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.
Read more about the article A novel LRSAM1 mutation is associated with autosomal dominant axonal Charcot-Marie-Tooth disease.
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A novel LRSAM1 mutation is associated with autosomal dominant axonal Charcot-Marie-Tooth disease.

Abstract Charcot-Marie-Tooth (CMT) disease is the most common hereditary neuropathy resulting from mutations in >30 genes expressed in either the Schwann cells or the axon of peripheral nerves. The disease…

Continue ReadingA novel LRSAM1 mutation is associated with autosomal dominant axonal Charcot-Marie-Tooth disease.
Read more about the article How do mutations in GJB1 cause X-linked Charcot-Marie-Tooth disease?
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How do mutations in GJB1 cause X-linked Charcot-Marie-Tooth disease?

Abstract The X-linked form of Charcot-Marie-Tooth disease (CMT1X) is the second most common form of hereditary motor and sensory neuropathy. The clinical phenotype is characterized by progressive weakness, atrophy, and…

Continue ReadingHow do mutations in GJB1 cause X-linked Charcot-Marie-Tooth disease?
Read more about the article Is suppression of cyst growth in PKD enough to preserve renal function?: STAT6 inhibition is a novel promising target.
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Is suppression of cyst growth in PKD enough to preserve renal function?: STAT6 inhibition is a novel promising target.

Abstract The autosomal dominant form of polycystic kidney disease (ADPKD) is one of the most frequent monogenic disorders and the most frequent among inherited kidney disorders. In fact it has…

Continue ReadingIs suppression of cyst growth in PKD enough to preserve renal function?: STAT6 inhibition is a novel promising target.
Read more about the article Homocysteine levels and MTHFR polymorphisms in young patients with acute myocardial infarction: a case control study.
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Homocysteine levels and MTHFR polymorphisms in young patients with acute myocardial infarction: a case control study.

Abstract Increased levels of homocysteine are known to be associated with coronary artery disease (CAD). The most common form of genetic hyperhomocysteinemia results from MTHFR polymorphisms. To examine the role…

Continue ReadingHomocysteine levels and MTHFR polymorphisms in young patients with acute myocardial infarction: a case control study.
Read more about the article Morphology and phylogeny of Reticulitermes sp. (Isoptera, Rhinotermitidae) from Cyprus.
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Morphology and phylogeny of Reticulitermes sp. (Isoptera, Rhinotermitidae) from Cyprus.

Abstract Taxonomy and phylogeny of termites of the genus Reticulitermes in central and eastern Mediterranean lands are poorly understood, partly due to insufficient sampling. This study aims to contribute to…

Continue ReadingMorphology and phylogeny of Reticulitermes sp. (Isoptera, Rhinotermitidae) from Cyprus.
Read more about the article Non-invasive prenatal diagnosis of aneuploidies: new technologies and clinical applications.
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Non-invasive prenatal diagnosis of aneuploidies: new technologies and clinical applications.

Abstract Non-invasive prenatal diagnosis (NIPD) has substantial medical importance as it targets the development of safer and more effective methods to avoid the risk of fetal loss associated with currently…

Continue ReadingNon-invasive prenatal diagnosis of aneuploidies: new technologies and clinical applications.
Read more about the article A single nucleotide polymorphism in the acetyl-coenzyme A acyltransferase 2 (ACAA2) gene is associated with milk yield in Chios sheep.
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A single nucleotide polymorphism in the acetyl-coenzyme A acyltransferase 2 (ACAA2) gene is associated with milk yield in Chios sheep.

Abstract The objective of this work was to identify single nucleotide polymorphisms (SNP) in the ovine acetyl-coenzyme A acyltransferase 2 (ACAA2) gene and investigate their association with milk production traits.…

Continue ReadingA single nucleotide polymorphism in the acetyl-coenzyme A acyltransferase 2 (ACAA2) gene is associated with milk yield in Chios sheep.
Read more about the article Reconstruction of paternal genotypes over multiple breeding seasons reveals male green turtles do not breed annually.
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Reconstruction of paternal genotypes over multiple breeding seasons reveals male green turtles do not breed annually.

Abstract For species of conservation concern, knowledge of key life-history and demographic components, such as the number and sex ratio of breeding adults, is essential for accurate assessments of population…

Continue ReadingReconstruction of paternal genotypes over multiple breeding seasons reveals male green turtles do not breed annually.