Cargando…
Validation of Mct8/Oatp1c1 dKO mice as a model organism for the Allan-Herndon-Dudley Syndrome
OBJECTIVE: The Allan-Herndon-Dudley syndrome (AHDS) is a severe disease caused by dysfunctional central thyroid hormone transport due to functional loss of the monocarboxylate transporter 8 (MCT8). In this study, we assessed whether mice with concomitant deletion of the thyroid hormone transporters...
Autores principales: | Maity-Kumar, Gandhari, Ständer, Lisa, DeAngelis, Meri, Lee, Sooyeon, Molenaar, Anna, Becker, Lore, Garrett, Lillian, Amerie, Oana V., Hoelter, Sabine M., Wurst, Wolfgang, Fuchs, Helmut, Feuchtinger, Annette, Gailus-Durner, Valerie, Garcia-Caceres, Cristina, Othman, Ahmed E., Brockmann, Caroline, Schöffling, Vanessa I., Beiser, Katja, Krude, Heiko, Mroz, Piotr A., Hofmann, Susanna, Tuckermann, Jan, DiMarchi, Richard D., Hrabe de Angelis, Martin, Tschöp, Matthias H., Pfluger, Paul T., Müller, Timo D. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9626936/ https://www.ncbi.nlm.nih.gov/pubmed/36270613 http://dx.doi.org/10.1016/j.molmet.2022.101616 |
Ejemplares similares
-
Allan-Herndon-Dudley syndrome in a female patient and related mechanisms
por: Olivati, Caroline, 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) -
SAT-081 Hidden in Plain Sight: Rethinking Our Approach to Allan-Herndon-Dudley Syndrome
por: Dye, Alyssa M, et al.
Publicado: (2020) -
Thyroid Hormone Transporter Defect: Allan Herndon Dudley Syndrome, Masquerading as Dyskinetic Cerebral Palsy
por: Gowda, Vykuntaraju Kammasandra, et al.
Publicado: (2021)