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1.
Sensors (Basel) ; 24(2)2024 Jan 07.
Artículo en Inglés | MEDLINE | ID: mdl-38257452

RESUMEN

This article presents the results of evaluating the possibility of conducting radio astronomy studies in the windows of atmospheric transparency ~100, ~230, and ~350 GHz using the optical Big Telescope Alt-Azimuthal (BTA) of the Special Astrophysical Observatory of the Russian Academy of Sciences (SAO RAS). A list of some promising astronomical tasks is proposed. The astroclimat conditions at the BTA site and possible optical, cryogenic, and mechanical interfaces for mounting a superconducting radio receiver at the focus of the optical telescope are considered. As a receiving system, arrays of detectors cooled to ~0.3 K based on the superconductor-insulator-normal metal-insulator-superconductor (SINIS) structure are proposed. The implementation of the project will make it possible to use the BTA site of the SAO RAS not only to solve some astronomical problems (it is possible to consider the implementation of a single observatory, the VLBI (very-long-baseline interferometry) mode in the Suffa, EHT (Event Horizon Telescope), and Millimetron projects), but it will also be used to test various cryogenic detectors in a real observatory.

2.
Nanomaterials (Basel) ; 12(22)2022 Nov 16.
Artículo en Inglés | MEDLINE | ID: mdl-36432315

RESUMEN

Usually in quantum optics, the theory of large- and small-scale waveguide beam splitters is the same. In this paper, it is shown that the theory of the nanoscale waveguide beamsplitter has a significant difference from a similar device, but of a larger scale. It is shown that the previously known theory of the waveguide beam splitter is a particular case of the theory presented here. The wave function at the output ports of the nanoscale beam splitter is analyzed. The results obtained are sensitive to the size of the beam splitter, the coupling parameter of the two waveguides, and the degree of nonmonochromaticity of the photons entering the first and second ports of the beam splitter. The results are important for quantum technologies using a nanosized beam splitter.

3.
Nanomaterials (Basel) ; 9(11)2019 Nov 08.
Artículo en Inglés | MEDLINE | ID: mdl-31717372

RESUMEN

The creation of hydrophobic anti-icing and self-cleaning coatings is a relevant task for many industrial sectors. The potential field of application includes production of liquid and gas separators and filters, the field of textiles and clothing, construction and new materials, optical and microelectronic devices, the field of automobile construction and maritime shipping as well as energy and agriculture. The article suggests a new approach to the creation of superhydrophobic anti-icing coatings, by drawing peeled multi-walled carbon nanotubes (MWCNTs) to the sample surface. This method allows you to combine the necessary factors: Low surface energy, micro-nano-roughness and hierarchical multi-scale. The authors investigated the dependence of the wetting angle of such a surface on the model of MWCNT, fractional composition and the polarity of the dissolvent. The suggested approach can be used to create superhydrophobic coatings with the additional function of removing static charge and heating the surface, which can be used in the field of energetics for protection against freezing of wind turbine blades and aircraft surfaces.

4.
Thromb Res ; 111(6): 351-6, 2003.
Artículo en Inglés | MEDLINE | ID: mdl-14698652

RESUMEN

Conflicting data from Western European and USA population studies led us to investigate hyperhomocysteinemia (HHcy), the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphisms and thrombotic disease in North Western Russia. Plasma total homocysteine (tHcy) levels, MTHFR C677T genotype, selected life style determinants and haemostatic factor activity were determined in patients with arterial (n = 33), venous (n = 40), arterial + venous (n = 11) thrombosis and healthy controls (n = 30). We found raised median tHcy levels in all patient groups vs. controls (p < 0.05), with odds ratios (95% CI) for vascular disease among patients with HHcy (defined as > 15 micromol/l) of 3.9 (0.6 - 14.3), 4.8 (1.2 - 18.8) and 15.8 (2.8 - 87.3) respectively. tHcy levels were a function of MTHFR C677T genotype, and all patients with tHcy levels > 30 micromol/l had the MTHFR C677T homozygous substitution. Elevated tHcy levels (p < 0.05) were identified in smokers and coffee drinkers, with the degree of elevation dependent on MTHFR C677T genotype. Of the studied haemostatic parameters increased factor VIII activity and vWF antigen and activity was observed in HHcy subjects. We conclude that HHcy and MTHFR C677T genotype are positively associated with arterial and venous thrombotic disease in the population of North Western Russia.


