Read more about the article Autism.
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Autism.

Abstract Autism is a set of heterogeneous neurodevelopmental conditions, characterised by early-onset difficulties in social communication and unusually restricted, repetitive behaviour and interests. The worldwide population prevalence is about 1%.…

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Read more about the article N-alpha-terminal acetylation of histone H4 regulates arginine methylation and ribosomal DNA silencing.
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N-alpha-terminal acetylation of histone H4 regulates arginine methylation and ribosomal DNA silencing.

Abstract Post-translational modifications of histones play a key role in DNA-based processes, like transcription, by modulating chromatin structure. N-terminal acetylation is unique among the numerous histone modifications because it is…

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Read more about the article Irisin mRNA and circulating levels in relation to other myokines in healthy and morbidly obese humans.
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Irisin mRNA and circulating levels in relation to other myokines in healthy and morbidly obese humans.

Abstract Skeletal muscle is considered to be an endocrine organ that secretes a number of myokines including follistatin (FST), myostatin (MSTN), activin A, and the newly identified irisin. Irisin's biology…

Continue ReadingIrisin mRNA and circulating levels in relation to other myokines in healthy and morbidly obese humans.
Read more about the article Family structure and childhood obesity: results of the IDEFICS Project.
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Family structure and childhood obesity: results of the IDEFICS Project.

Abstract To analyse the association between family structure and adiposity in children. Cross-sectional and longitudinal analysis of the IDEFICS (Identification and prevention of dietary- and lifestyle-induced health effects in children…

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Read more about the article A dominant-negative provides new insights into FAK regulation and function in early embryonic morphogenesis.
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A dominant-negative provides new insights into FAK regulation and function in early embryonic morphogenesis.

Abstract FAK is a non-receptor tyrosine kinase involved in a wide variety of biological processes and crucial for embryonic development. In this manuscript, we report the generation of a new…

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Read more about the article Molecular genetics of familial hematuric diseases.
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Molecular genetics of familial hematuric diseases.

Abstract The familial hematuric diseases are a genetically heterogeneous group of monogenic conditions, caused by mutations in one of several genes. The major genes involved are the following: (i) the…

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Read more about the article Association of genotypes at the matrix metalloproteinase (MMP) loci with carotid IMT and presence of carotid and femoral atherosclerotic plaques.
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Association of genotypes at the matrix metalloproteinase (MMP) loci with carotid IMT and presence of carotid and femoral atherosclerotic plaques.

Abstract We aimed to test the association between matrix metalloproteinase (MMP) genetic polymorphisms and (a) intima-media thickness in the common carotid (IMTcc) and (b) the presence of plaques in the…

Continue ReadingAssociation of genotypes at the matrix metalloproteinase (MMP) loci with carotid IMT and presence of carotid and femoral atherosclerotic plaques.
Read more about the article Identifying outcomes of clinical genetic services: qualitative evidence and methodological considerations.
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Identifying outcomes of clinical genetic services: qualitative evidence and methodological considerations.

Abstract Extensive research into the tangible and intangible implications of Clinical Genetic Services (CGSs) has confirmed the relevance of a multidimensional outcome of benefit conceptually linked to perceived control. This…

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Read more about the article Acaricide resistance in Tetranychus urticae (Acari: Tetranychidae) populations from Cyprus.
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Acaricide resistance in Tetranychus urticae (Acari: Tetranychidae) populations from Cyprus.

Abstract Five field and greenhouse populations of the twospotted spider mite, Tetranychus urticae Koch (Acari: Tetranychidae), were collected from five different districts across the island of Cyprus, both in field…

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Read more about the article The changing epidemiology of β-thalassemia in the Greek-Cypriot population.
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The changing epidemiology of β-thalassemia in the Greek-Cypriot population.

Abstract The first epidemiological study for thalassemia in Cyprus was performed by Fawdry in 1946. The study determined that the frequency of β-thalassemia (β-thal) carriers was around 18.0% and that…

Continue ReadingThe changing epidemiology of β-thalassemia in the Greek-Cypriot population.