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PUBMED FOR HANDHELDS

Journal Abstract Search


224 related items for PubMed ID: 10843192

  • 1.
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  • 2. Sodium iodide symporter and pendrin expression in human thyroid tissues.
    Mian C, Lacroix L, Alzieu L, Nocera M, Talbot M, Bidart JM, Schlumberger M, Caillou B.
    Thyroid; 2001 Sep; 11(9):825-30. PubMed ID: 11575851
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  • 3. Characterization and semiquantitative analyses of pendrin expressed in normal and tumoral human thyroid tissues.
    Porra V, Bernier-Valentin F, Trouttet-Masson S, Berger-Dutrieux N, Peix JL, Perrin A, Selmi-Ruby S, Rousset B.
    J Clin Endocrinol Metab; 2002 Apr; 87(4):1700-7. PubMed ID: 11932304
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  • 7. Expression pattern of the pendrin and sodium/iodide symporter genes in human thyroid carcinoma cell lines and human thyroid tumors.
    Arturi F, Russo D, Bidart JM, Scarpelli D, Schlumberger M, Filetti S.
    Eur J Endocrinol; 2001 Aug; 145(2):129-35. PubMed ID: 11454507
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  • 8. Genetics and phenomics of Pendred syndrome.
    Bizhanova A, Kopp P.
    Mol Cell Endocrinol; 2010 Jun 30; 322(1-2):83-90. PubMed ID: 20298745
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  • 9. The Pendred syndrome gene encodes a chloride-iodide transport protein.
    Scott DA, Wang R, Kreman TM, Sheffield VC, Karniski LP.
    Nat Genet; 1999 Apr 30; 21(4):440-3. PubMed ID: 10192399
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  • 11. Expression of the apical iodide transporter in human thyroid tissues: a comparison study with other iodide transporters.
    Lacroix L, Pourcher T, Magnon C, Bellon N, Talbot M, Intaraphairot T, Caillou B, Schlumberger M, Bidart JM.
    J Clin Endocrinol Metab; 2004 Mar 30; 89(3):1423-8. PubMed ID: 15001644
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  • 12. 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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  • 13. Pendred syndrome and iodide transport in the thyroid.
    Kopp P, Pesce L, Solis-S JC.
    Trends Endocrinol Metab; 2008 Sep 01; 19(7):260-8. PubMed ID: 18692402
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  • 15. Differential diagnosis between Pendred and pseudo-Pendred syndromes: clinical, radiologic, and molecular studies.
    Fugazzola L, Cerutti N, Mannavola D, Crino A, Cassio A, Gasparoni P, Vannucchi G, Beck-Peccoz P.
    Pediatr Res; 2002 Apr 01; 51(4):479-84. PubMed ID: 11919333
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  • 16. Expression of pendrin in benign and malignant human thyroid tissues.
    Skubis-Zegadło J, Nikodemska A, Przytuła E, Mikula M, Bardadin K, Ostrowski J, Wenzel BE, Czarnocka B.
    Br J Cancer; 2005 Jul 11; 93(1):144-51. PubMed ID: 15942636
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  • 19. Pendred syndrome.
    Glaser B.
    Pediatr Endocrinol Rev; 2003 Dec 11; 1 Suppl 2():199-204; discussion 204. PubMed ID: 16444159
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  • 20. Expression of the Na+/I- symporter gene in human thyroid tumors: a comparison study with other thyroid-specific genes.
    Lazar V, Bidart JM, Caillou B, Mahé C, Lacroix L, Filetti S, Schlumberger M.
    J Clin Endocrinol Metab; 1999 Sep 11; 84(9):3228-34. PubMed ID: 10487692
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