BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

183 related articles for article (PubMed ID: 31583102)

  • 1. Approaching two decades of cystic fibrosis research in Qatar: a historical perspective and future directions.
    Hammoudeh S; Gadelhak W; AbdulWahab A; Al-Langawi M; Janahi IA
    Multidiscip Respir Med; 2019; 14():29. PubMed ID: 31583102
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Serum zinc concentration in cystic fibrosis patients with CFTR I1234V mutation associated with pancreatic sufficiency.
    AbdulWahab A; Abushahin A; Allangawi M; Chandra P; Abdel Rahman MO; Soliman A
    Clin Respir J; 2017 May; 11(3):305-310. PubMed ID: 26096753
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Heterogeneity of the cystic fibrosis phenotype in a large kindred family in Qatar with cystic fibrosis mutation (I1234V).
    Abdul Wahab A; Al Thani G; Dawod ST; Kambouris M; Al Hamed M
    J Trop Pediatr; 2001 Apr; 47(2):110-2. PubMed ID: 11336127
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Advances in Cystic Fibrosis Research in Qatar: A Commentary.
    Hammoudeh S; Janahi IA
    J Pers Med; 2023 Feb; 13(3):. PubMed ID: 36983631
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Faecal elastase-1 concentration in cystic fibrosis patients with CFTR I1234V mutation.
    Abdel Rahman H; Abdul Wahab A; Abdel Rahman MO; Mostafa OA
    Acta Paediatr; 2006 Sep; 95(9):1066-9. PubMed ID: 16938751
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cystic fibrosis mutation I1234V in a Qatari lady.
    Wahab AA
    J Trop Pediatr; 2003 Feb; 49(1):54-5. PubMed ID: 12630722
    [TBL] [Abstract][Full Text] [Related]  

  • 7. First report of the cystic fibrosis transmembrane conductance regulator mutation c.1521_1523delCTT (p. Phe508del) in two Qatari patients with cystic fibrosis.
    AbdulWahab A; AlNaimi A; Habra B; Janahi I
    Qatar Med J; 2021; 2021(1):24. PubMed ID: 34377682
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Spectrum of mutations of cystic fibrosis in the 22 Arab countries: A systematic review.
    Al-Sadeq D; Abunada T; Dalloul R; Fahad S; Taleb S; Aljassim K; Al Hamed FA; Zayed H
    Respirology; 2019 Feb; 24(2):127-136. PubMed ID: 30419605
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Association of IVS6A GATT polymorphism of CFTR gene with cystic fibrosis: first study in CF and normal Tunisian population.
    Chaima S; Sondess HF; Khedija B; Ahmed M; Taieb M
    Ann Biol Clin (Paris); 2020 Jun; 78(3):314-318. PubMed ID: 32540817
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in pancreatitis.
    Ooi CY; Durie PR
    J Cyst Fibros; 2012 Sep; 11(5):355-62. PubMed ID: 22658665
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A mutation in the cystic fibrosis transmembrane conductance regulator gene associated with elevated sweat chloride concentrations in the absence of cystic fibrosis.
    Mickle JE; Macek M; Fulmer-Smentek SB; Egan MM; Schwiebert E; Guggino W; Moss R; Cutting GR
    Hum Mol Genet; 1998 Apr; 7(4):729-35. PubMed ID: 9499426
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Ivacaftor: the first therapy acting on the primary cause of cystic fibrosis.
    McPhail GL; Clancy JP
    Drugs Today (Barc); 2013 Apr; 49(4):253-60. PubMed ID: 23616952
    [TBL] [Abstract][Full Text] [Related]  

  • 13. CFTR dysfunction in cystic fibrosis and chronic obstructive pulmonary disease.
    Fernandez Fernandez E; De Santi C; De Rose V; Greene CM
    Expert Rev Respir Med; 2018 Jun; 12(6):483-492. PubMed ID: 29750581
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Distribution of Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Mutations in a Cohort of Patients Residing in Palestine.
    Siryani I; Jama M; Rumman N; Marzouqa H; Kannan M; Lyon E; Hindiyeh M
    PLoS One; 2015; 10(7):e0133890. PubMed ID: 26208274
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A cystic fibrosis transmembrane conductance regulator splice variant with partial penetrance associated with variable cystic fibrosis presentations.
    Kerem E; Rave-Harel N; Augarten A; Madgar I; Nissim-Rafinia M; Yahav Y; Goshen R; Bentur L; Rivlin J; Aviram M; Genem A; Chiba-Falek O; Kraemer MR; Simon A; Branski D; Kerem B
    Am J Respir Crit Care Med; 1997 Jun; 155(6):1914-20. PubMed ID: 9196095
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Pharmacological Correction of Cystic Fibrosis: Molecular Mechanisms at the Plasma Membrane to Augment Mutant CFTR Function.
    Arora K; Naren AP
    Curr Drug Targets; 2016; 17(11):1275-81. PubMed ID: 26648081
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cystic fibrosis transmembrane conductance regulator-modifying medications: the future of cystic fibrosis treatment.
    Pettit RS
    Ann Pharmacother; 2012; 46(7-8):1065-75. PubMed ID: 22739718
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Lumacaftor and ivacaftor in the management of patients with cystic fibrosis: current evidence and future prospects.
    Kuk K; Taylor-Cousar JL
    Ther Adv Respir Dis; 2015 Dec; 9(6):313-26. PubMed ID: 26416827
    [TBL] [Abstract][Full Text] [Related]  

  • 20. On the mechanism of gating defects caused by the R117H mutation in cystic fibrosis transmembrane conductance regulator.
    Yu YC; Sohma Y; Hwang TC
    J Physiol; 2016 Jun; 594(12):3227-44. PubMed ID: 26846474
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.