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Molecular Biology Reports, ISSN 0301-4851, 5/2014, Volume 41, Issue 5, pp. 2859 - 2864
The most important feature of abdominal aortic aneurysm (AAA) pathogenesis is an enzymatic degradation of elastic lamellae and extracellular matrix proteins... 
Life Sciences | PAI - 1 −844 G/A polymorphism | Animal Biochemistry | Abdominal aortic aneurysm | t - PA −7351 C/T polymorphism | PAI - 1 −675 4G/5G polymorphism | u - PA 1788 C/T polymorphism | Animal Anatomy / Morphology / Histology | RFLP | PAI -1 -844 G/A polymorphism | t-PA -7351 C/T polymorphism | PAI-1 -675 4G/5G polymorphism | u-PA 1788 C/T polymorphism | t-PA-7351 C/T polymorphism | MYOCARDIAL-INFARCTION | BIOCHEMISTRY & MOLECULAR BIOLOGY | PAI-1-844 G/A polymorphism | PLASMINOGEN-ACTIVATOR INHIBITOR-1 | ENHANCER POLYMORPHISM | FIBRINOLYTIC SYSTEM | PAI-1-675 4G/5G polymorphism | MATRIX METALLOPROTEINASES | 4G/5G POLYMORPHISM | ISCHEMIC-STROKE | ASSOCIATION | SINGLE-NUCLEOTIDE POLYMORPHISMS | CORONARY-ARTERY-DISEASE | Gene Frequency | Humans | Middle Aged | Genotype | Male | Aortic Aneurysm, Abdominal - genetics | Urokinase-Type Plasminogen Activator - genetics | Tissue Plasminogen Activator - genetics | Case-Control Studies | INDEL Mutation | Polymorphism, Genetic | Alleles | Adult | Female | Aged | Polymorphism, Single Nucleotide | Plasminogen Activator Inhibitor 1 - genetics | Fibrin | Enzymes | Care and treatment | Tissue plasminogen activator | Analysis | Genes | Genetic research | Genetic aspects | Abdominal aneurysm | Genetic polymorphisms | Aneurysms | Genotype & phenotype | Risk factors | Veins & arteries | Polymorphism | Index Medicus | PAI-1 −675 4G | u-PA 1788 C | T polymorphism | A polymorphism | PAI-1 −844 G | t-PA −7351 C | 5G polymorphism
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2014, Volume 9, Issue 9, p. e109222
Journal Article
2003, Methods in molecular biology, ISBN 9780896039681, Volume 212., xi, 269
Single nucleotide polymorphisms (SNPs) have become the markers of choice in elucidating the relationship between DNA sequence variation and susceptibility to... 
Chromosome polymorphism | Genetic markers | Variation | Human genetics | Laboratory manuals | Human Genetics | Biomedicine
Book
Journal Article
PLoS One, ISSN 1932-6203, 03/2012, Volume 7, Issue 3, pp. e31230 - e31230
Background: Behcet's disease is known as a recurrent, multisystem inflammation and immune-related disease. Protein tyrosine phosphatase non-receptor 22... 
RHEUMATOID-ARTHRITIS | IL10 | JAPANESE POPULATION | MULTIDISCIPLINARY SCIENCES | IL23R-IL12RB2 | TYROSINE-PHOSPHATASE PTPN22 | AUTOIMMUNE-DISEASE | GENE POLYMORPHISMS | VARIANT | GENOME-WIDE ASSOCIATION | SILK ROAD | Genetic Predisposition to Disease | Eye Diseases - ethnology | Gene Frequency | Humans | Middle Aged | Protein Tyrosine Phosphatase, Non-Receptor Type 22 - genetics | Genotype | Male | Case-Control Studies | Polymorphism, Genetic | Behcet Syndrome - ethnology | Eye Diseases - genetics | Immune System | Polymorphism, Restriction Fragment Length | China | Adolescent | Polymerase Chain Reaction | Adult | Female | Aged | Behcet Syndrome - genetics | Tyrosine | Medical research | Phosphatases | Analysis | Genes | Medicine, Experimental | Disease susceptibility | Genetic aspects | Single nucleotide polymorphisms | T cells | Behcet's syndrome | Haplotypes | Multiple sclerosis | Populations | Laboratories | Pathogenesis | Lymphocytes T | Single-nucleotide polymorphism | Kinases | Phosphatase | Proteins | Lymphocytes | Rheumatology | Inflammation | Regression analysis | Disease control | Patients | Minority & ethnic groups | Crohns disease | Polymerase chain reaction | Hospitals | Restriction fragment length polymorphism | Gene frequency | Rheumatoid arthritis | Diabetes | Autoimmune diseases | Health risk assessment | Protein-tyrosine-phosphatase | Polymorphism | Index Medicus
Journal Article
Molecular and Cellular Biochemistry, ISSN 0300-8177, 1/2011, Volume 347, Issue 1, pp. 201 - 208
Journal Article
PLoS ONE, ISSN 1932-6203, 06/2013, Volume 8, Issue 6, pp. e66592 - e66592
Background: Heroin dependence is a debilitating psychiatric disorder with complex inheritance. Since the dopaminergic system has a key role in rewarding... 
ASSOCIATION ANALYSIS | FUNCTIONAL POLYMORPHISM | DEFICIT HYPERACTIVITY DISORDER | TRANSPORTER GENE | MULTIDISCIPLINARY SCIENCES | PROMOTER REGION | NOVELTY SEEKING | FACTOR-KAPPA-B | RECEPTOR DRD4 GENE | EXON-III POLYMORPHISM | TANDEM DUPLICATION POLYMORPHISM | Haplotypes | Multivariate Analysis | Humans | Middle Aged | Male | Catechol O-Methyltransferase - genetics | Receptors, Dopamine D4 - genetics | Case-Control Studies | Young Adult | Adult | Female | Heroin Dependence - genetics | Genetic Predisposition to Disease | Genetic Association Studies | Risk Factors | Protein-Serine-Threonine Kinases - genetics | Dopamine Plasma Membrane Transport Proteins - genetics | Receptors, Dopamine D2 - genetics | Linkage Disequilibrium | Polymorphism, Restriction Fragment Length | Adolescent | Bayes Theorem | Aged | Models, Genetic | Polymorphism, Single Nucleotide | Catechin | Genes | Illegal drugs | Genetic research | Genetic aspects | Single nucleotide polymorphisms | Mental illness | Risk factors | Heroin | Heroin habit | Dopamine receptors | Attention deficit disorder | Drugs | Drug abuse | Brain | Neurobiology | Single-nucleotide polymorphism | Multivariate analysis | Kinases | Dopamine D4 receptors | Gene polymorphism | Information systems | Addictive behaviors | Dopamine transporter | Dopamine D2 receptors | Dopamine | Narcotics | Alcoholism | Catechol | Heredity | Risk analysis | Addictions | Studies | Hypotheses | Multilevel | Alleles | Cocaine | Ankyrin | Molecular biology | Psychiatry | Bayesian analysis | Transporter | Polymorphism | Smoking | Index Medicus
Journal Article