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Ines E Royaux Selected Research

Pendred syndrome

8/2004Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model.
9/2003Localization and functional studies of pendrin in the mouse inner ear provide insight about the etiology of deafness in pendred syndrome.
10/2002Retention of pendrin in the endoplasmic reticulum is a major mechanism for Pendred syndrome.
7/2002Pendrin is an iodide-specific apical porter responsible for iodide efflux from thyroid cells.
2/2002Expression of PDS/Pds, the Pendred syndrome gene, in endometrium.

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Ines E Royaux Research Topics

Disease

5Pendred syndrome
08/2004 - 02/2002
2Deafness (Deaf Mutism)
08/2004 - 10/2002
1Alkalosis
09/2003
1Hypertension (High Blood Pressure)
09/2003
1Goiter
10/2002

Drug/Important Bio-Agent (IBA)

3Proteins (Proteins, Gene)FDA Link
08/2004 - 07/2002
3IodidesIBA
10/2002 - 02/2002
1MineralocorticoidsIBA
09/2003
1Desoxycorticosterone (Deoxycorticosterone)IBA
09/2003
1AldosteroneIBA
09/2003
1Complementary DNA (cDNA)IBA
07/2002
1AcidsIBA
07/2002
1sodium-iodide symporter (sodium iodide symporter)IBA
07/2002