Reconstruction of plasma density profiles by measuring spectra of radiation emitted from oscillating plasma dipoles

We suggest a new method for characterising non-uniform density distributions of plasma by measuring the spectra of radiation emitted from a localised plasma dipole oscillator excited by colliding electromagnetic pulses. The density distribution can be determined by scanning the collision point in space. Two-dimensional particle-in-cell simulations demonstrate the reconstruction of linear and nonlinear density profiles corresponding to laser-produced plasma. The method can be applied to a wide range of plasma, including fusion and low temperature plasmas. It overcomes many of the disadvantages of existing methods that only yield average densities along the path of probe pulses, such as interferometry and spectroscopy

On electromagnetic interactions for massive mixed symmetry field

In this paper we investigate electromagnetic interactions for simplest massive mixed symmetry field. Using frame-like gauge invariant formulation we extend Fradkin-Vasiliev procedure, initially proposed for investigation of gravitational interactions for massless particles in AdS space, to the case of electromagnetic interactions for massive particles leaving in (A)dS space with arbitrary value of cosmological constant including flat Minkowski space. At first, as an illustration of general procedure, we re-derive our previous results on massive spin 2 electromagnetic interactions and then we apply this procedure to massive mixed symmetry field. These two cases are just the simplest representatives of two general class of fields, namely completely symmetric and mixed symmetry ones, and it is clear that the results obtained admit straightforward generalization to higher spins as well.Comment: 17 pages. Some clarifications added. Version to appear in JHE

Combination of angiotensin converting enzyme inhibitor and irbesartan for the treatment of heart failure

published_or_final_versio

Cardiac rehabilitation improves functional and clinical status of patients after AMI or PTCA - a randomised controlled study

published_or_final_versio

Influence of clinical parameters on short-term outcome in cardiac rehabilitation patients after actue myocardial infarction

published_or_final_versio

An analysis on reasons of non-compliant to cardiac rehabilitation programme

Abstract no. 09published_or_final_versio

Benefits of cardiac rehabilitation in patients with left ventricular systolic heart failure

published_or_final_versio

Active cardiac rehabilitation program is able to improve risk factors profile

Abstract no. 08published_or_final_versio

Cryotomography of budding influenza a virus reveals filaments with diverse morphologies that mostly do not bear a genome at their distal end

Influenza viruses exhibit striking variations in particle morphology between strains. Clinical isolates of influenza A virus have been shown to produce long filamentous particles while laboratory-adapted strains are predominantly spherical. However, the role of the filamentous phenotype in the influenza virus infectious cycle remains undetermined. We used cryo-electron tomography to conduct the first three-dimensional study of filamentous virus ultrastructure in particles budding from infected cells. Filaments were often longer than 10 microns and sometimes had bulbous heads at their leading ends, some of which contained tubules we attribute to M1 while none had recognisable ribonucleoprotein (RNP) and hence genome segments. Long filaments that did not have bulbs were infrequently seen to bear an ordered complement of RNPs at their distal ends. Imaging of purified virus also revealed diverse filament morphologies; short rods (bacilliform virions) and longer filaments. Bacilliform virions contained an ordered complement of RNPs while longer filamentous particles were narrower and mostly appeared to lack this feature, but often contained fibrillar material along their entire length. The important ultrastructural differences between these diverse classes of particles raise the possibility of distinct morphogenetic pathways and functions during the infectious process

Tumor innate immunity primed by specific interferon-stimulated endogenous retroviruses.

Mesenchymal tumor subpopulations secrete pro-tumorigenic cytokines and promote treatment resistance1-4. This phenomenon has been implicated in chemorefractory small cell lung cancer and resistance to targeted therapies5-8, but remains incompletely defined. Here, we identify a subclass of endogenous retroviruses (ERVs) that engages innate immune signaling in these cells. Stimulated 3 prime antisense retroviral coding sequences (SPARCS) are oriented inversely in 3' untranslated regions of specific genes enriched for regulation by STAT1 and EZH2. Derepression of these loci results in double-stranded RNA generation following IFN-γ exposure due to bi-directional transcription from the STAT1-activated gene promoter and the 5' long terminal repeat of the antisense ERV. Engagement of MAVS and STING activates downstream TBK1, IRF3, and STAT1 signaling, sustaining a positive feedback loop. SPARCS induction in human tumors is tightly associated with major histocompatibility complex class 1 expression, mesenchymal markers, and downregulation of chromatin modifying enzymes, including EZH2. Analysis of cell lines with high inducible SPARCS expression reveals strong association with an AXL/MET-positive mesenchymal cell state. While SPARCS-high tumors are immune infiltrated, they also exhibit multiple features of an immune-suppressed microenviroment. Together, these data unveil a subclass of ERVs whose derepression triggers pathologic innate immune signaling in cancer, with important implications for cancer immunotherapy