Rapid detection of the factor XIII Val34Leu (163 G→T) polymorphism by real-time PCR using fluorescence resonance energy transfer detection and melting curve analysis
Changes of matrix metalloproteinases (MMPs) and tissue inhibitors of metalloproteinases (TIMPs) in the serum of patients with autoimmune diseases: association with age and disease activity
A recombinant cell bioassay for measurement of overall estrogenic activity of serum: preliminary results in women with breast cancer
N-terminal pro-atrial natriuretic peptide as a biochemical marker of long-term interventional success after radiofrequency catheter ablation of paroxysmal supraventricular tachyarrhythmias1)
Preventing in vitro lipoperoxidation in the malondialdehydethiobarbituric assay
Oxidative stress: potential of distinct peroxide determination systems1)
Quality assessment in cytogenetic and molecular genetic testing: the experience of the Italian Project on Standardisation and Quality Assurance
Guidelines for blood smear preparation and staining procedure for setting up an external quality assessment scheme for blood smear interpretation. Part I: control material
Measurement of serum and plasma osmolality in healthy young humans - influence of time and storage conditions
High in-hospital mortality of intensive care patients with nucleated red blood cells in blood
Frequency of −163 C>A and 63 C>G single nucleotide polymorphism of cytochrome P450 1A2 in two African populations
Long-term stability of endogenous B-type natriuretic peptide (BNP) and amino terminal proBNP (NT-proBNP) in frozen plasma samples
Plasma or serum samples: measurements of cardiac troponin T and of other analytes compared
Antioxidant capacity of the human pericardial fluid: does gender have a role?
Comparison of serum digoxin concentration monitoring by fluorescence polarization immunoassay on the TDxFLx® and dry chemistry enzyme immunoassay on the Vitros 950
Multicenter analytical performance evaluation of the Elecsys® proBNP assay
Analytical evaluation and reference values of serum amyloid-A on the BN ProSpec
Reference values of soluble interleukin-2 receptor on the IMMULITE
Analysis of cystatin C, creatinine, albumin, lipids and lipoprotein concentrations in serum and acidified citrate plasma (StabilyteTM) tubes compared
Analysis of γ-globulins consisting of hepatitis C-associated cryoglobulins in the blood
Serum total glutathione-S-transferase in stroke, a preliminary report
Human Population Genetics, Evolution and Disease
Mitochondrial DNA Diversity in Health and Diseases
Genetic risk prediction
Pharmacogenomics and “Individualized Drug Therapy”: Exciting Challenges that Remain Ahead
The Mystery of Conserved Non-genic Sequences, and their Variation in Health and Disease
The International HapMap Project and its Impact on Pharmacogenomics
Significant Polymorphisms in the Stanislas Cohort
Predisposing Genes Linked to Obesity
Expressed Genome Signatures of Cardiovascular Disease
Muscle-dedicated DNA Chips for Cardiovascular Diseases
The Use of Transgenic Mice in Studying Polymorphisms Related to Cardiovascular Diseases
Inflammation and Cell Lipid Metabolism Regulation by the Interaction of Fatty Acids with Nuclear Receptors
Phenotypic and Genetic Dissection of Metabolic Syndrome: The GEMS Project
The Additive Effect of Coexistence more than one “Susceptibility Gene” Alleles on Development of Obesity, Insulin Resistance and Hypertension
Genetic Screening of Genes Affecting HDL Cholesterol Levels and Risk of Ischemic Heart Disease. The Copenhagen City Heart Study
Familial Hypercholesterolemia in Europe
Pharmacogenomics and Cardiovascular Drugs
Cardiovascular Pharmacogenomics
Cardiovascular Genomics - Update 2004
Pharmacogenomics and the Therapeutic Response to Statins in Hypercholesterolemia
Searching for SNP Profiles for Pharmaco-genetics of Hypertension
Are We Ready for Pharmacogenomics in Heart Failure?
