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1.
J Biol Regul Homeost Agents ; 25(3): 351-8, 2011.
Article in English | MEDLINE | ID: mdl-22023759

ABSTRACT

Reelin is an extracellular signaling glycoprotein, which plays a significant role in cytoarchitectonic pattern formation of different brain areas during development. Reelin gene is located on chromosome 7q22. The aim of this study is to investigate the possible association of the following reelin polymorphisms SNP Intron12A/C (rs727531), SNP Exon15A/G (rs2072403), SNP Intron15G/T (rs2072402), SNP Exon22c/g (rs362691), SNP Intron41G/T (rs362719) and SNP Intron59C/T (rs736707) in the pathogenesis of Alzheimer 's disease and the frequency of these polymorphisms in the population of Northern Greece. The study included two groups, A and B. Group A consisted of 50 patients with Alzheimer 's disease and group B of 70 healthy controls. Genomic DNA isolated from blood was used for PCR and subsequent RFLP analysis. According to our results, the exon 22 C/G marker of Reelin is significantly associated with Alzheimer 's disease in the Greek population but the Likelihood Ratio Test shows that the GT haplotype ++ this polymorphism does not affect the phenotype of group A in relation to Group B. This is the first report on a Greek population-based approach.


Subject(s)
Alzheimer Disease/genetics , Cell Adhesion Molecules, Neuronal/genetics , Exons/genetics , Extracellular Matrix Proteins/genetics , Haplotypes/genetics , Introns/genetics , Nerve Tissue Proteins/genetics , Polymorphism, Single Nucleotide , Serine Endopeptidases/genetics , Aged , Aged, 80 and over , Alzheimer Disease/epidemiology , Female , Genetic Markers/genetics , Greece/epidemiology , Humans , Male , Polymerase Chain Reaction/methods , Reelin Protein
2.
J Infect Dis ; 174(2): 407-10, 1996 Aug.
Article in English | MEDLINE | ID: mdl-8699076

ABSTRACT

Blood samples were collected from an Albanian and a Greek patient with hemorrhagic fever with renal syndrome and tested by reverse transcriptase-polymerase chain reaction. The genetic detection assay amplified hantavirus-specific DNA fragments from RNA extracted from the blood of the patients; nucleotide sequence analysis revealed that the causative agent of the disease was Dobrava virus. These findings suggest that Dobrava virus (which was originally isolated from the lungs of an Apodenws flavicollis mouse in Slovenia) is endemic throughout the Balkan States and causes overt human disease.


Subject(s)
Hemorrhagic Fever with Renal Syndrome/virology , Orthohantavirus/genetics , Adult , Albania/ethnology , Genetic Variation , Greece/epidemiology , Orthohantavirus/classification , Orthohantavirus/isolation & purification , Hemorrhagic Fever with Renal Syndrome/blood , Hemorrhagic Fever with Renal Syndrome/epidemiology , Humans , Male , Molecular Sequence Data , Polymerase Chain Reaction/methods , Sequence Analysis, DNA
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