These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

199 related articles for article (PubMed ID: 23344472)

  • 1. Common genetic variants of the human uromodulin gene regulate transcription and predict plasma uric acid levels.
    Han J; Liu Y; Rao F; Nievergelt CM; O'Connor DT; Wang X; Liu L; Bu D; Liang Y; Wang F; Zhang L; Zhang H; Chen Y; Wang H
    Kidney Int; 2013 Apr; 83(4):733-40. PubMed ID: 23344472
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 531(2):363-9. PubMed ID: 23988501
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Common variants of the UMOD promoter associated with blood pressure in a community-based Chinese cohort.
    Han J; Chen Y; Liu Y; Liang Y; Wang X; Liu L; Wang F; Zhang L; Zhang H; Wang H
    Hypertens Res; 2012 Jul; 35(7):769-74. PubMed ID: 22592667
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Quercetin regulates organic ion transporter and uromodulin expression and improves renal function in hyperuricemic mice.
    Hu QH; Zhang X; Wang X; Jiao RQ; Kong LD
    Eur J Nutr; 2012 Aug; 51(5):593-606. PubMed ID: 21909718
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Common variants in UMOD associate with urinary uromodulin levels: a meta-analysis.
    Olden M; Corre T; Hayward C; Toniolo D; Ulivi S; Gasparini P; Pistis G; Hwang SJ; Bergmann S; Campbell H; Cocca M; Gandin I; Girotto G; Glaudemans B; Hastie ND; Loffing J; Polasek O; Rampoldi L; Rudan I; Sala C; Traglia M; Vollenweider P; Vuckovic D; Youhanna S; Weber J; Wright AF; Kutalik Z; Bochud M; Fox CS; Devuyst O
    J Am Soc Nephrol; 2014 Aug; 25(8):1869-82. PubMed ID: 24578125
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Common noncoding UMOD gene variants induce salt-sensitive hypertension and kidney damage by increasing uromodulin expression.
    Trudu M; Janas S; Lanzani C; Debaix H; Schaeffer C; Ikehata M; Citterio L; Demaretz S; Trevisani F; Ristagno G; Glaudemans B; Laghmani K; Dell'Antonio G; ; Loffing J; Rastaldi MP; Manunta P; Devuyst O; Rampoldi L
    Nat Med; 2013 Dec; 19(12):1655-60. PubMed ID: 24185693
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Phenotype and outcome in hereditary tubulointerstitial nephritis secondary to UMOD mutations.
    Bollée G; Dahan K; Flamant M; Morinière V; Pawtowski A; Heidet L; Lacombe D; Devuyst O; Pirson Y; Antignac C; Knebelmann B
    Clin J Am Soc Nephrol; 2011 Oct; 6(10):2429-38. PubMed ID: 21868615
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A case of familial juvenile hyperuricemic nephropathy with novel uromodulin gene mutation, a novel heterozygous missense mutation in Korea.
    Lee DH; Kim JK; Oh SE; Noh JW; Lee YK
    J Korean Med Sci; 2010 Nov; 25(11):1680-2. PubMed ID: 21060763
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical, Genetic, and Urinary Factors Associated with Uromodulin Excretion.
    Troyanov S; Delmas-Frenette C; Bollée G; Youhanna S; Bruat V; Awadalla P; Devuyst O; Madore F
    Clin J Am Soc Nephrol; 2016 Jan; 11(1):62-9. PubMed ID: 26683887
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. A novel UMOD mutation (c.187T>C) in a Korean family with juvenile hyperuricemic nephropathy.
    Lee MN; Jun JE; Kwon GY; Huh WS; Ki CS
    Ann Lab Med; 2013 Jul; 33(4):293-6. PubMed ID: 23826568
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Wild-type uromodulin prevents NFkB activation in kidney cells, while mutant uromodulin, causing FJHU nephropathy, does not.
    Dinour D; Ganon L; Nomy LI; Ron R; Holtzman EJ
    J Nephrol; 2014 Jun; 27(3):257-64. PubMed ID: 24648000
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Autosomal dominant tubulointerstitial kidney disease caused by uromodulin mutations: seek and you will find.
    Raffler G; Zitt E; Sprenger-Mähr H; Nagel M; Lhotta K
    Wien Klin Wochenschr; 2016 Apr; 128(7-8):291-4. PubMed ID: 26810206
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Next generation sequencing search for uromodulin gene variants related with impaired renal function.
    Gómez J; Díaz-Corte C; Tranche S; Alvarez F; Iglesias S; Alonso B; Coto E
    Mol Biol Rep; 2015 Sep; 42(9):1353-8. PubMed ID: 26040415
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Primary hyperuricemia due to decreased renal uric acid excretion].
    Yamauchi T; Ueda T
    Nihon Rinsho; 2008 Apr; 66(4):679-81. PubMed ID: 18409514
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Elevated UMOD methylation level in peripheral blood is associated with gout risk.
    Yang Y; Chen X; Hu H; Jiang Y; Yu H; Dai J; Mao Y; Duan S
    Sci Rep; 2017 Sep; 7(1):11196. PubMed ID: 28894234
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Meta-GWAS Reveals Novel Genetic Variants Associated with Urinary Excretion of Uromodulin.
    Joseph CB; Mariniello M; Yoshifuji A; Schiano G; Lake J; Marten J; Richmond A; Huffman JE; Campbell A; Harris SE; Troyanov S; Cocca M; Robino A; Thériault S; Eckardt KU; Wuttke M; Cheng Y; Corre T; Kolcic I; Black C; Bruat V; Concas MP; Sala C; Aeschbacher S; Schaefer F; Bergmann S; Campbell H; Olden M; Polasek O; Porteous DJ; Deary IJ; Madore F; Awadalla P; Girotto G; Ulivi S; Conen D; Wuehl E; Olinger E; Wilson JF; Bochud M; Köttgen A; Hayward C; Devuyst O
    J Am Soc Nephrol; 2022 Mar; 33(3):511-529. PubMed ID: 35228297
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Association between SLC2A9 transporter gene variants and uric acid phenotypes in African American and white families.
    Rule AD; de Andrade M; Matsumoto M; Mosley TH; Kardia S; Turner ST
    Rheumatology (Oxford); 2011 May; 50(5):871-8. PubMed ID: 21186168
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hyperuricemia, gout and the kidney.
    Gibson T
    Curr Opin Rheumatol; 2012 Mar; 24(2):127-31. PubMed ID: 22157498
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.