Asunto(s)
Hiperhomocisteinemia/genética , Metilenotetrahidrofolato Reductasa (NADPH2)/genética , Adolescente , Adulto , Anciano , Coagulación Sanguínea , Femenino , Frecuencia de los Genes , Genotipo , Homocisteína/sangre , Humanos , Hiperhomocisteinemia/complicaciones , Hiperhomocisteinemia/enzimología , Hiperhomocisteinemia/epidemiología , Masculino , Persona de Mediana Edad , Mutación , Polimorfismo Genético , Estudios Retrospectivos , Federación de Rusia/epidemiología , Trombosis/complicaciones , Trombosis/epidemiología , Trombosis/genética , Trombosis de la Vena/complicaciones , Trombosis de la Vena/epidemiología , Trombosis de la Vena/genética
6.
Pathol Oncol Res ; 3(2): 106-108, 1997.
Artículo en Inglés | MEDLINE | ID: mdl-11173635

RESUMEN

The association between severe aplastic anemia (AA) and DR2 antigen seems to be well established. However, since discrimination between two DR2-associated splits, namely DR15 and DR16, rarely was performed, it remains unclear whether one or both of these subvariants are responsible for AA susceptibility. In this study, we have analyzed the HLA-DR allelic distribution in a group of 37 AA patients of slavic origin from North-Western Russia. The experimental design included PCR-based amplification of DRB-specific sequences, followed by reverse dot-blot hybridization of the biotinylated PCR-product with the set of sequence-specific oligonucleotide probes. HLA-DRB alleles were identified by non-radioactive enzymatic reaction, then standard serological specificities of HLA-DR antigen were estimated according to the WHO nomenclature. Whereas DR15 subtype occurred more often in the patients (23.0% vs. 13.3%, p< 0.05), DR16 split did not show the same tendency. The results, show the overall predominance of HLA-DR2 specificity (DR15+DR16) did not reach statistical significance (24.4% vs.17.5%, p<0.2). Thus, we conclude that repeatedly reported DR2 frequency increase in AA patients is mainly attributed to the prevalence of DR15 subtype.

7.
Clin Chem Lab Med ; 41(4): 496-500, 2003 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-12747593

RESUMEN

We undertook genetic and biochemical assays in patients with arterial (n = 146) and venous (n = 199) thromboembolism and survivors of pulmonary embolism (n = 58) to study causation and gene-life style interactions. In the clinical material from North Western Russia, factor V Leiden was found to be a risk factor in venous thrombosis (OR = 3.6), while the methylenetetrahydrofolate reductase (MTHFR) C677T mutation was a significant variable in both venous (p = 0.03) and arterial thrombosis (p = 0.004). Homocysteine levels were determined (n = 84) and hyperhomocysteinemia correlated with the T allele of the MTHFR gene, and with smoking and coffee consumption. Vitamin supplementation reduced homocysteine levels dependent on MTHFR genotype (36% TT, 25% CT, 22% CC). In pulmonary embolism patients, frequency of the -455G/A beta-fibrinogen dimorphism was studied. Carriers of this allele were significantly underrepresented (p < 0.02) among pulmonary embolism survivors (34.5%) compared to controls (56.7%). Additionally, -455AA homozygotes were found in 11.7% controls but only 1.7% of pulmonary embolism patients (p = 0.006). In venous and arterial thrombosis cases, MTHFR and homocysteine data led to effective dietary supplementation with a reduced risk of disease progression. Results from the pulmonary embolism study may indicate that screening tests for the -455G/A beta-fibrinogen genetic variation could be of prognostic value, and may point the way for novel anticoagulation strategies.


Asunto(s)
Arteriopatías Oclusivas/genética , Factor V/genética , Variación Genética/genética , Oxidorreductasas actuantes sobre Donantes de Grupo CH-NH/genética , Protrombina/genética , Tromboembolia/genética , Trombosis de la Vena/genética , Adulto , Arteriopatías Oclusivas/enzimología , Análisis Mutacional de ADN , Cartilla de ADN/química , Femenino , Fibrinógeno/genética , Genotipo , Humanos , Masculino , Metilenotetrahidrofolato Reductasa (NADPH2) , Persona de Mediana Edad , Mutación , Reacción en Cadena de la Polimerasa , Tromboembolia/enzimología , Trombosis de la Vena/enzimología
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