Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 4 de 4
Filter
Add more filters










Database
Language
Publication year range
1.
J Imaging ; 9(1)2023 Jan 10.
Article in English | MEDLINE | ID: mdl-36662113

ABSTRACT

The paper describes the construction of the neutron imaging facility at the very low-power research reactor VR-1. The training reactor VR-1 is operated by the Czech Technical University in Prague, Czech Republic. It is mainly used for the education of students in the field of nuclear engineering as well as for the training of professionals. Neutron imaging is the new field of VR-1 reactor utilisation currently under development. Extremely low reactor power at the level of 100 W brought many challenges that were necessary to overcome to build and commission a sustainable neutron radiography facility. The paper describes the reactor's neutron flux verification and the basic concept and design of the neutron imaging instrumentation. The first experimental results were mainly dedicated to testing the detection system for different radial beam port configurations, different L/D ratios, and different exposure times. Preliminary results of neutron radiography and tomography measurements at VR-1 clearly showed the potential of using neutron imaging in low-power reactors such as the VR-1 reactor.

2.
Exp Clin Cardiol ; 15(3): e52-6, 2010.
Article in English | MEDLINE | ID: mdl-20959880

ABSTRACT

BACKGROUND: The majority of acute coronary syndrome (ACS) cases cannot be explained by the analysis of commonly recognized risk factors; thus, the analysis of possible genetic predispositions is of interest. The genes for connexin-37, stromelysin-1, plasminogen activator-inhibitor type 1 (PAI-1) and lymphotoxin-alpha are among many presently known candidate genes that are associated with risk factors for ACS. OBJECTIVE: To identify the potential impact of the functional variants of connexin-37, stromelysin-1, PAI-1 and lymphotoxin-alpha on ACS in a Caucasian Czech population. METHODS: A total of 1399 consecutive patients (1016 men and 383 women) with ACS from five coronary care units located in Prague (Czech Republic) were analyzed; a representative sample of 2559 healthy individuals (1191 men and 1368 women) were also genotyped and served as controls. RESULTS: The gene variants analyzed were not significantly associated with the prevalence of ACS or the classical risk factors of ACS development such as high plasma lipid levels, hypertension, diabetes, high body mass index or smoking. CONCLUSION: In a Caucasian Czech population sample, genetic variants of connexin-37, stromelysin-1, PAI-1 and lymphotoxin-alpha were not significantly associated with a predisposition toward ACS.

3.
Clin Chim Acta ; 411(15-16): 1069-72, 2010 Aug 05.
Article in English | MEDLINE | ID: mdl-20362563

ABSTRACT

BACKGROUND: The FTO gene plays an important role in the determination of body weight and BMI and it has been suspected of being associated with all-case mortality. METHODS: We have analyzed the FTO rs17817449 variant in consecutive 1092 male patients with acute coronary syndrome (ACS) and in 1191 randomly selected Caucasian individuals (population controls). RESULTS: The FTO variant was significantly associated with BMI both in controls (P<0.02) and ACS patients (P<0.01). In both groups, BMI was highest in GG homozygotes and lowest in TT homozygotes. There was a significant difference between the ACS patients and controls in the frequency of the FTO genotype GG (21.4% vs. 15.9%, P<0.005). FTO GG homozygotes had a significantly increased risk of ACS, compared with TT homozygotes which was independent of age and BMI (odds ratio 1.49, 95% confidence interval 1.16-1.93). The odds ratio of ACS patients for the GG genotype remained significant even after the exclusion of diabetics (100 controls and 339 ACS patients), with OR 1.32 (95% CI 1.01-1.72). CONCLUSIONS: This study provides an evidence of an association between the FTO variant and risk of ACS in Caucasian males.


Subject(s)
Acute Coronary Syndrome/genetics , Genetic Predisposition to Disease , Genetic Variation , Proteins/genetics , Alpha-Ketoglutarate-Dependent Dioxygenase FTO , Case-Control Studies , Humans , Male , Middle Aged , Risk Factors
4.
Chembiochem ; 9(15): 2534-41, 2008 Oct 13.
Article in English | MEDLINE | ID: mdl-18785199

ABSTRACT

The knowledge of the molecular basis of communication in bumblebee communities is limited. None of the enzymes that participate in pheromone production have been characterized. Here, we cloned the gene encoding the Delta(9) desaturase from cDNA prepared from the total RNA of the pheromone gland and fat bodies of Bombus lucorum male. Functional expression of BlucNPVE desaturase in Saccharomyces cerevisiae and GC-MS analyses revealed its preference for C(18) saturated fatty acids. This suggests that Delta(9) desaturase is involved in the desaturation of metabolic fatty acids stored in triacylglyceroles (TAGs), because oleic acid is the most abundant fatty acid bound in TAG in B. lucorum and it is present in low concentration in the pheromone blend. The incubation of pheromone precursors with a dissected labial gland as well as direct injection of labelled pheromone substrates into B. lucorum males revealed that esterification of pheromone products occurs in the labial gland. These results support both the biosynthesis of pheromones from common lipids and the de novo synthesis of unsaturated pheromones in the labial gland.


Subject(s)
Bees/enzymology , Sex Attractants/biosynthesis , Stearoyl-CoA Desaturase/metabolism , Amino Acid Sequence , Animals , Bees/chemistry , Cloning, Molecular , Esters/metabolism , Male , Molecular Sequence Data , Sequence Alignment , Sequence Homology, Amino Acid , Sex Attractants/chemistry , Stearoyl-CoA Desaturase/chemistry , Stearoyl-CoA Desaturase/genetics
SELECTION OF CITATIONS
SEARCH DETAIL
...