4,564 research outputs found
Interacting double dark resonances in a hot atomic vapor of helium
We experimentally and theoretically study two different tripod configurations
using metastable helium (He*), with the probe field polarization
perpendicular and parallel to the quantization axis, defined by an applied weak
magnetic field. In the first case, the two dark resonances interact
incoherently and merge together into a single EIT peak with increasing coupling
power. In the second case, we observe destructive interference between the two
dark resonances inducing an extra absorption peak at the line center.Comment: 7 pages, 7 figure
Feasibility study of an Integrated Program for Aerospace vehicle Design (IPAD). Volume 4: IPAD system design
The computing system design of IPAD is described and the requirements which form the basis for the system design are discussed. The system is presented in terms of a functional design description and technical design specifications. The functional design specifications give the detailed description of the system design using top-down structured programming methodology. Human behavioral characteristics, which specify the system design at the user interface, security considerations, and standards for system design, implementation, and maintenance are also part of the technical design specifications. Detailed specifications of the two most common computing system types in use by the major aerospace companies which could support the IPAD system design are presented. The report of a study to investigate migration of IPAD software between the two candidate 3rd generation host computing systems and from these systems to a 4th generation system is included
Information Problems for Policy Analysis and Forecasting
Good information is required for policy analysis and forecasting. This paper reviews the broad range of information problems that face an analyst or forecaster. Two distinct situations are considered: (1) the need to explain the current structure of an economic sector, and (2) the requirement to predict the effects of structural changes. The difficulties considered include data revisions, conflicting results in published studies, publication biases and possibly inappropriate models and theories. Examples considered include computable general equilibrium analyses and forecasts of the effects of airline deregulation.Forecasting; Information
Microbiology of Urinary Tract Infections in Gaborone, Botswana
Objective
The microbiology and epidemiology of UTI pathogens are largely unknown in Botswana, a high prevalence HIV setting. Using laboratory data from the largest referral hospital and a private hospital, we describe the major pathogens causing UTI and their antimicrobial resistance patterns. Methods
This retrospective study examined antimicrobial susceptibility data for urine samples collected at Princess Marina Hospital (PMH), Bokamoso Private Hospital (BPH), or one of their affiliated outpatient clinics. A urine sample was included in our dataset if it demonstrated pure growth of a single organism and accompanying antimicrobial susceptibility and subject demographic data were available. Results
A total of 744 samples were included. Greater than 10% resistance was observed for amoxicillin, co-trimoxazole, amoxicillin-clavulanate, and ciprofloxacin. Resistance of E. coli isolates to ampicillin and co-trimoxazole was greater than 60% in all settings. HIV status did not significantly impact the microbiology of UTIs, but did impact antimicrobial resistance to co-trimoxazole. Conclusions
Data suggests that antimicrobial resistance has already emerged to most oral antibiotics, making empiric management of outpatient UTIs challenging. Ampicillin, co-trimoxazole, and ciprofloxacin should not be used as empiric treatment for UTI in this context. Nitrofurantoin could be used for simple cystitis; aminoglycosides for uncomplicated UTI in inpatients
Filamin C-related myopathies: pathology and mechanisms
The term filaminopathy was introduced after a truncating mutation in the dimerization domain of filamin C (FLNc) was shown to be responsible for a devastating muscle disease. Subsequently, the same mutation was found in patients from diverse ethnical origins, indicating that this specific alteration is a mutational hot spot. Patients initially present with proximal muscle weakness, while distal and respiratory muscles become affected with disease progression. Muscle biopsies of these patients show typical signs of myofibrillar myopathy, including disintegration of myofibrils and aggregation of several proteins into distinct intracellular deposits. Highly similar phenotypes were observed in patients with other mutations in Ig-like domains of FLNc that result in expression of a noxious protein. Biochemical and biophysical studies showed that the mutated domains acquire an abnormal structure causing decreased stability and eventually becoming a seed for abnormal aggregation with other proteins. The disease usually presents only after the fourth decade of life possibly as a result of ageing-related impairments in the machinery that is responsible for disposal of damaged proteins. This is confirmed by mutations in components of this machinery that cause a highly similar phenotype. Transfection studies of cultured muscle cells reflect the events observed in patient muscles and, therefore, may provide a helpful model for testing future dedicated therapeutic strategies. More recently, FLNC mutations were also found in families with a distal myopathy phenotype, caused either by mutations in the actin-binding domain of FLNc that result in increased actin-binding and non-specific myopathic abnormalities without myofibrillar myopathy pathology, or a nonsense mutation in the rod domain that leads to RNA instability, haploinsufficiency with decreased expression levels of FLNc in the muscle fibers and myofibrillar abnormalities, but not to the formation of desmin-positive protein aggregates required for the diagnosis of myofibrillar myopathy
