A CRISPR/Cas9-engineered avatar mouse model of monocarboxylate transporter 8 deficiency displays distinct neurological alterations
Open Access
- 13 October 2022
- journal article
- research article
- Published by Elsevier in Neurobiology of Disease
- Vol. 174, 105896
Abstract
No abstract availableKeywords
This publication has 78 references indexed in Scilit:
- Insights into molecular properties of the human monocarboxylate transporter 8 by combining functional with structural informationThyroid Research, 2011
- Essential Molecular Determinants for Thyroid Hormone Transport and First Structural Implications for Monocarboxylate Transporter 8Journal of Biological Chemistry, 2010
- Thyroid Hormone-Regulated Mouse Cerebral Cortex Genes Are Differentially Dependent on the Source of the Hormone: A Study in Monocarboxylate Transporter-8- and Deiodinase-2-Deficient MiceEndocrinology, 2010
- Neuronal 3′,3,5-Triiodothyronine (T3) Uptake and Behavioral Phenotype of Mice Deficient inMct8, the Neuronal T3Transporter Mutated in Allan–Herndon–Dudley SyndromeJournal of Neuroscience, 2009
- Importance of Monocarboxylate Transporter 8 for the Blood-Brain Barrier-Dependent Availability of 3,5,3′-Triiodo-l-ThyronineEndocrinology, 2009
- Locomotor Deficiencies and Aberrant Development of Subtype-Specific GABAergic Interneurons Caused by an Unliganded Thyroid Hormone Receptor α1Journal of Neuroscience, 2008
- The MCT8 thyroid hormone transporter and Allan–Herndon–Dudley syndromeBest Practice & Research Clinical Endocrinology & Metabolism, 2007
- Abnormal thyroid hormone metabolism in mice lacking the monocarboxylate transporter 8Journal of Clinical Investigation, 2007
- AQUA and PROCHECK-NMR: Programs for checking the quality of protein structures solved by NMRJournal of Biomolecular NMR, 1996
- Permanent defects in rat peripheral auditory function following perinatal hypothyroidism: Determination of a critical periodDevelopmental Brain Research, 1985