BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

192 related articles for article (PubMed ID: 10644529)

  • 1. Human pendrin expressed in Xenopus laevis oocytes mediates chloride/formate exchange.
    Scott DA; Karniski LP
    Am J Physiol Cell Physiol; 2000 Jan; 278(1):C207-11. PubMed ID: 10644529
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. An ion transporter involved in congenital deafness focus on "human pendrin expressed in Xenopus laevis oocytes mediates chloride/formate exchange".
    Cuppoletti J
    Am J Physiol Cell Physiol; 2000 Jan; 278(1):C11-2. PubMed ID: 10644505
    [No Abstract]   [Full Text] [Related]  

  • 5. Formate-stimulated NaCl absorption in the proximal tubule is independent of the pendrin protein.
    Karniski LP; Wang T; Everett LA; Green ED; Giebisch G; Aronson PS
    Am J Physiol Renal Physiol; 2002 Nov; 283(5):F952-6. PubMed ID: 12372770
    [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. 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]  

  • 8. 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]  

  • 9. Clinical and molecular characteristics of Pendred syndrome.
    Kopp P; Bizhanova A
    Ann Endocrinol (Paris); 2011 Apr; 72(2):88-94. PubMed ID: 21511235
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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; 279(13):13004-10. PubMed ID: 14715652
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Molecular and functional characterization of human pendrin and its allelic variants.
    Dossena S; Nofziger C; Tamma G; Bernardinelli E; Vanoni S; Nowak C; Grabmayer E; Kössler S; Stephan S; Patsch W; Paulmichl M
    Cell Physiol Biochem; 2011; 28(3):451-66. PubMed ID: 22116358
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. The ESF meeting on "The proteomics, epigenetics and pharmacogenetics of pendrin".
    Dossena S; Nofziger C; Lang F; Valenti G; Paulmichl M
    Cell Physiol Biochem; 2011; 28(3):377-84. PubMed ID: 22116352
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mechanism of iodide/chloride exchange by pendrin.
    Yoshida A; Hisatome I; Taniguchi S; Sasaki N; Yamamoto Y; Miake J; Fukui H; Shimizu H; Okamura T; Okura T; Igawa O; Shigemasa C; Green ED; Kohn LD; Suzuki K
    Endocrinology; 2004 Sep; 145(9):4301-8. PubMed ID: 15155570
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Pendrin: physiology, molecular biology and clinical importance].
    Grimaldi R; Capuano P; Miranda N; Wagner C; Capasso G
    G Ital Nefrol; 2007; 24(4):288-94. PubMed ID: 17659500
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Pendrin function and regulation in Xenopus oocytes.
    Reimold FR; Heneghan JF; Stewart AK; Zelikovic I; Vandorpe DH; Shmukler BE; Alper SL
    Cell Physiol Biochem; 2011; 28(3):435-50. PubMed ID: 22116357
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The role of pendrin in iodide regulation.
    Fugazzola L; Cerutti N; Mannavola D; Vannucchi G; Beck-Peccoz P
    Exp Clin Endocrinol Diabetes; 2001; 109(1):18-22. PubMed ID: 11573133
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular physiology of the renal chloride-formate exchanger.
    Soleimani M
    Curr Opin Nephrol Hypertens; 2001 Sep; 10(5):677-83. PubMed ID: 11496064
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.