280 research outputs found
The role of psychological correction in discogenic dorsopathies treatment
Chuhraev N., Zukow W., Samosiuk N., Danilova О. The role of psychological correction in discogenic dorsopathies treatment. Journal of Education, Health and Sport. 2016;6(11):262-270. eISSN 2391-8306. DOI http://dx.doi.org/10.5281/zenodo.166568http://ojs.ukw.edu.pl/index.php/johs/article/view/3995 The journal has had 7 points in Ministry of Science and Higher Education parametric evaluation. Part B item 755 (23.12.2015).755 Journal of Education, Health and Sport eISSN 2391-8306 7© The Author (s) 2016;This article is published with open access at Licensee Open Journal Systems of Kazimierz Wielki University in Bydgoszcz, PolandOpen Access. This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium,provided the original author(s) and source are credited. This is an open access article licensed under the terms of the Creative Commons Attribution Non Commercial License(http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted, non commercial use, distribution and reproduction in any medium, provided the work is properly cited.This is an open access article licensed under the terms of the Creative Commons Attribution Non Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted, non commercialuse, distribution and reproduction in any medium, provided the work is properly cited.The authors declare that there is no conflict of interests regarding the publication of this paper.Received: 01.11.2016. Revised 12.11.2016. Accepted: 13.11.2016. UDC 615.8 THE ROLE OF PSYCHOLOGICAL CORRECTION IN DISCOGENIC DORSOPATHIES TREATMENT Chuhraev N.1, Zukow W.2, Samosiuk N.3, Danilova О.4 1. LLC «NMZ Мedintech», Kiev, Ukraine. Email: [email protected]. Kazimierz Wielki University, Bydgoszcz, Poland3. National Medical Academy of Postgraduate Education named P. L. Shupik, Department of neurology №1, Kiev, Ukraine4. Private higher education institution «Interregional Academy of Personnel Management», Kiev, Ukraine Summary The article dials with the role of psychological correction in the treatment of discogenic dorsopathies based on zonal applicated ultraphonophoresis of analgesic drugs and psychological treatment of anxious depression (F41.2 Mixed anxiety and depressive disorder) with the use of binaural rhythms and magnetofotostimulation. Keywords: discogenic dorsopathy, anxious depression, binaural rhythms, magnetofotostimulation
High energy hadrons in EAS at mountain altitude
An extensive simulation has been carried out to estimate the physical
interpretation of dynamical factors such as , in terms of high
energy interaction features, concentrated in the present analysis on the
average transverse momentum. It appears that the large enhancement observed for
versus primary energy, suggesting in earliest analysis a significant
rise of with energy, is only the result of the limited resolution of the
detectors and remains in agreement with a wide range of models used in
simulations.Comment: 13 pages, 6 PostScript figures, LaTeX Subm. to JPhys
Features of Muon Arrival Time Distributions of High Energy EAS at Large Distances From the Shower Axis
In view of the current efforts to extend the KASCADE experiment
(KASCADE-Grande) for observations of Extensive Air Showers (EAS) of primary
energies up to 1 EeV, the features of muon arrival time distributions and their
correlations with other observable EAS quantities have been scrutinised on
basis of high-energy EAS, simulated with the Monte Carlo code CORSIKA and using
in general the QGSJET model as generator. Methodically various correlations of
adequately defined arrival time parameters with other EAS parameters have been
investigated by invoking non-parametric methods for the analysis of
multivariate distributions, studying the classification and misclassification
probabilities of various observable sets. It turns out that adding the arrival
time information and the multiplicity of muons spanning the observed time
distributions has distinct effects improving the mass discrimination. A further
outcome of the studies is the feature that for the considered ranges of primary
energies and of distances from the shower axis the discrimination power of
global arrival time distributions referring to the arrival time of the shower
core is only marginally enhanced as compared to local distributions referring
to the arrival of the locally first muon.Comment: 24 pages, Journal Physics G accepte
Atmospheric Muon Flux at Sea Level, Underground, and Underwater
The vertical sea-level muon spectrum at energies above 1 GeV and the
underground/underwater muon intensities at depths up to 18 km w.e. are
calculated. The results are particularly collated with a great body of the
ground-level, underground, and underwater muon data. In the hadron-cascade
calculations, the growth with energy of inelastic cross sections and pion,
kaon, and nucleon generation in pion-nucleus collisions are taken into account.
For evaluating the prompt muon contribution to the muon flux, we apply two
phenomenological approaches to the charm production problem: the recombination
quark-parton model and the quark-gluon string model. To solve the muon
transport equation at large depths of homogeneous medium, a semi-analytical
method is used. The simple fitting formulas describing our numerical results
are given. Our analysis shows that, at depths up to 6-7 km w. e., essentially
all underground data on the muon intensity correlate with each other and with
predicted depth-intensity relation for conventional muons to within 10%.
