Read more about the article Sudden unexpected death in epilepsy: experience from a tertiary epilepsy centre in Cyprus with review of the literature.
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Sudden unexpected death in epilepsy: experience from a tertiary epilepsy centre in Cyprus with review of the literature.

Abstract Sudden unexpected death in epilepsy (SUDEP) affects 0.09-9.3 per 1,000 person-years depending on the population studied and constitutes the most common cause of death in people with epilepsy. The…

Continue ReadingSudden unexpected death in epilepsy: experience from a tertiary epilepsy centre in Cyprus with review of the literature.
Read more about the article Functional assessment for elimination of mismatches in nuclear and whole cell extracts obtained from mouse and human blastocysts.
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Functional assessment for elimination of mismatches in nuclear and whole cell extracts obtained from mouse and human blastocysts.

Abstract Preimplantation embryos may have an increased risk of having mismatches due to the rates of cell proliferation and DNA replication. Elimination of mismatches in human gametes and embryos has…

Continue ReadingFunctional assessment for elimination of mismatches in nuclear and whole cell extracts obtained from mouse and human blastocysts.
Read more about the article Psychopathic personality traits in 5 year old twins: the importance of genetic and shared environmental influences.
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Psychopathic personality traits in 5 year old twins: the importance of genetic and shared environmental influences.

Abstract There is limited research on the genetic and environmental bases of psychopathic personality traits in children. In this study, psychopathic personality traits were assessed in a total of 1189…

Continue ReadingPsychopathic personality traits in 5 year old twins: the importance of genetic and shared environmental influences.
Read more about the article Whole-genome fetal and maternal DNA methylation analysis using MeDIP-NGS for the identification of differentially methylated regions.
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Whole-genome fetal and maternal DNA methylation analysis using MeDIP-NGS for the identification of differentially methylated regions.

Abstract DNA methylation is an epigenetic marker that has been shown to vary significantly across different tissues. Taking advantage of the methylation differences between placenta-derived cell-free DNA and maternal blood,…

Continue ReadingWhole-genome fetal and maternal DNA methylation analysis using MeDIP-NGS for the identification of differentially methylated regions.
Read more about the article Plasma pentraxin-3 is associated with endothelial dysfunction in non-alcoholic fatty liver disease.
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Plasma pentraxin-3 is associated with endothelial dysfunction in non-alcoholic fatty liver disease.

Abstract Pentraxin-3 (PTX-3) is an acute-phase protein belonging to the PTX family. It has been reported that PTX-3 is significantly associated with obesity, metabolic syndrome, and cardiovascular diseases (CVD). Non-alcoholic…

Continue ReadingPlasma pentraxin-3 is associated with endothelial dysfunction in non-alcoholic fatty liver disease.
Read more about the article Glucosinolate biosynthesis in Eruca sativa.
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Glucosinolate biosynthesis in Eruca sativa.

Abstract Glucosinolates (GSLs) are a highly important group of secondary metabolites in the Caparalles order, both due to their significance in plant-biome interactions and to their chemoprotective properties. This study…

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Read more about the article A Common Variant and the Transcript Levels of MC4R Gene Are Associated With Adiposity in Children: The IDEFICS Study.
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A Common Variant and the Transcript Levels of MC4R Gene Are Associated With Adiposity in Children: The IDEFICS Study.

Abstract The melanocortin-4 receptor gene (MC4R) plays a pivotal role in the regulation of body fat and food and energy intake. The objectives of the study were as follows: 1)…

Continue ReadingA Common Variant and the Transcript Levels of MC4R Gene Are Associated With Adiposity in Children: The IDEFICS Study.
Read more about the article Diagnosis and management of Silver-Russell syndrome: first international consensus statement.
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Diagnosis and management of Silver-Russell syndrome: first international consensus statement.

Abstract This Consensus Statement summarizes recommendations for clinical diagnosis, investigation and management of patients with Silver-Russell syndrome (SRS), an imprinting disorder that causes prenatal and postnatal growth retardation. Considerable overlap…

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Read more about the article Target-based drug discovery for [Formula: see text]-globin disorders: drug target prediction using quantitative modeling with hybrid functional Petri nets.
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Target-based drug discovery for [Formula: see text]-globin disorders: drug target prediction using quantitative modeling with hybrid functional Petri nets.

Abstract Recent molecular studies provide important clues into treatment of [Formula: see text]-thalassemia, sickle-cell anaemia and other [Formula: see text]-globin disorders revealing that increased production of fetal hemoglobin, that is…

Continue ReadingTarget-based drug discovery for [Formula: see text]-globin disorders: drug target prediction using quantitative modeling with hybrid functional Petri nets.
Read more about the article A novel COL4A1 frameshift mutation in familial kidney disease: the importance of the C-terminal NC1 domain of type IV collagen.
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A novel COL4A1 frameshift mutation in familial kidney disease: the importance of the C-terminal NC1 domain of type IV collagen.

Abstract Hereditary microscopic haematuria often segregates with mutations of COL4A3, COL4A4 or COL4A5 but in half of families a gene is not identified. We investigated a Cypriot family with autosomal…

Continue ReadingA novel COL4A1 frameshift mutation in familial kidney disease: the importance of the C-terminal NC1 domain of type IV collagen.