129 related articles for article (PubMed ID: 17182881)
1. Mechanism of injury in uromodulin-associated kidney disease.
Kumar S
J Am Soc Nephrol; 2007 Jan; 18(1):10-2. PubMed ID: 17182881
[No Abstract] [Full Text] [Related]
2. [Familial juvenile hyperuricemic nephropathy (FJHN)].
Kudo E; Itakura M
Nihon Rinsho; 2008 Apr; 66(4):683-6. PubMed ID: 18409515
[TBL] [Abstract][Full Text] [Related]
3. [Uromodulin mutation and hyperuricemia].
Kudo E; Itakura M
Nihon Rinsho; 2008 Apr; 66(4):778-83. PubMed ID: 18409531
[TBL] [Abstract][Full Text] [Related]
4. A novel heterozygous missense mutation in the UMOD gene responsible for Familial Juvenile Hyperuricemic Nephropathy.
Calado J; Gaspar A; Clemente C; Rueff J
BMC Med Genet; 2005 Jan; 6():5. PubMed ID: 15673476
[TBL] [Abstract][Full Text] [Related]
5. [Hyperuricemic nephropathy: Pathogenesis, pathophysiology, and therapy].
Ichida K; Hosoya T; Hosoyamada M
Nihon Rinsho; 2006 Feb; 64 Suppl 2():438-41. PubMed ID: 16523929
[No Abstract] [Full Text] [Related]
6. 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
[TBL] [Abstract][Full Text] [Related]
7. Uromodulin and translational medicine: will the SNPs bring zip to clinical practice?
Sedor JR
J Am Soc Nephrol; 2010 Feb; 21(2):204-6. PubMed ID: 20110381
[No Abstract] [Full Text] [Related]
8. Familial nephropathy associated with hyperuricemia in Spain: our experience with 3 families harbouring a UMOD mutation.
Puig JG; Prior C; Martínez-Ara J; Torres RJ
Nucleosides Nucleotides Nucleic Acids; 2006; 25(9-11):1295-300. PubMed ID: 17065110
[TBL] [Abstract][Full Text] [Related]
9. Type of uromodulin mutation and allelic status influence onset and severity of uromodulin-associated kidney disease in mice.
Kemter E; Prueckl P; Sklenak S; Rathkolb B; Habermann FA; Hans W; Gailus-Durner V; Fuchs H; Hrabě de Angelis M; Wolf E; Aigner B; Wanke R
Hum Mol Genet; 2013 Oct; 22(20):4148-63. PubMed ID: 23748428
[TBL] [Abstract][Full Text] [Related]
10. Production and characterization of transgenic mice harboring mutant human UMOD gene.
Takiue Y; Hosoyamada M; Yokoo T; Kimura M; Ochiai M; Kaneko K; Ichida K; Hosoya T; Shibasaki T
Nucleosides Nucleotides Nucleic Acids; 2008 Jun; 27(6):596-600. PubMed ID: 18600511
[TBL] [Abstract][Full Text] [Related]
11. Familial juvenile hyperuricaemic nephropathy.
Puig JG; Torres RJ
QJM; 2004 Jul; 97(7):457-8. PubMed ID: 15208434
[No Abstract] [Full Text] [Related]
12. [Familial juvenile hyperuricemic nephropathy].
Hummel A
Nephrol Ther; 2012 Apr; 8(2):117-25. PubMed ID: 22193138
[TBL] [Abstract][Full Text] [Related]
13. 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
[TBL] [Abstract][Full Text] [Related]
14. Familial juvenile hyperuricaemic nephropathy.
Bleyer AJ; Hart TC
QJM; 2003 Nov; 96(11):867-8. PubMed ID: 14566042
[No Abstract] [Full Text] [Related]
15. UROMODULIN mutations cause familial juvenile hyperuricemic nephropathy.
Turner JJ; Stacey JM; Harding B; Kotanko P; Lhotta K; Puig JG; Roberts I; Torres RJ; Thakker RV
J Clin Endocrinol Metab; 2003 Mar; 88(3):1398-401. PubMed ID: 12629136
[TBL] [Abstract][Full Text] [Related]
16. Novel missense mutation of uromodulin in mice causes renal dysfunction with alterations in urea handling, energy, and bone metabolism.
Kemter E; Rathkolb B; Rozman J; Hans W; Schrewe A; Landbrecht C; Klaften M; Ivandic B; Fuchs H; Gailus-Durner V; Klingenspor M; de Angelis MH; Wolf E; Wanke R; Aigner B
Am J Physiol Renal Physiol; 2009 Nov; 297(5):F1391-8. PubMed ID: 19692485
[TBL] [Abstract][Full Text] [Related]
17. Tamm-Horsfall protein or uromodulin: new ideas about an old molecule.
Devuyst O; Dahan K; Pirson Y
Nephrol Dial Transplant; 2005 Jul; 20(7):1290-4. PubMed ID: 15840660
[No Abstract] [Full Text] [Related]
18. Mutations in RPGRIP1L: extending the clinical spectrum of ciliopathies.
Devuyst O; Arnould VJ
Nephrol Dial Transplant; 2008 May; 23(5):1500-3. PubMed ID: 18281315
[No Abstract] [Full Text] [Related]
19. Improving the recognition of hereditary interstitial kidney disease.
Bleyer AJ
J Am Soc Nephrol; 2009 Jan; 20(1):11-3. PubMed ID: 19056873
[TBL] [Abstract][Full Text] [Related]
20. Membrane targeting and secretion of mutant uromodulin in familial juvenile hyperuricemic nephropathy.
Jennings P; Aydin S; Kotanko P; Lechner J; Lhotta K; Williams S; Thakker RV; Pfaller W
J Am Soc Nephrol; 2007 Jan; 18(1):264-73. PubMed ID: 17151335
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]