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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

365 related items for PubMed ID: 18692402

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  • 25. Pendrin: the thyrocyte apical membrane iodide transporter?
    Twyffels L, Massart C, Golstein PE, Raspe E, Van Sande J, Dumont JE, Beauwens R, Kruys V.
    Cell Physiol Biochem; 2011; 28(3):491-6. PubMed ID: 22116362
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  • 27. Molecular analysis of the PDS gene in a nonconsanguineous Sicilian family with Pendred's syndrome.
    Gillam MP, Bartolone L, Kopp P, Benvenga S.
    Thyroid; 2005 Jul; 15(7):734-41. PubMed ID: 16053392
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  • 28. Functional differences of the PDS gene product are associated with phenotypic variation in patients with Pendred syndrome and non-syndromic hearing loss (DFNB4).
    Scott DA, Wang R, Kreman TM, Andrews M, McDonald JM, Bishop JR, Smith RJ, Karniski LP, Sheffield VC.
    Hum Mol Genet; 2000 Jul 01; 9(11):1709-15. PubMed ID: 10861298
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  • 30. The immunohistochemical analysis of pendrin in the mouse inner ear.
    Yoshino T, Sato E, Nakashima T, Nagashima W, Teranishi MA, Nakayama A, Mori N, Murakami H, Funahashi H, Imai T.
    Hear Res; 2004 Sep 01; 195(1-2):9-16. PubMed ID: 15350275
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  • 31. Functional characterization of pendrin in a polarized cell system. Evidence for pendrin-mediated apical iodide efflux.
    Gillam MP, Sidhaye AR, Lee EJ, Rutishauser J, Stephan CW, Kopp P.
    J Biol Chem; 2004 Mar 26; 279(13):13004-10. PubMed ID: 14715652
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  • 32. Fast fluorometric method for measuring pendrin (SLC26A4) Cl-/I- transport activity.
    Dossena S, Rodighiero S, Vezzoli V, Bazzini C, Sironi C, Meyer G, Fürst J, Ritter M, Garavaglia ML, Fugazzola L, Persani L, Zorowka P, Storelli C, Beck-Peccoz P, Bottá G, Paulmichl M.
    Cell Physiol Biochem; 2006 Mar 26; 18(1-3):67-74. PubMed ID: 16914891
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  • 35. SLC26A4 mutation in Pendred syndrome with hypokalemia: A case report.
    Lu YT, Wang L, Hou LL, Zheng PP, Xu Q, Deng DT.
    Medicine (Baltimore); 2022 Sep 02; 101(35):e30253. PubMed ID: 36107570
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  • 36. Mutations in the SLC26A4 (pendrin) gene in patients with sensorineural deafness and enlarged vestibular aqueduct.
    Bogazzi F, Russo D, Raggi F, Ultimieri F, Berrettini S, Forli F, Grasso L, Ceccarelli C, Mariotti S, Pinchera A, Bartalena L, Martino E.
    J Endocrinol Invest; 2004 May 02; 27(5):430-5. PubMed ID: 15279074
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  • 37. [Pendred's syndrome: a cause of goiter associated with deafness].
    Vázquez AG, Montesinos IG, Jiménez AM, García JA, García JG, Hernández JA.
    Endocrinol Nutr; 2009 Oct 02; 56(8):428-30. PubMed ID: 19959154
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  • 38. Sulfate transport is not impaired in pendred syndrome thyrocytes.
    Kraiem Z, Heinrich R, Sadeh O, Shiloni E, Nassir E, Hazani E, Glaser B.
    J Clin Endocrinol Metab; 1999 Jul 02; 84(7):2574-6. PubMed ID: 10404839
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  • 39. [Pendrin: physiology, molecular biology and clinical importance].
    Grimaldi R, Capuano P, Miranda N, Wagner C, Capasso G.
    G Ital Nefrol; 2007 Jul 02; 24(4):288-94. PubMed ID: 17659500
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  • 40. Pendred syndrome.
    Lado Abeal J.
    Expert Rev Endocrinol Metab; 2008 Sep 02; 3(5):635-643. PubMed ID: 30290408
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