Cerebral Cortex Hyperthyroidism of Newborn Mct8-Deficient Mice Transiently Suppressed by Lat2 Inactivation

Thyroid hormone entry into cells is facilitated by transmembrane transporters. Mutations of the specific thyroid hormone transporter, MCT8 (Monocarboxylate Transporter 8, SLC16A2) cause an X-linked syndrome of profound neurological impairment and altered thyroid function known as the Allan-Herndon-D...

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Detalles Bibliográficos
Autores principales: Núñez, Bárbara, Martínez de Mena, Raquel, Obregon, Maria Jesus, Font-Llitjós, Mariona, Nunes, Virginia, Palacín, Manuel, Dumitrescu, Alexandra M., Morte, Beatriz, Bernal, Juan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4018440/
https://www.ncbi.nlm.nih.gov/pubmed/24819605
http://dx.doi.org/10.1371/journal.pone.0096915

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4018440/
https://www.ncbi.nlm.nih.gov/pubmed/24819605
http://dx.doi.org/10.1371/journal.pone.0096915

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