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Journal Abstract Search

207 related items for PubMed ID: 35093948

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  • 2. 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.
    Ohta A, Schumacher FR, Mehellou Y, Johnson C, Knebel A, Macartney TJ, Wood NT, Alessi DR, Kurz T.
    Biochem J; 2013 Apr 01; 451(1):111-22. PubMed ID: 23387299
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  • 3. Combined Kelch-like 3 and Cullin 3 Degradation is a Central Mechanism in Familial Hyperkalemic Hypertension in Mice.
    Maeoka Y, Ferdaus MZ, Cornelius RJ, Sharma A, Su XT, Miller LN, Robertson JA, Gurley SB, Yang CL, Ellison DH, McCormick JA.
    J Am Soc Nephrol; 2022 Mar 01; 33(3):584-600. PubMed ID: 35064051
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  • 4. Role of KLHL3 and dietary K+ in regulating KS-WNK1 expression.
    Ostrosky-Frid M, Chávez-Canales M, Zhang J, Andrukhova O, Argaiz ER, Lerdo-de-Tejada F, Murillo-de-Ozores A, Sanchez-Navarro A, Rojas-Vega L, Bobadilla NA, Vazquez N, Castañeda-Bueno M, Alessi DR, Gamba G.
    Am J Physiol Renal Physiol; 2021 May 01; 320(5):F734-F747. PubMed ID: 33682442
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  • 10. Mutation affecting the conserved acidic WNK1 motif causes inherited hyperkalemic hyperchloremic acidosis.
    Louis-Dit-Picard H, Kouranti I, Rafael C, Loisel-Ferreira I, Chavez-Canales M, Abdel-Khalek W, Argaiz ER, Baron S, Vacle S, Migeon T, Coleman R, Do Cruzeiro M, Hureaux M, Thurairajasingam N, Decramer S, Girerd X, O'Shaugnessy K, Mulatero P, Roussey G, Tack I, Unwin R, Vargas-Poussou R, Staub O, Grimm R, Welling PA, Gamba G, Clauser E, Hadchouel J, Jeunemaitre X.
    J Clin Invest; 2020 Dec 01; 130(12):6379-6394. PubMed ID: 32790646
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  • 11. WNK4 is indispensable for the pathogenesis of pseudohypoaldosteronism type II caused by mutant KLHL3.
    Susa K, Sohara E, Takahashi D, Okado T, Rai T, Uchida S.
    Biochem Biophys Res Commun; 2017 Sep 23; 491(3):727-732. PubMed ID: 28743496
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  • 12. Impaired degradation of WNK1 and WNK4 kinases causes PHAII in mutant KLHL3 knock-in mice.
    Susa K, Sohara E, Rai T, Zeniya M, Mori Y, Mori T, Chiga M, Nomura N, Nishida H, Takahashi D, Isobe K, Inoue Y, Takeishi K, Takeda N, Sasaki S, Uchida S.
    Hum Mol Genet; 2014 Oct 01; 23(19):5052-60. PubMed ID: 24821705
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  • 13. Kelch-like 3 and Cullin 3 regulate electrolyte homeostasis via ubiquitination and degradation of WNK4.
    Shibata S, Zhang J, Puthumana J, Stone KL, Lifton RP.
    Proc Natl Acad Sci U S A; 2013 May 07; 110(19):7838-43. PubMed ID: 23576762
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  • 14. Genotype-phenotype correlation in Gordon's syndrome: report of two cases carrying novel heterozygous mutations.
    Anglani F, Salviati L, Cassina M, Rigato M, Gobbi L, Calò LA.
    J Nephrol; 2022 Apr 07; 35(3):859-862. PubMed ID: 34089516
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  • 15. KLHL3 Knockout Mice Reveal the Physiological Role of KLHL3 and the Pathophysiology of Pseudohypoaldosteronism Type II Caused by Mutant KLHL3.
    Sasaki E, Susa K, Mori T, Isobe K, Araki Y, Inoue Y, Yoshizaki Y, Ando F, Mori Y, Mandai S, Zeniya M, Takahashi D, Nomura N, Rai T, Uchida S, Sohara E.
    Mol Cell Biol; 2017 Apr 01; 37(7):. PubMed ID: 28052936
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  • 18. Renal COP9 Signalosome Deficiency Alters CUL3-KLHL3-WNK Signaling Pathway.
    Cornelius RJ, Si J, Cuevas CA, Nelson JW, Gratreak BDK, Pardi R, Yang CL, Ellison DH.
    J Am Soc Nephrol; 2018 Nov 01; 29(11):2627-2640. PubMed ID: 30301860
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  • 19. Generation and analysis of a mouse model of pseudohypoaldosteronism type II caused by KLHL3 mutation in BTB domain.
    Lin CM, Cheng CJ, Yang SS, Tseng MH, Yen MT, Sung CC, Lin SH.
    FASEB J; 2019 Jan 01; 33(1):1051-1061. PubMed ID: 30148674
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  • 20. Familial Hyperkalemia and Hypertension (FHHt) and KLHL3: Description of a Family with a New Recessive Mutation (S553L) Compared to a Family with a Dominant Mutation, Q309R, with Analysis of Urinary Sodium Chloride Cotransporter.
    Kliuk-Ben Bassat O, Carmon V, Hanukoglu A, Ganon L, Massalha E, Holtzman EJ, Farfel Z, Mayan H.
    Nephron; 2017 Jan 01; 137(1):77-84. PubMed ID: 28511177
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