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Journal Abstract Search

390 related items for PubMed ID: 15327389

  • 1. Mutations in the uromodulin gene decrease urinary excretion of Tamm-Horsfall protein.
    Bleyer AJ, Hart TC, Shihabi Z, Robins V, Hoyer JR.
    Kidney Int; 2004 Sep; 66(3):974-7. PubMed ID: 15327389
    [Abstract] [Full Text] [Related]

  • 2. A cluster of mutations in the UMOD gene causes familial juvenile hyperuricemic nephropathy with abnormal expression of uromodulin.
    Dahan K, Devuyst O, Smaers M, Vertommen D, Loute G, Poux JM, Viron B, Jacquot C, Gagnadoux MF, Chauveau D, Büchler M, Cochat P, Cosyns JP, Mougenot B, Rider MH, Antignac C, Verellen-Dumoulin C, Pirson Y.
    J Am Soc Nephrol; 2003 Nov; 14(11):2883-93. PubMed ID: 14569098
    [Abstract] [Full Text] [Related]

  • 3. Clinical characterization of a family with a mutation in the uromodulin (Tamm-Horsfall glycoprotein) gene.
    Bleyer AJ, Woodard AS, Shihabi Z, Sandhu J, Zhu H, Satko SG, Weller N, Deterding E, McBride D, Gorry MC, Xu L, Ganier D, Hart TC.
    Kidney Int; 2003 Jul; 64(1):36-42. PubMed ID: 12787393
    [Abstract] [Full Text] [Related]

  • 4. Uromodulin-associated kidney disease.
    Bleyer AJ, Zivná M, Kmoch S.
    Nephron Clin Pract; 2011 Jul; 118(1):c31-6. PubMed ID: 21071970
    [Abstract] [Full Text] [Related]

  • 5. Mutations of the Uromodulin gene in MCKD type 2 patients cluster in exon 4, which encodes three EGF-like domains.
    Wolf MT, Mucha BE, Attanasio M, Zalewski I, Karle SM, Neumann HP, Rahman N, Bader B, Baldamus CA, Otto E, Witzgall R, Fuchshuber A, Hildebrandt F.
    Kidney Int; 2003 Nov; 64(5):1580-7. PubMed ID: 14531790
    [Abstract] [Full Text] [Related]

  • 6. Homozygosity for uromodulin disorders: FJHN and MCKD-type 2.
    Rezende-Lima W, Parreira KS, García-González M, Riveira E, Banet JF, Lens XM.
    Kidney Int; 2004 Aug; 66(2):558-63. PubMed ID: 15253706
    [Abstract] [Full Text] [Related]

  • 7. A novel pattern of mutation in uromodulin disorders: autosomal dominant medullary cystic kidney disease type 2, familial juvenile hyperuricemic nephropathy, and autosomal dominant glomerulocystic kidney disease.
    Lens XM, Banet JF, Outeda P, Barrio-Lucía V.
    Am J Kidney Dis; 2005 Jul; 46(1):52-7. PubMed ID: 15983957
    [Abstract] [Full Text] [Related]

  • 8. The Uromodulin C744G mutation causes MCKD2 and FJHN in children and adults and may be due to a possible founder effect.
    Wolf MT, Beck BB, Zaucke F, Kunze A, Misselwitz J, Ruley J, Ronda T, Fischer A, Eifinger F, Licht C, Otto E, Hoppe B, Hildebrandt F.
    Kidney Int; 2007 Mar; 71(6):574-81. PubMed ID: 17245395
    [Abstract] [Full Text] [Related]

  • 9. Urinary Tamm-Horsfall protein excretion in patients with primary vesicoureteral reflux.
    Uto I, Ishimatsu T, Hirayama H, Ueda S, Nishi K, Tsuruta J, Kambara T.
    Eur Urol; 1991 Mar; 19(4):315-8. PubMed ID: 1915538
    [Abstract] [Full Text] [Related]

