Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Peter Kubesch"'
Autor:
Liliana Luciano, Inka Brockhausen, Meike Lingner, Sonja Horatzek, Yu-Sing Tammy Bohn, Dietmar Schomburg, Joachim Greipel, Jens Klockgether, Christian Herrmann, Norbert Miethke, Peter Kubesch, Colin F. Davenport, Prabhakar Salunkhe, Lutz Wiehlmann, Maria Wehsling, Leo Eberl, Susanne Herrmann, Nina Cramer, Burkhard Tümmler
Publikováno v:
Environmental Microbiology. 15:191-210
Microevolution of closely related Pseudomonas aeruginosa was compared in the clone TB strains TBCF10839 and TBCF121838 which had been isolated from two unrelated individuals with cystic fibrosis who had acquired clone TB during a local outbreak. Comp
Autor:
Burkhard Tümmler, Rainer Fislage, Hubert Thole, Peter Kubesch, Annette Demmer, Tanja Brandt, Manfred Raida
Publikováno v:
The Journal of biological chemistry. 272(33)
P-glycoprotein, the overexpression of which is a major cause for the failure of cancer chemotherapy in man, recognizes and transports a broad range of structurally unrelated amphiphilic compounds. This study reports on the localization of the binding
Publikováno v:
European journal of pharmacology. 315(3)
The affinity of the multidrug resistance modulator S9788 to interact with P-glycoprotein was characterized by its ability to inhibit the photoaffinity labelling of plasma membranes of multidrug resistant chinese hamster ovary B30 cells by iodomycin.
Autor:
Horst von der Hardt, Ulrich Wulbrand, Gratiana Steinkamp, Rainer Fislage, Peter Kubesch, Nanette Kälin, Thomas Neumann, Burkhard Tümmler, Brigitte Wulf, Thilo Dörk
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 217(1)
The generalized exocrinopathy cystic fibrosis (CF) is the most common severe genetic disease in Caucasian populations. A panel of more than 700 chromosomes from German and Turkish CF patients was screened for disease-causing mutations in the cystic f
Autor:
Peter Kubesch, H. Geerlings, Thomas Neumann, H. Weißbrodt, Ulrich Wulbrand, Nanette Kälin, H. von der Hardt, Brigitte Wulf, Burkhard Tümmler, Thilo Dörk
Publikováno v:
Lancet (London, England). 341(8839)
Exocrine pancreatic insufficiency and lung infection with Pseudomonas aeruginosa are major features of cystic fibrosis (CF). This monogenic disease is caused by mutations in the CF transmembrane conductance regulator (CFTR) gene. 267 children and ado
Publikováno v:
Pediatric Research. 28:290-290
Averting initial colonization of the respiratory tract with P.aeruginosa would be of great benefit for patients with cystic fibrosis (CF). Our approach to this problem is mucosal immunization with a vaccine prepared from the OMP fraction of a PAO-1 s
Publikováno v:
Zentralblatt fur Bakteriologie, Mikrobiologie, und Hygiene. Series A, Medical microbiology, infectious diseases, virology, parasitology. 265(1-2)
The outer membrane-disorganizing agent polymyxin B nonapeptide sensitized Pseudomonas aeruginosa strains 2–40fold to ciprofloxacin, norfloxacin, and ofloxacin, and 80-200fold to nalidixic acid. Sensitized P. aeruginosa strains were nearly as suscep
Publikováno v:
Zentralblatt fur Bakteriologie, Mikrobiologie, und Hygiene. Series A, Medical microbiology, infectious diseases, virology, parasitology. 269(3)
The systemic humoral immune response in cystic fibrosis (CF) to outer membrane (OM) proteins of Pseudomonas aeruginosa was investigated as a function of the time of colonization by immunoblotting. OM proteins were prepared from bacteria grown in ion-