Pendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretion

Pendrin is an anion transporter encoded by the PDS/Pds gene. In humans, mutations in PDS cause the genetic disorder Pendred syndrome, which is associated with deafness and goiter. Previous studies have shown that this gene has a relatively restricted pattern of expression, with PDS/Pds mRNA detected...

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Detalhes bibliográficos
Main Authors: Royaux, Ines E., Wall, Susan M., Karniski, Lawrence P., Everett, Lorraine A., Suzuki, Koichi, Knepper, Mark A., Green, Eric D.
Formato: Artigo
Idioma:Inglês
Publicado em: The National Academy of Sciences 2001
Assuntos:
Biological Sciences
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC31206/
https://ncbi.nlm.nih.gov/pubmed/11274445
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.071516798
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