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Items: 1 to 20 of 197

1.

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.

PMID:
10650967
2.
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.

PMID:
10843192
4.

Pendrin is an iodide-specific apical porter responsible for iodide efflux from thyroid cells.

Yoshida A, Taniguchi S, Hisatome I, Royaux IE, Green ED, Kohn LD, Suzuki K.

J Clin Endocrinol Metab. 2002 Jul;87(7):3356-61.

PMID:
12107249
5.

Follicular thyroglobulin suppresses iodide uptake by suppressing expression of the sodium/iodide symporter gene.

Suzuki K, Mori A, Saito J, Moriyama E, Ullianich L, Kohn LD.

Endocrinology. 1999 Nov;140(11):5422-30.

PMID:
10537174
6.

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.

7.

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.

PMID:
10192399
8.

TSH regulates pendrin membrane abundance and enhances iodide efflux in thyroid cells.

Pesce L, Bizhanova A, Caraballo JC, Westphal W, Butti ML, Comellas A, Kopp P.

Endocrinology. 2012 Jan;153(1):512-21. doi: 10.1210/en.2011-1548.

9.

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. doi: 10.1159/000335103. Review.

10.

Genetics and phenomics of Pendred syndrome.

Bizhanova A, Kopp P.

Mol Cell Endocrinol. 2010 Jun 30;322(1-2):83-90. doi: 10.1016/j.mce.2010.03.006. Review.

PMID:
20298745
11.

Pendred syndrome and iodide transport in the thyroid.

Kopp P, Pesce L, Solis-S JC.

Trends Endocrinol Metab. 2008 Sep;19(7):260-8. doi: 10.1016/j.tem.2008.07.001. Review.

PMID:
18692402
12.

Anoctamin-1/TMEM16A is the major apical iodide channel of the thyrocyte.

Twyffels L, Strickaert A, Virreira M, Massart C, Van Sande J, Wauquier C, Beauwens R, Dumont JE, Galietta LJ, Boom A, Kruys V.

Am J Physiol Cell Physiol. 2014 Dec 15;307(12):C1102-12. doi: 10.1152/ajpcell.00126.2014.

13.

Pendrin and anoctamin as mediators of apical iodide efflux in thyroid cells.

Silveira JC, Kopp PA.

Curr Opin Endocrinol Diabetes Obes. 2015 Oct;22(5):374-80. doi: 10.1097/MED.0000000000000188. Review.

PMID:
26313899
14.
15.

Minireview: The sodium-iodide symporter NIS and pendrin in iodide homeostasis of the thyroid.

Bizhanova A, Kopp P.

Endocrinology. 2009 Mar;150(3):1084-90. doi: 10.1210/en.2008-1437. Review.

16.

Effects of thyroglobulin and pendrin on iodide flux through the thyrocyte.

Kohn LD, Suzuki K, Nakazato M, Royaux I, Green ED.

Trends Endocrinol Metab. 2001 Jan-Feb;12(1):10-6. Review.

PMID:
11137035
17.

Thyroglobulin (Tg) induces thyroid cell growth in a concentration-specific manner by a mechanism other than thyrotropin/cAMP stimulation.

Noguchi Y, Harii N, Giuliani C, Tatsuno I, Suzuki K, Kohn LD.

Biochem Biophys Res Commun. 2010 Jan 1;391(1):890-4. doi: 10.1016/j.bbrc.2009.11.158.

PMID:
19951699
18.

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. doi: 10.4274/jcrpe.v2i2.81.

19.

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. doi: 10.1159/000335110. Review.

20.

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.

PMID:
11932304

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