Pub. Date : 2009 Mar
PMID : 19018842
8 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
| 1 | Elevated serum triiodothyronine and intellectual and motor disability with paroxysmal dyskinesia caused by a monocarboxylate transporter 8 gene mutation. | Triiodothyronine | solute carrier family 16 member 2 | Homo sapiens |
| 2 | Monocarboxylate transporter 8 (MCT8 or SLC16A2) is important for the neuronal uptake of triiodothyronine (T3) in its function as a specific and active transporter of thyroid hormones across the cell membrane, thus being essential for human brain development. | Triiodothyronine | solute carrier family 16 member 2 | Homo sapiens |
| 3 | Monocarboxylate transporter 8 (MCT8 or SLC16A2) is important for the neuronal uptake of triiodothyronine (T3) in its function as a specific and active transporter of thyroid hormones across the cell membrane, thus being essential for human brain development. | Triiodothyronine | solute carrier family 16 member 2 | Homo sapiens |
| 4 | Monocarboxylate transporter 8 (MCT8 or SLC16A2) is important for the neuronal uptake of triiodothyronine (T3) in its function as a specific and active transporter of thyroid hormones across the cell membrane, thus being essential for human brain development. | Triiodothyronine | solute carrier family 16 member 2 | Homo sapiens |
| 5 | Monocarboxylate transporter 8 (MCT8 or SLC16A2) is important for the neuronal uptake of triiodothyronine (T3) in its function as a specific and active transporter of thyroid hormones across the cell membrane, thus being essential for human brain development. | Triiodothyronine | solute carrier family 16 member 2 | Homo sapiens |
| 6 | Monocarboxylate transporter 8 (MCT8 or SLC16A2) is important for the neuronal uptake of triiodothyronine (T3) in its function as a specific and active transporter of thyroid hormones across the cell membrane, thus being essential for human brain development. | Triiodothyronine | solute carrier family 16 member 2 | Homo sapiens |
| 7 | Monocarboxylate transporter 8 (MCT8 or SLC16A2) is important for the neuronal uptake of triiodothyronine (T3) in its function as a specific and active transporter of thyroid hormones across the cell membrane, thus being essential for human brain development. | Triiodothyronine | solute carrier family 16 member 2 | Homo sapiens |
| 8 | The identified MCT8 gene mutation (R271H) is very likely to be the genetic cause for neuronal hypothyroidism despite elevated serum T3 levels. | Triiodothyronine | solute carrier family 16 member 2 | Homo sapiens |