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Journal Abstract Search

114 related items for PubMed ID: 8566587

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  • 5. Abolition of Ca2+-mediated intestinal anion secretion and increased stool dehydration in mice lacking the intermediate conductance Ca2+-dependent K+ channel Kcnn4.
    Flores CA, Melvin JE, Figueroa CD, Sepúlveda FV.
    J Physiol; 2007 Sep 01; 583(Pt 2):705-17. PubMed ID: 17584847
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  • 6. Cl- transport by cystic fibrosis transmembrane conductance regulator (CFTR) contributes to the inhibition of epithelial Na+ channels (ENaCs) in Xenopus oocytes co-expressing CFTR and ENaC.
    Briel M, Greger R, Kunzelmann K.
    J Physiol; 1998 May 01; 508 ( Pt 3)(Pt 3):825-36. PubMed ID: 9518736
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  • 8. Physiological relevance of cell-specific distribution patterns of CFTR, NKCC1, NBCe1, and NHE3 along the crypt-villus axis in the intestine.
    Jakab RL, Collaco AM, Ameen NA.
    Am J Physiol Gastrointest Liver Physiol; 2011 Jan 01; 300(1):G82-98. PubMed ID: 21030607
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  • 9. Identification of new small molecule inhibitors of cystic fibrosis transmembrane conductance regulator protein: in vitro and in vivo studies.
    Muanprasat C, Kaewmokul S, Chatsudthipong V.
    Biol Pharm Bull; 2007 Mar 01; 30(3):502-7. PubMed ID: 17329846
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  • 10. Characterization of CFTR High Expresser cells in the intestine.
    Jakab RL, Collaco AM, Ameen NA.
    Am J Physiol Gastrointest Liver Physiol; 2013 Sep 15; 305(6):G453-65. PubMed ID: 23868408
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  • 11. Relationship of a non-cystic fibrosis transmembrane conductance regulator-mediated chloride conductance to organ-level disease in Cftr(-/-) mice.
    Clarke LL, Grubb BR, Yankaskas JR, Cotton CU, McKenzie A, Boucher RC.
    Proc Natl Acad Sci U S A; 1994 Jan 18; 91(2):479-83. PubMed ID: 7507247
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  • 13. A unique subset of rat and human intestinal villus cells express the cystic fibrosis transmembrane conductance regulator.
    Ameen NA, Ardito T, Kashgarian M, Marino CR.
    Gastroenterology; 1995 Apr 18; 108(4):1016-23. PubMed ID: 7535272
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  • 15. Residual chloride secretion in intestinal tissue of deltaF508 homozygous twins and siblings with cystic fibrosis. The European CF Twin and Sibling Study Consortium.
    Bronsveld I, Mekus F, Bijman J, Ballmann M, Greipel J, Hundrieser J, Halley DJ, Laabs U, Busche R, De Jonge HR, Tümmler B, Veeze HJ.
    Gastroenterology; 2000 Jul 18; 119(1):32-40. PubMed ID: 10889152
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  • 16. Liquid movement across the surface epithelium of large airways.
    Chambers LA, Rollins BM, Tarran R.
    Respir Physiol Neurobiol; 2007 Dec 15; 159(3):256-70. PubMed ID: 17692578
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  • 19. Normalization of raised sodium absorption and raised calcium-mediated chloride secretion by adenovirus-mediated expression of cystic fibrosis transmembrane conductance regulator in primary human cystic fibrosis airway epithelial cells.
    Johnson LG, Boyles SE, Wilson J, Boucher RC.
    J Clin Invest; 1995 Mar 15; 95(3):1377-82. PubMed ID: 7533790
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  • 20. Inhibition of epithelial Na+ currents by intracellular domains of the cystic fibrosis transmembrane conductance regulator.
    Kunzelmann K, Kiser GL, Schreiber R, Riordan JR.
    FEBS Lett; 1997 Jan 06; 400(3):341-4. PubMed ID: 9009227
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