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Journal Abstract Search

114 related items for PubMed ID: 16773427

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  • 2. A case of antenatal Bartter syndrome with sensorineural deafness.
    Lee HS, Cheong HI, Ki CS.
    J Pediatr Endocrinol Metab; 2010 Oct; 23(10):1077-81. PubMed ID: 21158220
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  • 5. 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; 21(5):643-8. PubMed ID: 16572343
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  • 9. 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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  • 10. Molecular mechanisms of Bartter syndrome caused by mutations in the BSND gene.
    Hayama A, Rai T, Sasaki S, Uchida S.
    Histochem Cell Biol; 2003 Jun 22; 119(6):485-93. PubMed ID: 12761627
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  • 11. Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness.
    Nozu K, Inagaki T, Fu XJ, Nozu Y, Kaito H, Kanda K, Sekine T, Igarashi T, Nakanishi K, Yoshikawa N, Iijima K, Matsuo M.
    J Med Genet; 2008 Mar 22; 45(3):182-6. PubMed ID: 18310267
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  • 15. Antenatal Bartter syndrome with sensorineural deafness: refinement of the locus on chromosome 1p31.
    Vollmer M, Jeck N, Lemmink HH, Vargas R, Feldmann D, Konrad M, Beekmann F, van Den Heuvel LP, Deschenes G, Guay-Woodford LM, Antignac C, Seyberth HW, Hildebrandt F, Knoers NV.
    Nephrol Dial Transplant; 2000 Jul 22; 15(7):970-4. PubMed ID: 10862633
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  • 16. 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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  • 18. Disease-causing dysfunctions of barttin in Bartter syndrome type IV.
    Janssen AG, Scholl U, Domeyer C, Nothmann D, Leinenweber A, Fahlke C.
    J Am Soc Nephrol; 2009 Jan 10; 20(1):145-53. PubMed ID: 18776122
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  • 19. Generation and analyses of R8L barttin knockin mouse.
    Nomura N, Tajima M, Sugawara N, Morimoto T, Kondo Y, Ohno M, Uchida K, Mutig K, Bachmann S, Soleimani M, Ohta E, Ohta A, Sohara E, Okado T, Rai T, Jentsch TJ, Sasaki S, Uchida S.
    Am J Physiol Renal Physiol; 2011 Aug 10; 301(2):F297-307. PubMed ID: 21593186
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  • 20. [Bartter disease with neurosensitive deafness (Bartter type IV). A clinical entity described 10 years ago].
    García Nieto V, Claverie-Martín F.
    Nefrologia; 2005 Aug 10; 25(6):596-601. PubMed ID: 16514898
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