetic and individual sensibility in response to warfarin
Multiplex genotyping of CYP2D6 polymorphisms by MALDI-TOF mass spectrometry
Transcriptional analysis of the endocrine heart under normal and chronic hemodynamic overload conditions
Atorvastatin down-regulates ABCA1 gene expression in peripheral blood mononuclear cells of Brazilian hypercholesterolemic patients
Analysis of gene polymorphisms by pharmacy biochip in newborn and elderly people from the North-West region of Russia
Multiplex PCR universal primers in biochip analysis of thrombosis genes polymorphism
The effect of the plasma n-3/n-6 PUFA ratio on the dietary LDL phenotype transformation and ischemia modified albumin (IMA) related to postprandial response. The LIPGENE study
PDXK expression in testes of rats under oxidative stress is affected by Toona sinensis extracts
Impact of apolipoprotein A5 gene variants on statin treatment efficacy
Haplotypes of APOA5 gene in the metabolic syndrome
Quantification of adhesion molecules and cytokins by flow cytometry in lymphocytes, monocytes and polynuclear cells - stimulation with PMA-ionomycin
Hypermethylation of the promoter region of the dihydropyrimidine dehydrogenase gene is not a predictor of severe toxicity in 5-fluorouracil based chemotherapy
The attitude towards genetic testing for disease predisposition in lay people in Russia
Genetic risk for metabolic syndrome: examination of ACE (I/D), AGTR1 (A1166C) and FGA (Thr312Ala) gene polymorphisms related to lipid metabolism and blood flow disorders in patients with metabolic syndrome
P-selectin polymorphisms' influences on P-selectin serum concentrations and on their familial correlation: the STANISLAS family study
Cytochrome P450 gene variations analysis using MALDI-TOF technology
Transcriptome profiling of toxicant exposure in whole blood from monozygotic twins discordant for smoking
Parental precocious influences on offspring's cardiovascular risk markers in the STANISLAS Cohort
The Association of APOE , CYP3A4 & HMGCR1 Genes Polymorphisms with effects of atorvastatin in patients with early coronary artery disease
Leptin and leptin receptor single nucleotide polymorphisms are associated with obesity and metabolic markers for heart disease in a sample population from Brazil
Signature of recent positive selection at the G-allele of the E1/A118G non-synonymous single nucleotide polymorphism in the mu opioid receptor gene
Influence of VKORC1 [G-1639A] [C1173T], CYP2C9*2/*3 and CYP2A6*2/*3/*4 polymorphisms on acenocoumarol (Sintrom ®) treatment response in a collective of Luxembourg patients treated
Polymorphic CYP2C19 but not CYP3A5 genotype affects pharmacokinetics and pharmacodynamics of clopidogrel: a possible mechanism for clopidogrel resistance
The effect of the factor II (F2) G20210A, factor V (F5) R506Q and factor VII (F7) R353Q polymorphism on the effectiveness of statins: the GenHAT study
Genetic deficiency in the renal expression of Cd36 increases blood pressure in the spontaneously hypertensive rat
Teststrip-based genotyping to assist in the prediction of anticoagulant dose requirement
Prevalence of the novel CYP2C19*17 allele variant in the Greek population
Development of a multiplex SNP detection assay for warfarin dosing
Alteration of the expression of efflux and uptake transporters during hypercholesterolemia. Role in variability of atorvastatin response
An intervention model for prevention of chronic and complex diseases
Capillary isotachophoresis as a lipoproteomic tool to reveal the apoE-concerted regulation of VLDL and HDL metabolism
Vitamin K epoxide reductase haplotypes in Roma and average Hungarian samples
Gene expression profiling of TNF and LPS stimulated monocytes in the whole blood and their imprint in monocytes isolated from rheumatoid arthritis patients
Glycated LDL enhance pro-oxidant and scavenger receptors gene expression in human vascular smooth muscle cells; effect of atorvastatin
The adiponectin gene polymorphisms in the metabolic syndrome patients
Sequence variations in the proprotein convertase subtilisin/kexin type 9 gene in a cohort of Czech hyper-cholesterollemic patients
Functional polymorphisms of apoE and CETP in a selected aged population
Glycated LDL is a potent modulator of specific genes involved in atherosclerosis and diabetes
Vasomotor dysfunction, increased TNF-alpha and endothelin- 1 levels in metabolic syndrome patients with insulin resistance
Ethanol extracts of S yzygium Aromaticum and Hyssopus officinalis induce PPAR-γ activation and lower blood glucose and triglyceride in high fat diet fed C57BL/6 mice
PBMCs (peripheral mononuclear blood cells) as a targettissue for studying hypertension and obesity in the context of inflammation
UGT1A6 (R184S) polymorphism in epileptic patients developing toxicity to sodium valproate in Indian population
Radiation effects as molecular models for pathophysiology and diseases pathways: a systems biology approach
CYP3A4 and CYP3A5 mRNA expression are affected by atorvastatin in HepG2 cell line
Multiplex measurement of soluble molecules involved in inflammation with the fully automated analyser Evidence®
Evaluation of genetic predisposition to insulin resistance by nutrient-induced insulin output ratio (NIOR)
Association with coronary infarct of the joint presence of genetic predisposition and non-genetic risk factors in a general population cohort study in Greece
Association of human cathelicidin (hCAP18/LL-37) gene expression with cardiovascular disease risk factors
Promoter polymorphism of protein C gene associated with unfavorable outcomes in patients after acute coronary syndrome: results of multicentral study based on 1143 Russian patients
High-dose atorvastatin lowers blood pressure in a CXCL5 genotype-dependent manner
Liver X receptor alpha (LXRA) gene polymorphism associates with baseline cholesterol but not statin response in healthy volunteers