Institution
Kazan Federal University
Education•Kazan’, Russia•
About: Kazan Federal University is a education organization based out in Kazan’, Russia. It is known for research contribution in the topics: Population & Chemistry. The organization has 9868 authors who have published 14390 publications receiving 135726 citations. The organization is also known as: Kazan (Volga region) Federal University & Kazan State University.
Papers published on a yearly basis
Papers
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TL;DR: It is found that prodigiosin-loaded halloysite nanotubes inhibit human epithelial colorectal adenocarcinoma and human colon carcinoma cells proliferative activity and a disorganization of the F-actin structure is observed.
Abstract: Prodigiosin, a bioactive secondary metabolite produced by Serratia marcescens, is an effective proapoptotic agent against various cancer cell lines, with little or no toxicity toward normal cells. The hydrophobicity of prodigiosin limits its use for medical and biotechnological applications, these limitations, however, can be overcome by using nanoscale drug carriers, resulting in promising formulations for target delivery systems with great potential for anticancer therapy. Here we report on prodigiosin-loaded halloysite-based nanoformulation and its effects on viability of malignant and non-malignant cells. We have found that prodigiosin-loaded halloysite nanotubes inhibit human epithelial colorectal adenocarcinoma (Caco-2) and human colon carcinoma (HCT116) cells proliferative activity. After treatment of Caco-2 cells with prodigiosin-loaded halloysite nanotubes, we have observed a disorganization of the F-actin structure. Comparison of this effects on malignant (Caco-2, HCT116) and non-malignant (MSC, HSF) cells suggests the selective cytotoxic and genotoxic activity of prodigiosin-HNTs nanoformulation.
37 citations
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TL;DR: A whole genome sequencing metagenomic/genomic study of the intestinal microbiota changes caused by Helicobacter pylori eradications therapy revealed a statistically significant decrease in alpha-diversity and relative abundance of Bifidobacterium adolescentis due to HP eradication therapy, while the relative abundances of Enterococcus faecium increased.
Abstract: The human gut microbiome plays an important role both in health and disease. Use of antibiotics can alter gut microbiota composition, which can lead to various deleterious events. Here we report a whole genome sequencing metagenomic/genomic study of the intestinal microbiota changes caused by Helicobacter pylori (HP) eradication therapy. Using approaches for metagenomic data analysis we revealed a statistically significant decrease in alpha-diversity and relative abundance of Bifidobacterium adolescentis due to HP eradication therapy, while the relative abundance of Enterococcus faecium increased. We have detected changes in general metagenome resistome profiles as well: after HP eradication therapy, the ermB, CFX group, and tetQ genes were overrepresented, while tetO and tetW genes were underrepresented. We have confirmed these results with genome-resolved metagenomic approaches. MAG (metagenome-assembled genomes) abundance profiles have changed dramatically after HP eradication therapy. Focusing on ermB gene conferring resistance to macrolides, which were included in the HP eradication therapy scheme, we have shown a connection between antibiotic resistance genes (ARGs) and some overrepresented MAGs. Moreover, some E. faecium strains isolated from stool samples obtained after HP eradication have manifested greater antibiotic resistance in vitro in comparison to other isolates, as well as the higher number of ARGs conferring resistance to macrolides and tetracyclines.
37 citations
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TL;DR: In this article, the authors evaluated the experience of active learning methods application in environmental education of school pupils and showed promising character of its application in the system of supplementary education of students in secondary schools.
37 citations
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27 Jan 2017-Materials Science and Engineering A-structural Materials Properties Microstructure and Processing
TL;DR: In this article, high pressure torsion was employed to deform Ti-6Al-4V (TC4) alloy to restrain grain growth, and the effect of this mechanism reduces at large strains due to the existing high-dense dislocations and non-equilibrium grain boundaries.
