1,284 research outputs found
Rank-Two Beamforming and Power Allocation in Multicasting Relay Networks
In this paper, we propose a novel single-group multicasting relay beamforming
scheme. We assume a source that transmits common messages via multiple
amplify-and-forward relays to multiple destinations. To increase the number of
degrees of freedom in the beamforming design, the relays process two received
signals jointly and transmit the Alamouti space-time block code over two
different beams. Furthermore, in contrast to the existing relay multicasting
scheme of the literature, we take into account the direct links from the source
to the destinations. We aim to maximize the lowest received quality-of-service
by choosing the proper relay weights and the ideal distribution of the power
resources in the network. To solve the corresponding optimization problem, we
propose an iterative algorithm which solves sequences of convex approximations
of the original non-convex optimization problem. Simulation results demonstrate
significant performance improvements of the proposed methods as compared with
the existing relay multicasting scheme of the literature and an algorithm based
on the popular semidefinite relaxation technique
Generic Invertibility of Multidimensional FIR Filter Banks and MIMO Systems
We study the invertibility of M-variate Laurent polynomial N Ă P matrices. Such matrices represent multidimensional systems in various settings such as filter banks, multiple-input multiple-output systems, and multirate systems. Given an N Ă P Laurent polynomial matrix H(z1,..., zM) of degree at most k, we want to find a P Ă N Laurent polynomial left inverse matrix G(z) of H(z) such that G(z)H(z) = I. We provide computable conditions to test the invertibility and propose algorithms to find a particular inverse. The main result of this paper is to prove that H(z) is generically invertible when N âP â„ M; whereas when N âP < M, then H(z) is generically noninvertible. As a result, we propose an algorithm to find a particular inverse of a Laurent polynomial matrix that is faster than current algorithms known to us
Language and social/emotional problems identified at a universal developmental assessment at 30 months
Non peer reviewedPublisher PD
Short-term efficacy of physical interventions in osteoarthritic knee pain. A systematic review and meta-analysis of randomised placebo-controlled trials.
BACKGROUND: Treatment efficacy of physical agents in osteoarthritis of the knee (OAK) pain has been largely unknown, and this systematic review was aimed at assessing their short-term efficacies for pain relief. METHODS: Systematic review with meta-analysis of efficacy within 1-4 weeks and at follow up at 1-12 weeks after the end of treatment. RESULTS: 36 randomised placebo-controlled trials (RCTs) were identified with 2434 patients where 1391 patients received active treatment. 33 trials satisfied three or more out of five methodological criteria (Jadad scale). The patient sample had a mean age of 65.1 years and mean baseline pain of 62.9 mm on a 100 mm visual analogue scale (VAS). Within 4 weeks of the commencement of treatment manual acupuncture, static magnets and ultrasound therapies did not offer statistically significant short-term pain relief over placebo. Pulsed electromagnetic fields offered a small reduction in pain of 6.9 mm [95% CI: 2.2 to 11.6] (n = 487). Transcutaneous electrical nerve stimulation (TENS, including interferential currents), electro-acupuncture (EA) and low level laser therapy (LLLT) offered clinically relevant pain relieving effects of 18.8 mm [95% CI: 9.6 to 28.1] (n = 414), 21.9 mm [95% CI: 17.3 to 26.5] (n = 73) and 17.7 mm [95% CI: 8.1 to 27.3] (n = 343) on VAS respectively versus placebo control. In a subgroup analysis of trials with assumed optimal doses, short-term efficacy increased to 22.2 mm [95% CI: 18.1 to 26.3] for TENS, and 24.2 mm [95% CI: 17.3 to 31.3] for LLLT on VAS. Follow-up data up to 12 weeks were sparse, but positive effects seemed to persist for at least 4 weeks after the course of LLLT, EA and TENS treatment was stopped. CONCLUSION: TENS, EA and LLLT administered with optimal doses in an intensive 2-4 week treatment regimen, seem to offer clinically relevant short-term pain relief for OAK
Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment
Peer reviewedPublisher PD
The elusive meningococcal meningitis serogroup: a systematic review of serogroup B epidemiology
<p>Abstract</p> <p>Background</p> <p>Invasive meningococcal disease (IMD), is a widely distributed, complex human disease affecting all age categories. The causative agent, <it>Neisseria meningitidis</it>, is spread through aerosol respiratory droplets. 13 different serogroups have been identified, each with varying epidemiological features including prevalence, virulence, immunogenicity, geographical and temporal distribution. Although preventative measures are available for several of the serogroups, meningococcal disease caused by serogroup B is of particular interest due to the challenge it presents concerning vaccine development.</p> <p>Methods</p> <p>A systematic review of peer reviewed studies and reports, the collection of data from national and international health resources, along with the analysis of the Multi Locus Sequence Typing database was carried out aimed at collecting information concerning serogroup B IMD and the epidemiology attached to it.</p> <p>Results</p> <p>A continuous output of related and novel STs occurring worldwide in terms of the hypervirulent clonal complexes was observed both in published studies and the MLST database in this case using the eburst software, which highlights the genetically diverse nature of serogroup B strains.</p> <p>Conclusions</p> <p>With the recent dominance of serogroup B IMD seen in many countries, along with the presence of antibiotic resistance, vaccine development needs to target areas of the bacterium which tackle this widespread and heterogeneous aspect of meningococcal meningitis disease.</p
Correlation between arterial blood volume obtained by arterial spin labelling and cerebral blood volume in intracranial tumours
The stellar halo of the Galaxy
Stellar halos may hold some of the best preserved fossils of the formation
history of galaxies. They are a natural product of the merging processes that
probably take place during the assembly of a galaxy, and hence may well be the
most ubiquitous component of galaxies, independently of their Hubble type. This
review focuses on our current understanding of the spatial structure, the
kinematics and chemistry of halo stars in the Milky Way. In recent years, we
have experienced a change in paradigm thanks to the discovery of large amounts
of substructure, especially in the outer halo. I discuss the implications of
the currently available observational constraints and fold them into several
possible formation scenarios. Unraveling the formation of the Galactic halo
will be possible in the near future through a combination of large wide field
photometric and spectroscopic surveys, and especially in the era of Gaia.Comment: 46 pages, 16 figures. References updated and some minor changes.
Full-resolution version available at
http://www.astro.rug.nl/~ahelmi/stellar-halo-review.pd
Reactivation of EpsteinâBarr virus by a dual-responsive fluorescent EBNA1-targeting agent with Zn2+-chelating function
EBNA1 is the only EpsteinâBarr virus (EBV) latent protein responsible for viral genome maintenance and is expressed in all EBV-infected cells. Zn2+ is essential for oligomerization of the functional EBNA1. We constructed an EBNA1 binding peptide with a Zn2+ chelator to create an EBNA1-specific inhibitor (ZRL5P4). ZRL5P4 by itself is sufficient to reactivate EBV from its latent infection. ZRL5P4 is able to emit unique responsive fluorescent signals once it binds with EBNA1 and a Zn2+ ion. ZRL5P4 can selectively disrupt the EBNA1 oligomerization and cause nasopharyngeal carcinoma (NPC) tumor shrinkage, possibly due to EBV lytic induction. Dicer1 seems essential for this lytic reactivation. As can been seen, EBNA1 is likely to maintain NPC cell survival by suppressing viral reactivation
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