| 1 |
35227018 | Functional interplay between CFTR and pendrin: physiological and pathophysiological relevance. | 2022 Feb 21 |
4 |
| 2 |
33806154 | Airway Surface Liquid pH Regulation in Airway Epithelium Current Understandings and Gaps in Knowledge. | 2021 Mar 25 |
1 |
| 3 |
32923987 | Pendrin stimulates a chloride absorption pathway to increase CFTR-mediated chloride secretion from Cystic Fibrosis airway epithelia. | 2020 Sep |
2 |
| 4 |
33182508 | Dietary Chloride Deficiency Syndrome: Pathophysiology, History, and Systematic Literature Review. | 2020 Nov 9 |
1 |
| 5 |
30744098 | Interleukin-Mediated Pendrin Transcriptional Regulation in Airway and Esophageal Epithelia. | 2019 Feb 9 |
2 |
| 6 |
31281021 | Synthesis and evaluation of tetrahydropyrazolopyridine inhibitors of anion exchange protein SLC26A4 (pendrin). | 2019 Aug 15 |
1 |
| 7 |
28648509 | Pendred syndrome. | 2017 Mar |
3 |
| 8 |
27509681 | [Pendred syndrome and nonsyndromic related deafness: a same entity?]. | 2015 Apr-May |
2 |
| 9 |
25141009 | IL-17A induces Pendrin expression and chloride-bicarbonate exchange in human bronchial epithelial cells. | 2014 |
1 |
| 10 |
23383138 | Regulation of two renal chloride transporters, AE1 and pendrin, by electrolytes and aldosterone. | 2013 |
1 |
| 11 |
21358184 | Hereditary hearing loss with thyroid abnormalities. | 2011 |
2 |
| 12 |
21511235 | Clinical and molecular characteristics of Pendred syndrome. | 2011 Apr |
2 |
| 13 |
21551164 | Life-threatening metabolic alkalosis in Pendred syndrome. | 2011 Jul |
2 |
| 14 |
22116353 | Transcriptional regulation of the pendrin gene. | 2011 |
3 |
| 15 |
22116359 | Identification of allelic variants of pendrin (SLC26A4) with loss and gain of function. | 2011 |
2 |
| 16 |
22116360 | Functional characterization of pendrin mutations found in the Israeli and Palestinian populations. | 2011 |
1 |
| 17 |
22116371 | Pendrin overexpression affects cell volume recovery, intracellular pH and chloride concentration after hypotonicity-induced cell swelling. | 2011 |
1 |
| 18 |
20298745 | Genetics and phenomics of Pendred syndrome. | 2010 Jun 30 |
2 |
| 19 |
19050049 | Pendrin is a novel autoantigen recognized by patients with autoimmune thyroid diseases. | 2009 Feb |
1 |
| 20 |
19277700 | Regulated acid-base transport in the collecting duct. | 2009 May |
3 |
| 21 |
18692402 | Pendred syndrome and iodide transport in the thyroid. | 2008 Sep |
2 |
| 22 |
30290408 | Pendred syndrome. | 2008 Sep |
4 |
| 23 |
17164396 | The emerging role of pendrin in renal chloride reabsorption. | 2007 Mar |
1 |
| 24 |
17659500 | [Pendrin: physiology, molecular biology and clinical importance]. | 2007 Jul-Aug |
2 |
| 25 |
17766716 | High phenotypic intrafamilial variability in patients with Pendred syndrome and a novel duplication in the SLC26A4 gene: clinical characterization and functional studies of the mutated SLC26A4 protein. | 2007 Sep |
1 |
| 26 |
16791000 | Functional characterization of wild-type and a mutated form of SLC26A4 identified in a patient with Pendred syndrome. | 2006 |
4 |
| 27 |
16914891 | Fast fluorometric method for measuring pendrin (SLC26A4) Cl-/I- transport activity. | 2006 |
3 |
| 28 |
15850642 | The BeWo choriocarcinoma cell line as a model of iodide transport by placenta. | 2005 May |
1 |
| 29 |
16260428 | The expression of wild-type pendrin (SLC26A4) in human embryonic kidney (HEK 293 Phoenix) cells leads to the activation of cationic currents. | 2005 Nov |
4 |
| 30 |
12533525 | Expression of human pendrin in diseased thyroids. | 2003 Feb |
1 |
| 31 |
11919333 | Differential diagnosis between Pendred and pseudo-Pendred syndromes: clinical, radiologic, and molecular studies. | 2002 Apr |
1 |
| 32 |
11496064 | Molecular physiology of the renal chloride-formate exchanger. | 2001 Sep |
2 |
| 33 |
11573133 | The role of pendrin in iodide regulation. | 2001 |
1 |
| 34 |
10644505 | An ion transporter involved in congenital deafness focus on "human pendrin expressed in Xenopus laevis oocytes mediates chloride/formate exchange". | 2000 Jan |
1 |
| 35 |
10843192 | Expression of pendrin and the Pendred syndrome (PDS) gene in human thyroid tissues. | 2000 May |
1 |
| 36 |
10861298 | Functional differences of the PDS gene product are associated with phenotypic variation in patients with Pendred syndrome and non-syndromic hearing loss (DFNB4). | 2000 Jul 1 |
4 |
| 37 |
11087667 | Mapping of five new putative anion transporter genes in human and characterization of SLC26A6, a candidate gene for pancreatic anion exchanger. | 2000 Nov 15 |
1 |
| 38 |
10192399 | The Pendred syndrome gene encodes a chloride-iodide transport protein. | 1999 Apr |
2 |
| 39 |
10571950 | Splice-site mutation in the PDS gene may result in intrafamilial variability for deafness in Pendred syndrome. | 1999 |
1 |