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Journal Abstract Search

161 related items for PubMed ID: 9786924

  • 1. Phenotype resembling Gitelman's syndrome in mice lacking the apical Na+-Cl- cotransporter of the distal convoluted tubule.
    Schultheis PJ, Lorenz JN, Meneton P, Nieman ML, Riddle TM, Flagella M, Duffy JJ, Doetschman T, Miller ML, Shull GE.
    J Biol Chem; 1998 Oct 30; 273(44):29150-5. PubMed ID: 9786924
    [Abstract] [Full Text] [Related]

  • 2. Abnormal reabsorption of Na+/CI- by the thiazide-inhibitable transporter of the distal convoluted tubule in Gitelman's syndrome.
    Colussi G, Rombolà G, Brunati C, De Ferrari ME.
    Am J Nephrol; 1997 Oct 30; 17(2):103-11. PubMed ID: 9096439
    [Abstract] [Full Text] [Related]

  • 3. Altered renal distal tubule structure and renal Na(+) and Ca(2+) handling in a mouse model for Gitelman's syndrome.
    Loffing J, Vallon V, Loffing-Cueni D, Aregger F, Richter K, Pietri L, Bloch-Faure M, Hoenderop JG, Shull GE, Meneton P, Kaissling B.
    J Am Soc Nephrol; 2004 Sep 30; 15(9):2276-88. PubMed ID: 15339977
    [Abstract] [Full Text] [Related]

  • 4. Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter.
    Simon DB, Nelson-Williams C, Bia MJ, Ellison D, Karet FE, Molina AM, Vaara I, Iwata F, Cushner HM, Koolen M, Gainza FJ, Gitleman HJ, Lifton RP.
    Nat Genet; 1996 Jan 30; 12(1):24-30. PubMed ID: 8528245
    [Abstract] [Full Text] [Related]

  • 5. [From gene to disease; mutations in the SLC12A3 gene as the cause of Gitelman's syndrome].
    Cornelissen EA, Bindels RJ, Hoefsloot LH, Knoers NV.
    Ned Tijdschr Geneeskd; 2005 Jun 11; 149(24):1330-3. PubMed ID: 16008036
    [Abstract] [Full Text] [Related]

  • 6. [Renal sodium transport abnormality: Gitelman's syndrome and renal sodium transporter].
    Takeuchi K, Taniyama Y, Ito S, Yasujima M.
    Rinsho Byori; 1999 Dec 11; 47(12):1128-33. PubMed ID: 10639822
    [Abstract] [Full Text] [Related]

  • 7. Loss of sodium chloride co-transporter impairs the outgrowth of the renal distal convoluted tubule during renal development.
    Schnoz C, Carrel M, Loffing J.
    Nephrol Dial Transplant; 2020 Mar 01; 35(3):411-432. PubMed ID: 31436795
    [Abstract] [Full Text] [Related]

  • 8. The molecular basis of inherited hypokalemic alkalosis: Bartter's and Gitelman's syndromes.
    Simon DB, Lifton RP.
    Am J Physiol; 1996 Nov 01; 271(5 Pt 2):F961-6. PubMed ID: 8945989
    [Abstract] [Full Text] [Related]

  • 9. Mouse model of type II Bartter's syndrome. II. Altered expression of renal sodium- and water-transporting proteins.
    Wagner CA, Loffing-Cueni D, Yan Q, Schulz N, Fakitsas P, Carrel M, Wang T, Verrey F, Geibel JP, Giebisch G, Hebert SC, Loffing J.
    Am J Physiol Renal Physiol; 2008 Jun 01; 294(6):F1373-80. PubMed ID: 18322017
    [Abstract] [Full Text] [Related]

  • 10. Association of a mutation in thiazide-sensitive Na-Cl cotransporter with familial Gitelman's syndrome.
    Takeuchi K, Kure S, Kato T, Taniyama Y, Takahashi N, Ikeda Y, Abe T, Narisawa K, Muramatsu Y, Abe K.
    J Clin Endocrinol Metab; 1996 Dec 01; 81(12):4496-9. PubMed ID: 8954067
    [Abstract] [Full Text] [Related]

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  • 12. Identification of a novel R642C mutation in Na/Cl cotransporter with Gitelman's syndrome.
    Yahata K, Tanaka I, Kotani M, Mukoyama M, Ogawa Y, Goto M, Nakagawa M, Sugawara A, Tanaka K, Shimatsu A, Nakao K.
    Am J Kidney Dis; 1999 Nov 01; 34(5):845-53. PubMed ID: 10561140
    [Abstract] [Full Text] [Related]

  • 13. [Regulation of kidney on potassium balance and its clinical significance].
    Xie QH, Hao CM.
    Sheng Li Xue Bao; 2023 Apr 25; 75(2):216-230. PubMed ID: 37089096
    [Abstract] [Full Text] [Related]

  • 14. Attenuated renal excretion in response to thiazide diuretics in Gitelman's syndrome: a case report.
    Yeum CH, Kim SW, Ma SK, Ko JH, Nah MY, Kim NH, Choi KC.
    J Korean Med Sci; 2002 Aug 25; 17(4):567-70. PubMed ID: 12172059
    [Abstract] [Full Text] [Related]

  • 15. Gitelman's syndrome (familial hypokalemia-hypomagnesemia).
    Barakat AJ, Rennert OM.
    J Nephrol; 2001 Aug 25; 14(1):43-7. PubMed ID: 11281344
    [Abstract] [Full Text] [Related]

  • 16. Molecular pathophysiology of Bartter's and Gitelman's syndromes.
    Koulouridis E, Koulouridis I.
    World J Pediatr; 2015 May 25; 11(2):113-25. PubMed ID: 25754753
    [Abstract] [Full Text] [Related]

  • 17. Functional expression of mutations in the human NaCl cotransporter: evidence for impaired routing mechanisms in Gitelman's syndrome.
    De Jong JC, Van Der Vliet WA, Van Den Heuvel LP, Willems PH, Knoers NV, Bindels RJ.
    J Am Soc Nephrol; 2002 Jun 25; 13(6):1442-8. PubMed ID: 12039972
    [Abstract] [Full Text] [Related]

  • 18. Three cases of Gitelman's syndrome possibly caused by different mutations in the thiazide-sensitive Na-Cl cotransporter.
    Takeuchi K, Kato T, Taniyama Y, Tsunoda K, Takahashi N, Ikeda Y, Omata K, Imai Y, Saito T, Ito S, Abe K.
    Intern Med; 1997 Aug 25; 36(8):582-5. PubMed ID: 9260778
    [Abstract] [Full Text] [Related]

  • 19. Mutations in the Na-Cl cotransporter reduce blood pressure in humans.
    Cruz DN, Simon DB, Nelson-Williams C, Farhi A, Finberg K, Burleson L, Gill JR, Lifton RP.
    Hypertension; 2001 Jun 25; 37(6):1458-64. PubMed ID: 11408395
    [Abstract] [Full Text] [Related]

  • 20. [Gitelman's syndrome: an important differential diagnosis of hypokalemia].
    Kurschat C, Heering P, Grabensee B.
    Dtsch Med Wochenschr; 2003 May 30; 128(22):1225-8. PubMed ID: 12772080
    [Abstract] [Full Text] [Related]

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