Search results for " Polymorphism."

showing 10 items of 1006 documents

CD14 C(-260)>T gene polymorphism is not a risk factor for myocardial infarction

2002

gene polymorphism risk factor myocardial infarction
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CD14 C(-260)>T gene polymorphism is not a risk factor for myocardial infarction

2002

gene polymorphism risk factors myocardial infarction
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Role of gene polymorphisms IL 10 (-1082 G/A) and TNFa (-308G/A) in susceptibility to acute myocardial infarction in young man.

2011

gene polymorphisms IL10 (-1082 G/A) and TNF a (-308G/A)acute myocardial infarctionSettore MED/05 - Patologia Clinicayoung man.
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Regulatory cytokine gene polymorphisms and risk of colorectal carcinoma.

2006

It is well established that cancer arises in chronically inflamed tissue, and this is particularly notable in the gastrointestinal tract. Classic examples include Helicobacter pylori-associated gastric cancer, hepatocellular carcinoma, and inflammatory bowel disease-associated colorectal cancer. Growing evidence suggests that these associations might be not casual findings. Focusing on individual cytokines has generated evidence that anti-inflammatory cytokine interleukin (IL)-10 and transforming growth factor-beta1 (TGF-beta1) may have a complex role in gastrointestinal carcinogenesis. As an example, IL-10-deficient mice develop severe atrophic gastritis and a chronic enterocolitis, develo…

gene polymorphismsMaleRiskProlineColorectal cancerAtrophic gastritisil-10colorectal cancerMouse model of colorectal and intestinal cancerBiologymedicine.disease_causePolymorphism Single NucleotideGeneral Biochemistry Genetics and Molecular BiologyMetastasisTransforming Growth Factor beta1colorectal cancercytokine genepolymorphismsHistory and Philosophy of ScienceGene FrequencyLeucineGenotypemedicineHumansGenetic Predisposition to DiseaseAllelesGeneral Neurosciencetgf-β1CarcinomaCancermedicine.diseaseInterleukin-10Amino Acid SubstitutionItalyTumor progressionCase-Control StudiesImmunologycolorectal cancer; gene polymorphisms; il-10; tgf-β1FemaleCarcinogenesisColorectal NeoplasmsAnnals of the New York Academy of Sciences
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The functional significance of colour polymorphism in the European common wall lizard (Podarcis muralis)

2021

Colour polymorphisms, the coexistence of two or more colour morphs of a species within a population, have long fascinated evolutionary biologists interested in the mechanisms generating and maintaining phenotypic variation in nature. The functional significance of colour polymorphisms (i.e. their adaptive value) is often linked to the selective mechanisms responsible for their maintenance over time. In lizards, the hypothesis that colour morphs may reflect alternative reproductive strategies involving differential sociosexual behaviour and/or alternative reproductive strategies has come to dominate the field. Wall lizards (family Lacertidae, genus Podarcis), with several geographically dist…

genetic structuresevoluciónpolimorfismo de colorlagartija roquerawall lizardestrategias alternativas de reproducciónalternative reproductive strategiescomportamiento:CIENCIAS DE LA VIDA [UNESCO]behaviourbody regionscolour polymorphismevolutionUNESCO::CIENCIAS DE LA VIDA
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TOTAL GENETIC SCORE: AN INSTRUMENT TO IMPROVE THE PERFORMANCE IN THE ELITE ATHLETES

2018

genetics analysis polymorphisms performance demands basketball soccer
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The implication of MBL deficient haplotypes in acute coronary syndrome

2014

haplotypeSettore BIO/12 - Biochimica Clinica E Biologia Molecolare ClinicaPhysiologyPhysiology (medical)mannose binding lectin 2mannose binding lectin 2 DNA acute coronary syndrome genetic polymorphism haplotypegenetic polymorphismDNACardiology and Cardiovascular Medicineacute coronary syndrome
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Polymorphism of immunoglobulin (Ig) enhancerelement HS1,2A: allele *2 associates with Systemicfrequency Sclerosis. Comparison with HLA-DR and DQ alle…

2007

OBJECTIVE: To investigate the relationship of the polymorphic enhancer HS1,2 central to the 3' enhancer complex regulatory region (IgH3'EC) of the immunoglobulin heavy chain genes with systemic sclerosis (SSc) disease and compare it with HLA-DR and DQ associations. METHODS: A total of 116 patients with SSc were classified as diffuse (dSSc) or limited (lSSc), and as carriers of antitopoisomerase I (anti-Scl70) or anticentromere (ACA) antibodies. Allele and genotype frequencies were assessed in the population as a whole and in the two major subsets, dSSc and lSSc. The concentration of peripheral blood immunoglobulin levels was also determined and analysed according to the genotypes. RESULTS: …

immunoglobulin (Ig) Polymorphism.
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Candidate gene study on nicotine dependence in Finnish sibpairs

2008

kaksosetsingle nucleotide polymorphismtupakointiriippuvuuscytochrome P450 genecandidate genenikotiininicotine dependencesisaruksetassociation analysis
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Hemostasis and ageing

2008

Abstract On March 19, 2008 a Symposium on Pathophysiology of Ageing and Age-Related Diseases was held in Palermo, Italy. The lecture of D. Mari on Hemostasis and ageing is summarized herein. Physiological ageing is associated with increased plasma levels of many proteins of blood coagulation together with fibrinolysis impairment. This may be of great concern in view of the known association between vascular and thromboembolic diseases and ageing. On the other hand, centenarians are characterized by a state of hypercoagulability and possession of several high-risk alleles and well-known atherothrombotic risk markers but this appears to be compatible with longevity and/or health. Parameters c…

lcsh:Immunologic diseases. AllergyAginggene polymorphismmedia_common.quotation_subjectmedicine.medical_treatmentImmunologyShort Reportlcsh:GeriatricsBioinformaticsFibrinolysisSettore MED/05 - Patologia ClinicaMedicinemedia_commonbusiness.industryGeriatrics gerontologyLongevityPlasma levelsHemostasilcsh:RC952-954.6ageingAgeingBiological significanceHemostasisImmunologylcsh:RC581-607businessImmunity & Ageing
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