医中誌リンクサービス


文献リスト

1)Kupper N, Willemsen G, Riese H, et al. Heritability of daytime ambulatory blood pressure in an extended twin design. Hypertension. 2005; 45: 80-5
PubMed CrossRef
医中誌リンクサービス
2)Katsuya T, Ishikawa K, Sugimoto K, et al. Salt sensitivity of Japanese from the viewpoint of gene polymorphism. Hypertens Res. 2003; 26: 521-5
医学中央雑誌刊行会  PubMed CrossRef J-Stage
医中誌リンクサービス
3)Choi M, Scholl UI, Yue P, et al. K+ channel mutations in adrenal aldosterone-producing adenomas and hereditary hypertension. Science. 2011; 331: 768-72
PubMed
医中誌リンクサービス
4)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
5)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
6)Gordon RD. Syndrome of hypertension and hyperkalemia with normal glomerular filtration rate. Hypertension. 1986; 8: 93-102
PubMed CrossRef
医中誌リンクサービス
7)Wilson FH, Disse-Nicodème S, Choate KA, et al. Human hypertension caused by mutations in WNK kinases. Science. 2001; 293: 1107-12
PubMed
医中誌リンクサービス
8)Xu B, English JM, Wilsbacher JL, et al. WNK1, a novel mammalian serine/threonine protein kinase lacking the catalytic lysine in subdomain II. J Biol Chem. 2000; 275: 16795-801
PubMed CrossRef
医中誌リンクサービス
9)Ohno M, Uchida K, Ohashi T, et al. Immunolocalization of WNK4 in mouse kidney. Histochem Cell Biol. 2011; 136: 25-35
PubMed CrossRef
医中誌リンクサービス
10)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
医中誌リンクサービス
11)Vitari AC, Deak M, Morrice NA, et al. The WNK1 and WNK4 protein kinases that are mutated in Gordonʼs hypertension syndrome phosphorylate and activate SPAK and OSR1 protein kinases. Biochem J. 2005; 391: 17-24
PubMed CrossRef
医中誌リンクサービス
12)Rafiqi FH, Zuber AM, Glover M, et al. Role of the WNK-activated SPAK kinase in regulating blood pressure. EMBO Mol Med. 2010; 2: 63-75
PubMed CrossRef
医中誌リンクサービス
13)Yang SS, Lo YF, Wu CC, et al. SPAK-knockout mice manifest Gitelman syndrome and impaired vasoconstriction. J Am Soc Nephrol. 2010; 21: 1868-77
PubMed CrossRef
医中誌リンクサービス
14)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
15)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
16)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
17)Castañeda-Bueno M, Cervantes-Pérez LG, Vázquez 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
医中誌リンクサービス
18)Chiga M, Rai T, Yang SS, et al. Dietary salt regulates the phosphorylation of OSR1/SPAK kinases and the sodium chloride cotransporter through aldosterone. Kidney Int. 2008; 74: 1403-9
PubMed CrossRef
医中誌リンクサービス
19)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
20)Mutig K, Saritas T, Uchida S, et al. Short-term stimulation of the thiazide-sensitive Na+-Cl− cotransporter by vasopressin involves phosphorylation and membrane translocation. Am J Physiol Renal Physiol. 2010; 298: F502-9
PubMed
医中誌リンクサービス
21)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
22)Naito S, Ohta A, Sohara E, et al. Regulation of WNK1 kinase by extracellular potassium. Clin Exp Nephrol. 2011; 15: 195-202
医学中央雑誌刊行会  PubMed CrossRef
医中誌リンクサービス
23)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
24)Nishida H, Sohara E, Nomura N, et al. Phosphatidylinositol 3-kinase/Akt signaling pathway activates the WNK-OSR1/SPAK-NCC phosphorylation cascade in hyperinsulinemic db/db mice. Hypertension. 2012; 60: 981-90
PubMed CrossRef
医中誌リンクサービス
25)Albagli O, Dhordain P, Deweindt C, et al. The BTB/POZ domain: a new protein-protein interaction motif common to DNA- and actin-binding proteins. Cell Growth Differ. 1995; 6: 1193-8
PubMed
医中誌リンクサービス
26)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
27)Furukawa M, He YJ, Borchers C, et al. Targeting of protein ubiquitination by BTB-Cullin 3-Roc1 ubiquitin ligases. Nat Cell Biol. 2003; 5: 1001-7
PubMed CrossRef
医中誌リンクサービス
28)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
29)Dhanoa BS, Cogliati T, Satish AG, et al. Update on the Kelch-like (KLHL) gene family. Hum Genomics. 2013; 7: 13
PubMed CrossRef
医中誌リンクサービス
30)Ohta T, Iijima K, Miyamoto M, et al. Loss of Keap1 function activates Nrf2 and provides advantages for lung cancer cell growth. Cancer Res. 2008; 68: 1303-9
PubMed CrossRef
医中誌リンクサービス
31)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
32)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
33)Ohta A, Schumacher FR, Mehellou Y, et al. The CUL3-KLHL3 E3 ligase complex mutated in Gordonʼs 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
34)Takahashi D, Mori T, Wakabayashi M, et al. KLHL2 interacts with and ubiquitinates WNK kinases. Biochem Biophys Res Commun. 2013; 437: 457-62
PubMed CrossRef
医中誌リンクサービス


NPO医学中央雑誌刊行会
https://www.jamas.or.jp/
info@jamas.or.jp