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1) Preston GM, Carroll TP, Guggino WB, et al. Appearance of water channels in Xenopus oocytes expressing red cell CHIP28 protein. Science. 1992; 256: 385-7
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2) Agre P, Sasaki S, Chrispeels MJ. Aquaporins: a family of water channel proteins. Am J Physiol. 1993; 265: F461
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3) Agre P, King LS, Yasui M, et al. Aquaporin water channels-from atomic structure to clinical medicine. J Physiol. 2002; 542(Pt 1): 3-16
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4) Noda Y, Sohara E, Ohta E, et al. Aquaporins in kidney pathophysiology. Nat Rev Nephrol. 2010; 6(3); 168-78
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5) King LS, Choi M, Fernandez PC, et al. Defective urinary-concentrating ability due to a complete deficiency of aquaporin-1. N Engl J Med. 2001; 345: 175-9
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6) Verkman AS. Physiological importance of aquaporin water channels. Ann Med. 2002; 34: 192-200
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7) Saadoun S, Papadopoulos MC, Hara-Chikuma M, et al. Impairment of angiogenesis and cell migration by targeted aquaporin-1 gene disruption. Nature. 2005; 434: 786-92
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8) Noda Y, Horikawa S, Kanda E, et al. Reciprocal interaction with G-actin and tropomyosin is essential for aquaporin-2 trafficking. J Cell Biol. 2008; 182: 587-601
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9) Kuwahara M, Iwai K, Ooeda T, et al. Three families with autosomal dominant nephrogenic diabetes insipidus caused by aquaporin-2 mutations in the C-terminus. Am J Hum Genet. 2001; 69: 738-48
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10) Sohara E, Rai T, Yang SS, et al. Pathogenesis and treatment of autosomal-dominant nephrogenic diabetes insipidus caused by an aquaporin 2 mutation. Proc Natl Acad Sci U S A. 2006; 103: 14217-22
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11) Roudier N, Ripoche P, Gane P, et al. AQP3 deficiency in humans and the molecular basis of a novel blood group system, GIL. J Biol Chem. 2002; 277: 45854-9
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12) Manley GT, Fujimura M, Ma T, et al. Aquaporin-4 deletion in mice reduces brain edema after acute water intoxication and ischemic stroke. Nat Med. 2000; 6: 159-63
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13) Yasui M, Kwon TH, Knepper MA, et al. Aquaporin-6: An intracellular vesicle water channel protein in renal epithelia. Proc Natl Acad Sci U S A. 1999; 96: 5808-13
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14) 安井正人. アクアポリン研究の最前線. Annual Review 腎臓2008. 東京: 中外医学社; 2008. p.31-5
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15) Kondo H, Shimomura I, Kishida K, et al. Human aquaporin adipose (AQPap) gene. Genomic structure, promoter analysis and functional mutation. Eur J Biochem. 2002; 269: 1814-26
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16) Sohara E, Rai T, Miyazaki J, et al. Defective water and glycerol transport in the proximal tubules of AQP7 knockout mice. Am J Physiol Renal Physiol. 2005; 289: F1195-200
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17) Maeda N, Funahashi T, Hibuse T, et al. Adaptation to fasting by glycerol transport through aquaporin 7 in adipose tissue. Proc Natl Acad Sci U S A. 2004; 101: 17801-6
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18) Hara-Chikuma M, Sohara E, Rai T, et al. Progressive adipocyte hypertrophy in aquaporin-7-deficient mice: adipocyte glycerol permeability as a novel regulator of fat accumulation. J Biol Chem. 2005; 280: 15493-6
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19) Morishita Y, Sakube Y, Sasaki S, et al. Molecular mechanisms and drug development in aquaporin water channel diseases: aquaporin superfamily (superaquaporins): expansion of aquaporins restricted to multicellular organisms. J Pharmacol Sci. 2004; 96: 276-9
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20) Yakata K, Hiroaki Y, Ishibashi K, et al. Aquaporin-11 containing a divergent NPA motif has normal water channel activity. Biochim Biophys Acta. 2007; 1768: 688-93
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21) Morishita Y, Matsuzaki T, Hara-Chikuma M, et al. Disruption of aquaporin-11 produces polycystic kidneys following vacuolization of the proximal tubule. Mol Cell Biol. 2005; 25: 7770-9
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