Nutrigenetics, Lipid Metabolism and Cardio-vascular Disease: The Framingham Heart Study
Imprinted Genes and Transposons: Epigenomic Targets Linking Prenatal Nutrition with Adult Disease Susceptibility
The Omega-6/Omega-3 Essential Fatty Acid Ratio and Gene Expression
Alcohol and Gene Interactions
A-204C Polymorphism in Cholesterol 7alpha-hydroxylase and Cholesterol Responsiveness to the Dietary Changes
Detecting Gene-environment Interaction using Familial Aggregation Stratified on Proband Exposure
A Functional-genetics Approach to Unravel Molecular Pathways in Celiac Disease
Physiogenomics and the Response to Exercise
Folic Acid Intake and of MTHFR Polymorphism in Egyptian Mothers of Children with Down Syndrome
FABP2 Gene Polymorphism and Insulin Resistance
Molecular Analysis of Cancer in the Post-genome Era
Identification and Tracing of Low-level Mutations in Tumors and their Potential Influence on Drug Resistance
Xenobiotic Metabolizing Enzyme Polymorphisms and Cancer Risk
CYP2A6 Polymorphism and Tobacco Related Cancer
Cancer Proteomics: From Discovery to Diagnostics
Messenger mRNAs and Leukemias: Diagnosis, Follow up and Therapy Monitoring
Implications of Acquired Mutations on Therapeutic Response and Drug Resistance
A Proteomic Approach to Chemoresistance in the Squamous Cell Carcinoma Cell Line A431 Treated with Cisplatin
Case-control Study of Polymorphism of Drug Metabolizing Enzymes and Human Hormone-dependent Cancer
Genotyping of Thymidylate Synthase, Dihydropyrimidine Dehydrogenase and p53 Polymorphisms in ORL Cancers Associated to 5-fluorouracil Based-chemotherapy
CYP3A4 and PXR Gene Polymorphisms in Breast Cancer Patients
N-Acetylcysteine Enhances Multidrug Resistance-associated Protein 1 (MRP 1) Mediated Doxorubicin Resistance
Flow Cytometric Analysis of Signal Transduction Pathways
Identification of Diagnostic Markers for Colorectal Cancer by Expression Profiling of Human Tumors
The Beta-carotene and the Umbilical Cord Progenitor Cell Activation During Angiogenesis
New Diagnostic Protein Markers for Chagas' Disease (American Trypanosomiasis) Discovered and Identified using Seldi Protein Chip ® Technology
Identification, Functional and Structural Characterization of Novel Bacterial RNAs; Putative Targets to Develop Antibiotics
Association of Polymorphisms in Carbohydrate Recognition Domain of Surfactant Protein D Gene with Pulmonary Tuberculosis in Indian Population
Obesity-related Leptin Regulates Alzheimer's Ab
Main CYP Polymorphisms Implicated in Drug Metabolism
CYP2D6 Polymorphisms in Xenobiotic and Endobiotic Substrates Responses
Polymorphisms of Human Aldehyde Dehydrogenases: Impact on Metabolism and Disease
ABC Transporter Polymorphisms, Xenobiotic, and Endogenous Substrates Responses
Integration of Preclinical and Clinical Pharmacogenomics in Drug Development
Population Genetics and High-throuput Expression Analysis: A Powerful Hybrid Approach to the Genetics of Drug Response
Depression and Cardiovascular Diseases. Shared Genetic Substrates
Adrenergic Receptor Polymorphisms
Pharmacogenomics for Pain Management and Forensic Toxicology
Pharmacogenetics and Schizophrenia
CYP2D6 and CYP2C9 and QTc Interval Lengthening During Treatment with Antipsychotic Drugs.
Candidate Genes Mapping in Korean Schizophrenia: Preliminary Study
Pharmacogenomics Approaches in Alzheimer's Disease
Functional Genomics and Proteomics for Cancer Analysis
Proteomics and Its Applications in Pharmaceutical Industry
Mapping the Molecular Diversity of Tumor Blood Vessels for the Development of Targeted Therapies and Imaging Agents
Integrated Health Care - An Industrial Vision
Glutathione S-transferase Genes and Coronary Artery Disease
Genotyping of Cytochrome P4502D6 Mutations in a Greek Population Using PCR-RFLP Method
Alcohol Consumption does not Modulate the Impact of CETP Gene Polymorphisms on Lipid Levels and the Risk of Coronary Heart Disease
Evidences of the Impact of Water Quality on Gel Electrophoresis
Homogenous SNP Genotyping Based on Restriction Endonuclease Cleavage
Study of Apo E Genotypes in a Hypercholesterolemic Young Adults
The GGC Repeat of eRF3/GSPT1 Gene is Associated with Susceptibility to Gastric Cancer
CYP2D6 and CYP2C9 among Patients Treated with Psychotropic Drugs: Potential Risk of Interactions
“OptiFECTIN”: A Novel, Robust, Broad Spectrum Transfection Reagent for Delivery of siRNA in Cultured Cells
Characterization of 67 Single Nucle otide of the Human Mismatch Repair Genes in a Pooled DNA of Korean People
Polymorphism of Vascular System Genes (ACE, eNOS, PLAT, PAI-1) in Women with Preeclampsia. Case-control Study.
