Read more about the article Arrhythmic risk assessment in genotyped families with arrhythmogenic right ventricular cardiomyopathy.
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Arrhythmic risk assessment in genotyped families with arrhythmogenic right ventricular cardiomyopathy.

Abstract Arrhythmogenic right-ventricular cardiomyopathy (ARVC) is a genetically determined disorder, mostly caused by mutations in genes encoding desmosomal proteins. We evaluated phenotype/genotype characteristics to predict the risk for the first…

Continue ReadingArrhythmic risk assessment in genotyped families with arrhythmogenic right ventricular cardiomyopathy.
Read more about the article BRCA genetic screening in Middle Eastern and North African: mutational spectrum and founder BRCA1 mutation (c.798_799delTT) in North African.
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BRCA genetic screening in Middle Eastern and North African: mutational spectrum and founder BRCA1 mutation (c.798_799delTT) in North African.

Abstract The contribution of BRCA1 mutations to both hereditary and sporadic breast and ovarian cancer (HBOC) has not yet been thoroughly investigated in MENA. To establish the knowledge about BRCA1…

Continue ReadingBRCA genetic screening in Middle Eastern and North African: mutational spectrum and founder BRCA1 mutation (c.798_799delTT) in North African.
Read more about the article Phylogenetic relationships among four new complete mitogenome sequences of Pelophylax (Amphibia: Anura) from the Balkans and Cyprus.
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Phylogenetic relationships among four new complete mitogenome sequences of Pelophylax (Amphibia: Anura) from the Balkans and Cyprus.

Abstract We present the full-length mitogenome sequences of four European water frog species: Pelophylax cypriensis, P. epeiroticus, P. kurtmuelleri and P. shqipericus. The mtDNA size varied from 17,363 to 17,895 bp,…

Continue ReadingPhylogenetic relationships among four new complete mitogenome sequences of Pelophylax (Amphibia: Anura) from the Balkans and Cyprus.
Read more about the article Gene expression changes in HLA mismatched mixed lymphocyte cultures reveal genes associated with allorecognition.
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Gene expression changes in HLA mismatched mixed lymphocyte cultures reveal genes associated with allorecognition.

Abstract Human leucocyte antigen (HLA) compatibility is the main factor determining the occurrence of graft-vs-host disease (GVHD) in patients. It has also been shown that minor histocompatibility antigen differences as…

Continue ReadingGene expression changes in HLA mismatched mixed lymphocyte cultures reveal genes associated with allorecognition.
Read more about the article Molecular characterization and phylogeny of Kalotermes populations from the Levant, and description of Kalotermes phoeniciae sp. nov.
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Molecular characterization and phylogeny of Kalotermes populations from the Levant, and description of Kalotermes phoeniciae sp. nov.

Abstract The presence of the yellow-necked drywood termite, Kalotermes flavicollis Fabr., has been reported along most of the Mediterranean coasts of Europe, Africa and Asia. While morphological and genetic data…

Continue ReadingMolecular characterization and phylogeny of Kalotermes populations from the Levant, and description of Kalotermes phoeniciae sp. nov.
Read more about the article MicroRNA responses to environmental liver carcinogens: Biological and clinical significance.
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MicroRNA responses to environmental liver carcinogens: Biological and clinical significance.

Abstract A large number of biological, chemical, and dietary factors have been implicated in the development of liver cancer. These involve complex and protracted interactions between genetic, epigenetic, and environmental…

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Read more about the article A start codon CMT1X mutation associated with transient encephalomyelitis causes complete loss of Cx32.
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A start codon CMT1X mutation associated with transient encephalomyelitis causes complete loss of Cx32.

Abstract X-linked Charcot-Marie-Tooth disease (CMTX1) results from numerous mutations in the GJB1 gene encoding the gap junction protein connexin32 (Cx32) and is one of the commonest forms of inherited neuropathy.…

Continue ReadingA start codon CMT1X mutation associated with transient encephalomyelitis causes complete loss of Cx32.
Read more about the article Anti-inflammatory and cytoprotective properties of hydrogen sulfide.
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Anti-inflammatory and cytoprotective properties of hydrogen sulfide.

Abstract Hydrogen sulfide is an endogenous gaseous mediator that plays important roles in many physiological processes in microbes, plants, and animals. This chapter focuses on the important roles of hydrogen…

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Read more about the article In vivo allergenic activity of a hypoallergenic mutant of the major fish allergen Cyp c 1 evaluated by means of skin testing.
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In vivo allergenic activity of a hypoallergenic mutant of the major fish allergen Cyp c 1 evaluated by means of skin testing.

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Abstract

Continue ReadingIn vivo allergenic activity of a hypoallergenic mutant of the major fish allergen Cyp c 1 evaluated by means of skin testing.
Read more about the article Prediction of autism by translation and immune/inflammation coexpressed genes in toddlers from pediatric community practices.
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Prediction of autism by translation and immune/inflammation coexpressed genes in toddlers from pediatric community practices.

Abstract The identification of genomic signatures that aid early identification of individuals at risk for autism spectrum disorder (ASD) in the toddler period remains a major challenge because of the…

Continue ReadingPrediction of autism by translation and immune/inflammation coexpressed genes in toddlers from pediatric community practices.