Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 93

1.

Genome Sequence of Pseudomonas aeruginosa Strain DK1-NH57388A, a Stable Mucoid Cystic Fibrosis Isolate.

Norman A, Ciofu O, Amador CI, Høiby N, Jelsbak L.

Genome Announc. 2016 Feb 25;4(1). pii: e00008-16. doi: 10.1128/genomeA.00008-16.

2.

Bacteriophages φMR299-2 and φNH-4 can eliminate Pseudomonas aeruginosa in the murine lung and on cystic fibrosis lung airway cells.

Alemayehu D, Casey PG, McAuliffe O, Guinane CM, Martin JG, Shanahan F, Coffey A, Ross RP, Hill C.

MBio. 2012 Mar 6;3(2):e00029-12. doi: 10.1128/mBio.00029-12. Print 2012.

3.

Draft Genome Sequence of a Mucoid Isolate of Pseudomonas aeruginosa Strain C7447m from a Patient with Cystic Fibrosis.

Yin Y, Withers TR, Johnson SL, Yu HD.

Genome Announc. 2013 Oct 10;1(5). pii: e00837-13. doi: 10.1128/genomeA.00837-13.

4.

Investigation of the algT operon sequence in mucoid and non-mucoid Pseudomonas aeruginosa isolates from 115 Scandinavian patients with cystic fibrosis and in 88 in vitro non-mucoid revertants.

Ciofu O, Lee B, Johannesson M, Hermansen NO, Meyer P, Høiby N; Scandinavian Cystic Fibrosis Study Consortium.

Microbiology. 2008 Jan;154(Pt 1):103-13. doi: 10.1099/mic.0.2007/010421-0.

PMID:
18174130
6.

Effects of intratracheal administration of novispirin G10 on a rat model of mucoid Pseudomonas aeruginosa lung infection.

Song Z, Wu H, Mygind P, Raventos D, Sonksen C, Kristensen HH, Høiby N.

Antimicrob Agents Chemother. 2005 Sep;49(9):3868-74.

7.

Mucoid conversion of Pseudomonas aeruginosa by hydrogen peroxide: a mechanism for virulence activation in the cystic fibrosis lung.

Mathee K, Ciofu O, Sternberg C, Lindum PW, Campbell JI, Jensen P, Johnsen AH, Givskov M, Ohman DE, Molin S, Høiby N, Kharazmi A.

Microbiology. 1999 Jun;145 ( Pt 6):1349-57.

PMID:
10411261
8.

Strain-specific proteome responses of Pseudomonas aeruginosa to biofilm-associated growth and to calcium.

Patrauchan MA, Sarkisova SA, Franklin MJ.

Microbiology. 2007 Nov;153(Pt 11):3838-51.

PMID:
17975093
9.

Genome Sequence of Mucoid Pseudomonas aeruginosa Strain FRD1.

Wang D, Hildebrand F, Ye L, Wei Q, Ma LZ.

Genome Announc. 2015 Apr 23;3(2). pii: e00376-15. doi: 10.1128/genomeA.00376-15.

10.

Longitudinal development of mucoid Pseudomonas aeruginosa infection and lung disease progression in children with cystic fibrosis.

Li Z, Kosorok MR, Farrell PM, Laxova A, West SE, Green CG, Collins J, Rock MJ, Splaingard ML.

JAMA. 2005 Feb 2;293(5):581-8.

PMID:
15687313
11.

Complete Genome Sequence of Persistent Cystic Fibrosis Isolate Pseudomonas aeruginosa Strain RP73.

Jeukens J, Boyle B, Bianconi I, Kukavica-Ibrulj I, Tümmler B, Bragonzi A, Levesque RC.

Genome Announc. 2013 Aug 1;1(4). pii: e00568-13. doi: 10.1128/genomeA.00568-13.

12.

Pseudomonas aeruginosa exploits lipid A and muropeptides modification as a strategy to lower innate immunity during cystic fibrosis lung infection.

Cigana C, Curcurù L, Leone MR, Ieranò T, Lorè NI, Bianconi I, Silipo A, Cozzolino F, Lanzetta R, Molinaro A, Bernardini ML, Bragonzi A.

PLoS One. 2009 Dec 23;4(12):e8439. doi: 10.1371/journal.pone.0008439.

14.

Estrogen aggravates inflammation in Pseudomonas aeruginosa pneumonia in cystic fibrosis mice.

Wang Y, Cela E, Gagnon S, Sweezey NB.

Respir Res. 2010 Nov 30;11:166. doi: 10.1186/1465-9921-11-166.

15.
16.

Complete Genome Sequence of Pseudomonas aeruginosa Mucoid Strain FRD1, Isolated from a Cystic Fibrosis Patient.

Silo-Suh LA, Suh SJ, Ohman DE, Wozniak DJ, Pridgeon JW.

Genome Announc. 2015 Mar 19;3(2). pii: e00153-15. doi: 10.1128/genomeA.00153-15.

17.

Genotypic and phenotypic analyses of a Pseudomonas aeruginosa chronic bronchiectasis isolate reveal differences from cystic fibrosis and laboratory strains.

Varga JJ, Barbier M, Mulet X, Bielecki P, Bartell JA, Owings JP, Martinez-Ramos I, Hittle LE, Davis MR Jr, Damron FH, Liechti GW, Puchałka J, dos Santos VA, Ernst RK, Papin JA, Albertí S, Oliver A, Goldberg JB.

BMC Genomics. 2015 Oct 30;16:883. doi: 10.1186/s12864-015-2069-0.

20.

Supplemental Content

Support Center