Read more about the article Serum total homocysteine, folate, 5,10-methylenetetrahydrofolate reductase (MTHFR) 677C–>T genotype and subclinical atherosclerosis.
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Serum total homocysteine, folate, 5,10-methylenetetrahydrofolate reductase (MTHFR) 677C–>T genotype and subclinical atherosclerosis.

Abstract To determine the relationship of serum total homocysteine (tHcy), serum folate and 5,10-methylenetetrahydrofolate reductase (MTHFR) 677C-->T genotype with ultrasonic arterial wall measurements associated with subclinical atherosclerosis. Cross-sectional analysis of…

Continue ReadingSerum total homocysteine, folate, 5,10-methylenetetrahydrofolate reductase (MTHFR) 677C–>T genotype and subclinical atherosclerosis.
Read more about the article Generation of an ABCG2(GFPn-puro) transgenic line–a tool to study ABCG2 expression in mice.
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Generation of an ABCG2(GFPn-puro) transgenic line–a tool to study ABCG2 expression in mice.

Abstract The ATP-binding cassette (ABC) transporter 2 (ABCG2) is expressed by stem cells in many organs and in stem cells of solid tumors. These cells are isolated based on the…

Continue ReadingGeneration of an ABCG2(GFPn-puro) transgenic line–a tool to study ABCG2 expression in mice.
Read more about the article Low HDL cholesterol, smoking and IL-13 R130Q polymorphism are associated with myocardial infarction in Greek Cypriot males. A pilot study.
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Low HDL cholesterol, smoking and IL-13 R130Q polymorphism are associated with myocardial infarction in Greek Cypriot males. A pilot study.

Abstract This study was carried out in Greek Cypriot males to identify risk factors that predispose to myocardial infarction (MI). Genetic and lipid risk factors were investigated for the first…

Continue ReadingLow HDL cholesterol, smoking and IL-13 R130Q polymorphism are associated with myocardial infarction in Greek Cypriot males. A pilot study.
Read more about the article Population programs for the detection of couples at risk for severe monogenic genetic diseases.
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Population programs for the detection of couples at risk for severe monogenic genetic diseases.

Abstract Population genetic screening programs for carrier detection of severe genetic disorders exist worldwide, mainly for beta-thalassemia. These screening programs are either mandatory or voluntary. In several Arab countries and…

Continue ReadingPopulation programs for the detection of couples at risk for severe monogenic genetic diseases.
Read more about the article The paraphyletic composition of Leishmania donovani zymodeme MON-37 revealed by multilocus microsatellite typing.
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The paraphyletic composition of Leishmania donovani zymodeme MON-37 revealed by multilocus microsatellite typing.

Abstract Multilocus microsatellite typing (MLMT) was employed to compare strains of Leishmania donovani belonging to the MON-37 zymodeme (MON-37 strains) from Cyprus and Israel to MON-37 strains from the Indian…

Continue ReadingThe paraphyletic composition of Leishmania donovani zymodeme MON-37 revealed by multilocus microsatellite typing.
Read more about the article Hemoglobin variants in Cyprus.
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Hemoglobin variants in Cyprus.

Abstract Cyprus, located at the eastern end of the Mediterranean region, has been a place of eastern and western civilizations, and the presence of various hemoglobin (Hb) variants can be…

Continue ReadingHemoglobin variants in Cyprus.
Read more about the article Clinico-pathological correlations in 127 patients in 11 large pedigrees, segregating one of three heterozygous mutations in the COL4A3/ COL4A4 genes associated with familial haematuria and significant late progression to proteinuria and chronic kidney disease from focal segmental glomerulosclerosis.
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Clinico-pathological correlations in 127 patients in 11 large pedigrees, segregating one of three heterozygous mutations in the COL4A3/ COL4A4 genes associated with familial haematuria and significant late progression to proteinuria and chronic kidney disease from focal segmental glomerulosclerosis.

Abstract Heterozygous mutations in the COL4A3/ COL4A4 genes are currently thought to be responsible for familial benign microscopic haematuria and maintenance of normal long-term kidney function. We report on 11…

Continue ReadingClinico-pathological correlations in 127 patients in 11 large pedigrees, segregating one of three heterozygous mutations in the COL4A3/ COL4A4 genes associated with familial haematuria and significant late progression to proteinuria and chronic kidney disease from focal segmental glomerulosclerosis.
Read more about the article Sites of differential DNA methylation between placenta and peripheral blood: molecular markers for noninvasive prenatal diagnosis of aneuploidies.
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Sites of differential DNA methylation between placenta and peripheral blood: molecular markers for noninvasive prenatal diagnosis of aneuploidies.

Abstract The use of epigenetic differences between maternal whole blood and fetal (placental) DNA is one of the main areas of interest for the development of noninvasive prenatal diagnosis of…

Continue ReadingSites of differential DNA methylation between placenta and peripheral blood: molecular markers for noninvasive prenatal diagnosis of aneuploidies.
Read more about the article Epidemiological, clinical and genetic study of familial amyloidotic polyneuropathy in Cyprus.
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Epidemiological, clinical and genetic study of familial amyloidotic polyneuropathy in Cyprus.

Abstract OBJECTIVES. To define the incidence and prevalence of familial amyloidotic polyneuropathy (FAP) TTRVal30Met on the island of Cyprus. To study the clinical phenotype and genetic features of FAP TTRVal30Met…

Continue ReadingEpidemiological, clinical and genetic study of familial amyloidotic polyneuropathy in Cyprus.
Read more about the article Spatially distinct functions of PAX6 and NKX2.2 during gliogenesis in the ventral spinal cord.
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Spatially distinct functions of PAX6 and NKX2.2 during gliogenesis in the ventral spinal cord.

Abstract During ventral spinal cord (vSC) development, the p3 and pMN progenitor domain boundary is thought to be maintained by cross-repressive interactions between NKX2.2 and PAX6. Using loss-of-function analysis during…

Continue ReadingSpatially distinct functions of PAX6 and NKX2.2 during gliogenesis in the ventral spinal cord.