However, the high-energy sea-level data as well as the data at large depths are
contradictory and cannot be quantitatively decribed by a single nuclear-cascade
model.Comment: 47 pages, REVTeX, 15 EPS figures included; recent experimental data
and references added, typos correcte
Sour Taste Responses in Mice Lacking PKD Channels
The polycystic kidney disease-like ion channel PKD2L1 and its associated
partner PKD1L3 are potential candidates for sour taste receptors. PKD2L1 is
expressed in type III taste cells that respond to sour stimuli and genetic
elimination of cells expressing PKD2L1 substantially reduces chorda tympani
nerve responses to sour taste stimuli. However, the contribution of PKD2L1
and PKD1L3 to sour taste responses remains unclear.We made mice lacking PKD2L1 and/or PKD1L3 gene and investigated whole nerve
responses to taste stimuli in the chorda tympani or the glossopharyngeal
nerve and taste responses in type III taste cells. In mice lacking PKD2L1
gene, chorda tympani nerve responses to sour, but not sweet, salty, bitter,
and umami tastants were reduced by 25–45% compared with those
in wild type mice. In contrast, chorda tympani nerve responses in PKD1L3
knock-out mice and glossopharyngeal nerve responses in single- and
double-knock-out mice were similar to those in wild type mice. Sour taste
responses of type III fungiform taste cells (GAD67-expressing taste cells)
were also reduced by 25–45% by elimination of PKD2L1.These findings suggest that PKD2L1 partly contributes to sour taste responses
in mice and that receptors other than PKDs would be involved in sour
detection
Mutation in utp15 Disrupts Vascular Patterning in a p53-Dependent Manner in Zebrafish Embryos
Angiogenesis is the process by which the highly branched and functional vasculature arises from the major vessels, providing developing tissues with nutrients, oxygen, and removing metabolic waste. During embryogenesis, vascular patterning is dependent on a tightly regulated balance between pro- and anti-angiogenic signals, and failure of angiogenesis leads to embryonic lethality. Using the zebrafish as a model organism, we sought to identify genes that influence normal vascular patterning.In a forward genetic screen, we identified mutant LA1908, which manifests massive apoptosis during early embryogenesis, abnormal expression of several markers of arterial-venous specification, delayed angiogenic sprouting of the intersegmental vessels (ISV), and malformation of the caudal vein plexus (CVP), indicating a critical role for LA1908 in cell survival and angiogenesis. Genetic mapping and sequencing identified a G to A transition in the splice site preceding exon 11 of utp15 in LA1908 mutant embryos. Overexpression of wild type utp15 mRNA suppresses all observed mutant phenotypes, demonstrating a causative relationship between utp15 and LA1908. Furthermore, we found that injecting morpholino oligonucleotides inhibiting p53 translation prevents cell death and rescues the vascular abnormalities, indicating that p53 is downstream of Utp15 deficiency in mediating the LA1908 phenotypes.Taken together, our data demonstrate an early embryonic effect of Utp15 deficiency on cell survival and the normal patterning of the vasculature and highlight an anti-angiogenic role of p53 in developing embryos
An Integrated TCGA Pan-Cancer Clinical Data Resource to Drive High-Quality Survival Outcome Analytics
For a decade, The Cancer Genome Atlas (TCGA) program collected clinicopathologic annotation data along with multi-platform molecular profiles of more than 11,000 human tumors across 33 different cancer types. TCGA clinical data contain key features representing the democratized nature of the data collection process. To ensure proper use of this large clinical dataset associated with genomic features, we developed a standardized dataset named the TCGA Pan-Cancer Clinical Data Resource (TCGA-CDR), which includes four major clinical outcome endpoints. In addition to detailing major challenges and statistical limitations encountered during the effort of integrating the acquired clinical data, we present a summary that includes endpoint usage recommendations for each cancer type. These TCGA-CDR findings appear to be consistent with cancer genomics studies independent of the TCGA effort and provide opportunities for investigating cancer biology using clinical correlates at an unprecedented scale. Analysis of clinicopathologic annotations for over 11,000 cancer patients in the TCGA program leads to the generation of TCGA Clinical Data Resource, which provides recommendations of clinical outcome endpoint usage for 33 cancer types
Mismatch repair deficiency predicts response of solid tumors to PD-1 blockade.
The genomes of cancers deficient in mismatch repair contain exceptionally high numbers of somatic mutations. In a proof-of-concept study, we previously showed that colorectal cancers with mismatch repair deficiency were sensitive to immune checkpoint blockade with antibodies to programmed death receptor-1 (PD-1). We have now expanded this study to evaluate the efficacy of PD-1 blockade in patients with advanced mismatch repair-deficient cancers across 12 different tumor types. Objective radiographic responses were observed in 53% of patients, and complete responses were achieved in 21% of patients. Responses were durable, with median progression-free survival and overall survival still not reached. Functional analysis in a responding patient demonstrated rapid in vivo expansion of neoantigen-specific T cell clones that were reactive to mutant neopeptides found in the tumor. These data support the hypothesis that the large proportion of mutant neoantigens in mismatch repair-deficient cancers make them sensitive to immune checkpoint blockade, regardless of the cancers\u27 tissue of origin
Genomic, Pathway Network, and Immunologic Features Distinguishing Squamous Carcinomas
This integrated, multiplatform PanCancer Atlas study co-mapped and identified distinguishing
molecular features of squamous cell carcinomas (SCCs) from five sites associated with smokin
Pan-cancer Alterations of the MYC Oncogene and Its Proximal Network across the Cancer Genome Atlas
Although theMYConcogene has been implicated incancer, a systematic assessment of alterations ofMYC, related transcription factors, and co-regulatoryproteins, forming the proximal MYC network (PMN),across human cancers is lacking. Using computa-tional approaches, we define genomic and proteo-mic features associated with MYC and the PMNacross the 33 cancers of The Cancer Genome Atlas.Pan-cancer, 28% of all samples had at least one ofthe MYC paralogs amplified. In contrast, the MYCantagonists MGA and MNT were the most frequentlymutated or deleted members, proposing a roleas tumor suppressors.MYCalterations were mutu-ally exclusive withPIK3CA,PTEN,APC,orBRAFalterations, suggesting that MYC is a distinct onco-genic driver. Expression analysis revealed MYC-associated pathways in tumor subtypes, such asimmune response and growth factor signaling; chro-matin, translation, and DNA replication/repair wereconserved pan-cancer. This analysis reveals insightsinto MYC biology and is a reference for biomarkersand therapeutics for cancers with alterations ofMYC or the PMN
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