Iodides

solute carrier family 26 member 4 ; Homo sapiens







62 Article(s)
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Title
Pub. Year
#Total Relationships
51 11932304 Characterization and semiquantitative analyses of pendrin expressed in normal and tumoral human thyroid tissues. 2002 Apr 1
52 11932316 Mutations of the PDS gene, encoding pendrin, are associated with protein mislocalization and loss of iodide efflux: implications for thyroid dysfunction in Pendred syndrome. 2002 Apr 2
53 12107249 Pendrin is an iodide-specific apical porter responsible for iodide efflux from thyroid cells. 2002 Jul 2
54 12354788 Retention of pendrin in the endoplasmic reticulum is a major mechanism for Pendred syndrome. 2002 Oct 1 1
55 11137035 Effects of thyroglobulin and pendrin on iodide flux through the thyrocyte. 2001 Jan-Feb 1
56 11248751 Na(+)/I(-) symporter and Pendred syndrome gene and protein expressions in human extra-thyroidal tissues. 2001 Mar 2
57 11573132 Iodide handling by the thyroid epithelial cell. 2001 1
58 11573133 The role of pendrin in iodide regulation. 2001 2
59 10843192 Expression of pendrin and the Pendred syndrome (PDS) gene in human thyroid tissues. 2000 May 1
60 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 5
61 10192399 The Pendred syndrome gene encodes a chloride-iodide transport protein. 1999 Apr 2
62 10571950 Splice-site mutation in the PDS gene may result in intrafamilial variability for deafness in Pendred syndrome. 1999 1