8,728 research outputs found
Scheduling strategies for LTE uplink with flow behaviour analysis
Long Term Evolution (LTE) is a cellular technology developed to support\ud
diversity of data traffic at potentially high rates. It is foreseen to extend the capacity and improve the performance of current 3G cellular networks. A key\ud
mechanism in the LTE traffic handling is the packet scheduler, which is in charge of allocating resources to active flows in both the frequency and time dimension. In this paper we present a performance comparison of two distinct scheduling schemes for LTE uplink (fair fixed assignment and fair work-conserving) taking into account both packet level characteristics and flow level dynamics due to the random user behaviour. For that purpose, we apply a combined analytical/simulation approach which enables fast evaluation of performance measures such as mean flow transfer times manifesting the impact of resource allocation strategies. The results show that the resource allocation strategy has a crucial impact on performance and that some trends are observed only if flow level dynamics are considered
Changes in pathogen prevalence and resistance related to the introduction of macrolide maintenance therapy in cystic fibrosis patients
Out of Equilibrium Solutions in the -Hamiltonian Mean Field model
Out of equilibrium magnetised solutions of the -Hamiltonian Mean Field
(-HMF) model are build using an ensemble of integrable uncoupled pendula.
Using these solutions we display an out-of equilibrium phase transition using a
specific reduced set of the magnetised solutions
High orders of Weyl series for the heat content
This article concerns the Weyl series of spectral functions associated with
the Dirichlet Laplacian in a -dimensional domain with a smooth boundary. In
the case of the heat kernel, Berry and Howls predicted the asymptotic form of
the Weyl series characterized by a set of parameters. Here, we concentrate on
another spectral function, the (normalized) heat content. We show on several
exactly solvable examples that, for even , the same asymptotic formula is
valid with different values of the parameters. The considered domains are
-dimensional balls and two limiting cases of the elliptic domain with
eccentricity : A slightly deformed disk () and an
extremely prolonged ellipse (). These cases include 2D domains
with circular symmetry and those with only one shortest periodic orbit for the
classical billiard. We analyse also the heat content for the balls in odd
dimensions for which the asymptotic form of the Weyl series changes
significantly.Comment: 20 pages, 1 figur
Genetics of Amyotrophic Lateral Sclerosis
La sclérose latérale amyotrophique (SLA) est la maladie des neurones moteurs la plus fréquente, affectant 4-6 individus par 100,000 habitants à l’échelle mondiale. La maladie se caractérise par une faiblesse et une atrophie musculaire suite à la dégénérescence des neurones du cortex moteur, tronc cérébral et moelle épinière. Les personnes atteintes développent les premiers symptômes à l’âge adulte et la maladie progresse sur une période de trois à cinq ans. Il a été répertorié qu’environ 10% des patients ont une histoire familiale de SLA; 90% des gens affectés le sont donc de façon sporadique. La découverte il y a 19 ans de mutations dans le gène zinc/copper superoxide dismutase (SOD1), présentes dans 15-20% des cas familiaux de SLA et environ 2% du total des individus affectés, a été l’événement déclencheur pour la découverte de variations génétiques responsables de la maladie. La recherche sur la génétique de la SLA a connu une progression rapide ces quatre dernières années avec l’identification de mutations dans de nouveaux gènes. Toutefois, même si certains de ces gènes ont été démontrés comme réellement liés à la maladie, la contribution d’autres gènes demeure incertaine puisque les résultats publiés de ceux-ci n’ont pas, à ce jour, été répliqués. Une portion substantielle de cas reste cependant à être génétiquement expliquée, et aucun traitement à ce jour n’a été démontré comme étant efficace pour remédier, atténuer ou prévenir la maladie.
Le but du projet de recherche de doctorat était d’identifier de nouveaux gènes mutés dans la SLA, tout en évaluant la contribution de gènes nouvellement identifiés chez une importante cohorte multiethnique de cas familiaux et sporadiques. Les résultats présentés sont organisés en trois sections différentes. Dans un premier temps, la contribution de mutations présentes dans le gène FUS est évaluée chez les patients familiaux, sporadiques et juvéniles de SLA. Précisément, de nouvelles mutations sont rapportées et la proportion de mutations retrouvées chez les cas familiaux et sporadiques de SLA est évaluée. De plus, une nouvelle mutation est rapportée dans un cas juvénile de SLA; cette étude de cas est discutée. Dans un deuxième temps, de nouvelles avenues génétiques sont explorées concernant le gène SOD1. En effet, une nouvelle mutation complexe est rapportée chez une famille française de SLA. De plus, la possibilité qu’une mutation présente dans un autre gène impliqué dans la SLA ait un impact sur l’épissage du gène SOD1 est évaluée. Finalement, la dernière section explique la contribution de nouveaux gènes candidats chez les patients atteints de SLA. Spécifiquement, le rôle des gènes OPTN, SIGMAR1 et SORT1 dans le phénotype de SLA est évalué.
