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1)Gordon RD. Syndrome of hypertension and hyperkalemia with normal glomerular filtration rate. Hypertension. 1986; 8: 93-102
PubMed CrossRef
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2)Wilson FH, Disse-Nicodème S, Choate KA, et al. Human hypertension caused by mutations in WNK kinases. Science. 2001; 293: 1107-12
PubMed CrossRef
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3)Moriguchi T, Urushiyama S, Hisamoto N, et al. WNK1 regulates phosphorylation of cation-chloride-coupled cotransporters via the STE20-related kinases, SPAK and OSR1. J Biol Chem. 2005; 280: 42685-93
PubMed CrossRef
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4)Yang SS, Morimoto T, Rai T, et al. Molecular pathogenesis of pseudohypoaldosteronism type II: generation and analysis of a Wnk4(D561A/.) knockin mouse model. Cell Metab. 2007; 5: 331-44
PubMed CrossRef
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5)Ohta A, Rai T, Yui N, et al. Targeted disruption of the Wnk4 gene decreases phosphorylation of Na-Cl cotransporter, increases Na excretion and lowers blood pressure. Hum Mol Genet. 2009; 18: 3978-86
PubMed CrossRef
医中誌リンクサービス
6)Castaneda-Bueno M, Cervantes-Perez LG, Vazquez N, et al. Activation of the renal Na.:Cl_ cotransporter by angiotensin II is a WNK4-dependent process. Proc Natl Acad Sci U S A. 2012; 109: 7929-34
PubMed CrossRef
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7)Boyden LM, Choi M, Choate KA, et al. Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities. Nature. 2012; 482: 98-102
PubMed CrossRef
医中誌リンクサービス
8)Louis-Dit-Picard H, Barc J, Trujillano D, et al. KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron. Nat Genet. 2012; 44: 456-60
PubMed CrossRef
医中誌リンクサービス
9)Genschik P, Sumara I, Lechner E. The emerging family of CULLIN3-RING ubiquitin ligases (CRL3 s): cellular functions and disease implications. EMBO J. 2013; 32: 2307-20
PubMed CrossRef
医中誌リンクサービス
10)Adams J, Kelso R, Cooley L. The kelch repeat superfamily of proteins: propellers of cell function. Trends Cell Biol. 2000; 10: 17-24
PubMed CrossRef
医中誌リンクサービス
11)Kigoshi Y, Tsuruta F, Chiba T. Ubiquitin ligase activity of Cul3-KLHL7 protein is attenuated by autosomal dominant retinitis pigmentosa causative mutation. J Biol Chem. 2011; 286: 33613-21
PubMed CrossRef
医中誌リンクサービス
12)Cirak S, von Deimling F, Sachdev S, et al. Kelch-like homologue 9 mutation is associated with an early onset autosomal dominant distal myopathy. Brain. 2010; 133: 2123-35
PubMed CrossRef
医中誌リンクサービス
13)Bomont P, Cavalier L, Blondeau F, et al. The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy. Nat Genet. 2000; 26: 370-4
PubMed CrossRef
医中誌リンクサービス
14)Ohta A, Schumacher FR, Mehellou Y, et al. The CUL3-KLHL3 E3 ligase complex mutated in Gordon’s hypertension syndrome interacts with and ubiquitylates WNK isoforms: disease-causing mutations in KLHL3 and WNK4 disrupt interaction. Biochem J. 2013; 451: 111-22
PubMed CrossRef
医中誌リンクサービス
15)Wakabayashi M, Mori T, Isobe K, et al. Impaired KLHL3-mediated ubiquitination of WNK4 causes human hypertension. Cell Rep. 2013; 3: 858-68
PubMed
医中誌リンクサービス
16)Shibata S, Zhang J, Puthumana J, et al. Kelch-like 3 and Cullin 3 regulate electrolyte homeostasis via ubiquitination and degradation of WNK4. Proc Natl Acad Sci U S A. 2013; 110: 7838-43
PubMed CrossRef
医中誌リンクサービス
17)Wu G, Peng JB. Disease-causing mutations in KLHL3 impair its effect on WNK4 degradation. FEBS Lett. 2013; 587: 1717-22
PubMed CrossRef
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18)Mori Y, Wakabayashi M, Mori T, et al. Decrease of WNK4 ubiquitination by disease-causing mutations of KLHL3 through different molecular mechanisms. Biochem Biophys Res Commun. 2013; 439: 30-4
PubMed CrossRef
医中誌リンクサービス
19)Osawa M, Ogura Y, Isobe K, et al. CUL3 gene analysis enables early intervention for pediatric pseudohypoaldosteronism type II in infancy. Pediatr Nephrol. 2013; 28: 1881-4
PubMed CrossRef
医中誌リンクサービス
20)Tsuji S, Yamashita M, Unishi G, et al. A young child with pseudohypoaldosteronism type II by a mutation of Cullin 3. BMC Nephrol. 2013; 14: 166
PubMed
医中誌リンクサービス
21)Susa K, Sohara E, Rai T, et al. Impaired degradation of WNK1 and WNK4 kinases causes PHAII in mutant KLHL3 knock-in mice. Hum Mol Genet. 2014; 23: 5052-60
CrossRef
医中誌リンクサービス
22)Chiga M, Rafiqi FH, Alessi DR, et al. Phenotypes of pseudohypoaldosteronism type II caused by the WNK4 D561A missense mutation are dependent on the WNK-OSR1/SPAK kinase cascade. J Cell Sci. 2011; 124: 1391-5
PubMed CrossRef
医中誌リンクサービス
23)Vallon V, Schroth J, Lang F, et al. Expression and phosphorylation of the Na+-Cl- cotransporter NCC in vivo is regulated by dietary salt, potassium, and SGK1. Am J Physiol Renal Physiol. 2009; 297: F704-12
PubMed
医中誌リンクサービス
24)Sohara E, Rai T, Yang SS, et al. Acute insulin stimulation induces phosphorylation of the Na-Cl cotransporter in cultured distal mpkDCT cells and mouse kidney. PLoS One. 2011; 6: e24277
CrossRef
医中誌リンクサービス
25)Talati G, Ohta A, Rai T, et al. Effect of angiotensin II on the WNK-OSR1/SPAK-NCC phosphorylation cascade in cultured mpkDCT cells and in vivo mouse kidney. Biochem Biophys Res Commun. 2010; 393: 844-8
PubMed CrossRef
医中誌リンクサービス
26)McCormick JA, Ellison DH. The WNKs: atypical protein kinases with pleiotropic actions. Physiol Rev. 2011; 91: 177-219
PubMed CrossRef
医中誌リンクサービス
27)Wilson FH, Kahle KT, Sabath E, et al. Molecular pathogenesis of inherited hypertension with hyperkalemia: the Na-Cl cotransporter is inhibited by wildtype but not mutant WNK4. Proc Natl Acad Sci U S A. 2003; 100: 680-4
PubMed CrossRef
医中誌リンクサービス
28)Yang CL, Angell J, Mitchell R, et al. WNK kinases regulate thiazide-sensitive Na-Cl cotransport. J Clin Invest. 2003; 111: 1039-45
PubMed CrossRef
医中誌リンクサービス
29)Lalioti MD, Zhang J, Volkman HM, et al. Wnk4 controls blood pressure and potassium homeostasis via regulation of mass and activity of the distal convoluted tubule. Nat Genet. 2006; 38: 1124-32
PubMed CrossRef
医中誌リンクサービス
30)Uchida S. Regulation of blood pressure and renal electrolyte balance by Cullin-RING ligases. Curr Opin Nephrol Hypertens. 2014; 23: 487-93
CrossRef
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