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Journal Abstract Search

173 related items for PubMed ID: 28555110

  • 1. Reduced Membrane Insertion of CLC-K by V33L Barttin Results in Loss of Hearing, but Leaves Kidney Function Intact.
    Tan H, Bungert-Plümke S, Fahlke C, Stölting G.
    Front Physiol; 2017; 8():269. PubMed ID: 28555110
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  • 2. Activation of renal ClC-K chloride channels depends on an intact N terminus of their accessory subunit barttin.
    Wojciechowski D, Thiemann S, Schaal C, Rahtz A, de la Roche J, Begemann B, Becher T, Fischer M.
    J Biol Chem; 2018 Jun 01; 293(22):8626-8637. PubMed ID: 29674316
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  • 6. Human CLC-K Channels Require Palmitoylation of Their Accessory Subunit Barttin to Be Functional.
    Steinke KV, Gorinski N, Wojciechowski D, Todorov V, Guseva D, Ponimaskin E, Fahlke C, Fischer M.
    J Biol Chem; 2015 Jul 10; 290(28):17390-400. PubMed ID: 26013830
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  • 14. Role of zebrafish ClC-K/barttin channels in apical kidney chloride reabsorption.
    Pérez-Rius C, Castellanos A, Gaitán-Peñas H, Navarro A, Artuch R, Barrallo-Gimeno A, Estévez R.
    J Physiol; 2019 Aug 10; 597(15):3969-3983. PubMed ID: 31177533
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  • 17. Regulation of CLC-Ka/barttin by the ubiquitin ligase Nedd4-2 and the serum- and glucocorticoid-dependent kinases.
    Embark HM, Böhmer C, Palmada M, Rajamanickam J, Wyatt AW, Wallisch S, Capasso G, Waldegger P, Seyberth HW, Waldegger S, Lang F.
    Kidney Int; 2004 Nov 10; 66(5):1918-25. PubMed ID: 15496163
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  • 18. Regulation of ClC-K/barttin by endocytosis influences distal convoluted tubule hyperplasia.
    Mayayo-Vallverdú C, Gaitán-Peñas H, Armand-Ugon M, Muhaisen A, Prat E, Castellanos A, Elorza-Vidal X, de Heredia ML, Alonso-Gardón M, Pérez-Rius C, Vecino-Pérez M, Mallen A, Errasti-Murugarren E, Hueso M, Artuch R, Nunes V, Estévez R.
    J Physiol; 2024 Sep 10; 602(17):4291-4307. PubMed ID: 39106251
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  • 19. Treatment with 17-allylamino-17-demethoxygeldanamycin ameliorated symptoms of Bartter syndrome type IV caused by mutated Bsnd in mice.
    Nomura N, Kamiya K, Ikeda K, Yui N, Chiga M, Sohara E, Rai T, Sakaki S, Uchida S.
    Biochem Biophys Res Commun; 2013 Nov 22; 441(3):544-9. PubMed ID: 24189473
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  • 20. Mutation G47R in the BSND gene causes Bartter syndrome with deafness in two Spanish families.
    García-Nieto V, Flores C, Luis-Yanes MI, Gallego E, Villar J, Claverie-Martín F.
    Pediatr Nephrol; 2006 May 22; 21(5):643-8. PubMed ID: 16572343
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