Cargando…
Molecular docking studies of human MCT8 protein with soy isoflavones in Allan-Herndon-Dudley syndrome (AHDS)
Monocarboxylate transporter-8 (MCT8) is a specific thyroid hormone transporter, essential for the uptake of thyroid hormone into target tissues. Mutations in the MCT8 gene have been identified as the cause of Allan-Herndon-Dudley syndrome (AHDS). It has been reported that soy isoflavones influence t...
Autor principal: | Shaji, Divya |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Xi'an Jiaotong University
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6191963/ https://www.ncbi.nlm.nih.gov/pubmed/30345146 http://dx.doi.org/10.1016/j.jpha.2018.07.001 |
Ejemplares similares
-
Further Insights into the Allan-Herndon-Dudley Syndrome: Clinical and Functional Characterization of a Novel MCT8 Mutation
por: Armour, Christine M., et al.
Publicado: (2015) -
Allan-Herndon-Dudley syndrome in a female patient and related mechanisms
por: Olivati, Caroline, et al.
Publicado: (2022) -
Validation of Mct8/Oatp1c1 dKO mice as a model organism for the Allan-Herndon-Dudley Syndrome
por: Maity-Kumar, Gandhari, et al.
Publicado: (2022) -
Mathematical modeling and simulation of thyroid homeostasis: Implications for the Allan-Herndon-Dudley syndrome
por: Wolff, Tobias M., et al.
Publicado: (2022) -
SLC16A2 mutations in two Japanese patients with Allan–Herndon–Dudley syndrome
por: Yamamoto, Toshiyuki, et al.
Publicado: (2014)