62 Article(s)Download |
PMID | 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 |