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XB-ANAT-86
Papers associated with tail region (and aqp2)
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Aquaporin-2: new mutations responsible for autosomal-recessive nephrogenic diabetes insipidus-update and epidemiology., Bichet DG., Clin Kidney J. June 1, 2012; 5 (3): 195-202.  |
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Role of multiple phosphorylation sites in the COOH-terminal tail of aquaporin-2 for water transport: evidence against channel gating., Moeller HB., Am J Physiol Renal Physiol. March 1, 2009; 296 (3): F649-57. |
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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., Hum Mol Genet. December 15, 2004; 13 (24): 3045-56. |
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Three families with autosomal dominant nephrogenic diabetes insipidus caused by aquaporin-2 mutations in the C-terminus., Kuwahara M., Am J Hum Genet. October 1, 2001; 69 (4): 738-48. |
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An aquaporin-2 water channel mutant which causes autosomal dominant nephrogenic diabetes insipidus is retained in the Golgi complex., Mulders SM., J Clin Invest. July 1, 1998; 102 (1): 57-66. |
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