Meshless methods for âgas â evaporating dropletâ flow modelling
The main ideas of simulation of two-phase flows, based on a combination of the conventional Lagrangian method or fully Lagrangian method (FLM) for the dispersed phase and the mesh-free vortex and thermal blob methods for the carrier phase, are summarised. A meshless method for modelling of 2D transient, non-isothermal, gasdroplet flows with phase transitions, based on a combination of the viscous-vortex and thermal-blob methods for the carrier phase with the Lagrangian approach for the dispersed phase, is described. The one-way coupled, two-fluid approach is used in the analysis. The method makes it possible to avoid the `remeshing' procedure (recalculation of flow parameters from Eulerian to Lagrangian grids) and reduces the problem to the solution of three systems of ordinary differential equations, describing the motion of viscous-vortex blobs, thermal blobs, and evaporating droplets. The gas velocity field is restored using the Biot-Savart integral. The numerical algorithm is verified against the analytical solution for a non-isothermal Lamb vortex. The method is applied to modelling of an impulse two-phase cold jet injected into a quiescent hot gas, taking into account droplet evaporation. Various flow patterns are obtained in the calculations, depending on the initial droplet size: (i) low-inertia droplets, evaporating at a higher rate, form ring-like structures and are accumulated only behind the vortex pair; (ii) large droplets move closer to the jet axis, with their sizes remaining almost unchanged; and (iii) intermediate-size droplets are accumulated in a curved band whose ends trail in the periphery behind the head of the cloud, with larger droplets being collected at the front of the two-phase region
Evidence for a Pathogenic Role of Different Mutations at Codon 188 of PRNP
Clinical and pathological changes in familial Creutzfeldt-Jakob disease (CJD) cases may be similar or indistinguishable from sporadic CJD. Therefore determination of novel mutations in PRNP remains of major importance
Generating mice with targeted mutations.
Journal ArticleMutational analysis is one of the most informative approaches available for the study of complex biological processes. It has been particularly successful in the analysis of the biology of bacteria, yeast, the nematode worm Caenorhabditis elegans and the fruit fly Drosophila melanogaster. Extension of this approach to the mouse, through informative, was far less successful relative to what has been achieved with these simpler model organisms. This is because it is not numerically practical in mice to use random mutagenesis to isolate mutations that affect a specified biological process of interest. Nonetheless, biological phenomena such as a sophisticated immune response, cancer, vascular disease or higher-order cognitive function, to mention just a few, must analyzed in organisms that show such phenomena, and for this reason geneticists and other researchers have turned to the mouse. Gene targeting, the means for creating mice with designed mutations in almost any gene, was developed as an alternative to the impractical use of random mutgenesis for pursing genetic analysis in the mouse. Now gene targeting has advanced the genomic manipulations possible in mice to a level that can be matched only in far simple organisms such as bacteria and yeast
New insights into the protein aggregation pathology in myotilinopathy by combined proteomic and immunolocalization analyses
Introduction: Myofibrillar myopathies are characterized by progressive muscle weakness and impressive abnormal protein aggregation in muscle fibers. In about 10 % of patients, the disease is caused by mutations in the MYOT gene encoding myotilin. The aim of our study was to decipher the composition of protein deposits in myotilinopathy to get new information about aggregate pathology. Results: Skeletal muscle samples from 15 myotilinopathy patients were included in the study. Aggregate and control samples were collected from muscle sections by laser microdissection and subsequently analyzed by a highly sensitive proteomic approach that enables a relative protein quantification. In total 1002 different proteins were detected. Seventy-six proteins showed a significant over-representation in aggregate samples including 66 newly identified aggregate proteins. Z-disc-associated proteins were the most abundant aggregate components, followed by sarcolemmal and extracellular matrix proteins, proteins involved in protein quality control and degradation, and proteins with a function in actin dynamics or cytoskeletal transport. Forty over-represented proteins were evaluated by immunolocalization studies. These analyses validated our mass spectrometric data and revealed different regions of protein accumulation in abnormal muscle fibers. Comparison of data from our proteomic analysis in myotilinopathy with findings in other myofibrillar myopathy subtypes indicates a characteristic basic pattern of aggregate composition and resulted in identification of a highly sensitive and specific diagnostic marker for myotilinopathy. Conclusions: Our findings i) indicate that main protein components of aggregates belong to a network of interacting proteins, ii) provide new insights into the complex regulation of protein degradation in myotilinopathy that may be relevant for new treatment strategies, iii) imply a combination of a toxic gain-of-function leading to myotilin-positive protein aggregates and a loss-of-function caused by a shift in subcellular distribution with a deficiency of myotilin at Z-discs that impairs the integrity of myofibrils, and iv) demonstrate that proteomic analysis can be helpful in differential diagnosis of protein aggregate myopathies
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