| Pendred s syndrome | 9723 | Pendred Syndrom |
SLC26A4 Pendrin |
| 1996 1 | Pendred syndrome. [9004139] J Med Genet 33(12):1037-40 (1996) |
| 2009 2 | Functional characterization of wild-type and mutated pendrin (SLC26A4), the anion transporter involved in Pendred syndrome. [19608655] J Mol Endocrinol 43(3):93-103 (2009) |
| 2007 3 | Functional cross talk between ENaC and pendrin. [17855481] Am J Physiol Renal Physiol 293(5):F1439-40 (2007) |
| 2007 4 | The emerging role of pendrin in renal chloride reabsorption. [17164396] Am J Physiol Renal Physiol 292(3):F912-3 (2007) |
| 2006 5 | Supporting sensory transduction: cochlear fluid homeostasis and the endocochlear potential. [16857713] J Physiol 576(Pt 1):11-21 (2006) |
| 2009 6 | Minireview: The sodium-iodide symporter NIS and pendrin in iodide homeostasis of the thyroid. [19196800] Endocrinology 150(3):1084-90 (2009) |
| 2007 7 | Loss of cochlear HCO3- secretion causes deafness via endolymphatic acidification and inhibition of Ca2+ reabsorption in a Pendred syndrome mouse model. [17299139] Am J Physiol Renal Physiol 292(5):F1345-53 (2007) |
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