| 1 |
34679181 | Long-Term Efficacy of T3 Analogue Triac in Children and Adults With MCT8 Deficiency: A Real-Life Retrospective Cohort Study. | 2022 Feb 17 |
1 |
| 2 |
34850364 | Screening for drugs potentially interfering with MCT8-mediated T3 transport in vitro identifies dexamethasone and some commonly used drugs as inhibitors of MCT8 activity. | 2022 Apr |
4 |
| 3 |
32687511 | Intranasal delivery of Thyroid hormones in MCT8 deficiency. | 2020 |
2 |
| 4 |
30369548 | Functional analysis of monocarboxylate transporter 8 mutations in Japanese Allan-Herndon-Dudley syndrome patients. | 2019 Jan 28 |
1 |
| 5 |
31809508 | Intracerebroventricular administration of the thyroid hormone analog TRIAC increases its brain content in the absence of MCT8. | 2019 |
1 |
| 6 |
25896225 | Clinical and endocrine features of two Allan-Herndon-Dudley syndrome patients with monocarboxylate transporter 8 mutations. | 2015 |
4 |
| 7 |
24479416 | Authentic bosutinib inhibits triiodothyronine transport by monocarboxylate transporter 8. | 2014 May |
1 |
| 8 |
25231447 | Thyroid hormone cell membrane transport defect. | 2014 |
1 |
| 9 |
22723621 | Thyroid hormone transporters and deiodinases in the developing human hypothalamus. | 2012 Sep |
1 |
| 10 |
21468521 | Novel mutation in MCT8 gene in a Brazilian boy with thyroid hormone resistance and severe neurologic abnormalities. | 2011 Feb |
1 |
| 11 |
21813593 | Monocarboxylate transporter 8 deficiency: altered thyroid morphology and persistent high triiodothyronine/thyroxine ratio after thyroidectomy. | 2011 Oct |
3 |
| 12 |
21835056 | Molecules important for thyroid hormone synthesis and action - known facts and future perspectives. | 2011 Aug 3 |
2 |
| 13 |
21896621 | A child with a deletion in the monocarboxylate transporter 8 gene: 7-year follow-up and effects of thyroid hormone treatment. | 2011 Nov |
9 |
| 14 |
20713192 | Allan-Herndon-Dudley syndrome (AHDS) caused by a novel SLC16A2 gene mutation showing severe neurologic features and unexpectedly low TRH-stimulated serum TSH. | 2010 Nov-Dec |
1 |
| 15 |
18636565 | Novel pathogenic mechanism suggested by ex vivo analysis of MCT8 (SLC16A2) mutations. | 2009 Jan |
4 |
| 16 |
19018842 | Elevated serum triiodothyronine and intellectual and motor disability with paroxysmal dyskinesia caused by a monocarboxylate transporter 8 gene mutation. | 2009 Mar |
8 |
| 17 |
19022891 | Monocarboxylate transporter 8 in neuronal cell growth. | 2009 Apr |
2 |
| 18 |
19648159 | Surface translocation and tri-iodothyronine uptake of mutant MCT8 proteins are cell type-dependent. | 2009 Dec |
1 |
| 19 |
18166539 | A novel monocarboxylate transporter 8 gene mutation as a cause of severe neonatal hypotonia and developmental delay. | 2008 Jan |
1 |
| 20 |
18187543 | Genotype-phenotype relationship in patients with mutations in thyroid hormone transporter MCT8. | 2008 May |
1 |
| 21 |
18334584 | Beneficial effects of propylthiouracil plus L-thyroxine treatment in a patient with a mutation in MCT8. | 2008 Jun |
1 |
| 22 |
18337592 | Effective cellular uptake and efflux of thyroid hormone by human monocarboxylate transporter 10. | 2008 Jun |
1 |
| 23 |
18418673 | Thyroid hormone transporters in the brain. | 2008 |
1 |
| 24 |
17356046 | Functional analysis of monocarboxylate transporter 8 mutations identified in patients with X-linked psychomotor retardation and elevated serum triiodothyronine. | 2007 Jun |
6 |
| 25 |
17574005 | Thyroid hormone transport by monocarboxylate transporters. | 2007 Jun |
2 |
| 26 |
18174701 | Thyroid hormone transporters. | 2007 |
5 |
| 27 |
15980113 | Decreased cellular uptake and metabolism in Allan-Herndon-Dudley syndrome (AHDS) due to a novel mutation in the MCT8 thyroid hormone transporter. | 2006 May |
2 |
| 28 |
16957765 | Mechanisms of disease: psychomotor retardation and high T3 levels caused by mutations in monocarboxylate transporter 8. | 2006 Sep |
2 |
| 29 |
15727804 | Thyroid hormone transporters. | 2005 |
1 |
| 30 |
16131319 | Thyroid hormone transporters in health and disease. | 2005 Aug |
2 |
| 31 |
15488219 | Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation. | 2004 Oct 16-22 |
2 |