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Journal Abstract Search

177 related items for PubMed ID: 16798114

  • 1. Elevated hepatic SULT1E1 activity in mouse models of cystic fibrosis alters the regulation of estrogen responsive proteins.
    Li L, Falany CN.
    J Cyst Fibros; 2007 Jan; 6(1):23-30. PubMed ID: 16798114
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  • 2. Regulation of hepatic sulfotransferase (SULT) 1E1 expression and effects on estrogenic activity in cystic fibrosis (CF).
    Falany CN, He D, Li L, Falany JL, Wilborn TW, Kocarek TA, Runge-Morris M.
    J Steroid Biochem Mol Biol; 2009 Mar; 114(1-2):113-9. PubMed ID: 19429440
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  • 3. Repression of CFTR activity in human MMNK-1 cholangiocytes induces sulfotransferase 1E1 expression in co-cultured HepG2 hepatocytes.
    He D, Wilborn TW, Falany JL, Li L, Falany CN.
    Biochim Biophys Acta; 2008 Dec; 1783(12):2391-7. PubMed ID: 18817817
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  • 4. Increased SULT1E1 activity in HepG2 hepatocytes decreases growth hormone stimulation of STAT5b phosphorylation.
    Li L, He D, Wilborn TW, Falany JL, Falany CN.
    Steroids; 2009 Jan; 74(1):20-9. PubMed ID: 18831980
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  • 5. Increased expression of cystic fibrosis transmembrane conductance regulator in rat liver after common bile duct ligation.
    Shen H, Fan Y, Yang X, Burczynski FJ, Li P, Gong Y.
    J Cell Physiol; 2005 Jun; 203(3):599-603. PubMed ID: 15605366
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  • 7. Cystic fibrosis is associated with a defect in apical receptor-mediated endocytosis in mouse and human kidney.
    Jouret F, Bernard A, Hermans C, Dom G, Terryn S, Leal T, Lebecque P, Cassiman JJ, Scholte BJ, de Jonge HR, Courtoy PJ, Devuyst O.
    J Am Soc Nephrol; 2007 Mar; 18(3):707-18. PubMed ID: 17287432
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  • 11. Cystic fibrosis transmembrane conductance regulator deficiency exacerbates islet cell dysfunction after beta-cell injury.
    Stalvey MS, Muller C, Schatz DA, Wasserfall CH, Campbell-Thompson ML, Theriaque DW, Flotte TR, Atkinson MA.
    Diabetes; 2006 Jul; 55(7):1939-45. PubMed ID: 16804061
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  • 12. CFTR mutations impart elevated immune reactivity in a murine model of cystic fibrosis related diabetes.
    Stalvey MS, Brusko TM, Mueller C, Wasserfall CH, Schatz DA, Atkinson MA, Flotte TR.
    Cytokine; 2008 Oct; 44(1):154-9. PubMed ID: 18778952
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  • 13. Expression of CFTR from a ciliated cell-specific promoter is ineffective at correcting nasal potential difference in CF mice.
    Ostrowski LE, Yin W, Diggs PS, Rogers TD, O'Neal WK, Grubb BR.
    Gene Ther; 2007 Oct; 14(20):1492-501. PubMed ID: 17637798
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  • 14. Abnormally up-regulated cystic fibrosis transmembrane conductance regulator expression and uterine fluid accumulation contribute to Chlamydia trachomatis-induced female infertility.
    He Q, Tsang LL, Ajonuma LC, Chan HC.
    Fertil Steril; 2010 May 15; 93(8):2608-14. PubMed ID: 20227074
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  • 15. Decreased expression of peroxisome proliferator activated receptor gamma in cftr-/- mice.
    Ollero M, Junaidi O, Zaman MM, Tzameli I, Ferrando AA, Andersson C, Blanco PG, Bialecki E, Freedman SD.
    J Cell Physiol; 2004 Aug 15; 200(2):235-44. PubMed ID: 15174093
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  • 17. Cholangiocyte biology and cystic fibrosis liver disease.
    Feranchak AP, Sokol RJ.
    Semin Liver Dis; 2001 Nov 15; 21(4):471-88. PubMed ID: 11745036
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  • 18. Hepatic iodothyronine deiodinase type 1 activity is decreased in two DeltaF508 cystic fibrosis mouse models.
    Klaren PH, Looijmans PH.
    J Cyst Fibros; 2004 Jun 15; 3(2):125-8. PubMed ID: 15463895
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  • 19. Intestinal phenotype of variable-weight cystic fibrosis knockout mice.
    Canale-Zambrano JC, Poffenberger MC, Cory SM, Humes DG, Haston CK.
    Am J Physiol Gastrointest Liver Physiol; 2007 Jul 15; 293(1):G222-9. PubMed ID: 17615178
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  • 20. Ursodeoxycholic acid stimulates cholangiocyte fluid secretion in mice via CFTR-dependent ATP secretion.
    Fiorotto R, Spirlì C, Fabris L, Cadamuro M, Okolicsanyi L, Strazzabosco M.
    Gastroenterology; 2007 Nov 15; 133(5):1603-13. PubMed ID: 17983806
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