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PUBMED FOR HANDHELDS

Journal Abstract Search


176 related items for PubMed ID: 7564126

  • 1. Expression studies of two vasopressin V2 receptor gene mutations, R202C and 804insG, in nephrogenic diabetes insipidus.
    Tsukaguchi H, Matsubara H, Inada M.
    Kidney Int; 1995 Aug; 48(2):554-62. PubMed ID: 7564126
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  • 5. The role of conserved extracellular cysteine residues in vasopressin V2 receptor function and properties of two naturally occurring mutant receptors with additional extracellular cysteine residues.
    Schülein R, Zühlke K, Oksche A, Hermosilla R, Furkert J, Rosenthal W.
    FEBS Lett; 2000 Jan 21; 466(1):101-6. PubMed ID: 10648821
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  • 6. Two novel mutations in the vasopressin V2 receptor gene in unrelated Japanese kindreds with nephrogenic diabetes insipidus.
    Tsukaguchi H, Matsubara H, Aritaki S, Kimura T, Abe S, Inada M.
    Biochem Biophys Res Commun; 1993 Dec 15; 197(2):1000-10. PubMed ID: 8267567
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  • 9. AVPR2 variants and V2 vasopressin receptor function in nephrogenic diabetes insipidus.
    Wildin RS, Cogdell DE, Valadez V.
    Kidney Int; 1998 Dec 15; 54(6):1909-22. PubMed ID: 9853256
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  • 10. Vasopressin V2 receptor mutants that cause X-linked nephrogenic diabetes insipidus: analysis of expression, processing, and function.
    Oksche A, Schülein R, Rutz C, Liebenhoff U, Dickson J, Müller H, Birnbaumer M, Rosenthal W.
    Mol Pharmacol; 1996 Oct 15; 50(4):820-8. PubMed ID: 8863826
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  • 13. Six novel mutations in the vasopressin V2 receptor gene causing nephrogenic diabetes insipidus.
    Cheong HI, Park HW, Ha IS, Moon HN, Choi Y, Ko KW, Jun JK.
    Nephron; 1997 Oct 15; 75(4):431-7. PubMed ID: 9127330
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  • 18. Mutations in the vasopressin V2 receptor gene in two families with nephrogenic diabetes insipidus.
    Holtzman EJ, Kolakowski LF, Geifman-Holtzman O, O'Brien DG, Rasoulpour M, Guillot AP, Ausiello DA.
    J Am Soc Nephrol; 1994 Aug 15; 5(2):169-76. PubMed ID: 7993996
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  • 20. Nephrogenic diabetes insipidus caused by mutation of Tyr205: a key residue of V2 vasopressin receptor function.
    Sangkuhl K, Römpler H, Busch W, Karges B, Schöneberg T.
    Hum Mutat; 2005 May 15; 25(5):505. PubMed ID: 15841479
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