BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

139 related articles for article (PubMed ID: 10404839)

  • 1. 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; 84(7):2574-6. PubMed ID: 10404839
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pendred syndrome.
    Glaser B
    Pediatr Endocrinol Rev; 2003 Dec; 1 Suppl 2():199-204; discussion 204. PubMed ID: 16444159
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Expression of pendrin and the Pendred syndrome (PDS) gene in human thyroid tissues.
    Bidart JM; Mian C; Lazar V; Russo D; Filetti S; Caillou B; Schlumberger M
    J Clin Endocrinol Metab; 2000 May; 85(5):2028-33. PubMed ID: 10843192
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The Pendred syndrome gene encodes a chloride-iodide transport protein.
    Scott DA; Wang R; Kreman TM; Sheffield VC; Karniski LP
    Nat Genet; 1999 Apr; 21(4):440-3. PubMed ID: 10192399
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutations of the PDS gene, encoding pendrin, are associated with protein mislocalization and loss of iodide efflux: implications for thyroid dysfunction in Pendred syndrome.
    Taylor JP; Metcalfe RA; Watson PF; Weetman AP; Trembath RC
    J Clin Endocrinol Metab; 2002 Apr; 87(4):1778-84. PubMed ID: 11932316
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetics and phenomics of Pendred syndrome.
    Bizhanova A; Kopp P
    Mol Cell Endocrinol; 2010 Jun; 322(1-2):83-90. PubMed ID: 20298745
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Pendrin, the protein encoded by the Pendred syndrome gene (PDS), is an apical porter of iodide in the thyroid and is regulated by thyroglobulin in FRTL-5 cells.
    Royaux IE; Suzuki K; Mori A; Katoh R; Everett LA; Kohn LD; Green ED
    Endocrinology; 2000 Feb; 141(2):839-45. PubMed ID: 10650967
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Phenocopies for deafness and goiter development in a large inbred Brazilian kindred with Pendred's syndrome associated with a novel mutation in the PDS gene.
    Kopp P; Arseven OK; Sabacan L; Kotlar T; Dupuis J; Cavaliere H; Santos CL; Jameson JL; Medeiros-Neto G
    J Clin Endocrinol Metab; 1999 Jan; 84(1):336-41. PubMed ID: 9920104
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Pendred syndrome and iodide transport in the thyroid.
    Kopp P; Pesce L; Solis-S JC
    Trends Endocrinol Metab; 2008 Sep; 19(7):260-8. PubMed ID: 18692402
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The PDS gene, Pendred syndrome and non-syndromic deafness DFNB4.
    Wilcox ER; Everett LA; Li XC; Lalwani AK; Green ED
    Adv Otorhinolaryngol; 2000; 56():145-51. PubMed ID: 10868226
    [No Abstract]   [Full Text] [Related]  

  • 11. 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; 9(11):1709-15. PubMed ID: 10861298
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Pendred's syndrome: identification of the genetic defect a century after its recognition.
    Kopp P
    Thyroid; 1999 Jan; 9(1):65-9. PubMed ID: 10037079
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Controversies concerning the role of pendrin as an apical iodide transporter in thyroid follicular cells.
    Bizhanova A; Kopp P
    Cell Physiol Biochem; 2011; 28(3):485-90. PubMed ID: 22116361
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Two common and three novel PDS mutations in Thai patients with Pendred syndrome.
    Snabboon T; Plengpanich W; Saengpanich S; Sirisalipoch S; Keelawat S; Sunthornyothin S; Khovidhunkit W; Suwanwalaikorn S; Sridama V; Shotelersuk V
    J Endocrinol Invest; 2007 Dec; 30(11):907-13. PubMed ID: 18250610
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS).
    Everett LA; Glaser B; Beck JC; Idol JR; Buchs A; Heyman M; Adawi F; Hazani E; Nassir E; Baxevanis AD; Sheffield VC; Green ED
    Nat Genet; 1997 Dec; 17(4):411-22. PubMed ID: 9398842
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Enlarged vestibular aqueduct: a radiological marker of pendred syndrome, and mutation of the PDS gene.
    Reardon W; OMahoney CF; Trembath R; Jan H; Phelps PD
    QJM; 2000 Feb; 93(2):99-104. PubMed ID: 10700480
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 51(4):479-84. PubMed ID: 11919333
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Syndromic and non-syndromic deafness, molecular aspects of Pendred syndrome and its reported mutations.
    Shaukat S; Fatima Z; Zehra U; Waqar AB
    J Ayub Med Coll Abbottabad; 2003; 15(3):59-64. PubMed ID: 14727345
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Pendred syndrome.
    Wémeau JL; Kopp P
    Best Pract Res Clin Endocrinol Metab; 2017 Mar; 31(2):213-224. PubMed ID: 28648509
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Congenital goitrous hypothyroidism, deafness and iodide organification defect in four siblings: Pendred or pseudo-Pendred syndrome?
    Kara C; Kılıç M; Uçaktürk A; Aydın M
    J Clin Res Pediatr Endocrinol; 2010; 2(2):81-4. PubMed ID: 21274344
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.