These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

222 related articles for article (PubMed ID: 20927127)

  • 1. PTX3 genetic variations affect the risk of Pseudomonas aeruginosa airway colonization in cystic fibrosis patients.
    Chiarini M; Sabelli C; Melotti P; Garlanda C; Savoldi G; Mazza C; Padoan R; Plebani A; Mantovani A; Notarangelo LD; Assael BM; Badolato R
    Genes Immun; 2010 Dec; 11(8):665-70. PubMed ID: 20927127
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Proteolytic cleavage of the long pentraxin PTX3 in the airways of cystic fibrosis patients.
    Hamon Y; Jaillon S; Person C; Giniès JL; Garo E; Bottazzi B; Ghamrawi S; Urban T; Subra JF; Bouchara JP; Mantovani A; Jeannin P; Delneste Y
    Innate Immun; 2013 Dec; 19(6):611-22. PubMed ID: 23475792
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Association of beta-defensin-1 gene polymorphisms with Pseudomonas aeruginosa airway colonization in cystic fibrosis.
    Tesse R; Cardinale F; Santostasi T; Polizzi A; Manca A; Mappa L; Iacoviello G; De Robertis F; Logrillo VP; Armenio L
    Genes Immun; 2008 Jan; 9(1):57-60. PubMed ID: 17960157
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical and microbiological characteristics of cystic fibrosis adults never colonized by Pseudomonas aeruginosa: Analysis of the French CF registry.
    Vongthilath R; Richaud Thiriez B; Dehillotte C; Lemonnier L; Guillien A; Degano B; Dalphin ML; Dalphin JC; Plésiat P
    PLoS One; 2019; 14(1):e0210201. PubMed ID: 30620748
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Response of CFTR-deficient mice to long-term chronic Pseudomonas aeruginosa infection and PTX3 therapy.
    Paroni M; Moalli F; Nebuloni M; Pasqualini F; Bonfield T; Nonis A; Mantovani A; Garlanda C; Bragonzi A
    J Infect Dis; 2013 Jul; 208(1):130-8. PubMed ID: 23087427
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cystic fibrosis transmembrane conductance regulator (CFTR)-mediated residual chloride secretion does not protect against early chronic Pseudomonas aeruginosa infection in F508del homozygous cystic fibrosis patients.
    Derichs N; Mekus F; Bronsveld I; Bijman J; Veeze HJ; von der Hardt H; Tummler B; Ballmann M
    Pediatr Res; 2004 Jan; 55(1):69-75. PubMed ID: 14605249
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Harnessing Neutrophil Survival Mechanisms during Chronic Infection by
    Marteyn BS; Burgel PR; Meijer L; Witko-Sarsat V
    Front Cell Infect Microbiol; 2017; 7():243. PubMed ID: 28713772
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Pseudomonas aeruginosa triggers CFTR-mediated airway surface liquid secretion in swine trachea.
    Luan X; Campanucci VA; Nair M; Yilmaz O; Belev G; Machen TE; Chapman D; Ianowski JP
    Proc Natl Acad Sci U S A; 2014 Sep; 111(35):12930-5. PubMed ID: 25136096
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The therapeutic potential of the humoral pattern recognition molecule PTX3 in chronic lung infection caused by Pseudomonas aeruginosa.
    Moalli F; Paroni M; Véliz Rodriguez T; Riva F; Polentarutti N; Bottazzi B; Valentino S; Mantero S; Nebuloni M; Mantovani A; Bragonzi A; Garlanda C
    J Immunol; 2011 May; 186(9):5425-34. PubMed ID: 21441447
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Infections with Pseudomonas aeruginosa in patients with cystic fibrosis.
    Tümmler B; Bosshammer J; Breitenstein S; Brockhausen I; Gudowius P; Herrmann C; Herrmann S; Heuer T; Kubesch P; Mekus F; Römling U; Schmidt KD; Spangenberg C; Walter S
    Behring Inst Mitt; 1997 Feb; (98):249-55. PubMed ID: 9382747
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Fcgamma receptor IIA genotype and susceptibility to P. aeruginosa infection in patients with cystic fibrosis.
    De Rose V; Arduino C; Cappello N; Piana R; Salmin P; Bardessono M; Goia M; Padoan R; Bignamini E; Costantini D; Pizzamiglio G; Bennato V; Colombo C; Giunta A; Piazza A
    Eur J Hum Genet; 2005 Jan; 13(1):96-101. PubMed ID: 15367919
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cysteamine re-establishes the clearance of Pseudomonas aeruginosa by macrophages bearing the cystic fibrosis-relevant F508del-CFTR mutation.
    Ferrari E; Monzani R; Villella VR; Esposito S; Saluzzo F; Rossin F; D'Eletto M; Tosco A; De Gregorio F; Izzo V; Maiuri MC; Kroemer G; Raia V; Maiuri L
    Cell Death Dis; 2017 Jan; 8(1):e2544. PubMed ID: 28079883
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cystic fibrosis transmembrane conductance regulator and caveolin-1 regulate epithelial cell internalization of Pseudomonas aeruginosa.
    Bajmoczi M; Gadjeva M; Alper SL; Pier GB; Golan DE
    Am J Physiol Cell Physiol; 2009 Aug; 297(2):C263-77. PubMed ID: 19386787
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Analysis of DEFB1 regulatory SNPs in cystic fibrosis patients from North-Eastern Italy.
    Segat L; Morgutti M; Athanasakis E; Trevisiol C; Amaddeo A; Poli F; Crovella S
    Int J Immunogenet; 2010 Jun; 37(3):169-75. PubMed ID: 20193032
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Phagocytic and signaling innate immune receptors: are they dysregulated in cystic fibrosis in the fight against Pseudomonas aeruginosa?
    Sallenave JM
    Int J Biochem Cell Biol; 2014 Jul; 52():103-7. PubMed ID: 24508137
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The role of the CFTR in susceptibility to Pseudomonas aeruginosa infections in cystic fibrosis.
    Goldberg JB; Pier GB
    Trends Microbiol; 2000 Nov; 8(11):514-20. PubMed ID: 11121762
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Innate lung defenses and compromised Pseudomonas aeruginosa clearance in the malnourished mouse model of respiratory infections in cystic fibrosis.
    Yu H; Nasr SZ; Deretic V
    Infect Immun; 2000 Apr; 68(4):2142-7. PubMed ID: 10722612
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cystic fibrosis transmembrane conductance regulator channel dysfunction in non-cystic fibrosis bronchiectasis.
    Bienvenu T; Sermet-Gaudelus I; Burgel PR; Hubert D; Crestani B; Bassinet L; Dusser D; Fajac I
    Am J Respir Crit Care Med; 2010 May; 181(10):1078-84. PubMed ID: 20167849
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Association of interleukin-10 gene haplotypes with Pseudomonas aeruginosa airway colonization in cystic fibrosis.
    Tesse R; Cardinale F; Santostasi T; Polizzi A; Mappa L; Manca A; De Robertis F; Silecchia O; Armenio L
    J Cyst Fibros; 2008 Jul; 7(4):329-332. PubMed ID: 18093884
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic Association With
    Nourkami-Tutdibi N; Freitag K; Zemlin M; Tutdibi E
    Front Immunol; 2021; 12():587313. PubMed ID: 33679736
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 12.