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 *

144 related articles for article (PubMed ID: 29052568)

  • 21. 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]  

  • 22. Autosomal dominant tubulointerstitial kidney disease (ADTKD) in Ireland.
    Cormican S; Connaughton DM; Kennedy C; Murray S; Živná M; Kmoch S; Fennelly NK; O'Kelly P; Benson KA; Conlon ET; Cavalleri G; Foley C; Doyle B; Dorman A; Little MA; Lavin P; Kidd K; Bleyer AJ; Conlon PJ
    Ren Fail; 2019 Nov; 41(1):832-841. PubMed ID: 31509055
    [No Abstract]   [Full Text] [Related]  

  • 23. Analysis of Yak MUC1 Protein Polymorphisms and the Corresponding VNTR Structure.
    Zheng Y; Fan Q; Liu Y; Zhao X; He X; Jin S
    Anim Biotechnol; 2009; 20(4):231-7. PubMed ID: 19937497
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Autosomal Dominant Tubulointerstitial Kidney Disease.
    Bleyer AJ; Kidd K; Živná M; Kmoch S
    Adv Chronic Kidney Dis; 2017 Mar; 24(2):86-93. PubMed ID: 28284384
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Medullary cystic kidney disease type 1 in a large Native-American kindred.
    Kiser RL; Wolf MT; Martin JL; Zalewski I; Attanasio M; Hildebrandt F; Klemmer P
    Am J Kidney Dis; 2004 Oct; 44(4):611-7. PubMed ID: 15384011
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The polymorphism in MUC1 gene in Nelore cattle.
    de Souza FR; Dentillo DB; Meola J; Biase FH; Andréa MV; Vozzi PA; Lôbo RB; Martelli LR
    J Anim Breed Genet; 2007 Feb; 124(1):42-6. PubMed ID: 17302961
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Bovine Muc1 is a highly polymorphic gene encoding an extensively glycosylated mucin that binds bacteria.
    Sando L; Pearson R; Gray C; Parker P; Hawken R; Thomson PC; Meadows JR; Kongsuwan K; Smith S; Tellam RL
    J Dairy Sci; 2009 Oct; 92(10):5276-91. PubMed ID: 19762846
    [TBL] [Abstract][Full Text] [Related]  

  • 28. From juvenile hyperuricaemia to dysfunctional uromodulin: an ongoing metamorphosis.
    Venkat-Raman G; Gast C; Marinaki A; Fairbanks L
    Pediatr Nephrol; 2016 Nov; 31(11):2035-42. PubMed ID: 26872483
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Two additional polymorphisms within the hypervariable MUC1 gene: association of alleles either side of the VNTR region.
    Pratt WS; Islam I; Swallow DM
    Ann Hum Genet; 1996 Jan; 60(1):21-28. PubMed ID: 8835095
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Is MUC1 polymorphism associated with female infertility?
    Goulart LR; Vieira GS; Martelli L; Inácio J; Goulart IM; Franco JG
    Reprod Biomed Online; 2004 Apr; 8(4):477-82. PubMed ID: 15149576
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Detecting
    Okada E; Morisada N; Horinouchi T; Fujii H; Tsuji T; Miura M; Katori H; Kitagawa M; Morozumi K; Toriyama T; Nakamura Y; Nishikomori R; Nagai S; Kondo A; Aoto Y; Ishiko S; Rossanti R; Sakakibara N; Nagano C; Yamamura T; Ishimori S; Usui J; Yamagata K; Iijima K; Imasawa T; Nozu K
    Kidney Int Rep; 2022 Apr; 7(4):857-866. PubMed ID: 35497811
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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; 50(3):155-158. PubMed ID: 27729211
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Refinement of the gene locus for autosomal dominant medullary cystic kidney disease type 1 (MCKD1) and construction of a physical and partial transcriptional map of the region.
    Fuchshuber A; Kroiss S; Karle S; Berthold S; Huck K; Burton C; Rahman N; Koptides M; Deltas C; Otto E; Rüschendorf F; Feest T; Hildebrandt F
    Genomics; 2001 Mar; 72(3):278-84. PubMed ID: 11401443
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Plasma Mucin-1 (CA15-3) Levels in Autosomal Dominant Tubulointerstitial Kidney Disease due to MUC1 Mutations.
    Vylet'al P; Kidd K; Ainsworth HC; Springer D; Vrbacká A; Přistoupilová A; Hughey RP; Alper SL; Lennon N; Harrison S; Harden M; Robins V; Taylor A; Martin L; Howard K; Bitar I; Langefeld CD; Barešová V; Hartmannová H; Hodaňová K; Zima T; Živná M; Kmoch S; Bleyer AJ
    Am J Nephrol; 2021; 52(5):378-387. PubMed ID: 34098564
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Induction of immune response and anti-tumor activities in mice with a DNA vaccine encoding human mucin 1 variable-number tandem repeats.
    Zhang S; Zhang H; Shi H; Yu X; Kong W; Li W
    Hum Immunol; 2008; 69(4-5):250-8. PubMed ID: 18486759
    [TBL] [Abstract][Full Text] [Related]  

  • 36. UMOD gene mutations in Chinese patients with autosomal dominant tubulointerstitial kidney disease: a pediatric case report and literature review.
    Yang J; Zhang Y; Zhou J
    BMC Pediatr; 2019 May; 19(1):145. PubMed ID: 31068150
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. MUC1 and estrogen receptor alpha gene polymorphisms in dry eye patients.
    Imbert Y; Foulks GN; Brennan MD; Jumblatt MM; John G; Shah HA; Newton C; Pouranfar F; Young WW
    Exp Eye Res; 2009 Mar; 88(3):334-8. PubMed ID: 18619437
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Identification of a novel UMOD mutation (c.163G>A) in a Brazilian family with autosomal dominant tubulointerstitial kidney disease.
    Lopes LB; Abreu CC; Souza CF; Guimaraes LER; Silva AA; Aguiar-Alves F; Kidd KO; Kmoch S; Bleyer AJ; Almeida JR
    Braz J Med Biol Res; 2018 Mar; 51(3):e6560. PubMed ID: 29513881
    [TBL] [Abstract][Full Text] [Related]  

  • 40.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.