Read more about the article Geographical distribution of plakophilin-2 mutation prevalence in patients with arrhythmogenic cardiomyopathy.
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Geographical distribution of plakophilin-2 mutation prevalence in patients with arrhythmogenic cardiomyopathy.

Abstract Arrhythmogenic cardiomyopathy (AC) is characterised by myocardial fibrofatty tissue infiltration and presents with palpitations, ventricular arrhythmias, syncope and sudden cardiac death. AC is associated with mutations in genes encoding…

Continue ReadingGeographical distribution of plakophilin-2 mutation prevalence in patients with arrhythmogenic cardiomyopathy.
Read more about the article A new non-invasive prenatal diagnosis of Down syndrome through epigenetic markers and real-time qPCR.
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A new non-invasive prenatal diagnosis of Down syndrome through epigenetic markers and real-time qPCR.

Abstract Non-invasive prenatal diagnosis (NIPD) of Down syndrome is rapidly evolving. Currently, two applications for NIPD of Down syndrome have been developed with potential and have displayed positive results; the…

Continue ReadingA new non-invasive prenatal diagnosis of Down syndrome through epigenetic markers and real-time qPCR.
Read more about the article Significant enrichment of Y-bearing chromosome human spermatozoa using a modified centrifugation technique.
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Significant enrichment of Y-bearing chromosome human spermatozoa using a modified centrifugation technique.

Abstract The effective separation of X- and Y-bearing chromosome spermatozoa has been a topic of major attraction to a number of scientific disciplines. Approaches have typically been based upon either…

Continue ReadingSignificant enrichment of Y-bearing chromosome human spermatozoa using a modified centrifugation technique.
Read more about the article Gap junction pathology in multiple sclerosis lesions and normal-appearing white matter.
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Gap junction pathology in multiple sclerosis lesions and normal-appearing white matter.

Abstract Oligodendrocyte gap junctions (GJs) are vital for central nervous system myelination, but their involvement in multiple sclerosis (MS) pathology remains unknown. The aim of this study was to examine…

Continue ReadingGap junction pathology in multiple sclerosis lesions and normal-appearing white matter.
Read more about the article Activation of endogenous FAK via expression of its amino terminal domain in Xenopus embryos.
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Activation of endogenous FAK via expression of its amino terminal domain in Xenopus embryos.

Abstract The Focal Adhesion Kinase is a well studied tyrosine kinase involved in a wide number of cellular processes including cell adhesion and migration. It has also been shown to…

Continue ReadingActivation of endogenous FAK via expression of its amino terminal domain in Xenopus embryos.
Read more about the article Disruption of oligodendrocyte gap junctions in experimental autoimmune encephalomyelitis.
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Disruption of oligodendrocyte gap junctions in experimental autoimmune encephalomyelitis.

Abstract Gap junctions (GJs) are vital for oligodendrocyte survival and myelination. In order to examine how different stages of inflammatory demyelination affect oligodendrocyte GJs, we studied the expression of oligodendrocytic…

Continue ReadingDisruption of oligodendrocyte gap junctions in experimental autoimmune encephalomyelitis.
Read more about the article Generation of a selectively cytotoxic fusion protein against p53 mutated cancers.
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Generation of a selectively cytotoxic fusion protein against p53 mutated cancers.

Abstract A significant number of cancers are caused by defects in p21 causing functional defects in p21 or p53 tumour-suppressor proteins. This has led to many therapeutic approaches including restoration…

Continue ReadingGeneration of a selectively cytotoxic fusion protein against p53 mutated cancers.
Read more about the article Overview of genetic defects in endocrinopathies in the island of Cyprus; evidence of a founder effect.
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Overview of genetic defects in endocrinopathies in the island of Cyprus; evidence of a founder effect.

Abstract Hereditary endocrinopathies in Cyprus exhibit evidence of a founder effect and display the influence of past migration patterns. The genetic frequency and mutation pattern of a specific disorder of…

Continue ReadingOverview of genetic defects in endocrinopathies in the island of Cyprus; evidence of a founder effect.
Read more about the article MeDIP real-time qPCR of maternal peripheral blood reliably identifies trisomy 21.
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MeDIP real-time qPCR of maternal peripheral blood reliably identifies trisomy 21.

Abstract To reevaluate the efficiency of the 12 differentially methylated regions (DMRs) used in the methylated DNA immunoprecipitation (MeDIP) real-time quantitative polymerase chain reaction (real-time qPCR) based approach, develop an…

Continue ReadingMeDIP real-time qPCR of maternal peripheral blood reliably identifies trisomy 21.
Read more about the article In vivo, site-specific, covalent conjugation of quantum dots to proteins via split-intein splicing.
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In vivo, site-specific, covalent conjugation of quantum dots to proteins via split-intein splicing.

Abstract The ability to target proteins with nanostructures and/or nanodevices in vivo is important for understanding and controlling their biological function. Quantum dots (QDs) serve as an ideal model nanostructure…

Continue ReadingIn vivo, site-specific, covalent conjugation of quantum dots to proteins via split-intein splicing.