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 *

446 related articles for article (PubMed ID: 12647363)

  • 21. Common regulatory elements in the polycystic kidney disease 1 and 2 promoter regions.
    Lantinga-van Leeuwen IS; Leonhard WN; Dauwerse H; Baelde HJ; van Oost BA; Breuning MH; Peters DJ
    Eur J Hum Genet; 2005 May; 13(5):649-59. PubMed ID: 15770226
    [TBL] [Abstract][Full Text] [Related]  

  • 22. PKD1 interacts with PKD2 through a probable coiled-coil domain.
    Qian F; Germino FJ; Cai Y; Zhang X; Somlo S; Germino GG
    Nat Genet; 1997 Jun; 16(2):179-83. PubMed ID: 9171830
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Pax2 gene dosage influences cystogenesis in autosomal dominant polycystic kidney disease.
    Stayner C; Iglesias DM; Goodyer PR; Ellis L; Germino G; Zhou J; Eccles MR
    Hum Mol Genet; 2006 Dec; 15(24):3520-8. PubMed ID: 17082250
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The role of the polycystins in kidney development.
    van Adelsberg JS
    Pediatr Nephrol; 1999 Jun; 13(5):454-9. PubMed ID: 10412869
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Molecular genetics of polycystic kidney disease.
    Calvet JP
    J Nephrol; 1998; 11(1):24-34. PubMed ID: 9561482
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Toxic tubular injury in kidneys from Pkd1-deletion mice accelerates cystogenesis accompanied by dysregulated planar cell polarity and canonical Wnt signaling pathways.
    Happé H; Leonhard WN; van der Wal A; van de Water B; Lantinga-van Leeuwen IS; Breuning MH; de Heer E; Peters DJ
    Hum Mol Genet; 2009 Jul; 18(14):2532-42. PubMed ID: 19401297
    [TBL] [Abstract][Full Text] [Related]  

  • 27. PKD1 haploinsufficiency causes a syndrome of inappropriate antidiuresis in mice.
    Ahrabi AK; Terryn S; Valenti G; Caron N; Serradeil-Le Gal C; Raufaste D; Nielsen S; Horie S; Verbavatz JM; Devuyst O
    J Am Soc Nephrol; 2007 Jun; 18(6):1740-53. PubMed ID: 17475819
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Co-inheritance of a PKD1 mutation and homozygous PKD2 variant: a potential modifier in autosomal dominant polycystic kidney disease.
    Dedoussis GV; Luo Y; Starremans P; Rossetti S; Ramos AJ; Cantiello HF; Katsareli E; Ziroyannis P; Lamnissou K; Harris PC; Zhou J
    Eur J Clin Invest; 2008 Mar; 38(3):180-90. PubMed ID: 18257781
    [TBL] [Abstract][Full Text] [Related]  

  • 29. In vitro cystogenesis: the search for drugs antagonizing cyst development.
    Ibraghimov-Beskrovnaya O; Bukanov NO
    Nephrol Ther; 2006 Jan; 2 Suppl 2():S109-14. PubMed ID: 17373209
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Polycystic kidney disease: new understanding in the pathogenesis.
    Wilson PD
    Int J Biochem Cell Biol; 2004 Oct; 36(10):1868-73. PubMed ID: 15203099
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A truncated polycystin-2 protein causes polycystic kidney disease and retinal degeneration in transgenic rats.
    Gallagher AR; Hoffmann S; Brown N; Cedzich A; Meruvu S; Podlich D; Feng Y; Könecke V; de Vries U; Hammes HP; Gretz N; Witzgall R
    J Am Soc Nephrol; 2006 Oct; 17(10):2719-30. PubMed ID: 16943309
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Association of PKD2 (polycystin 2) mutations with left-right laterality defects.
    Bataille S; Demoulin N; Devuyst O; Audrézet MP; Dahan K; Godin M; Fontès M; Pirson Y; Burtey S
    Am J Kidney Dis; 2011 Sep; 58(3):456-60. PubMed ID: 21719175
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Polycystins, calcium signaling, and human diseases.
    Delmas P; Padilla F; Osorio N; Coste B; Raoux M; Crest M
    Biochem Biophys Res Commun; 2004 Oct; 322(4):1374-83. PubMed ID: 15336986
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Trans-heterozygous Pkd1 and Pkd2 mutations modify expression of polycystic kidney disease.
    Wu G; Tian X; Nishimura S; Markowitz GS; D'Agati V; Park JH; Yao L; Li L; Geng L; Zhao H; Edelmann W; Somlo S
    Hum Mol Genet; 2002 Aug; 11(16):1845-54. PubMed ID: 12140187
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Curcumin inhibits cystogenesis by simultaneous interference of multiple signaling pathways: in vivo evidence from a Pkd1-deletion model.
    Leonhard WN; van der Wal A; Novalic Z; Kunnen SJ; Gansevoort RT; Breuning MH; de Heer E; Peters DJ
    Am J Physiol Renal Physiol; 2011 May; 300(5):F1193-202. PubMed ID: 21345977
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Deletion of the TSC2 and PKD1 genes associated with severe infantile polycystic kidney disease--a contiguous gene syndrome.
    Brook-Carter PT; Peral B; Ward CJ; Thompson P; Hughes J; Maheshwar MM; Nellist M; Gamble V; Harris PC; Sampson JR
    Nat Genet; 1994 Dec; 8(4):328-32. PubMed ID: 7894481
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells.
    Nauli SM; Alenghat FJ; Luo Y; Williams E; Vassilev P; Li X; Elia AE; Lu W; Brown EM; Quinn SJ; Ingber DE; Zhou J
    Nat Genet; 2003 Feb; 33(2):129-37. PubMed ID: 12514735
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Autosomal recessive and dominant polycystic kidney diseases.
    Sessa A; Righetti M; Battini G
    Minerva Urol Nefrol; 2004 Dec; 56(4):329-38. PubMed ID: 15785425
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Polycystic liver and kidney diseases.
    Tahvanainen E; Tahvanainen P; Kääriäinen H; Höckerstedt K
    Ann Med; 2005; 37(8):546-55. PubMed ID: 16338757
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Lowering of Pkd1 expression is sufficient to cause polycystic kidney disease.
    Lantinga-van Leeuwen IS; Dauwerse JG; Baelde HJ; Leonhard WN; van de Wal A; Ward CJ; Verbeek S; Deruiter MC; Breuning MH; de Heer E; Peters DJ
    Hum Mol Genet; 2004 Dec; 13(24):3069-77. PubMed ID: 15496422
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 23.