  • 10. Uromodulin levels associate with a common UMOD variant and risk for incident CKD.
    Köttgen A, Hwang SJ, Larson MG, Van Eyk JE, Fu Q, Benjamin EJ, Dehghan A, Glazer NL, Kao WH, Harris TB, Gudnason V, Shlipak MG, Yang Q, Coresh J, Levy D, Fox CS.
    J Am Soc Nephrol; 2010 Feb; 21(2):337-44. PubMed ID: 19959715
    [Abstract] [Full Text] [Related]

  • 11. Novel UMOD mutations in familial juvenile hyperuricemic nephropathy lead to abnormal uromodulin intracellular trafficking.
    Liu M, Chen Y, Liang Y, Liu Y, Wang S, Hou P, Zhang H, Zhao M.
    Gene; 2013 Dec 01; 531(2):363-9. PubMed ID: 23988501
    [Abstract] [Full Text] [Related]

  • 12. Novel uromodulin mutation in familial juvenile hyperuricemic nephropathy.
    Wei X, Xu R, Yang Z, Li Z, Liao Y, Johnson RJ, Yu X, Chen W.
    Am J Nephrol; 2012 Dec 01; 36(2):114-20. PubMed ID: 22776760
    [Abstract] [Full Text] [Related]

  • 13. A new missense mutation in UMOD gene leads to severely reduced serum uromodulin concentrations - A tool for the diagnosis of uromodulin-associated kidney disease.
    Satanovskij R, Bader A, Block M, Herbst V, Schlumberger W, Haack T, Nockher WA, Heemann U, Renders L, Schmaderer C, Angermann S, Wen M, Meitinger T, Scherberich J, Steubl D.
    Clin Biochem; 2017 Feb 01; 50(3):155-158. PubMed ID: 27729211
    [Abstract] [Full Text] [Related]

  • 14. Functional consequences of a novel uromodulin mutation in a family with familial juvenile hyperuricaemic nephropathy.
    Tinschert S, Ruf N, Bernascone I, Sacherer K, Lamorte G, Neumayer HH, Nürnberg P, Luft FC, Rampoldi L.
    Nephrol Dial Transplant; 2004 Dec 01; 19(12):3150-4. PubMed ID: 15575003
    [Abstract] [Full Text] [Related]

  • 15. Tamm-Horsfall protein in urine after uninephrectomy/transplantation in kidney donors and their recipients.
    Torffvit O, Kamper AL, Strandgaard S.
    Scand J Urol Nephrol; 1997 Dec 01; 31(6):555-9. PubMed ID: 9458515
    [Abstract] [Full Text] [Related]

  • 16. A novel homozygous UMOD mutation reveals gene dosage effects on uromodulin processing and urinary excretion.
    Edwards N, Olinger E, Adam J, Kelly M, Schiano G, Ramsbottom SA, Sandford R, Devuyst O, Sayer JA.
    Nephrol Dial Transplant; 2017 Dec 01; 32(12):1994-1999. PubMed ID: 28605509
    [Abstract] [Full Text] [Related]

  • 17. Urinary excretion of epidermal growth factor and Tamm-Horsfall protein in three rat models with increased renal excretion of urine.
    Thulesen J, Jørgensen PE, Torffvit O, Nexø E, Poulsen SS.
    Regul Pept; 1997 Oct 31; 72(2-3):179-86. PubMed ID: 9652978
    [Abstract] [Full Text] [Related]

  • 18. [Urinary excretion of Tamm-Horsfall protein by patients with acute renal failure].
    Kokot M, Duława J, Nowicki M, Kokot F, Machowska J.
    Pol Arch Med Wewn; 1992 Oct 31; 88(4):225-9. PubMed ID: 1488322
    [Abstract] [Full Text] [Related]

  • 19. Determinants of urinary excretion of Tamm-Horsfall protein in non-selected kidney stone formers and healthy subjects.
    Glauser A, Hochreiter W, Jaeger P, Hess B.
    Nephrol Dial Transplant; 2000 Oct 31; 15(10):1580-7. PubMed ID: 11007825
    [Abstract] [Full Text] [Related]

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