Search Results - "Tümmler, B."

ECFS standards of care on CFTR-related disorders: Diagnostic criteria of CFTR dysfunction by Sermet-Gaudelus, I., Girodon, E., Vermeulen, F., Solomon, G.M., Melotti, P., Graeber, S.Y., Bronsveld, I., Rowe, S.M., Wilschanski, M., Tümmler, B., Cutting, G.R., Gonska, T.

“…•CFTR-related disorders are clinical entities with features of CF and evidence for CFTR dysfunction but not meeting criteria for diagnosis of CF.•The spectrum…”
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Complete genome sequence and comparative analysis of the metabolically versatile Pseudomonas putida KT2440 by Nelson, K. E., Weinel, C., Paulsen, I. T., Dodson, R. J., Hilbert, H., Martins dos Santos, V. A. P., Fouts, D. E., Gill, S. R., Pop, M., Holmes, M., Brinkac, L., Beanan, M., DeBoy, R. T., Daugherty, S., Kolonay, J., Madupu, R., Nelson, W., White, O., Peterson, J., Khouri, H., Hance, I., Lee, P. Chris, Holtzapple, E., Scanlan, D., Tran, K., Moazzez, A., Utterback, T., Rizzo, M., Lee, K., Kosack, D., Moestl, D., Wedler, H., Lauber, J., Stjepandic, D., Hoheisel, J., Straetz, M., Heim, S., Kiewitz, C., Eisen, J., Timmis, K. N., Düsterhöft, A., Tümmler, B., Fraser, C. M.

“…Summary Pseudomonas putida is a metabolically versatile saprophytic soil bacterium that has been certified as a biosafety host for the cloning of foreign…”
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Sinonasal persistence of Pseudomonas aeruginosa after lung transplantation by Mainz, J.G, Hentschel, J, Schien, C, Cramer, N, Pfister, W, Beck, J.F, Tümmler, B

“…ABSTRACT We report on two CF patients who received double lung transplantation (LTX) due to Pseudomonas aeruginosa related pulmonary destruction. Prior to LTX…”
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Friend or foe: genetic and functional characterization of plant endophytic Pseudomonas aeruginosa by Kumar, A., Munder, A., Aravind, R., Eapen, S. J., Tümmler, B., Raaijmakers, J. M.

“…Summary Endophytic Pseudomonas aeruginosa strain BP35 was originally isolated from black pepper grown in the rain forest in Kerala, India. Strain PaBP35 was…”
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200 A novel entity of a CFTR-related respiratory disease by Schulz, A, Tümmler, B

“…Objectives Nasal transepithelial potential difference measurements (NPD) ascertain the conductance of the upper respiratory epithelium for sodium and chloride…”
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ePS01.9 Nasal potential difference in adults with idiopathic non-cystic fibrosis bronchiectasis by Tümmler, B, Schulz, A, Rademacher, J, Welte, T, Ringshausen, F.C

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WS13.1 Microevolution of Pseudomonas aeruginosa in cystic fibrosis lungs by Cramer, N, Klockgether, J, Davenport, C.F, Tümmler, B

“…Objectives Serial P. aeruginosa isolates in half year intervals from 35 CF patients at our local CF clinic who became colonized with P. aeruginosa in the 1980s…”
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WS07.1 Comparison of T-RFLP, 16S rDNA sequencing and metagenomics of respiratory microbiota in patients with cystic fibrosis by Losada, P. Moran, Yang, I, Chouvarine, P, Woltemate, S, Wiehlmann, L, Hermann, M, Bals, R, Müller, L. von, Suerbaum, S, Tümmler, B

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98 The cystic fibrosis lower airways microbial metagenome by Losada, P. Moran, Chouvarine, P, Dorda, M, Hedtfeld, S, Mielke, S, Schulz, A, Wiehlmann, L, Tümmler, B

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81 Specific IgE production against Staphylococcus aureus, Escherichia coli, Hemophilus influenzae and pneumococci in cystic fibrosis patients by Dittrich, A.-M, Dzoro, S, Albrecht, M, Dopfer, C, Sauer-Heilborn, A, Ringshausen, F, Tümmler, B, Valenta, R, Hales, B.J, Mitterman, I

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138 Dysregulation of epithelial miR-148b contributes to goblet cell metaplasia, inflammation and alveolar damage in cystic fibrosis lung disease by Agrawal, R, Altamura, S, Stanke, F, Meister, M, Muley, T, Randell, S.H, Greene, C.M, Tümmler, B, Muckenthaler, M.U, Mall, M.A

“…Cystic fibrosis (CF) lung disease is primarily characterized by chronic mucus obstruction, inflammation and structural damage. While mutations in the CFTR gene…”
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37 The microbial metagenome of cystic fibrosis lower airways by Losada, P.M, Chouvarine, P, Schulz, A, Hedtfeld, S, Mielke, S, Dorda, M, Wiehlmann, L, Tümmler, B

“…The use of culture-independent microbiome analysis is expanding our view of respiratory tract infection in Cystic fibrosis (CF). The lower airways of people…”
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WS19.4 Molecular epidemiology of hot-spots of mutation in antimicrobial resistance loci of Pseudomonas aeruginosa isolates from cystic fibrosis airways by Greipel, L, Cramer, N, Klockgether, J, Dorda, M, Mielke, S, Chouvarine, P, Wiehlmann, L, Tümmler, B

“…High-throughput genome sequencing of serial isolates from cystic fibrosis (CF) airways collected over a 30-year period uncovered targets of antipseudomonal…”
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WS23.3 ICM is sensitive to detect potentiation of CFTR-mediated Cl− secretion in patients with cystic fibrosis and the G551D mutation treated with ivacaftor by Graeber, S.Y, Hug, M.J, Sommerburg, O, Mainz, J.G, Heinzmann, A, Tümmler, B, Mall, M.A

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224 Genotype-phenotype correlation of pancreatic function in children with cystic fibrosis by Sciuca, S, Turcu, O, Posselt, G, Tümmler, B

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38 Sphingoid long chain bases prevent lung infection by Pseudomonas aeruginosa by Pewzner-Jung, Y, Tabazavareh, S.T, Grassmé, H, Becker, K.A, Japtok, L, Steinmann, J, Joseph, T, Lang, S, Tümmler, B, Schuchman, E.H, Lentsch, A.B, Kleuser, B, Edwards, M.J, Futerman, A.H, Gulbins, E

“…Physiological innate defense mechanisms against lung pathogens, and their alterations in lung diseases, are mostly unknown. Tracheal and bronchial sphingosine…”
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52 Evaluation of marker proteins for quantitation of CFTR by van Barneveld, A, Stolpe, C, Schulz, A, Dittrich, A.-M, Müller, C, Tümmler, B

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152 Microevolution of the major common Pseudomonas aeruginosa clones C and PA14 in cystic fibrosis lungs by Cramer, N, Klockgether, J, Davenport, C.F, Tümmler, B

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58 Route of application plays a distinct role for the outcome of a Pseudomonas aeruginosa airway infection in cystic fibrosis mouse models by Munder, A, Wölbeling, F, Baumann, U, Gulbins, E, Tümmler, B

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WS22.6 The Pseudomonas aeruginosa pangenome: Impact of genomic diversity on bacterial pathogenicity and host response in airway infections by Dethlefsen, S, Munder, A, Bezuidt, O, Fischer, S, Hilker, R, Klockgether, J, Voigt, B, Wiölbeling, F, Hecker, M, Goesmann, A, Gulbins, E, Tümmler, B

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