Πλοήγηση ανά Θέμα "FAMILY"
Αποτελέσματα 1-13 από 13
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Analysis of SLC40A1 gene at the mRNA level reveals rapidly the causative mutations in patients with hereditary hemochromatosis type IV
(2008)Mutations in the SLC40Al gene result in a dominant genetic disorder [ferroportin disease; hereditary hemochromatosis type (HH) IV], characterized by iron overload with two different clinical manifestations, normal transferrin ... -
Cloning and characterization of an alternatively spliced form of SR protein kinase 1 that interacts specifically with scaffold attachment factor-B
(2001)Serine/arginine protein kinases have been conserved throughout evolution and are thought to play important roles in the regulation of mRNA processing, nuclear import, germline development, polyamine transport, and ion ... -
A Comprehensive Phylogenetic Analysis of Deadenylases
(2013)Deadenylases catalyze the shortening of the poly(A) tail at the messenger ribonucleic acid (mRNA) 3'-end in eukaryotes. Therefore, these enzymes influence mRNA decay, and constitute a major emerging group of promising ... -
Does land property structure affect local development patterns? Evidence from a Greek tourist area
(2008)This paper attempts to clarify the institutional context and local framework of landed property relations in the local development patterns of a rural space converted into an urban tourist resort on the island of Rhodes, ... -
Eating habits and factors affecting food choice of adolescents living in rural areas
(2013)OBJECTIVE: To establish factors that affect food choices among adolescents living in rural areas and to identify their food choices. DESIGN: A random sample of adolescents living in a Greek rural area (n=382) aged 12-18 ... -
Extrachromosomal genetic elements detected in Escherichia coli treated with the antibacterial agents kanamycin and benzenetriol
(2013)Resistance to kanamycin was induced in Escherichia coli cells subjected to gradually increasing concentrations of the amino glycoside antibiotic kanamycin. The frequency of the appearance of resistance is not in agreement ... -
Genetics of restless legs syndrome (RLS): State-of-the-art and future directions
(2007)Several studies demonstrated that 60% of restless legs syndrome (RLS) patients have a positive family history and it has been suggested that RLS is a highly hereditary trait. To date, several loci have been mapped but no ... -
Greek adolescents, fitness, fatness, fat intake, activity, and coronary heart disease risk
(2004)Background: A dramatic increase in adult mortality rates from coronary heart disease (CHD) in Greece, accompanied by increased prevalence of CHD risk factors in children, has been documented. However, there is controversy ... -
Hereditary Angioedema in Greece: The First Results of the Greek Hereditary Angioedema Registry
(2014)Background: No published data presently exist concerning hereditary angioedema (HAE) in Greece. The aim of this study was to present the results from patients recorded by the Greek Hereditary Angioedema Registry over the ... -
The Psychopathology of Parents of Children and Adolescents with Obsessive-Compulsive Disorder
(2010)Objective: Our purpose was to determine the rates of psychopathology in parents of children and adolescents with obsessive-compulsive disorder (OCD) and compare these with that found in parents of children with learning ... -
Survivin regulation by HER2 through NF-kappa B and c-myc in irradiated breast cancer cells
(2011)Radiotherapy is an important treatment modality against cancer resulting in apoptosis and inhibition of cell growth. Survivin is an important cancer biomarker conferring to tumour cells increased survival potential by ... -
THAP1 mutations and dystonia phenotypes: Genotype phenotype correlations
(2012)THAP1 mutations have been shown to be the cause of DYT6. A number of different mutation types and locations in the THAP1 gene have been associated with a range of severity and dystonia phenotypes, but, as yet, it has been ...