Histopathological Features of Pendred Syndrome Thyroids Align with Differences in the Expression of Thyroid-Specific Markers, Apical Iodide Transporters, and Ciliogenesis Process

Pendred syndrome (PDS) is an autosomal recessive disorder caused by mutations in the gene that encodes pendrin. Pendred thyroid tissue is supposedly altered by the absence of functional pendrin, but it is still unknown whether other iodide exchangers could compensate for the loss of the protein. Mor...

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Detalles Bibliográficos
Autores principales: Vázquez-Román, V., Cameselle-Teijeiro, J. M., Fernández-Santos, J. M., Ríos-Moreno, M. J., Loidi, L., Ortiz, T., Martín-Lacave, I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9712347/
https://www.ncbi.nlm.nih.gov/pubmed/36242759
http://dx.doi.org/10.1007/s12022-022-09732-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9712347/
https://www.ncbi.nlm.nih.gov/pubmed/36242759
http://dx.doi.org/10.1007/s12022-022-09732-2

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