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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

751 related items for PubMed ID: 23613805

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Gut microbiota in adults with cystic fibrosis: Implications for the severity of the CFTR gene mutation and nutritional status.
    Durda-Masny M, Goździk-Spychalska J, Morańska K, Pawłowska N, Mazurkiewicz M, Skrzypczak I, Cofta S, Szwed A.
    J Cyst Fibros; 2024 Sep; 23(5):977-983. PubMed ID: 38960841
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. The altered gut microbiota in adults with cystic fibrosis.
    Burke DG, Fouhy F, Harrison MJ, Rea MC, Cotter PD, O'Sullivan O, Stanton C, Hill C, Shanahan F, Plant BJ, Ross RP.
    BMC Microbiol; 2017 Mar 09; 17(1):58. PubMed ID: 28279152
    [Abstract] [Full Text] [Related]

  • 5. Cystic fibrosis transmembrane conductance regulator mutations at a referral center for cystic fibrosis.
    Coutinho CA, Marson FA, Ribeiro AF, Ribeiro JD, Bertuzzo CS.
    J Bras Pneumol; 2013 Mar 09; 39(5):555-61. PubMed ID: 24310628
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Gut microbiota signatures in cystic fibrosis: Loss of host CFTR function drives the microbiota enterophenotype.
    Vernocchi P, Del Chierico F, Russo A, Majo F, Rossitto M, Valerio M, Casadei L, La Storia A, De Filippis F, Rizzo C, Manetti C, Paci P, Ercolini D, Marini F, Fiscarelli EV, Dallapiccola B, Lucidi V, Miccheli A, Putignani L.
    PLoS One; 2018 Mar 09; 13(12):e0208171. PubMed ID: 30521551
    [Abstract] [Full Text] [Related]

  • 11. An association study on contrasting cystic fibrosis endophenotypes recognizes KRT8 but not KRT18 as a modifier of cystic fibrosis disease severity and CFTR mediated residual chloride secretion.
    Stanke F, Hedtfeld S, Becker T, Tümmler B.
    BMC Med Genet; 2011 May 06; 12():62. PubMed ID: 21548936
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. 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 01; 78(3):314-318. PubMed ID: 32540817
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. 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 01; 540(2):183-90. PubMed ID: 24583165
    [Abstract] [Full Text] [Related]

  • 17. Efficacy and Safety of CFTR Corrector and Potentiator Combination Therapy in Patients with Cystic Fibrosis for the F508del-CFTR Homozygous Mutation: A Systematic Review and Meta-analysis.
    Wu HX, Zhu M, Xiong XF, Wei J, Zhuo KQ, Cheng DY.
    Adv Ther; 2019 Feb 01; 36(2):451-461. PubMed ID: 30554331
    [Abstract] [Full Text] [Related]

  • 18. Prevalence of meconium ileus marks the severity of mutations of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene.
    Dupuis A, Keenan K, Ooi CY, Dorfman R, Sontag MK, Naehrlich L, Castellani C, Strug LJ, Rommens JM, Gonska T.
    Genet Med; 2016 Apr 01; 18(4):333-40. PubMed ID: 26087176
    [Abstract] [Full Text] [Related]

  • 19. Ivacaftor in subjects with cystic fibrosis who are homozygous for the F508del-CFTR mutation.
    Flume PA, Liou TG, Borowitz DS, Li H, Yen K, Ordoñez CL, Geller DE, VX 08-770-104 Study Group.
    Chest; 2012 Sep 01; 142(3):718-724. PubMed ID: 22383668
    [Abstract] [Full Text] [Related]

  • 20. Two Small Molecules Restore Stability to a Subpopulation of the Cystic Fibrosis Transmembrane Conductance Regulator with the Predominant Disease-causing Mutation.
    Meng X, Wang Y, Wang X, Wrennall JA, Rimington TL, Li H, Cai Z, Ford RC, Sheppard DN.
    J Biol Chem; 2017 Mar 03; 292(9):3706-3719. PubMed ID: 28087700
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 38.