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 *

102 related articles for article (PubMed ID: 24388274)

  • 21. 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]  

  • 22. TG15 T5 allele in clinically discordant monozygotic twins with cystic fibrosis.
    Picci L; Cameran M; Scarpa M; Pradal U; Melotti P; Assael BM; Castellani C
    Am J Med Genet A; 2007 Aug; 143A(16):1936-7. PubMed ID: 17632788
    [No Abstract]   [Full Text] [Related]  

  • 23. [Genotype and phenotype of gastrointestinal symptoms analysis in children with cystic fibrosis].
    Iwańczak F; Smigiel R; Stawarski A; Pawłowicz J; Stembalska A; Mowszet K; Sasiadek M
    Pol Merkur Lekarski; 2005 Feb; 18(104):205-9. PubMed ID: 17877132
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genotype-phenotype relationship in 12 patients carrying cystic fibrosis mutation R334W.
    Antiñolo G; Borrego S; Gili M; Dapena J; Alfageme I; Reina F
    J Med Genet; 1997 Feb; 34(2):89-91. PubMed ID: 9039981
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. The Pseudomonas aeruginosa secreted protein PA2934 decreases apical membrane expression of the cystic fibrosis transmembrane conductance regulator.
    MacEachran DP; Ye S; Bomberger JM; Hogan DA; Swiatecka-Urban A; Stanton BA; O'Toole GA
    Infect Immun; 2007 Aug; 75(8):3902-12. PubMed ID: 17502391
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Phenotypic expression of genotype-phenotype correlation in cystic fibrosis patients carrying the 852del22 mutation.
    Polizzi A; Francavilla R; Castaldo G; Santostasi T; Tomaiuolo R; Manca A; De Robertis F; Mappa L; Oliverio FP; Salvatore F; Rigillo N
    Am J Med Genet A; 2005 Feb; 132A(4):434-40. PubMed ID: 15633186
    [TBL] [Abstract][Full Text] [Related]  

  • 28. HLA class II polymorphism in cystic fibrosis. A possible modifier of pulmonary phenotype.
    Aron Y; Polla BS; Bienvenu T; Dall'ava J; Dusser D; Hubert D
    Am J Respir Crit Care Med; 1999 May; 159(5 Pt 1):1464-8. PubMed ID: 10228112
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Twins and cystic fibrosis.
    Banjar H
    Saudi Med J; 2000 Sep; 21(9):889-91. PubMed ID: 11376374
    [No Abstract]   [Full Text] [Related]  

  • 30. Frequency of common CFTR gene mutations in Venezuelan patients with cystic fibrosis.
    Sánchez K; Arcia O; Matute X; Mindiola L; Chaustre I; Takiff H
    Invest Clin; 2014 Mar; 55(1):44-54. PubMed ID: 24758101
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Recurrent nasal polyps as a monosymptomatic form of cystic fibrosis associated with a novel in-frame deletion (591del18) in the CFTR gene.
    Varon R; Magdorf K; Staab D; Wahn HU; Krawczak M; Sperling K; Reis A
    Hum Mol Genet; 1995 Aug; 4(8):1463-4. PubMed ID: 7581390
    [No Abstract]   [Full Text] [Related]  

  • 33. Modulatory effect of the SLC9A3 gene on susceptibility to infections and pulmonary function in children with cystic fibrosis.
    Dorfman R; Taylor C; Lin F; Sun L; Sandford A; Paré P; Berthiaume Y; Corey M; Durie P; Zielenski J;
    Pediatr Pulmonol; 2011 Apr; 46(4):385-92. PubMed ID: 20967843
    [TBL] [Abstract][Full Text] [Related]  

  • 34. IL8 gene as modifier of cystic fibrosis: unraveling the factors which influence clinical variability.
    Furlan LL; Marson FA; Ribeiro JD; Bertuzzo CS; Salomão Junior JB; Souza DR
    Hum Genet; 2016 Aug; 135(8):881-94. PubMed ID: 27209008
    [TBL] [Abstract][Full Text] [Related]  

  • 35. CFTR mutations and host susceptibility to Pseudomonas aeruginosa lung infection.
    Pier GB
    Curr Opin Microbiol; 2002 Feb; 5(1):81-6. PubMed ID: 11834374
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Outcome of intracytoplasmic sperm injection for a couple in which the man is carrier of CFTR p.[R74W;V201M;D1270N] and p.P841R mutations and his spouse a heterozygous carrier of p.F508del mutation of the cystic fibrosis transmembrane conductance regulator gene.
    Brugnon F; Bilan F; Heraud MC; Grizard G; Janny L; Creveaux I
    Fertil Steril; 2008 Nov; 90(5):2004.e23-6. PubMed ID: 18703181
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Cystic fibrosis modifier genes related to Pseudomonas aeruginosa infection.
    Park JE; Yung R; Stefanowicz D; Shumansky K; Akhabir L; Durie PR; Corey M; Zielenski J; Dorfman R; Daley D; Sandford AJ
    Genes Immun; 2011 Jul; 12(5):370-7. PubMed ID: 21270830
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Convergent evolution and adaptation of Pseudomonas aeruginosa within patients with cystic fibrosis.
    Marvig RL; Sommer LM; Molin S; Johansen HK
    Nat Genet; 2015 Jan; 47(1):57-64. PubMed ID: 25401299
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Cystic fibrosis transmembrane conductance regulator (CFTR) gene: mutations and clinical phenotypes].
    Schwartz M
    Ugeskr Laeger; 2003 Feb; 165(9):912-6. PubMed ID: 12661515
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Pseudomonas aeruginosa-induced apoptosis is defective in respiratory epithelial cells expressing mutant cystic fibrosis transmembrane conductance regulator.
    Cannon CL; Kowalski MP; Stopak KS; Pier GB
    Am J Respir Cell Mol Biol; 2003 Aug; 29(2):188-97. PubMed ID: 12878584
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.