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Journal Abstract Search

379 related items for PubMed ID: 9171830

  • 1. 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
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  • 6. PKD2 mutations in a Czech population with autosomal dominant polycystic kidney disease.
    Stekrová J, Reiterová J, Merta M, Damborsky J, Zidovská J, Kebrdlová V, Kohoutová M.
    Nephrol Dial Transplant; 2004 May; 19(5):1116-22. PubMed ID: 14993477
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  • 7. Co-assembly of polycystin-1 and -2 produces unique cation-permeable currents.
    Hanaoka K, Qian F, Boletta A, Bhunia AK, Piontek K, Tsiokas L, Sukhatme VP, Guggino WB, Germino GG.
    Nature; 2004 May; 408(6815):990-4. PubMed ID: 11140688
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  • 10. Molecular genetics and mechanism of autosomal dominant polycystic kidney disease.
    Wu G, Somlo S.
    Mol Genet Metab; 2000 Jan; 69(1):1-15. PubMed ID: 10655152
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  • 11. Autosomal dominant polycystic kidney disease: clinical and genetic aspects.
    Sessa A, Ghiggeri GM, Turco AE.
    J Nephrol; 1997 Jan; 10(6):295-310. PubMed ID: 9442442
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  • 12. 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
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  • 14. Mutations of the human polycystic kidney disease 2 (PKD2) gene.
    Deltas CC.
    Hum Mutat; 2001 May; 18(1):13-24. PubMed ID: 11438989
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  • 15. Molecular genetics of polycystic kidney disease.
    Calvet JP.
    J Nephrol; 1998 May; 11(1):24-34. PubMed ID: 9561482
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  • 17. A splice form of polycystin-2, lacking exon 7, does not interact with polycystin-1.
    Hackmann K, Markoff A, Qian F, Bogdanova N, Germino GG, Pennekamp P, Dworniczak B, Horst J, Gerke V.
    Hum Mol Genet; 2005 Nov 01; 14(21):3249-62. PubMed ID: 16192288
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  • 18. Mutations of PKD1 in ADPKD2 cysts suggest a pathogenic effect of trans-heterozygous mutations.
    Watnick T, He N, Wang K, Liang Y, Parfrey P, Hefferton D, St George-Hyslop P, Germino G, Pei Y.
    Nat Genet; 2000 Jun 01; 25(2):143-4. PubMed ID: 10835625
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  • 19. Novel method for genomic analysis of PKD1 and PKD2 mutations in autosomal dominant polycystic kidney disease.
    Tan YC, Blumenfeld JD, Anghel R, Donahue S, Belenkaya R, Balina M, Parker T, Levine D, Leonard DG, Rennert H.
    Hum Mutat; 2009 Feb 01; 30(2):264-73. PubMed ID: 18837007
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  • 20. Diagnostic approach in autosomal dominant polycystic kidney disease.
    Pei Y.
    Clin J Am Soc Nephrol; 2006 Sep 01; 1(5):1108-14. PubMed ID: 17699332
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