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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
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 | Variabilité génétique | Marqueurs génétiques | Polymorphisme chromosomique | Variation | Human genetics | Laboratory manuals | Human Genetics | Biomedicine
Book
PLoS ONE, ISSN 1932-6203, 09/2014, Volume 9, Issue 9, p. e109222
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
2003, Methods in molecular biology, ISBN 9780896035485, Volume 210., xii, 340
Many of the genes found in the human major histocompatibility complex (MHC:HLA region) are subject to extreme polymorphism. HLA polymorphism has been used... 
Immunogenetics | Genetic aspects | Major histocompatibility complex | Genetic polymorphisms | Laboratory manuals | Immunology | Biomedicine
Book
Medychni Perspektyvy, ISSN 2307-0404, 01/2018, Volume 23, Issue 3 part1, p. 11
COPD is multifactorial disease, in which hereditary predisposition and environmental factors (including work conditions) play an important role. Among the... 
Polymorphism
Journal Article
Journal Article
1965, All Souls studies, Volume 5., 101
Book
Journal Article
Journal Article
RESEARCH NOTE - Human Genetic Bi-allelic Sequences, HGBASE, a Database of Intra-genic Polymorphisms, 12/1998
The Human Genome Project is providing a wealth of information about the human gene repertoire, and promises to furnish a complete genome sequence (and thereby... 
single nucleotide polymorphisms - polymorphisms - intra-genic polymorphisms - databases - bioinformatics
Journal