Read more about the article Fanconi anemia-D1 due to homozygosity for the BRCA2 gene Cypriot founder mutation: A case report.
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Fanconi anemia-D1 due to homozygosity for the BRCA2 gene Cypriot founder mutation: A case report.

Abstract Fanconi anemia (FA) is a rare disorder characterized by multiple congenital malformations, progressive bone marrow failure and susceptibility to malignancies. Biallelic mutations in the breast cancer 2, early onset…

Continue ReadingFanconi anemia-D1 due to homozygosity for the BRCA2 gene Cypriot founder mutation: A case report.
Read more about the article Double faced role of human mesenchymal stem cells and their role challenges in cancer therapy.
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Double faced role of human mesenchymal stem cells and their role challenges in cancer therapy.

Abstract Human mesenchymal stem cells (hMSCs) are multipotent non-hematopoietic precursor cells with the ability to differentiate into several tissue types. The use of hMSCs has gained significant importance in cancer…

Continue ReadingDouble faced role of human mesenchymal stem cells and their role challenges in cancer therapy.
Read more about the article Human and primate-specific microRNAs in cancer: Evolution, and significance in comparison with more distantly-related research models: The great potential of evolutionary young microRNA in cancer research.
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Human and primate-specific microRNAs in cancer: Evolution, and significance in comparison with more distantly-related research models: The great potential of evolutionary young microRNA in cancer research.

Abstract The largest proportion of microRNAs in humans (ca. 40-50%) originated in the phylogenetic grouping defined as primates. The dynamic evolution of this family of non-coding RNA is further demonstrated…

Continue ReadingHuman and primate-specific microRNAs in cancer: Evolution, and significance in comparison with more distantly-related research models: The great potential of evolutionary young microRNA in cancer research.
Read more about the article Polyamine oxidase 5 loss-of-function mutations in Arabidopsis thaliana trigger metabolic and transcriptional reprogramming and promote salt stress tolerance.
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Polyamine oxidase 5 loss-of-function mutations in Arabidopsis thaliana trigger metabolic and transcriptional reprogramming and promote salt stress tolerance.

Abstract The family of polyamine oxidases (PAO) in Arabidopsis (AtPAO1-5) mediates polyamine (PA) back-conversion, which reverses the PA biosynthetic pathway from spermine and its structural isomer thermospermine (tSpm) into spermidine…

Continue ReadingPolyamine oxidase 5 loss-of-function mutations in Arabidopsis thaliana trigger metabolic and transcriptional reprogramming and promote salt stress tolerance.
Read more about the article Special Issue–Towards Understanding the Mechanisms and Curing of Muscular Dystrophy Diseases.
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Special Issue–Towards Understanding the Mechanisms and Curing of Muscular Dystrophy Diseases.

Abstract Muscular dystrophies are a heterogeneous group of inherited diseases with different molecular basss, but sharing similar clinical features and dystrophic changes.

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Read more about the article Aetiology of Acute Respiratory Tract Infections in Hospitalised Children in Cyprus.
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Aetiology of Acute Respiratory Tract Infections in Hospitalised Children in Cyprus.

Abstract In order to improve clinical management and prevention of viral infections in hospitalised children improved etiological insight is needed. The aim of the present study was to assess the…

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Read more about the article Whole-blood fatty acids and inflammation in European children: the IDEFICS Study.
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Whole-blood fatty acids and inflammation in European children: the IDEFICS Study.

Abstract Fatty acids are hypothesized to influence cardiovascular disease risk because of their effect on inflammation. The aim of this study is to assess the relationship between whole-blood fatty acids…

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Read more about the article A unique mosaic Turner syndrome patient with androgen receptor gene derived marker chromosome.
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A unique mosaic Turner syndrome patient with androgen receptor gene derived marker chromosome.

Abstract Patients with Turner syndrome are generally characterized by having short stature with no secondary sexual characteristics. Some abnormalities, such as webbed neck, renal malformations (>50%) and cardiac defects (10%)…

Continue ReadingA unique mosaic Turner syndrome patient with androgen receptor gene derived marker chromosome.
Read more about the article Recommendations for presymptomatic genetic testing and management of individuals at risk for hereditary transthyretin amyloidosis.
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Recommendations for presymptomatic genetic testing and management of individuals at risk for hereditary transthyretin amyloidosis.

Abstract These recommendations highlight recent experience in genetic counselling for the severe autosomal-dominant, late-onset transthyretin familial amyloid polyneuropathy (TTR-FAP) disease, and present a structured approach towards identification and monitoring of…

Continue ReadingRecommendations for presymptomatic genetic testing and management of individuals at risk for hereditary transthyretin amyloidosis.
Read more about the article Sixty years of transthyretin familial amyloid polyneuropathy (TTR-FAP) in Europe: where are we now? A European network approach to defining the epidemiology and management patterns for TTR-FAP.
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Sixty years of transthyretin familial amyloid polyneuropathy (TTR-FAP) in Europe: where are we now? A European network approach to defining the epidemiology and management patterns for TTR-FAP.

Abstract Transthyretin familial amyloid polyneuropathy (TTR-FAP) is a highly disabling, life-threatening disease characterized by progressive sensorimotor and autonomic neuropathy. The profile of the disease across Europe is inadequately understood at…

Continue ReadingSixty years of transthyretin familial amyloid polyneuropathy (TTR-FAP) in Europe: where are we now? A European network approach to defining the epidemiology and management patterns for TTR-FAP.