| 1 |
35227018 | Functional interplay between CFTR and pendrin: physiological and pathophysiological relevance. | 2022 Feb 21 |
2 |
| 2 |
31971949 | Computational analysis of functional single nucleotide polymorphisms associated with SLC26A4 gene. | 2020 |
3 |
| 3 |
33055303 | Re-visiting autoimmunity to sodium-iodide symporter and pendrin in thyroid disease. | 2020 Dec |
2 |
| 4 |
30744098 | Interleukin-Mediated Pendrin Transcriptional Regulation in Airway and Esophageal Epithelia. | 2019 Feb 9 |
2 |
| 5 |
30774121 | An Iodide-Yellow Fluorescent Protein-Gap Junction-Intercellular Communication Assay. | 2019 Feb 1 |
1 |
| 6 |
31372509 | Congenital goitrous hypothyroidism is caused by dysfunction of the iodide transporter SLC26A7. | 2019 |
2 |
| 7 |
29772533 | Homology of pendrin, sodium-iodide symporter and apical iodide transporter. | 2018 Jun 1 |
1 |
| 8 |
28648509 | Pendred syndrome. | 2017 Mar |
3 |
| 9 |
27161422 | Effect of Known Inhibitors of Ion Transport on Pendrin (SLC26A4) Activity in a Human Kidney Cell Line. | 2016 |
2 |
| 10 |
26285906 | Iodide transport and breast cancer. | 2015 Oct |
1 |
| 11 |
26313899 | Pendrin and anoctamin as mediators of apical iodide efflux in thyroid cells. | 2015 Oct |
4 |
| 12 |
26444544 | A new high-throughput screening-compatible gap junctional intercellular communication assay. | 2015 Oct 6 |
1 |
| 13 |
23322815 | Low frequency of pendrin autoantibodies detected using a radioligand binding assay in patients with autoimmune thyroid disease. | 2013 Feb |
1 |
| 14 |
25960948 | SLC26A4 mutation testing for hearing loss associated with enlargement of the vestibular aqueduct. | 2013 May 28 |
2 |
| 15 |
22109890 | TSH regulates pendrin membrane abundance and enhances iodide efflux in thyroid cells. | 2012 Jan |
2 |
| 16 |
21358184 | Hereditary hearing loss with thyroid abnormalities. | 2011 |
2 |
| 17 |
21511235 | Clinical and molecular characteristics of Pendred syndrome. | 2011 Apr |
1 |
| 18 |
21550633 | Pendrin mediates uptake of perchlorate in a mammalian in vitro system. | 2011 Sep |
4 |
| 19 |
21551164 | Life-threatening metabolic alkalosis in Pendred syndrome. | 2011 Jul |
3 |
| 20 |
22116353 | Transcriptional regulation of the pendrin gene. | 2011 |
3 |
| 21 |
22116356 | Analysis of cellular localization and function of carboxy-terminal mutants of pendrin. | 2011 |
4 |
| 22 |
22116358 | Molecular and functional characterization of human pendrin and its allelic variants. | 2011 |
1 |
| 23 |
22116359 | Identification of allelic variants of pendrin (SLC26A4) with loss and gain of function. | 2011 |
1 |
| 24 |
22116360 | Functional characterization of pendrin mutations found in the Israeli and Palestinian populations. | 2011 |
2 |
| 25 |
22116361 | Controversies concerning the role of pendrin as an apical iodide transporter in thyroid follicular cells. | 2011 |
3 |
| 26 |
22116362 | Pendrin: the thyrocyte apical membrane iodide transporter? | 2011 |
2 |
| 27 |
20298745 | Genetics and phenomics of Pendred syndrome. | 2010 Jun 30 |
2 |
| 28 |
30780803 | Role of iodine in thyroid physiology. | 2010 Jul |
1 |
| 29 |
19050049 | Pendrin is a novel autoantigen recognized by patients with autoimmune thyroid diseases. | 2009 Feb |
2 |
| 30 |
19196800 | Minireview: The sodium-iodide symporter NIS and pendrin in iodide homeostasis of the thyroid. | 2009 Mar |
2 |
| 31 |
19429184 | An association study of the SLC26A4 gene in children with mental retardation. | 2009 Jul 3 |
1 |
| 32 |
18322141 | Molecular mechanisms of epithelial cell-specific expression and regulation of the human anion exchanger (pendrin) gene. | 2008 May |
2 |
| 33 |
18538122 | Profound hypokalemia and hypochloremic metabolic alkalosis during thiazide therapy in a child with Pendred syndrome. | 2008 Jun |
2 |
| 34 |
18692402 | Pendred syndrome and iodide transport in the thyroid. | 2008 Sep |
3 |
| 35 |
30290408 | Pendred syndrome. | 2008 Sep |
2 |
| 36 |
16648292 | Differential regulation of apical and basal iodide transporters in the thyroid by thyroglobulin. | 2006 May |
1 |
| 37 |
16684826 | Goitrous congenital hypothyroidism and hearing impairment associated with mutations in the TPO and SLC26A4/PDS genes. | 2006 Jul |
1 |
| 38 |
16791000 | Functional characterization of wild-type and a mutated form of SLC26A4 identified in a patient with Pendred syndrome. | 2006 |
2 |
| 39 |
16914891 | Fast fluorometric method for measuring pendrin (SLC26A4) Cl-/I- transport activity. | 2006 |
3 |
| 40 |
16924389 | Association of SLC26A4 mutations with clinical features and thyroid function in deaf infants with enlarged vestibular aqueduct. | 2006 |
1 |
| 41 |
15942636 | Expression of pendrin in benign and malignant human thyroid tissues. | 2005 Jul 11 |
1 |
| 42 |
16053392 | Molecular analysis of the PDS gene in a nonconsanguineous Sicilian family with Pendred's syndrome. | 2005 Jul |
1 |
| 43 |
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 |
2 |
| 44 |
14715652 | Functional characterization of pendrin in a polarized cell system. Evidence for pendrin-mediated apical iodide efflux. | 2004 Mar 26 |
3 |
| 45 |
15001644 | Expression of the apical iodide transporter in human thyroid tissues: a comparison study with other iodide transporters. | 2004 Mar |
1 |
| 46 |
12533525 | Expression of human pendrin in diseased thyroids. | 2003 Feb |
1 |
| 47 |
12727986 | PDS is a new susceptibility gene to autoimmune thyroid diseases: association and linkage study. | 2003 May |
1 |
| 48 |
14530519 | Pendrin transporter carries out iodide uptake into MCF-7 human mammary cancer cells. | 2003 Oct |
1 |
| 49 |
11836344 | Expression of PDS/Pds, the Pendred syndrome gene, in endometrium. | 2002 Feb |
2 |
| 50 |
11919333 | Differential diagnosis between Pendred and pseudo-Pendred syndromes: clinical, radiologic, and molecular studies. | 2002 Apr |
1 |