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165 related items for PubMed ID: 9678538

  • 21. Vasopressin-stimulated CFTR Cl- currents are increased in the renal collecting duct cells of a mouse model of Liddle's syndrome.
    Chang CT, Bens M, Hummler E, Boulkroun S, Schild L, Teulon J, Rossier BC, Vandewalle A.
    J Physiol; 2005 Jan 01; 562(Pt 1):271-84. PubMed ID: 15513933
    [Abstract] [Full Text] [Related]

  • 22. Defective regulation of the epithelial Na+ channel by Nedd4 in Liddle's syndrome.
    Abriel H, Loffing J, Rebhun JF, Pratt JH, Schild L, Horisberger JD, Rotin D, Staub O.
    J Clin Invest; 1999 Mar 01; 103(5):667-73. PubMed ID: 10074483
    [Abstract] [Full Text] [Related]

  • 23. Liddle's syndrome mutations increase Na+ transport through dual effects on epithelial Na+ channel surface expression and proteolytic cleavage.
    Knight KK, Olson DR, Zhou R, Snyder PM.
    Proc Natl Acad Sci U S A; 2006 Feb 21; 103(8):2805-8. PubMed ID: 16477034
    [Abstract] [Full Text] [Related]

  • 24. Liddle's syndrome: prospective genetic screening and suppressed aldosterone secretion in an extended kindred.
    Findling JW, Raff H, Hansson JH, Lifton RP.
    J Clin Endocrinol Metab; 1997 Apr 21; 82(4):1071-4. PubMed ID: 9100575
    [Abstract] [Full Text] [Related]

  • 25. Liddle's syndrome mechanisms, diagnosis and management.
    Enslow BT, Stockand JD, Berman JM.
    Integr Blood Press Control; 2019 Apr 21; 12():13-22. PubMed ID: 31564964
    [Abstract] [Full Text] [Related]

  • 26. Mechanism by which Liddle's syndrome mutations increase activity of a human epithelial Na+ channel.
    Snyder PM, Price MP, McDonald FJ, Adams CM, Volk KA, Zeiher BG, Stokes JB, Welsh MJ.
    Cell; 1995 Dec 15; 83(6):969-78. PubMed ID: 8521520
    [Abstract] [Full Text] [Related]

  • 27. WW domains of Nedd4 bind to the proline-rich PY motifs in the epithelial Na+ channel deleted in Liddle's syndrome.
    Staub O, Dho S, Henry P, Correa J, Ishikawa T, McGlade J, Rotin D.
    EMBO J; 1996 May 15; 15(10):2371-80. PubMed ID: 8665844
    [Abstract] [Full Text] [Related]

  • 28. Conservation of pH sensitivity in the epithelial sodium channel (ENaC) with Liddle's syndrome mutation.
    Konstas AA, Mavrelos D, Korbmacher C.
    Pflugers Arch; 2000 Dec 15; 441(2-3):341-50. PubMed ID: 11211122
    [Abstract] [Full Text] [Related]

  • 29. Epithelial Na+ channel mutants causing Liddle's syndrome retain ability to respond to aldosterone and vasopressin.
    Auberson M, Hoffmann-Pochon N, Vandewalle A, Kellenberger S, Schild L.
    Am J Physiol Renal Physiol; 2003 Sep 15; 285(3):F459-71. PubMed ID: 12759227
    [Abstract] [Full Text] [Related]

  • 30. Expression and regulation of normal and polymorphic epithelial sodium channel by human lymphocytes.
    Bubien JK, Watson B, Khan MA, Langloh AL, Fuller CM, Berdiev B, Tousson A, Benos DJ.
    J Biol Chem; 2001 Mar 16; 276(11):8557-66. PubMed ID: 11113130
    [Abstract] [Full Text] [Related]

  • 31. Liddle's syndrome in an African male due to a novel frameshift mutation in the beta-subunit of the epithelial sodium channel gene.
    Freercks R, Meldau S, Jones E, Ensor J, Weimers-Willard C, Rayner B.
    Cardiovasc J Afr; 2017 Sep 23; 28(4):e4-e6. PubMed ID: 29144530
    [Abstract] [Full Text] [Related]

  • 32. Liddle's syndrome caused by a novel missense mutation (P617L) of the epithelial sodium channel beta subunit.
    Rossi E, Farnetti E, Debonneville A, Nicoli D, Grasselli C, Regolisti G, Negro A, Perazzoli F, Casali B, Mantero F, Staub O.
    J Hypertens; 2008 May 23; 26(5):921-7. PubMed ID: 18398334
    [Abstract] [Full Text] [Related]

  • 33. The diagnosis of Liddle syndrome by identification of a mutation in the beta subunit of the epithelial sodium channel.
    Jackson SN, Williams B, Houtman P, Trembath RC.
    J Med Genet; 1998 Jun 23; 35(6):510-2. PubMed ID: 9643296
    [Abstract] [Full Text] [Related]

  • 34. The activity of the epithelial sodium channel is regulated by clathrin-mediated endocytosis.
    Shimkets RA, Lifton RP, Canessa CM.
    J Biol Chem; 1997 Oct 10; 272(41):25537-41. PubMed ID: 9325269
    [Abstract] [Full Text] [Related]

  • 35. Peptide block of constitutively activated Na+ channels in Liddle's disease.
    Ismailov II, Berdiev BK, Fuller CM, Bradford AL, Lifton RP, Warnock DG, Bubien JK, Benos DJ.
    Am J Physiol; 1996 Jan 10; 270(1 Pt 1):C214-23. PubMed ID: 8772447
    [Abstract] [Full Text] [Related]

  • 36. Disorders of the epithelial Na(+) channel in Liddle's syndrome and autosomal recessive pseudohypoaldosteronism type 1.
    Oh YS, Warnock DG.
    Exp Nephrol; 2000 Jan 10; 8(6):320-5. PubMed ID: 11014928
    [Abstract] [Full Text] [Related]

  • 37. Liddle's disease: abnormal regulation of amiloride-sensitive Na+ channels by beta-subunit mutation.
    Bubien JK, Ismailov II, Berdiev BK, Cornwell T, Lifton RP, Fuller CM, Achard JM, Benos DJ, Warnock DG.
    Am J Physiol; 1996 Jan 10; 270(1 Pt 1):C208-13. PubMed ID: 8772446
    [Abstract] [Full Text] [Related]

  • 38. Molecular genetics of Liddle's syndrome.
    Yang KQ, Xiao Y, Tian T, Gao LG, Zhou XL.
    Clin Chim Acta; 2014 Sep 25; 436():202-6. PubMed ID: 24882431
    [Abstract] [Full Text] [Related]

  • 39. Plasma aldosterone level in a female case of pseudohyperaldosteronism (Liddle's syndrome).
    Takeuchi K, Abe K, Sato M, Yasujima M, Omata K, Murakami O, Yoshinaga K.
    Endocrinol Jpn; 1989 Feb 25; 36(1):167-73. PubMed ID: 2659310
    [Abstract] [Full Text] [Related]

  • 40. Juvenile hypertension, the role of genetically altered steroid metabolism.
    Ferrari P, Bianchetti M, Frey FJ.
    Horm Res; 2001 Feb 25; 55(5):213-23. PubMed ID: 11740142
    [Abstract] [Full Text] [Related]

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