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Results: 1 to 20 of 96

Similar articles for PubMed (Select 24429826)

1.

A FRET-based approach for quantitative evaluation of forskolin-induced pendrin trafficking at the plasma membrane in bronchial NCI H292 cells.

Tamma G, Ranieri M, Dossena S, Di Mise A, Nofziger C, Svelto M, Paulmichl M, Valenti G.

Cell Physiol Biochem. 2013;32(7):200-9. doi: 10.1159/000356639. Epub 2013 Dec 18.

PMID:
24429826
2.

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. Epub 2011 Nov 22.

3.

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. doi: 10.1159/000335107. Epub 2011 Nov 18. Review.

PMID:
22116358
4.

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. Epub 2011 Nov 18. Review.

PMID:
22116361
5.

Salicylate restores transport function and anion exchanger activity of missense pendrin mutations.

Ishihara K, Okuyama S, Kumano S, Iida K, Hamana H, Murakoshi M, Kobayashi T, Usami S, Ikeda K, Haga Y, Tsumoto K, Nakamura H, Hirasawa N, Wada H.

Hear Res. 2010 Dec 1;270(1-2):110-8. doi: 10.1016/j.heares.2010.08.015. Epub 2010 Sep 6.

PMID:
20826203
6.

Clinical and molecular characteristics of Pendred syndrome.

Kopp P, Bizhanova A.

Ann Endocrinol (Paris). 2011 Apr;72(2):88-94. doi: 10.1016/j.ando.2011.03.010. Epub 2011 Apr 20.

PMID:
21511235
7.

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. Epub 2010 Mar 15. Review.

PMID:
20298745
8.

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. doi: 10.1159/000335101. Epub 2011 Nov 16.

PMID:
22116352
9.

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. doi: 10.1159/000335106. Epub 2011 Nov 16. Erratum in: Cell Physiol Biochem. 2012;29(1-2). doi:10.1159/000337613.

10.

Hereditary hearing loss with thyroid abnormalities.

Choi BY, Muskett J, King KA, Zalewski CK, Shawker T, Reynolds JC, Butman JA, Brewer CC, Stewart AK, Alper SL, Griffith AJ.

Adv Otorhinolaryngol. 2011;70:43-9. doi: 10.1159/000322469. Epub 2011 Feb 24. Review.

PMID:
21358184
11.
12.

Sgk1 sensitive pendrin expression in murine platelets.

Pelzl L, Fakhri H, Umbach AT, Gawaz M, Paulmichl M, Lang F.

Cell Physiol Biochem. 2013;32(7):210-20. doi: 10.1159/000356640. Epub 2013 Dec 18.

PMID:
24429827
13.

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. Epub 2010 May 6.

14.

Identification of a novel mutation in the SLC26A4 gene in an Italian with fluctuating sensorineural hearing loss.

Cama E, Alemanno MS, Bellacchio E, Santarelli R, Carella M, Zelante L, Palladino T, Inches I, di Paola F, Arslan E, Melchionda S.

Int J Pediatr Otorhinolaryngol. 2009 Oct;73(10):1458-63. doi: 10.1016/j.ijporl.2009.06.003. Epub 2009 Jul 16.

PMID:
19615760
15.

[Current status and perspectives of the research in Pendred syndrome].

Matsunaga T, Fujioka M, Hosoya M.

Nihon Rinsho. 2013 Dec;71(12):2215-22. Review. Japanese.

PMID:
24437281
16.

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. Epub 2008 Aug 7. Review.

PMID:
18692402
17.

Life-threatening metabolic alkalosis in Pendred syndrome.

Kandasamy N, Fugazzola L, Evans M, Chatterjee K, Karet F.

Eur J Endocrinol. 2011 Jul;165(1):167-70. doi: 10.1530/EJE-11-0101. Epub 2011 May 6.

18.

Pendred syndrome in two Galician families: insights into clinical phenotypes through cellular, genetic, and molecular studies.

Palos F, García-Rendueles ME, Araujo-Vilar D, Obregon MJ, Calvo RM, Cameselle-Teijeiro J, Bravo SB, Perez-Guerra O, Loidi L, Czarnocka B, Alvarez P, Refetoff S, Dominguez-Gerpe L, Alvarez CV, Lado-Abeal J.

J Clin Endocrinol Metab. 2008 Jan;93(1):267-77. Epub 2007 Oct 16.

19.

[Pendrin: physiology, molecular biology and clinical importance].

Grimaldi R, Capuano P, Miranda N, Wagner C, Capasso G.

G Ital Nefrol. 2007 Jul-Aug;24(4):288-94. Review. Italian.

PMID:
17659500
20.

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 1;9(11):1709-15.

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