Overcoming Monocarboxylate Transporter 8 (MCT8)-Deficiency to Promote Human Oligodendrocyte Differentiation and Myelination

Cell membrane thyroid hormone (TH) transport can be facilitated by the monocarboxylate transporter 8 (MCT8), encoded by the solute carrier family 16 member 2 (SLC16A2) gene. Human mutations of the gene, SLC16A2, result in the X-linked-inherited psychomotor retardation and hypomyelination disorder, A...

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Detalles Bibliográficos
Autores principales: Lee, Jae Young, Kim, Min Joung, Deliyanti, Devy, Azari, Michael F., Rossello, Fernando, Costin, Adam, Ramm, Georg, Stanley, Edouard G., Elefanty, Andrew G., Wilkinson-Berka, Jennifer L., Petratos, Steven
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5704066/
https://www.ncbi.nlm.nih.gov/pubmed/29111262
http://dx.doi.org/10.1016/j.ebiom.2017.10.016

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5704066/
https://www.ncbi.nlm.nih.gov/pubmed/29111262
http://dx.doi.org/10.1016/j.ebiom.2017.10.016

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