This work presents a study of the conditions and possibilities for the intercalation of hexafluorophosphate anions into CNT-based electrodes. For this, cathodes based on CNTs synthesized on different ...catalysts (Co–Mo)/(Al
2
O
3
–MgO) and (Fe–Co)/
2.1
Al
2
O
3
were produced. As a result, electrode materials were obtained at various concentrations of CNT/graphite: CNT-4F, CNT-6, and CNT-6F. The resulting electrodes were studied by cyclic voltammetry (CVA) in an electrolyte of a dissolved LiPF 6 salt based on EC : DEC (ethylene carbonate : diethylene carbonate) solvents (in the ratio 1 : 1 : 1) with an admixture of 3% VC at a sweep speed of 4 mV/s. On the basis of the obtained CVA dependences, the specific charge/discharge capacity of the electrodes CNT-4F, CNT-6, and CNT-6F was determined. The largest specific charge/discharge capacity calculated per mass of CNTs was 292 and 164.22 (mA h)/g for CNT-4/graphite electrodes, and the minimum specific charge/discharge capacity was 41.67 and 1.5 (mA h)/g for CNT-4 electrodes without graphite, respectively. Also, the dependences of the average electrode utilization coefficient on the charge time at constant current on the cycle number at a charge of 300 s were obtained. For chronoamperograms of individual steps of the СNT-6F electrode, the values of lithium diffusion coefficients were calculated.
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EMUNI, FIS, FZAB, GEOZS, GIS, IJS, IMTLJ, KILJ, KISLJ, MFDPS, NLZOH, NUK, OILJ, PNG, SAZU, SBCE, SBJE, SBMB, SBNM, UKNU, UL, UM, UPUK, VKSCE, ZAGLJ
Intensive glucose lowering targeting glycated hemoglobin levels of less than 6.0% was unexpectedly associated with an increase in overall mortality in high-risk patients with type 2 diabetes in the ...ACCORD trial. The findings identify a previously unrecognized risk of intensive glucose lowering in such patients.
Intensive glucose lowering targeting glycated hemoglobin levels to less than 6.0% was unexpectedly associated with an increase in overall mortality in high-risk patients with type 2 diabetes.
Type 2 diabetes mellitus is a metabolic disease that is diagnosed on the basis of sustained hyperglycemia. People with type 2 diabetes are at elevated risk for a number of serious health problems, including cardiovascular disease, premature death, blindness, kidney failure, amputations, fractures, frailty, depression, and cognitive decline.
1
In prospective epidemiologic studies, the incidence of many of these outcomes is directly associated with the degree of hyperglycemia, as measured by the plasma glucose or the glycated hemoglobin level, a measure of the mean blood glucose level during the previous 2 to 3 months. Thus, after adjustment for other risk factors, . . .
Mosquito-borne infections cause some of the most debilitating human diseases, including yellow fever and malaria, yet we lack an understanding of how disease risk scales with human-driven habitat ...changes. We present an approach to study variation in mosquito distribution and concomitant viral infections on the landscape level. In a pilot study we analyzed mosquito distribution along a 10-km transect of a West African rainforest area, which included primary forest, secondary forest, plantations, and human settlements. Variation was observed in the abundance of
Anopheles
,
Aedes,
Culex
, and
Uranotaenia
mosquitoes between the different habitat types. Screening of trapped mosquitoes from the different habitats led to the isolation of five uncharacterized viruses of the families
Bunyaviridae, Coronaviridae, Flaviviridae,
and
Rhabdoviridae
, as well as an unclassified virus. Polymerase chain reaction screening for these five viruses in individual mosquitoes indicated a trend toward infection with specific viruses in specific mosquito genera that differed by habitat. Based on these initial analyses, we believe that further work is indicated to investigate the impact of anthropogenic landscape changes on mosquito distribution and accompanying arbovirus infection.
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EMUNI, FIS, FZAB, GEOZS, GIS, IJS, IMTLJ, KILJ, KISLJ, MFDPS, NLZOH, NUK, OILJ, PNG, SAZU, SBCE, SBJE, SBMB, SBNM, UKNU, UL, UM, UPUK, VKSCE, ZAGLJ
Numerous electrochemical and chemical methods are suitable for preparation of tungsten trioxide (WO.sub.3) films. Many of these methods, however, have not been carefully studied, so information on ...the specific features of the WO.sub.3 film deposition technology is lacking. This paper describes the preparation of WO.sub.3 films by cathodic electrodeposition from the synthesized solution of peroxotungstic acid (PTA) on the surface of thermally expanded graphite (TEG) and titanium electrodes designed as foils. A stepwise pattern of reduction of tungsten oxides from PTA was revealed. The suitability of the WO.sub.3 film electrode as a material for electrochemical power industry was experimentally demonstrated. Specifically, WO.sub.3/Ti was found to be applicable as a protective coating for hydrogen fuel cells, and WO.sub.3/TEG, as a cathode material for asymmetric supercapacitors. Based on the charge-discharge curves for the WO.sub.3/TEG electrode used as a cathode in the free volume of th KOH electrolyte, the specific capacitance of the supercapacitor was estimated at 630 F/g. Electrochemical analysis showed that that WO.sub.3 films deposited on the titanium surface afford enhancement of the hydrogen overpotential and protection against pitting corrosion during potentiostatic polarization tests at the cathode potential of a fuel cell.
