BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

400 related articles for article (PubMed ID: 11025834)

  • 1. Mutation in the gene responsible for cystic fibrosis and predisposition to chronic rhinosinusitis in the general population.
    Wang X; Moylan B; Leopold DA; Kim J; Rubenstein RC; Togias A; Proud D; Zeitlin PL; Cutting GR
    JAMA; 2000 Oct; 284(14):1814-9. PubMed ID: 11025834
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Increased prevalence of chronic rhinosinusitis in carriers of a cystic fibrosis mutation.
    Wang X; Kim J; McWilliams R; Cutting GR
    Arch Otolaryngol Head Neck Surg; 2005 Mar; 131(3):237-40. PubMed ID: 15781764
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Increased prevalence of mutations in the cystic fibrosis transmembrane conductance regulator in children with chronic rhinosinusitis.
    Raman V; Clary R; Siegrist KL; Zehnbauer B; Chatila TA
    Pediatrics; 2002 Jan; 109(1):E13. PubMed ID: 11773581
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The prevalence of CFTR mutations in patients with chronic rhinosinusitis: A systematic review and meta-analysis.
    Yong M; Hernaiz-Leonardo JC; Alqunaee M; Quon BS; Javer A
    Clin Otolaryngol; 2022 Jan; 47(1):24-33. PubMed ID: 34664411
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Paranasal sinus size is decreased in CFTR heterozygotes with chronic rhinosinusitis.
    Calton JB; Koripella PC; Willis AL; Le CH; Chiu AG; Chang EH
    Int Forum Allergy Rhinol; 2017 Mar; 7(3):256-260. PubMed ID: 27860385
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Chronic Rhinosinusitis in Patients with Cystic Fibrosis.
    Hamilos DL
    J Allergy Clin Immunol Pract; 2016; 4(4):605-12. PubMed ID: 27393775
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Application of multiplex ARMS and SSCP/HD analysis in molecular diagnosis of cystic fibrosis in Indian patients.
    Ashavaid TF; Kondkar AA; Dherai AJ; Raghavan R; Udani SV; Udwadia ZF; Desai D
    Mol Diagn; 2005; 9(2):59-66. PubMed ID: 16137181
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Correlations between cystic fibrosis genotype and sinus disease severity in chronic rhinosinusitis.
    Abuzeid WM; Song C; Fastenberg JH; Fang CH; Ayoub N; Jerschow E; Mohabir PK; Hwang PH
    Laryngoscope; 2018 Aug; 128(8):1752-1758. PubMed ID: 29193105
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prospective analysis of cystic fibrosis transmembrane regulator mutations in adults with bronchiectasis or pulmonary nontuberculous mycobacterial infection.
    Ziedalski TM; Kao PN; Henig NR; Jacobs SS; Ruoss SJ
    Chest; 2006 Oct; 130(4):995-1002. PubMed ID: 17035430
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cystic fibrosis in Korean children:a case report identified by a quantitative pilocarpine iontophoresis sweat test and genetic analysis.
    Ahn KM; Park HY; Lee JH; Lee MG; Kim JH; Kang IJ; Lee SI
    J Korean Med Sci; 2005 Feb; 20(1):153-7. PubMed ID: 15716623
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic diagnosis in practice: From cystic fibrosis to CFTR-related disorders.
    Pagin A; Sermet-Gaudelus I; Burgel PR
    Arch Pediatr; 2020 Feb; 27 Suppl 1():eS25-eS29. PubMed ID: 32172933
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Acid and base secretion in freshly excised nasal tissue from cystic fibrosis patients with ΔF508 mutation.
    Cho DY; Hwang PH; Illek B; Fischer H
    Int Forum Allergy Rhinol; 2011; 1(2):123-7. PubMed ID: 22034590
    [TBL] [Abstract][Full Text] [Related]  

  • 13. CFTR genotype and clinical outcomes of adult patients carried as cystic fibrosis disease.
    Bonadia LC; de Lima Marson FA; Ribeiro JD; Paschoal IA; Pereira MC; Ribeiro AF; Bertuzzo CS
    Gene; 2014 May; 540(2):183-90. PubMed ID: 24583165
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Lack of association of common cystic fibrosis transmembrane conductance regulator gene mutations with primary sclerosing cholangitis.
    Gallegos-Orozco JF; E Yurk C; Wang N; Rakela J; Charlton MR; Cutting GR; Balan V
    Am J Gastroenterol; 2005 Apr; 100(4):874-8. PubMed ID: 15784035
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Comparison of radiographic and clinical characteristics of low-risk and high-risk cystic fibrosis genotypes.
    Ferril GR; Nick JA; Getz AE; Barham HP; Saavedra MT; Taylor-Cousar JL; Nichols DP; Curran-Everett D; Kingdom TT; Ramakrishnan VR
    Int Forum Allergy Rhinol; 2014 Nov; 4(11):915-20. PubMed ID: 25224556
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Population-based newborn screening for genetic disorders when multiple mutation DNA testing is incorporated: a cystic fibrosis newborn screening model demonstrating increased sensitivity but more carrier detections.
    Comeau AM; Parad RB; Dorkin HL; Dovey M; Gerstle R; Haver K; Lapey A; O'Sullivan BP; Waltz DA; Zwerdling RG; Eaton RB
    Pediatrics; 2004 Jun; 113(6):1573-81. PubMed ID: 15173476
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Role of CFTR mutation analysis in the diagnostic algorithm for cystic fibrosis.
    Ratkiewicz M; Pastore M; McCoy KS; Thompson R; Hayes D; Sheikh SI
    World J Pediatr; 2017 Apr; 13(2):129-135. PubMed ID: 28194692
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Comprehensive mutation screening in a cystic fibrosis center.
    Wine JJ; Kuo E; Hurlock G; Moss RB
    Pediatrics; 2001 Feb; 107(2):280-6. PubMed ID: 11158459
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Clinical manifestations and gene analysis of 2 Chinese children with cystic fibrosis].
    Liu JR; Peng Y; Zhao YH; Wang W; Guo Y; He JX; Zhao SY; Jiang ZF
    Zhonghua Er Ke Za Zhi; 2012 Nov; 50(11):829-33. PubMed ID: 23302613
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The cystic fibrosis transmembrane conductance regulator gene and ion channel function in patients with idiopathic pancreatitis.
    Bishop MD; Freedman SD; Zielenski J; Ahmed N; Dupuis A; Martin S; Ellis L; Shea J; Hopper I; Corey M; Kortan P; Haber G; Ross C; Tzountzouris J; Steele L; Ray PN; Tsui LC; Durie PR
    Hum Genet; 2005 Dec; 118(3-4):372-81. PubMed ID: 16193325
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.