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420 related items for PubMed ID: 15509592

  • 41. Effect of the cGMP pathway on AQP2 expression and translocation: potential implications for nephrogenic diabetes insipidus.
    Boone M, Kortenoeven M, Robben JH, Deen PM.
    Nephrol Dial Transplant; 2010 Jan; 25(1):48-54. PubMed ID: 19666909
    [Abstract] [Full Text] [Related]

  • 42. Characterization of an aquaporin-2 water channel gene mutation causing partial nephrogenic diabetes insipidus in a Mexican family: evidence of increased frequency of the mutation in the town of origin.
    Boccalandro C, De Mattia F, Guo DC, Xue L, Orlander P, King TM, Gupta P, Deen PM, Lavis VR, Milewicz DM.
    J Am Soc Nephrol; 2004 May; 15(5):1223-31. PubMed ID: 15100362
    [Abstract] [Full Text] [Related]

  • 43. Vasopressin receptor mutations causing nephrogenic diabetes insipidus.
    Bichet DG, Turner M, Morin D.
    Proc Assoc Am Physicians; 1998 May; 110(5):387-94. PubMed ID: 9756088
    [Abstract] [Full Text] [Related]

  • 44. Novel mutations in aquaporin-2 gene in female siblings with nephrogenic diabetes insipidus: evidence of disrupted water channel function.
    Goji K, Kuwahara M, Gu Y, Matsuo M, Marumo F, Sasaki S.
    J Clin Endocrinol Metab; 1998 Sep; 83(9):3205-9. PubMed ID: 9745427
    [Abstract] [Full Text] [Related]

  • 45. Neonatal mortality in an aquaporin-2 knock-in mouse model of recessive nephrogenic diabetes insipidus.
    Yang B, Gillespie A, Carlson EJ, Epstein CJ, Verkman AS.
    J Biol Chem; 2001 Jan 26; 276(4):2775-9. PubMed ID: 11035038
    [Abstract] [Full Text] [Related]

  • 46. Ser-256 phosphorylation dynamics of Aquaporin 2 during maturation from the ER to the vesicular compartment in renal cells.
    Procino G, Carmosino M, Marin O, Brunati AM, Contri A, Pinna LA, Mannucci R, Nielsen S, Kwon TH, Svelto M, Valenti G.
    FASEB J; 2003 Oct 26; 17(13):1886-8. PubMed ID: 12897058
    [Abstract] [Full Text] [Related]

  • 47. Effects of missense mutations on rat aquaporin-2 in LLC-PK1 porcine kidney cells.
    Yamauchi K, Fushimi K, Yamashita Y, Shinbo I, Sasaki S, Marumo F.
    Kidney Int; 1999 Jul 26; 56(1):164-71. PubMed ID: 10411689
    [Abstract] [Full Text] [Related]

  • 48. Diffusion in the endoplasmic reticulum of an aquaporin-2 mutant causing human nephrogenic diabetes insipidus.
    Levin MH, Haggie PM, Vetrivel L, Verkman AS.
    J Biol Chem; 2001 Jun 15; 276(24):21331-6. PubMed ID: 11297561
    [Abstract] [Full Text] [Related]

  • 49. Missorting of the Aquaporin-2 mutant E258K to multivesicular bodies/lysosomes in dominant NDI is associated with its monoubiquitination and increased phosphorylation by PKC but is due to the loss of E258.
    Kamsteeg EJ, Savelkoul PJ, Hendriks G, Konings IB, Nivillac NM, Lagendijk AK, van der Sluijs P, Deen PM.
    Pflugers Arch; 2008 Mar 15; 455(6):1041-54. PubMed ID: 17965877
    [Abstract] [Full Text] [Related]

  • 50. Genetic forms of nephrogenic diabetes insipidus (NDI): Vasopressin receptor defect (X-linked) and aquaporin defect (autosomal recessive and dominant).
    Bichet DG, Bockenhauer D.
    Best Pract Res Clin Endocrinol Metab; 2016 Mar 15; 30(2):263-76. PubMed ID: 27156763
    [Abstract] [Full Text] [Related]

  • 51. Misfolding of mutant aquaporin-2 water channels in nephrogenic diabetes insipidus.
    Tamarappoo BK, Yang B, Verkman AS.
    J Biol Chem; 1999 Dec 03; 274(49):34825-31. PubMed ID: 10574954
    [Abstract] [Full Text] [Related]

  • 52. Molecular mechanisms and drug development in aquaporin water channel diseases: molecular mechanism of water channel aquaporin-2 trafficking.
    Noda Y, Sasaki S.
    J Pharmacol Sci; 2004 Nov 03; 96(3):249-54. PubMed ID: 15539762
    [Abstract] [Full Text] [Related]

  • 53. Patients with autosomal nephrogenic diabetes insipidus homozygous for mutations in the aquaporin 2 water-channel gene.
    van Lieburg AF, Verdijk MA, Knoers VV, van Essen AJ, Proesmans W, Mallmann R, Monnens LA, van Oost BA, van Os CH, Deen PM.
    Am J Hum Genet; 1994 Oct 03; 55(4):648-52. PubMed ID: 7524315
    [Abstract] [Full Text] [Related]

  • 54. 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 03; 292(5):F1334-44. PubMed ID: 17229678
    [Abstract] [Full Text] [Related]

  • 55. Methyl-beta-cyclodextrin induces vasopressin-independent apical accumulation of aquaporin-2 in the isolated, perfused rat kidney.
    Russo LM, McKee M, Brown D.
    Am J Physiol Renal Physiol; 2006 Jul 03; 291(1):F246-53. PubMed ID: 16449354
    [Abstract] [Full Text] [Related]

  • 56. Molecular characterization of an aquaporin-2 mutation causing a severe form of nephrogenic diabetes insipidus.
    Saglar Ozer E, Moeller HB, Karaduman T, Fenton RA, Mergen H.
    Cell Mol Life Sci; 2020 Mar 03; 77(5):953-962. PubMed ID: 31302751
    [Abstract] [Full Text] [Related]

  • 57. [Nephrogenic diabetes insipidus associated with mutations of vasopressin V2 receptors and aquaporin-2].
    Ishikawa SE.
    Nihon Rinsho; 2002 Feb 03; 60(2):350-5. PubMed ID: 11857925
    [Abstract] [Full Text] [Related]

  • 58. Aquaporin-2: COOH terminus is necessary but not sufficient for routing to the apical membrane.
    Deen PM, Van Balkom BW, Savelkoul PJ, Kamsteeg EJ, Van Raak M, Jennings ML, Muth TR, Rajendran V, Caplan MJ.
    Am J Physiol Renal Physiol; 2002 Feb 03; 282(2):F330-40. PubMed ID: 11788448
    [Abstract] [Full Text] [Related]

  • 59. Molecular Characterization of an Aquaporin-2 Mutation Causing Nephrogenic Diabetes Insipidus.
    Li Q, Lu B, Yang J, Li C, Li Y, Chen H, Li N, Duan L, Gu F, Zhang J, Xia W.
    Front Endocrinol (Lausanne); 2021 Feb 03; 12():665145. PubMed ID: 34512542
    [Abstract] [Full Text] [Related]

  • 60. Nephrogenic diabetes insipidus.
    Knoers NV, Monnens LL.
    Semin Nephrol; 1999 Jul 03; 19(4):344-52. PubMed ID: 10435672
    [Abstract] [Full Text] [Related]

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