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Analysis of the core part of the LPS from several strains of Proteus revealed that P. penneri strains 2, 11, 19, 107, and P. vulgaris serotypes O4 and O8 have the same structure with a new type of linkage between monosaccharides–an open-chain acetal — that was previously determined for P. vulgaris OX2 and P. penneri 17. The LPS from P. penneri strain 40 contains the same structure substituted with one additional monosaccharide:
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where (1S)-GalaNAc1 is a residue of N-acetyl- -galactosamine in the open-chain form. It is connected as a cyclic acetal to positions 4 and 6 of the galactosamine residue having a free amino group. All other sugars are in the pyranose form.  相似文献   

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The O-methylation pattern of the O polysaccharide (OPS) of the lipopolysaccharide of Pseudomonas syringae pv. phaseolicola GSPB 1552 was revealed by methylation (CD3I) analysis, Smith degradation, and NMR spectroscopy. Together with the major O repeats consisting of -rhamnopyranose ( -Rhap) and -fucofuranose ( -Fucf), there are minor repeats (30%) containing 3-O-methyl- -rhamnose ( -acofriose), which is 2-substituted in the interior repeats and occupies the terminal non-reducing end of the OPS. It was suggested that the methylated O repeats are linked to each other nearby the non-reducing end of the OPS and that the ‘biological’ O repeat of the OPS has the following structure:
Full-size image (2K)
Author Keywords: Lipopolysaccharides; O polysaccharides; O-Methylation; Phytopathogens; Pseudomonas syringae  相似文献   

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The basic idea of the source simulation technique is to replace the scatterer (or radiator by a system of simple sources located within the envelope of the original body. The extent to which the simulated field reproduces the original field depends on the degree of correspondence between the simulated and the given boundary conditions. Numerical simulations have shown that: (1) the shape of the auxiliary surface, (2) the number of sources, and (3) the way the sources are distributed are the most relevant parameters to ensure an accurate solution for the problem. In the case of the single-layer method, sources should not be positioned close to the center of the body, because the problem becomes ill-conditioned. The auxiliary surface and the scatterer should be as similar as possible in order to minimize the boundary error. With respect to the number of sources (N), there are two opposite effects: (1) if (N) is too small, the sound field is not reproduced accurately; (2) if (N) is too large, computing time increases and solution accuracy decreases. The method beaks down when excitation frequency coincides with the eigenfrequencies — a narrow range of frequencies — of the space formed by the auxiliary surface. As the auxiliary surface is frequently represented by simple surfaces (cylinder, sphere), one can easily calculate the eigenfrequencies and therefore avoid them.
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doi:10.1078/1439-1791-00125
Copyright © 2003 Urban & Fischer Verlag Published by Elsevier GmbH
Pre-dispersal seed predation and seed limitation in an annual legume
Arpád Szentesia, , and Tibor Jermya
aZoology Department, Plant Protection Institute, Hungarian Academy of Sciences, Budapest, Hungary  相似文献   

