Genotyping Method for Point Mutation Detection in the Endothelial Nitric Oxide Synthase Exon 7 Using Fluorescent Probes. Clinical Validation in Systemic Sclerosis Patients

Articles in the same Issue

1. Autoantibodies Associated with Rheumatic Diseases
2. Simultaneous Detection of Multiple Proteins with an Array-Based Enzyme-Linked Immunosorbent Assay (ELISA) and Enhanced Chemiluminescence (ECL)
3. Hippuric Acid Test Using 13C-Labelling and NMR Spectroscopy
4. Hippuric Acid as a Modifier of Calcium Oxalate Crystallisation
5. Excretion of Sweat and Urine Pyridinoline Crosslinks in Healthy Controls and Subjects with Established Metabolic Bone Disease
6. Hyperhomocysteinemia and Changed Plasma Thiol Redox Status in Chronic Obstructive Pulmonary Disease
7. Biochemical Evaluation of Oxidative Stress during Exercise in Patients with Coronary Heart Disease
8. Prognostic Significance of the Presence of Erythroblasts in Blood after Cardiothoracic Surgery
9. Exploratory Biochemical Data Analysis: a Comparison of Two Sample Means and Diagnostic Displays
10. Standardization of Laboratory Data and Establishment of Reference Intervals in the Fukuoka Prefecture: A Japanese Perspective
11. Calibration, Specificity and Trueness of a Postheparin Plasma Lipoprotein Lipase Assay
12. Analytical Performance of a Direct Assay for LDL-Cholesterol
13. Genotyping Method for Point Mutation Detection in the Endothelial Nitric Oxide Synthase Exon 7 Using Fluorescent Probes. Clinical Validation in Systemic Sclerosis Patients
14. IFCC Reference Measurement Procedure for Substance Concentration Determination of Total Carbon Dioxide in Blood, Plasma or Serum
15. Joshua Lederberg (Editor-in-Chief): Encyclopedia of Microbiology, 2nd Edition, Vol 1-4