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 *

99 related articles for article (PubMed ID: 8585925)

  • 21. Prime suspect for cystic kidneys.
    Nat Genet; 1994 Jul; 7(3):341-2. PubMed ID: 7920647
    [No Abstract]   [Full Text] [Related]  

  • 22. Phenotypic variability in PKD1: the family as a starting point.
    Guay-Woodford LM
    Kidney Int; 1999 Jul; 56(1):344-6. PubMed ID: 10411712
    [No Abstract]   [Full Text] [Related]  

  • 23. Tuberous sclerosis complex and early-onset autosomal dominant polycystic kidney disease as a 'contiguous gene' syndrome: report of a case.
    Mancino C; Balducci A
    Contrib Nephrol; 1997; 122():96-7. PubMed ID: 9399047
    [No Abstract]   [Full Text] [Related]  

  • 24. Identification of a gene for autosomal dominant polycystic kidney disease: implications for understanding the pathogenesis and treatment of the disease.
    Harris PC
    Nephrol Dial Transplant; 1996 Feb; 11(2):258-62. PubMed ID: 8700362
    [No Abstract]   [Full Text] [Related]  

  • 25. Genetic Complexity of Autosomal Dominant Polycystic Kidney and Liver Diseases.
    Cornec-Le Gall E; Torres VE; Harris PC
    J Am Soc Nephrol; 2018 Jan; 29(1):13-23. PubMed ID: 29038287
    [TBL] [Abstract][Full Text] [Related]  

  • 26. New amino acid polymorphism, Ala/Val4058, in exon 45 of the polycystic kidney disease 1 gene: evolution of alleles.
    Constantinides R; Xenophontos S; Neophytou P; Nomura S; Pierides A; Deltas CC
    Hum Genet; 1997 May; 99(5):644-7. PubMed ID: 9150733
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A novel cyclin gene (CCNF) in the region of the polycystic kidney disease gene (PKD1).
    Kraus B; Pohlschmidt M; Leung AL; Germino GG; Snarey A; Schneider MC; Reeders ST; Frischauf AM
    Genomics; 1994 Nov; 24(1):27-33. PubMed ID: 7896286
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Medullary cystic kidney disease with hyperuricemia and gout in a large Cypriot family: no allelism with nephronophthisis type 1.
    Stavrou C; Pierides A; Zouvani I; Kyriacou K; Antignac C; Neophytou P; Christodoulou K; Deltas CC
    Am J Med Genet; 1998 May; 77(2):149-54. PubMed ID: 9605289
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genetic heterogeneity of polycystic kidney disease in Bulgaria.
    Bogdanova N; Dworniczak B; Dragova D; Todorov V; Dimitrakov D; Kalinov K; Hallmayer J; Horst J; Kalaydjieva L
    Hum Genet; 1995 Jun; 95(6):645-50. PubMed ID: 7789949
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Autosomal dominant polycystic kidney disease: molecular analysis.
    Harris PC; Ward CJ; Peral B; Hughes J
    Hum Mol Genet; 1995; 4 Spec No():1745-9. PubMed ID: 8541874
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Interpretation of renal volume in autosomal dominant polycystic kidney disease and relevant clinical implications.
    Masoumi A; Elhassan E; Schrier RW
    Iran J Kidney Dis; 2011 Jan; 5(1):1-8. PubMed ID: 21189426
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Linkage disequilibrium between D16S94 and the locus for adult polycystic kidney disease (PKD1).
    Elles RG
    J Med Genet; 1992 Oct; 29(10):758. PubMed ID: 1433243
    [No Abstract]   [Full Text] [Related]  

  • 33. [Adult dominant polycystic kidney disease: molecular mechanisms and new therapeutic possibilities].
    Rodríguez Pérez JC; Torres MJ
    Nefrologia; 2006; 26(6):651-2. PubMed ID: 17227240
    [No Abstract]   [Full Text] [Related]  

  • 34. Type identification of autosomal dominant polycystic kidney disease by analysis of fluorescent short tandem repeat markers.
    Lin WD; Wu JY; Tsai FJ; Gau MT; Lee CC
    J Formos Med Assoc; 2002 Aug; 101(8):567-71. PubMed ID: 12440087
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Evidence of linkage disequilibrium in the Spanish polycystic kidney disease I population.
    Peral B; Ward CJ; San Millán JL; Thomas S; Stallings RL; Moreno F; Harris PC
    Am J Hum Genet; 1994 May; 54(5):899-908. PubMed ID: 7909986
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Recurrent fetal loss associated with bilineal inheritance of type 1 autosomal dominant polycystic kidney disease.
    Paterson AD; Wang KR; Lupea D; St George-Hyslop P; Pei Y
    Am J Kidney Dis; 2002 Jul; 40(1):16-20. PubMed ID: 12087556
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Autosomal dominant polycystic kidney disease unlinked to the PKD1 and PKD2 loci presenting as familial cerebral aneurysm.
    McConnell RS; Rubinsztein DC; Fannin TF; McKinstry CS; Kelly B; Bailey IC; Hughes AE
    J Med Genet; 2001 Apr; 38(4):238-40. PubMed ID: 11368027
    [No Abstract]   [Full Text] [Related]  

  • 38. Loss of the polycystic kidney disease (PKD1) region of chromosome 16p13 in renal cyst cells supports a loss-of-function model for cyst pathogenesis.
    Brasier JL; Henske EP
    J Clin Invest; 1997 Jan; 99(2):194-9. PubMed ID: 9005987
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Ultrasonographic study of pancreatic cysts in autosomal dominant polycystic kidney disease.
    Torra R; Nicolau C; Badenas C; Navarro S; Pérez L; Estivill X; Darnell A
    Clin Nephrol; 1997 Jan; 47(1):19-22. PubMed ID: 9021236
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Cutaneous white spots in a child with polycystic kidneys: a clue to TSC2/PKD1 gene mutation.
    Sperandio M; Weber L; Jauch A; Janssen B; Mehls O; Schaefer F
    Nephrol Dial Transplant; 2000 Jun; 15(6):909-12. PubMed ID: 10831653
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.