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Journal Abstract Search

161 related items for PubMed ID: 10718825

  • 1. A novel mutation in the pendrin gene associated with Pendred's syndrome.
    Bogazzi F, Raggi F, Ultimieri F, Campomori A, Cosci C, Berrettini S, Neri E, La Rocca R, Ronca G, Martino E, Bartalena L.
    Clin Endocrinol (Oxf); 2000 Mar; 52(3):279-85. PubMed ID: 10718825
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  • 8. Mutations in the PDS gene in German families with Pendred's syndrome: V138F is a founder mutation.
    Borck G, Roth C, Martiné U, Wildhardt G, Pohlenz J.
    J Clin Endocrinol Metab; 2003 Jun; 88(6):2916-21. PubMed ID: 12788906
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  • 10. [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; 56(8):428-30. PubMed ID: 19959154
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  • 11. Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear.
    Everett LA, Morsli H, Wu DK, Green ED.
    Proc Natl Acad Sci U S A; 1999 Aug 17; 96(17):9727-32. PubMed ID: 10449762
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  • 12. Aggressive metastatic follicular thyroid carcinoma with anaplastic transformation arising from a long-standing goiter in a patient with Pendred's syndrome.
    Camargo R, Limbert E, Gillam M, Henriques MM, Fernandes C, Catarino AL, Soares J, Alves VA, Kopp P, Medeiros-Neto G.
    Thyroid; 2001 Oct 17; 11(10):981-8. PubMed ID: 11716048
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  • 13. 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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  • 14. The role of pendrin in iodide regulation.
    Fugazzola L, Cerutti N, Mannavola D, Vannucchi G, Beck-Peccoz P.
    Exp Clin Endocrinol Diabetes; 2001 Mar 26; 109(1):18-22. PubMed ID: 11573133
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  • 15. Pendred's syndrome with goiter and enlarged vestibular aqueducts diagnosed by PDS gene mutation.
    Ishinaga H, Shimizu T, Yuta A, Tsukamoto K, Usami S, Majima Y.
    Head Neck; 2002 Jul 26; 24(7):710-3. PubMed ID: 12112546
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  • 16. [Pendred's syndrome. Current features].
    Wémeau JL, Vlaeminck-Guillem V, Dubrulle F, Dumur V, Vincent C.
    Presse Med; 2001 Nov 17; 30(34):1689-94. PubMed ID: 11760600
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  • 18. Surprising news: a putative sulfate transporter is defective in Pendred's syndrome.
    Rutishauser J, Kopp P.
    Eur J Endocrinol; 1998 Jun 17; 138(6):623-4. PubMed ID: 9678527
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  • 19. SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis.
    Anwar S, Riazuddin S, Ahmed ZM, Tasneem S, Ateeq-ul-Jaleel, Khan SY, Griffith AJ, Friedman TB, Riazuddin S.
    J Hum Genet; 2009 May 17; 54(5):266-70. PubMed ID: 19287372
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