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753 results on '"de Vos, D."'

202. Selection and characterization of a candidate therapeutic bacteriophage that lyses the Escherichia coli 0104: H4 strain from the 2011 outbrak in Germany

Author

Meribishvili, Maia, De Vos, D., Verbeken, Gilbert, Kropinski, Andrew, Vandenheuvel, D., Lavigne, R., Wattiau, P., Mast, J., Ragimbeau, Catherine, Mossong, Joel, Scheres, Jacques, Chanishvili, N., Vaneechoutte, M, Pirnay, Jean-Paul, Hosp, Queen Astrid Mil, Mol, Lab, Technol, Cellular, Brussels, [No Value], Belgium, [No Value], Surgical clinical sciences, Specialities, Skin function and permeability, and Vriendenkring VUB

Subjects
phage therapy
Abstract

In 2011, a novel strain of O104:H4 Escherichia coli caused a serious outbreak of foodborne hemolytic uremic syndrome and bloody diarrhea in Germany. Antibiotics were of questionable use and 54 deaths occurred. Candidate therapeutic bacteriophages that efficiently lyse the E. coli O104:H4 outbreak strain could be selected rather easily from a phage bank or isolated from the environment. It is argued that phage therapy should be more considered as a potential armament against the growing threat of (resistant) bacterial infections.

Published
1970

203. Vertical systems biology: from DNA to flux and back

Author

Bevilacqua A, Sj, Wilkinson, Dimelow R, Murabito E, Rehman S, Nardelli M, van Eunen K, Rossell S, Fj, Bruggeman, Blüthgen N, De Vos D, Bouwman J, Barbara Bakker, Hv, Westerhoff, and Molecular Cell Physiology

204. Tetrasomy 15q: two marker chromosomes with no detectable alpha-satellite DNA

Author

Blennow E, Telenius H, de Vos D, Larsson C, Henriksson P, Johansson O, Np, Carter, and Magnus Nordenskjöld

Subjects
Adult, Chromosome Aberrations, Genetic Markers, Male, congenital, hereditary, and neonatal diseases and abnormalities, Chromosomes, Human, Pair 15, Chromosome Mapping, Trisomy, DNA, Satellite, Polymerase Chain Reaction, Phenotype, Child, Preschool, Karyotyping, Humans, Abnormalities, Multiple, Female, Lymphocytes, In Situ Hybridization, Fluorescence, DNA Primers, Research Article
Abstract

Two patients with specific and similar phenotypes were both found to have an unusual marker chromosome present in 70%-80% of their lymphocytes at routine cytogenetic examination. The marker chromosomes were isolated by flow sorting and were amplified by degenerate oligonucleotide-primed PCR. These libraries and a cosmid probe located at 15q26 were used to characterize the marker chromosomes by FISH. Both marker chromosomes were found to consist of duplicated chromosome material from the distal part of chromosome 15q and were identified as inv dup(15) (qter-->q23::q23-->qter) and inv dup(15) (qter-->q24::q24-->qter), respectively. Hence, the markers did not include any known centromere region, and no alpha-satellite DNA could be detected at the site of the primary constriction. Tetrasomy 15q may be a new syndrome, associated with a specific type of marker chromosome. In addition, further analyses of this type of marker chromosome might give new insight into the structure and function of the mammalian centromere.

210. Lead

Author

Wolters, J., primary and de Vos, D., additional

Published
1988
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241. Abstracts of papers Clinical Pharmacological meeting

Author

van Meyel, J. J. M., primary, Smits, P., additional, Gribnau, F. W. J., additional, Van Bortel, L. H. A. B., additional, van Herode, T., additional, Smeets, F. A. H., additional, Reneman, R. S., additional, Struyker Boudler, H. A. J., additional, Aengevaeren, W., additional, Corstens, F., additional, v. d. Werf, T., additional, Thien, Th., additional, Buijsrogge, J -P. H. C., additional, Thien, Th, additional, Hooymans, P. M., additional, Pouwels, M. J., additional, v. d. Aa, G. C. H. M., additional, Pouwbls, M. J., additional, Diepstraten, J. M. W. J., additional, Koopmans, P. P., additional, van der Aa, G. C. H. M., additional, Leeuwenkamp, O. R., additional, Van Per Wiel, H. E., additional, van der Vijgh, W. J. F., additional, Greuter, H., additional, Barto, R., additional, Netelenbos, J. C., additional, Lips, P., additional, de Vos, D., additional, Siee, P. H. Th. J., additional, Stevenson, D., additional, de Vos, P., additional, Slee, P. H. Th. J., additional, Ooslerhuis, B., additional, Nehmiz, G., additional, Cornelissen, P. J. G., additional, Zuiderwijk, P. B. M., additional, Jeuring, H. J., additional, Jonkman, J. H. G., additional, Su, C. A. P. F., additional, van Tol, R. G. L., additional, van Riel, A., additional, Kerremans, A. L. H., additional, van Kalken, C. K., additional, de Jong, J., additional, van der Hoeven, J. J. M., additional, Pinedo, H. M., additional, Kroon, C., additional, de Boer, A., additional, van der Meer, F. J. M., additional, Edelbroek, P. M., additional, Schoemaker, H. C., additional, Cohen, A. F., additional, van Steveninck, A. L., additional, Kroon, J. M., additional, Pieters, M. S. M., additional, Breimer, D. D., additional, Tukker, J. J., additional, and Mculendijk, A. J. M., additional

Published
1989
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242. Lead

Author

Wolters, J., primary and de Vos, D., additional

Published
1984
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