BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

142 related articles for article (PubMed ID: 16987934)

  • 1. The 8.1 ancestral MHC haplotype is associated with delayed onset of colonization in cystic fibrosis.
    Laki J; Laki I; Németh K; Ujhelyi R; Bede O; Endreffy E; Bolbás K; Gyurkovits K; Csiszér E; Sólyom E; Dobra G; Halász A; Pozsonyi E; Rajczy K; Prohászka Z; Fekete G; Füst G
    Int Immunol; 2006 Nov; 18(11):1585-90. PubMed ID: 16987934
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Relations between the frequency of the DeltaF 508 mutation and the course of pulmonary disease in cystic fibrosis patients infected with Pseudomonas aeruginosa.
    Rosenecker J
    Eur J Med Res; 2000 Aug; 5(8):356-9. PubMed ID: 10958769
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Analysis of the CFTR gene in Iranian cystic fibrosis patients: identification of eight novel mutations.
    Alibakhshi R; Kianishirazi R; Cassiman JJ; Zamani M; Cuppens H
    J Cyst Fibros; 2008 Mar; 7(2):102-9. PubMed ID: 17662673
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Polymorphisms in the lectin pathway genes as a possible cause of early chronic Pseudomonas aeruginosa colonization in cystic fibrosis patients.
    Haerynck F; Van Steen K; Cattaert T; Loeys B; Van Daele S; Schelstraete P; Claes K; Van Thielen M; De Canck I; Mahachie John JM; De Baets F
    Hum Immunol; 2012 Nov; 73(11):1175-83. PubMed ID: 22940091
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [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]  

  • 10. Ancestral haplotype 8.1 and lung disease severity in European cystic fibrosis patients.
    Corvol H; Beucher J; Boëlle PY; Busson PF; Muselet-Charlier C; Clement A; Ratjen F; Grasemann H; Laki J; Palmer CN; Elborn JS; Mehta A
    J Cyst Fibros; 2012 Jan; 11(1):63-7. PubMed ID: 21993476
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Early aggressive eradication therapy for intermittent Pseudomonas aeruginosa airway colonization in cystic fibrosis patients: 15 years experience.
    Hansen CR; Pressler T; Høiby N
    J Cyst Fibros; 2008 Nov; 7(6):523-30. PubMed ID: 18693078
    [TBL] [Abstract][Full Text] [Related]  

  • 12. National survey of molecular epidemiology of Staphylococcus aureus colonization in Belgian cystic fibrosis patients.
    Vergison A; Denis O; Deplano A; Casimir G; Claeys G; DeBaets F; DeBoeck K; Douat N; Franckx H; Gigi J; Ieven M; Knoop C; Lebeque P; Lebrun F; Malfroot A; Paucquay F; Pierard D; Van Eldere J; Struelens MJ
    J Antimicrob Chemother; 2007 May; 59(5):893-9. PubMed ID: 17341469
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Post-operative infections in cystic fibrosis and non-cystic fibrosis patients after lung transplantation.
    Bonvillain RW; Valentine VG; Lombard G; LaPlace S; Dhillon G; Wang G
    J Heart Lung Transplant; 2007 Sep; 26(9):890-7. PubMed ID: 17845927
    [TBL] [Abstract][Full Text] [Related]  

  • 14. HLA frequencies and associations in cystic fibrosis.
    Adriaanse MP; Vreugdenhil AC; Groeneweg M; Brüggenwirth HT; Castelijns SJ; van der Ent CK; Voorter CE; Tilanus MG
    Tissue Antigens; 2014 Jan; 83(1):27-31. PubMed ID: 24355005
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The 8.1 ancestral MHC haplotype is strongly associated with colorectal cancer risk.
    Tóth EK; Kocsis J; Madaras B; Bíró A; Pocsai Z; Fust G; Blaskó B; Karádi I; Adány R; Laki J
    Int J Cancer; 2007 Oct; 121(8):1744-8. PubMed ID: 17594690
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Implication of the cystic fibrosis transmembrane conductance regulator gene in infertile family members of Indian CF patients.
    Sharma N; Singh M; Acharya N; Singh SK; Thapa BR; Kaur G; Prasad R
    Biochem Genet; 2008 Dec; 46(11-12):847-56. PubMed ID: 18810634
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The combination of PCR and serology increases the diagnosis of Pseudomonas aeruginosa colonization/infection in cystic fibrosis.
    da Silva Filho LV; Tateno AF; Martins KM; Azzuz Chernishev AC; Garcia Dde O; Haug M; Meisner C; Rodrigues JC; Döring G
    Pediatr Pulmonol; 2007 Oct; 42(10):938-44. PubMed ID: 17722007
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Maintenance azithromycin treatment in pediatric patients with cystic fibrosis: long-term outcomes related to macrolide resistance and pulmonary function.
    Tramper-Stranders GA; Wolfs TF; Fleer A; Kimpen JL; van der Ent CK
    Pediatr Infect Dis J; 2007 Jan; 26(1):8-12. PubMed ID: 17195698
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cystic fibrosis is a risk factor for celiac disease.
    Walkowiak J; Blask-Osipa A; Lisowska A; Oralewska B; Pogorzelski A; Cichy W; Sapiejka E; Kowalska M; Korzon M; Szaflarska-Popławska A
    Acta Biochim Pol; 2010; 57(1):115-8. PubMed ID: 20300660
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Association of improved pulmonary phenotype in Irish cystic fibrosis patients with a 3' enhancer polymorphism in alpha-1-antitrypsin.
    Courtney JM; Plant BJ; Morgan K; Rendall J; Gallagher C; Ennis M; Kalsheker N; Elborn S; O'Connor CM
    Pediatr Pulmonol; 2006 Jun; 41(6):584-91. PubMed ID: 16617455
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.