Relationship between CYP2D6 Pheno and Genotyes among Spaniards
Antisense Oligonucleotide Inhibition of Hepatitis C virus Genotype 4 Replication in HepG2 Cells
The CETP Taq 1B Polymorphism Significantly Predicts the HDL-C Response to Fenofibrate Treatment in Subjects with Type 2 Diabetes Mellitus (T2DM). Results from the DAIS
Association of CYP2A6*1B Genetic Variant with the Amount of Smoking in French Adults from the Stanislas Cohort
Myosin Binding Protein-c Gene Analysis by DHPLC: Novel Mutations and Prevalence of Compound Heterozygosis Associated with Hypertrophic Cardiomyopathy
Analysis of ACE, AGT, AGTR1, ENOS, MTHFR Genes Polymorphisms in the Elderly People, Athletes and Population of North-West Region of Russia
Diagnostic Biochip Development for Polymorphism Detection of Biotransformation System Genes.
Factor VII (FVII) Haplotype Specific Reference Intervals for more Precise Interpretation of Plasma FVII Levels
DrugMEt TM Genotyping Microarray for the Major Drug Metabolising Enzymes
The Leu554Phe Polymorphism in the E-selectin Gene is Associated with Blood Pressure in Overweight People
P-selectin Serum Concentrations in the Stanislas Family Study: Familial Correlations and Genetic Influences
Microarray Analysis of the Ob/Ob and Fasting Mice; No Association of Peroxisome Proliferator Activated Receptor Gamma Coactivator-1 (PGC-1) Polymorphism between Obese and Non-obese Women in Korean Population
Sex-specific Effect of APOAV Variant Val153>Met on Plasma Levels of HDL-cholesterol
A New Family of KIAA1245 Genes with and without the HERV-K LTRs in their Introns
Metabolic Properties of Risperidone by CYP2D6 Genotype in Korean
Polymorphisms in Carcinogen-metabolism and DNA Repair Enzymes and Susceptibility to Hepatocellular Carcinoma
CYP2A6 Gene Polymorphisms and Smoking Behaviour
Association Study of HLA System and Nasopharyngeal Carcinoma in South Tunisia
Alpha 1-Antitrypsin Deficiency: a Model of Interaction Between Genetic and Environmental Factors
Study of the HLA Class I and Class II Polymorphism in a Sample of South Tunisian Population
Association Between Gly241Arg ICAM-1 Gene Polymorphism and Serum ICAM-1 Concentration in the Stanislas Cohort
Homozygous Deletion in GSTt1 Gene is Associated with the Increased Risk of AML
In-depth Detection of Somatic Mosaicism with a Combined Mutation Scanning Strategy that Utilizes Surveyor TM Mismatch Endonuclease and WAVE TM -HS DHPLC
Efficacy of Anti-obesity Therapy among Carriers of the Gln27Glu Beta2 Adrenoreceptor Gene Polymorphism. Study in Polish Caucasians with Familial Obesity
A New Approach to Detect Interactions Involving Lipid Genes by Combining Data Mining and Statistics in the STANISLAS Cohort
Chromosomal Aberrations in Breast Cancer: The Value of FISH for Therapy Decision Making
CYP1A1 and CYP1A2 Genetic Polymorphisms: Lack of Association with Reproductive System Abnormalities
Microarray Gene Expression Profiling in Human Mesothelioma
The Analysis of Main Genes of Calcified Tissue in the Athletes and Men of North-West Region of Russia
Association of MTHFR and GNB3 Genes with Coronary Artery Disease Among Russians
Coagulation Factor VII Genetic Variations in Tunisian Arabic Population and Association to Factor VII Plasma Levels
Real Time PCR: Applications in Oncology
SNP Genotyping by Using Microarray: A New Methodological Approach to Improve Sensitivity and Specificity with a Dual-laser Scanner
A Phenotypic-genotypic Acute Myocardial Infarction Risk Assessment Test: A Genome Wide Diagnostic Marker Discover Program
The Colorectal Cancer Susceptibility is Associated with the Polymorphism of APC Gene at Codon 1822 and Nutritional Factors
Peptidomic Analysis of Plasma Samples After Oral Administration of Glucose
Gain-of-function Mutation in the KCNMB1 Potassium Channel Subunit is Associated with Low Prevalence of Diastolic Hypertension
Haptoglobin Polymorphism in Type 2 Diabetes Mellitus
Relation between Vitamin Status, the C677T Polymorphism in the Methylenetetrahydrofolate Reductase (MTHFR) Gene, and Plasma Homocysteine Concentrations in Children
Gene Expression Profile of Alcohol-treated Neuroblastoma Using cDNA Microarray and ACE Gene Polymorphism in Korean Alcoholics
Effect of Some Calcium Channels Blockers in Experimentally Induced Diabetic Nephropathy in Rats
APOB, FGB and PROC Genes Implicated in the Genetic Predisposition to Long-term Bad Outcomes in Patients with Unstable Angina
Resistance to Imatinib Mesylate in CML Patients Resulting from Point Mutations of the ABL-kinase Domain
ABI PRISM7000 and Lightcycler Technologies for the Quantification of Minimal Residual Disease in Chronic Myelogenous Leukemia (CML)