Abstract: The high-pressure torsion method was employed to deform Ti-6Al-4V (TC4) alloy. The ambient temperature and high pressure were used to restrain the grain growth. Clear images showing the microstructure evolution of the deformed TC4 alloys were obtained using SEM, TEM and HRTEM. It was found that the HPT-deformed TC4 alloys contain a high density of dislocations and many defect structures. These dislocations were found to be generated on one or both sides of the elongated grains, and the dislocation lines were able to move across the elongated grains (mostly at ~60°) to form an uncondensed dislocation wall. Although deformation twins did not appear in the alloys deformed at intermediate strains (γ≤23.1), quantities of (10−12) tensile twins containing prismatic stacking faults were observed in the specimens deformed at a much larger plastic strain (γ≥157). The hardness-strain behaviors of the TC4 alloys were similar to those of pure Ti, which have a maximum hardness followed by a strain softening at large strains. In addition, the formation of the omega phase was suppressed due to the dissolution of substitutional Al and V. The alloy that received the highest levels of strain (γ~357) was found to have a nanoscale structure (~49.41 nm) with non-equilibrium GBs, as well as an increased microhardness (~424 HV) and yield strength (σ S ~960 MPa). The effects of these defect-structures on the mechanical behaviors of a TC4 alloy are mainly determined by their structures’ sizes according to Hall–Petch relationship. However, the effect of this mechanism reduces at large strains due to the existing high-dense dislocations and non-equilibrium grain boundaries.
37 citations
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06 Feb 2016TL;DR: The observations suggest that there are at least three types of mouths in deuterostomes, and that the new acquisition of chordate mouths was likely related to the dorso-ventral inversion that occurred in the last common ancestor of chordates.
Abstract: Deuterostomes (animals with ‘secondary mouths’) are generally accepted to develop the mouth independently of the blastopore. However, it remains largely unknown whether mouths are homologous among all deuterostome groups. Unlike other bilaterians, in amphioxus the mouth initially opens on the left lateral side. This peculiar morphology has not been fully explained in the evolutionary developmental context. We studied the developmental process of the amphioxus mouth to understand whether amphioxus acquired a new mouth, and if so, how it is related to or differs from mouths in other deuterostomes. The left first somite in amphioxus produces a coelomic vesicle between the epidermis and pharynx that plays a crucial role in the mouth opening. The vesicle develops in association with the amphioxus-specific Hatschek nephridium, and first opens into the pharynx and then into the exterior as a mouth. This asymmetrical development of the anterior-most somites depends on the Nodal-Pitx signaling unit, and the perturbation of laterality-determining Nodal signaling led to the disappearance of the vesicle, producing a symmetric pair of anterior-most somites that resulted in larvae lacking orobranchial structures. The vesicle expressed bmp2/4, as seen in ambulacrarian coelomic pore-canals, and the mouth did not open when Bmp2/4 signaling was blocked. We conclude that the amphioxus mouth, which uniquely involves a mesodermal coelomic vesicle, shares its evolutionary origins with the ambulacrarian coelomic pore-canal. Our observations suggest that there are at least three types of mouths in deuterostomes, and that the new acquisition of chordate mouths was likely related to the dorso-ventral inversion that occurred in the last common ancestor of chordates.
37 citations
Authors
Showing all 10096 results
Name | H-index | Papers | Citations |
---|---|---|---|
Richard G. Pestell | 130 | 479 | 54210 |
Alexander Spiridonov | 126 | 1198 | 77296 |
V. Stolyarov | 119 | 238 | 79004 |
Sergei D. Odintsov | 112 | 609 | 62524 |
Hans-Uwe Simon | 96 | 461 | 51698 |
Yuri Lvov | 89 | 342 | 27397 |
Alexei A. Starobinsky | 88 | 340 | 42331 |
Yakov Kuzyakov | 87 | 667 | 37050 |
V. E. Semenov | 74 | 372 | 22577 |
John W. Weisel | 73 | 323 | 17866 |
Klaus T. Preissner | 72 | 333 | 21289 |
Alexander Tropsha | 71 | 288 | 22898 |
Roland Winter | 68 | 468 | 15193 |
Christoph Schick | 68 | 443 | 16664 |
Marat Gilfanov | 62 | 350 | 14987 |