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 *

176 related articles for article (PubMed ID: 19726878)

  • 1. Pass the bicarb: the importance of HCO3- for mucin release.
    De Lisle RC
    J Clin Invest; 2009 Sep; 119(9):2535-7. PubMed ID: 19726878
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Normal mouse intestinal mucus release requires cystic fibrosis transmembrane regulator-dependent bicarbonate secretion.
    Garcia MA; Yang N; Quinton PM
    J Clin Invest; 2009 Sep; 119(9):2613-22. PubMed ID: 19726884
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Normal mucus formation requires cAMP-dependent HCO3- secretion and Ca2+-mediated mucin exocytosis.
    Yang N; Garcia MA; Quinton PM
    J Physiol; 2013 Sep; 591(18):4581-93. PubMed ID: 23818690
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Bicarbonate and functional CFTR channel are required for proper mucin secretion and link cystic fibrosis with its mucus phenotype.
    Gustafsson JK; Ermund A; Ambort D; Johansson ME; Nilsson HE; Thorell K; Hebert H; Sjövall H; Hansson GC
    J Exp Med; 2012 Jul; 209(7):1263-72. PubMed ID: 22711878
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mucus, mucins, and cystic fibrosis.
    Morrison CB; Markovetz MR; Ehre C
    Pediatr Pulmonol; 2019 Nov; 54 Suppl 3(Suppl 3):S84-S96. PubMed ID: 31715083
    [TBL] [Abstract][Full Text] [Related]  

  • 6. CFTR, mucins, and mucus obstruction in cystic fibrosis.
    Kreda SM; Davis CW; Rose MC
    Cold Spring Harb Perspect Med; 2012 Sep; 2(9):a009589. PubMed ID: 22951447
    [TBL] [Abstract][Full Text] [Related]  

  • 7. CFTR, bicarbonate, and the pathophysiology of cystic fibrosis.
    Borowitz D
    Pediatr Pulmonol; 2015 Oct; 50 Suppl 40():S24-S30. PubMed ID: 26335950
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Role of epithelial HCO3⁻ transport in mucin secretion: lessons from cystic fibrosis.
    Quinton PM
    Am J Physiol Cell Physiol; 2010 Dec; 299(6):C1222-33. PubMed ID: 20926781
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Eradication of small intestinal bacterial overgrowth in the cystic fibrosis mouse reduces mucus accumulation.
    De Lisle RC; Roach EA; Norkina O
    J Pediatr Gastroenterol Nutr; 2006 Jan; 42(1):46-52. PubMed ID: 16385253
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cystic fibrosis transmembrane conductance regulator is expressed in mucin granules from Calu-3 and primary human airway epithelial cells.
    LeSimple P; Goepp J; Palmer ML; Fahrenkrug SC; O'Grady SM; Ferraro P; Robert R; Hanrahan JW
    Am J Respir Cell Mol Biol; 2013 Oct; 49(4):511-6. PubMed ID: 23742042
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Intestinal bicarbonate secretion in cystic fibrosis mice.
    Clarke LL; Stien X; Walker NM
    JOP; 2001 Jul; 2(4 Suppl):263-7. PubMed ID: 11875269
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Selective activation of cystic fibrosis transmembrane conductance regulator Cl- and HCO3- conductances.
    Reddy MM; Quinton PM
    JOP; 2001 Jul; 2(4 Suppl):212-8. PubMed ID: 11875262
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Treatment of cystic fibrosis airway cells with CFTR modulators reverses aberrant mucus properties
    Morrison CB; Shaffer KM; Araba KC; Markovetz MR; Wykoff JA; Quinney NL; Hao S; Delion MF; Flen AL; Morton LC; Liao J; Hill DB; Drumm ML; O'Neal WK; Kesimer M; Gentzsch M; Ehre C
    Eur Respir J; 2022 Feb; 59(2):. PubMed ID: 34172469
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Bicarbonate conductance and pH regulatory capability of cystic fibrosis transmembrane conductance regulator.
    Poulsen JH; Fischer H; Illek B; Machen TE
    Proc Natl Acad Sci U S A; 1994 Jun; 91(12):5340-4. PubMed ID: 7515498
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cystic fibrosis: impaired bicarbonate secretion and mucoviscidosis.
    Quinton PM
    Lancet; 2008 Aug; 372(9636):415-7. PubMed ID: 18675692
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mucin secretion mediated by the cystic fibrosis gene protein, CFTR.
    Pereira MM; Dormer RL; McPherson MA
    Biochem Soc Trans; 1995 Nov; 23(4):532S. PubMed ID: 8654717
    [No Abstract]   [Full Text] [Related]  

  • 17. Bicarbonate in cystic fibrosis.
    Kunzelmann K; Schreiber R; Hadorn HB
    J Cyst Fibros; 2017 Nov; 16(6):653-662. PubMed ID: 28732801
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Acid-stimulated duodenal bicarbonate secretion involves a CFTR-mediated transport pathway in mice.
    Hogan DL; Crombie DL; Isenberg JI; Svendsen P; Schaffalitzky de Muckadell OB; Ainsworth MA
    Gastroenterology; 1997 Aug; 113(2):533-41. PubMed ID: 9247473
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Microbial-induced meprin β cleavage in MUC2 mucin and a functional CFTR channel are required to release anchored small intestinal mucus.
    Schütte A; Ermund A; Becker-Pauly C; Johansson ME; Rodriguez-Pineiro AM; Bäckhed F; Müller S; Lottaz D; Bond JS; Hansson GC
    Proc Natl Acad Sci U S A; 2014 Aug; 111(34):12396-401. PubMed ID: 25114233
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Bicarbonate secretion in the murine gallbladder--lessons for the treatment of cystic fibrosis.
    Cuthbert AW
    JOP; 2001 Jul; 2(4 Suppl):257-62. PubMed ID: 11875268
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.