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DOBA, EMUNI, FIS, FZAB, GEOZS, GIS, IJS, IMTLJ, IZUM, KILJ, KISLJ, MFDPS, NLZOH, NUK, OILJ, PILJ, PNG, SAZU, SBCE, SBJE, SBMB, SBNM, UILJ, UKNU, UL, UM, UPUK, VKSCE, ZAGLJ
A common feature of all the known cancer genetic syndromes is that they predispose only to selective types of malignancy. However, many of the genes mutated in these syndromes are ubiquitously ...expressed, and influence seemingly universal processes such as DNA repair or cell cycle control. The tissue specificity of cancers that arise from malfunction of these apparently universal traits remains a key puzzle in cancer genetics. Mutations in DNA mismatch repair (MMR) genes cause the most common known cancer genetic syndrome, hereditary non-polyposis colorectal cancer, and the fundamental biology of MMR is one of the most intensively studied processes in laboratories all around the world. This review uses MMR as a model system to understand mechanisms that may explain the selective development of tumors in particular cell types despite the universal nature of this process. We evaluate recent data giving insights into the specific tumor types that are attributable to defective MMR in humans and mice under different modes of inheritance, and propose models that may explain the spectrum of cancer types observed.
Specific features of synthesis and capacity for reversible electrochemical intercalation of lithium were studied for the electrode composite material on a carbon support, based on cobalt-vanadium ...oxide and oxide molybdenum compounds deposited from aqueous solutions of their salts under polarization with an alternating asymmetric current.
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EMUNI, FIS, FZAB, GEOZS, GIS, IJS, IMTLJ, KILJ, KISLJ, MFDPS, NLZOH, NUK, OBVAL, OILJ, PNG, SAZU, SBCE, SBJE, SBMB, SBNM, UKNU, UL, UM, UPUK, VKSCE, ZAGLJ
We present evidence that the human thyroid hormone receptor forms a heterodimer with the human retinoic acid receptor. This interaction results in a cooperative increase in binding of the alpha ...retinoic acid receptor to a subset of thyroid hormone response elements. Mutations within the DNA binding domain or near the C-terminus abolish either receptor's ability to interact cooperatively on these elements. The thyroid hormone-retinoic acid receptor heterodimer exhibits novel transcriptional properties in that coexpression of both receptors at low levels in Green monkey kidney (CV1) cells results in a positive transcriptional effect on promoters containing a palindromic thyroid hormone response element, but has a surprisingly negative effect on a thyroid hormone response element derived from the alpha myosin heavy chain gene. These results suggest that by forming heterodimers, more elab-orate control of transcription can be achieved by creating receptor combinations with differing activities.
Purpose: To assess costs and healthcare resource utilization (HCRU) associated with the use of idarucizumab for the reversal of dabigatran and andexanet alfa for the reversal of direct oral Factor Xa ...inhibitors. Methods: This retrospective study utilizing Premier Healthcare Database (PHD) included patients aged ≥18 years on direct oral anticoagulants (DOACs) who experienced life-threatening bleeds, discharged from the hospital during 5/1/2018–6/30/2019, and received idarucizumab or andexanet alfa. Inverse of treatment probability weighting (IPTW) method was used to balance patient and clinical characteristics between treatment cohorts. Results: Idarucizumab patients were older than andexanet alfa patients (median age 81 vs 77 years; p < 0.001), and less likely to experience intracranial hemorrhage (ICH) (37.1%vs 73.8%; p = 0.001). After IPTW adjustment, idarucizumab patients incurred lower mean total hospital costs ($30,413 ± $33,028 vs $44,477 ± $30,036; p < 0.001),and mean intensive care unit (ICU) cost ($25,114 ± $30,433 vs $43,484 ± $29,335; p < 0.001). Conclusions: Anticoagulant reversal therapy with idarucizumab was associated with significantly lower adjusted mean total hospital and ICU costs compared with andexanet alfa. However, a higher prevalence of ICH bleeds was noted in the andexanet alfa group. Trial Registration: Not applicable.
Mammalian MutL homologues function in DNA mismatch repair (MMR) after replication errors and in meiotic recombination. Both functions are initiated by a heterodimer of MutS homologues specific to ...either MMR (MSH2-MSH3 or MSH2-MSH6) or crossing over (MSH4-MSH5). Mutations of three of the four MutL homologues (Mlh1, Mlh3, and Pms2) result in meiotic defects. We show herein that two distinct complexes involving MLH3 are formed during murine meiosis. The first is a stable association between MLH3 and MLH1 and is involved in promoting crossing over in conjunction with MSH4-MSH5. The second complex involves MLH3 together with MSH2-MSH3 and localizes to repetitive sequences at centromeres and the Y chromosome. This complex is up-regulated in Pms2⁻superscript /⁻ males, but not females, providing an explanation for the sexual dimorphism seen in Pms2⁻superscript /⁻ mice. The association of MLH3 with repetitive DNA sequences is coincident with MSH2-MSH3 and is decreased in Msh2⁻superscript /⁻ and Msh3⁻superscript /⁻ mice, suggesting a novel role for the MMR family in the maintenance of repeat unit integrity during mammalian meiosis.
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