Il est souhaité que nos résultats combinés avec les récents développements en génétique et biologie moléculaire permettent une meilleure compréhension du mécanisme pathologique responsable de cette terrible maladie tout en guidant le déploiement de thérapies suite à l’identification des cibles appropriées.Amyotrophic lateral sclerosis (ALS) is the most common of motor neuron diseases, affecting 4-6 individuals per 100,000 individuals worldwide. ALS is characterized by muscle weakness and atrophy caused by the degeneration of neurons located in the motor cortex, brain stem and spinal cord. This fatal disease generally has an adult onset and progresses over a three to five year period. While 10% of patients affected have a family history of the disease, 90% of cases do not and are considered sporadic. The finding of mutations in the zinc/copper superoxide dismutase gene (SOD1) gene 19 years ago in about 15-20% of familial ALS (FALS) patients and approximately 2% of overall cases developed the interest of identifying rare genetics variants causing the disease. The ALS research field experienced a rapid progression during the last four years as mutations in new genes have been identified. While mutations in some of those new genes have been clearly linked to ALS, the role of others is still questionable and so far has not been positively replicated in other populations. Importantly, a significant portion of cases still need to be genetically explained and, unfortunately, there is still no effective treatment to cure, attenuate or prevent the disease.
The aim of this Ph.D research project was to identify new ALS mutated genes while analysing the causative role of other newly identified genes in a large familial and sporadic ALS cohort of different origins. The results presented here are categorized into three different sections. First, the contribution of FUS mutations to familial, sporadic and juvenile ALS is analysed. Specifically, new FUS mutations are reported in ALS cases and the proportions of variants present in the tested familial and sporadic ALS cohorts are assessed. In addition, a new mutation is reported in a juvenile ALS patient, and this interesting case is discussed. Second, new genetic avenues are explored for the SOD1 gene. Precisely, a new and complex SOD1 mutation is reported in a French ALS family. Moreover, the possibility that other ALS mutated genes influence SOD1 splicing events is evaluated. Third, the contribution of new candidate genes is evaluated. Precisely, the contribution of OPTN, SIGMAR1 and SORT1 genes to the ALS phenotype is assessed.
Hopefully, our different findings combined with recent developments in genetics and molecular biology will permit a better understanding of the pathological mechanisms involved in the disease and will lead to the identification of the right targets in order to develop appropriate therapeutics for ALS patients
Hospital-related costs of sepsis around the world:A systematic review exploring the economic burden of sepsis
Aim: The aim of this study was to examine the quality of manuscripts reporting sepsis health care costs and to provide an overview of hospital-related expenditures for sepsis in adult patients around the world. Methods: We systematically searched the PubMed, EMBASE, Cochrane and Google Scholar to identify relevant studies between January 2010 and January 2022. We selected articles that provided costs and cost-effectiveness analyses, defined sepsis and described their cost calculation method. All costs were adjusted to 2020 US dollars. Medians and interquartile ranges (IQRs) for various costs of sepsis were calculated. The quality of economic studies was assessed using the Drummond 10-item checklist. Results: Overall, 26 studies met our eligibility criteria. The mean total hospital costs per patient varied largely, between €1101 and €91,951. The median (IQR) of the total sepsis costs per country were €36,191 (€17,158 - €53,349), which equals €50 (€34 - €84) per capita annually. The relative amount of healthcare budget spent on sepsis was 2.65%, which equals 0.33% of the gross national product (GNP). Conclusion: While general sepsis costs are high, there is considerable variability between countries regarding the costs of sepsis. Further studies examining the impact on sepsis costs, especially on the general ward, can help justify, design and monitor initiatives on prevention, diagnosis, and treatment of this time-critical and potentially preventable disease
Rigorous investigation of the reduced density matrix for the ideal Bose gas in harmonic traps by a loop-gas-like approach
In this paper, we rigorously investigate the reduced density matrix (RDM)
associated to the ideal Bose gas in harmonic traps. We present a method based
on a sum-decomposition of the RDM allowing to treat not only the isotropic
trap, but also general anisotropic traps. When focusing on the isotropic trap,
the method is analogous to the loop-gas approach developed by W.J. Mullin in
[38]. Turning to the case of anisotropic traps, we examine the RDM for some
anisotropic trap models corresponding to some quasi-1D and quasi-2D regimes.
For such models, we bring out an additional contribution in the local density
of particles which arises from the mesoscopic loops. The close connection with
the occurrence of generalized-BEC is discussed. Our loop-gas-like approach
provides relevant information which can help guide numerical investigations on
highly anisotropic systems based on the Path Integral Monte Carlo (PIMC)
method.Comment: v3: Minor modifications of v2. v2: Major modifications: the former
version (v1) has been completely rewritten. New results concerning the
anisotropic traps and generalized Bose-Einstein condensation have been added.
The connection with the loop-gas approach is further discussed. 40 page
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