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Storage of human lymphocytes by freezing in serum alone     
S. C. Knight  J. Farrant  L. E. M. McGann 《Cryobiology》1976,13(6):656-657
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Edred John Henry Corner (1906–1996): a pioneer in tropical mycology     
Roy Watling   《Mycological Research》2001,105(12):1533-1536
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Diazomethane as a highly selective fatty acid methylating reagent for use in gas chromatographic analysis     
Hans W. Mueller 《Journal of chromatography. B, Analytical technologies in the biomedical and life sciences》1996,679(1-2)
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RREB1, a Ras Responsive Element Binding Protein, Maps to Human Chromosome 6p25     
Arunthathi Thiagalingam  Christoph Lengauer  Stephen B. Baylin  Barry D. Nelkin 《Genomics》1997,45(3):630
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Immune responses to protozoan parasites and its relevance to diagnosis in immunocompromised patients     
Alexander W. Pfaff  Ermanno Candolfi 《European journal of protistology》2003,39(4):428-434
The parasitology includes different parasites, of which some are very severe, which have a development in the blood, inside the cells and visible after coloration (Plasmodium, Babesia, Leishmania, Toxoplasma) or mobiles, outside the cells (Trypanosoma, microfilariae). The diagnosis of these parasites is the first aim of the biological technics. Direct diagnosis, under the microscope, allows to identifie the parasite, its stage of development, and the parasitaemia, which is essential to the prognosis and the therapeutic outcome.The technics include the direct examination to identify the extra cellular parasites, which are mobile among the blood red cells, or thin and thick smear, after coloration. It is often useful to use other technics, such as filtration, culture or animal inoculation. Recently, the molecular biology increased the sensitivity and the specificity of classical methods. Such progress, available by some laboratories, must be adapted to the methods of emergency and low cost diagnosis. In some cases of pauciparasitism or retrospective diagnosis, serological methods are useful to detect the trail of parasites by circulating antigens or antibodies.
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doi:10.1078/0932-4739-00016
Copyright © 2003 Urban & Fischer Verlag Published by Elsevier GmbH
Immune responses to protozoan parasites and its relevance to diagnosis in immunocompromised patients
Alexander W. Pfaffa, , and Ermanno Candolfia
aInstitut de Parasitologie et Pathologie Tropicale, 3 rue Koeberlé, 67000 Strasbourg, France  相似文献   

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Risk management in the hospital, which is one of the referentiels of the ANAES accreditation manual, may be considered on two levels. Firstly, risk management may be approached globally, in the same way as it is tackled in the accreditation process. Secondly, risk management may be more definite. A specific risk chosen in accordance with the priorities of a particular plan may be dealt with individually. In this respect, the tranfusion process allows the risk management method to be tested and developed.

Résumé

La gestion des risques est mise en œuvre dans le cadre d'un projet d'établissement. Elle représente l'un des référentiels du manuel d'accréditation de l'ANAES. Le dispositif de gestion des risques peut être envisagé selon deux niveaux. Le premier concerne l'approche globale du risque, telle qu'elle a été expérimentée, conformément au référentiel d'accréditation. Le second, dans l'objectif d'une approche globale, consiste à gérer un risque spécifique choisi selon les priorités, les besoins, ou encore dans le cadre d'une planification. À cet égard, le processus transfusionnel permet l'expérimentation et le développement d'une culture du risque transposable. © 1999 Elsevier, Paris
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doi:10.1016/S1297-9570(05)80036-6
Copyright © 2005 Published by Elsevier SAS
Convergence des référentiels de qualité et implications pour la fonction technique biomédicale
A. Achmirowicz, P.-Y. Delobel, C. Kichenassamy-Appou and G. Farges,

Available online 10 March 2006.

References

Paris Anaes, Manuel d'accréditation des établissements de santé http://www.anaes.fr (avril 1999).
Décret no 2001-1154 du 5 décembre 2001 relatif à l'obligation, à la maintenance et au contrôle de qualité des dispositifs médicaux, prévu à l'article L.5212-1 du Code de la santé publique, JO no 284 du 7 décembre 2001. http://www.legifrance.gouv.fr.
Loi no 2004-810 du 13 août 2004 relative à l'Assurance maladie, JO no 190 du 17 août 2004. http://www.legifrance.gouv.fr.
Ordonnance no 96-346 du 24 avril 1996 portant réforme de l'hospitalisation publique et privée, JO no 98 du 25 avril 1996. http://www. legifrance.gouv.fr.
NF Norme, EN ISO 9001, Système de management de la qualité, Éditions Afnor (Décembre 2002).
G. Farges, G. Wahart, J.-M. Denax and H. Métayer, Guide des bonnes pratiques biomédicales en établissements de santé, ITBM-RBM News Vol. 23, Éditions Elsevier (2002) Suppl. 2.
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