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

146 related items for PubMed ID: 18369642

  • 1. Characterisation of electrogenic nutrient absorption in the Cftr TgH(neoim)Hgu mouse model.
    Tóth B, Leonhard-Marek S, Hedrich HJ, Breves G.
    J Comp Physiol B; 2008 Aug; 178(6):705-12. PubMed ID: 18369642
    [Abstract] [Full Text] [Related]

  • 2. Very mild disease phenotype of congenic CftrTgH(neoim)Hgu cystic fibrosis mice.
    Tóth B, Wilke M, Stanke F, Dorsch M, Jansen S, Wedekind D, Charizopoulou N, Bot A, Burmester M, Leonhard-Marek S, de Jonge HR, Hedrich HJ, Breves G, Tümmler B.
    BMC Genet; 2008 Apr 09; 9():28. PubMed ID: 18400105
    [Abstract] [Full Text] [Related]

  • 3. Spontaneous rescue from cystic fibrosis in a mouse model.
    Charizopoulou N, Wilke M, Dorsch M, Bot A, Jorna H, Jansen S, Stanke F, Hedrich HJ, de Jonge HR, Tümmler B.
    BMC Genet; 2006 Mar 29; 7():18. PubMed ID: 16571105
    [Abstract] [Full Text] [Related]

  • 4. Instability of the insertional mutation in CftrTgH(neoim)Hgu cystic fibrosis mouse model.
    Charizopoulou N, Jansen S, Dorsch M, Stanke F, Dorin JR, Hedrich HJ, Tümmler B.
    BMC Genet; 2004 Apr 21; 5():6. PubMed ID: 15102331
    [Abstract] [Full Text] [Related]

  • 5. Characterisation of chloride currents across the proximal colon in CftrTgH(neoim)1Hgu congenic mice.
    Bleich EM, Leonhard-Marek S, Beyerbach M, Breves G.
    J Comp Physiol B; 2007 Jan 21; 177(1):61-73. PubMed ID: 16868751
    [Abstract] [Full Text] [Related]

  • 6. Small intestinal glucose absorption in cystic fibrosis: a study in human and transgenic DeltaF508 cystic fibrosis mouse tissues.
    Hardcastle J, Harwood MD, Taylor CJ.
    J Pharm Pharmacol; 2004 Mar 21; 56(3):329-38. PubMed ID: 15025858
    [Abstract] [Full Text] [Related]

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

  • 8. Strain-dependent pulmonary gene expression profiles of a cystic fibrosis mouse model.
    Haston CK, Cory S, Lafontaine L, Dorion G, Hallett MT.
    Physiol Genomics; 2006 Apr 13; 25(2):336-45. PubMed ID: 16614460
    [Abstract] [Full Text] [Related]

  • 9. Identification of transport abnormalities in duodenal mucosa and duodenal enterocytes from patients with cystic fibrosis.
    Pratha VS, Hogan DL, Martensson BA, Bernard J, Zhou R, Isenberg JI.
    Gastroenterology; 2000 Jun 13; 118(6):1051-60. PubMed ID: 10833480
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Quantitative expression analyses of candidates for alternative anion conductance in cystic fibrosis mouse models.
    Braun J, Mundhenk L, Range F, Gruber AD.
    J Cyst Fibros; 2010 Sep 13; 9(5):351-64. PubMed ID: 20624691
    [Abstract] [Full Text] [Related]

  • 12. Intestinal bicarbonate secretion in cystic fibrosis mice.
    Clarke LL, Stien X, Walker NM.
    JOP; 2001 Jul 13; 2(4 Suppl):263-7. PubMed ID: 11875269
    [Abstract] [Full Text] [Related]

  • 13. Defective CFTR promotes intestinal proliferation via inhibition of the hedgehog pathway during cystic fibrosis.
    Liu K, Wang X, Zou C, Zhang J, Chen H, Tsang L, Yu MK, Chung YW, Wang J, Dai Y, Liu Y, Zhang X.
    Cancer Lett; 2019 Apr 01; 446():15-24. PubMed ID: 30639531
    [Abstract] [Full Text] [Related]

  • 14. Rectal potential difference and the functional expression of CFTR in the gastrointestinal epithelia in cystic fibrosis mouse models.
    Weiner SA, Caputo C, Bruscia E, Ferreira EC, Price JE, Krause DS, Egan ME.
    Pediatr Res; 2008 Jan 01; 63(1):73-8. PubMed ID: 18043508
    [Abstract] [Full Text] [Related]

  • 15. Biokinetics of nanoparticles and susceptibility to particulate exposure in a murine model of cystic fibrosis.
    Geiser M, Stoeger T, Casaulta M, Chen S, Semmler-Behnke M, Bolle I, Takenaka S, Kreyling WG, Schulz H.
    Part Fibre Toxicol; 2014 Apr 24; 11():19. PubMed ID: 24758489
    [Abstract] [Full Text] [Related]

  • 16. Extracellular UTP stimulates electrogenic bicarbonate secretion across CFTR knockout gallbladder epithelium.
    Clarke LL, Harline MC, Gawenis LR, Walker NM, Turner JT, Weisman GA.
    Am J Physiol Gastrointest Liver Physiol; 2000 Jul 24; 279(1):G132-8. PubMed ID: 10898755
    [Abstract] [Full Text] [Related]

  • 17. Cystic fibrosis mouse model-dependent intestinal structure and gut microbiome.
    Bazett M, Honeyman L, Stefanov AN, Pope CE, Hoffman LR, Haston CK.
    Mamm Genome; 2015 Jun 24; 26(5-6):222-34. PubMed ID: 25721416
    [Abstract] [Full Text] [Related]

  • 18. Aberrant CFTR-dependent HCO3- transport in mutations associated with cystic fibrosis.
    Choi JY, Muallem D, Kiselyov K, Lee MG, Thomas PJ, Muallem S.
    Nature; 2001 Mar 01; 410(6824):94-7. PubMed ID: 11242048
    [Abstract] [Full Text] [Related]

  • 19. Linaclotide improves gastrointestinal transit in cystic fibrosis mice by inhibiting sodium/hydrogen exchanger 3.
    McHugh DR, Cotton CU, Moss FJ, Vitko M, Valerio DM, Kelley TJ, Hao S, Jafri A, Drumm ML, Boron WF, Stern RC, McBennett K, Hodges CA.
    Am J Physiol Gastrointest Liver Physiol; 2018 Nov 01; 315(5):G868-G878. PubMed ID: 30118317
    [Abstract] [Full Text] [Related]

  • 20. Normal mouse intestinal mucus release requires cystic fibrosis transmembrane regulator-dependent bicarbonate secretion.
    Garcia MA, Yang N, Quinton PM.
    J Clin Invest; 2009 Sep 01; 119(9):2613-22. PubMed ID: 19726884
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.