Project information
Molecular pathophysiology of multigene diseases
- Project Identification
- MSM 141100002
- Project Period
- 1/1999 - 1/2004
- Investor / Pogramme / Project type
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Ministry of Education, Youth and Sports of the CR
- Research Intents
- MU Faculty or unit
- Faculty of Medicine
- Keywords
- Multigenic disease, essential hypertension, ischemia, atopy, diabetes type II, late complications of diabetes, matrix metalloproteinase, gene polymorphism, remodeling, gene derepression, case-control study, PCR, SSCP, RFLP, sequencing.
Effects of allelic variability of the genes coding for matrix metalloproteinases (MMPs) on the etiopathogenesis of the essential hypertension, myocardial ischemia, atopic diseases, and late complications of diabetes II will be studied. Genotyping of individuals will be performed using molecular biological methods, especially PCR, SSCP, RFLP, and/or direct sequencing. Groups of diseased persons will be compared with the appropriate control groups (case-control study).
Publications
Total number of publications: 231
2006
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Variabilita receptorů RXRA a RXRB u pacintů s psoriázou
Kniha abstraktov, II. kongres slovenských a českých dermatovenerológov s medzinárodnou účasťou, year: 2006
2005
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Asociace inzerčně-delečního polymorfismu v genu pro angiotenzin-konvertující enzym (ID ACE) s gestačním diabetem
Praktická Gynekologie, year: 2005
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Association of the Cluster of Genetic Risk Factors in Loci Related to Glycoxidation with Diabetic Nephropathy in Type 2 Diabetes Mellitus
Year: 2005, type: Conference abstract
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Association of tumour necrosis factor-alpha, lymphotoxin-alpha and HLA-DRB1 gene polymorphisms with Lofgrens syndrome in Czech patients with sarcoidosis
Tissue Antigens, year: 2005, volume: 65, edition: 2
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Editorial: Regulation of pathogenetic aspects of allergic diseases
Current Drug Targets - Inflammation and Allergy, year: 2005, volume: 4, edition: 2
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Extracellular volume regulation and growth
Medical Hypotheses, year: 2005, volume: 64, edition: 2
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Gender specific association of the endothelial nitric oxide synthase (NOS3) gene polymorphisms with allergic diseases
European Respiratory Journal, year: 2005
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Genetic variability in the RAGE gene: Possible implications for nutrigenetics, nutrigenomics and understanding the susceptibility to diabetic complications
Molecular Nutrition & Food Research, year: 2005, volume: 49, edition: 7
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Genetic variations in the human gelatinase A (MMP-2) promoter are not associated with susceptibility to, and severity of, chronic periodontitis
J Periodontol, year: 2005, volume: 76, edition: 7
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Haplotype analysis of the RAGE gene: identification of a haplotype marker for diabetic nephropathy in type 2 diabetes mellitus
Nephrology Dialysis Transplantation, year: 2005, volume: 20, edition: 6