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Journal Abstract Search

382 related items for PubMed ID: 8140421

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  • 5. Water channels encoded by mutant aquaporin-2 genes in nephrogenic diabetes insipidus are impaired in their cellular routing.
    Deen PM, Croes H, van Aubel RA, Ginsel LA, van Os CH.
    J Clin Invest; 1995 May; 95(5):2291-6. PubMed ID: 7537761
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  • 10. [Vasopressin type 2 receptor mutations in congenital diabetes insipidus].
    Tsukaguchi H, Matsubara H, Inada M.
    Nihon Rinsho; 1998 Jul; 56(7):1848-55. PubMed ID: 9702064
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  • 14. A novel mechanism in recessive nephrogenic diabetes insipidus: wild-type aquaporin-2 rescues the apical membrane expression of intracellularly retained AQP2-P262L.
    de Mattia F, Savelkoul PJ, Bichet DG, Kamsteeg EJ, Konings IB, Marr N, Arthus MF, Lonergan M, van Os CH, van der Sluijs P, Robertson G, Deen PM.
    Hum Mol Genet; 2004 Dec 15; 13(24):3045-56. PubMed ID: 15509592
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  • 20. Nephrogenic diabetes insipidus in mice caused by deleting COOH-terminal tail of aquaporin-2.
    Shi PP, Cao XR, Qu J, Volk KA, Kirby P, Williamson RA, Stokes JB, Yang B.
    Am J Physiol Renal Physiol; 2007 May 15; 292(5):F1334-44. PubMed ID: 17229678
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