triiodothyronine has been researched along with Genetic Diseases, X-Chromosome Linked in 5 studies
Triiodothyronine: A T3 thyroid hormone normally synthesized and secreted by the thyroid gland in much smaller quantities than thyroxine (T4). Most T3 is derived from peripheral monodeiodination of T4 at the 5' position of the outer ring of the iodothyronine nucleus. The hormone finally delivered and used by the tissues is mainly T3.
3,3',5-triiodo-L-thyronine : An iodothyronine compound having iodo substituents at the 3-, 3'- and 5-positions. Although some is produced in the thyroid, most of the 3,3',5-triiodo-L-thyronine in the body is generated by mono-deiodination of L-thyroxine in the peripheral tissues. Its metabolic activity is about 3 to 5 times that of L-thyroxine. The sodium salt is used in the treatment of hypothyroidism.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (60.00) | 29.6817 |
| 2010's | 2 (40.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| López-Marín, L | 1 |
| Martín-Belinchón, M | 1 |
| Gutiérrez-Solana, LG | 1 |
| Morte-Molina, B | 1 |
| Duat-Rodríguez, A | 1 |
| Bernal, J | 1 |
| Sun, Y | 1 |
| Bak, B | 1 |
| Schoenmakers, N | 1 |
| van Trotsenburg, AS | 1 |
| Oostdijk, W | 1 |
| Voshol, P | 1 |
| Cambridge, E | 1 |
| White, JK | 1 |
| le Tissier, P | 1 |
| Gharavy, SN | 1 |
| Martinez-Barbera, JP | 1 |
| Stokvis-Brantsma, WH | 1 |
| Vulsma, T | 1 |
| Kempers, MJ | 1 |
| Persani, L | 1 |
| Campi, I | 1 |
| Bonomi, M | 1 |
| Beck-Peccoz, P | 1 |
| Zhu, H | 1 |
| Davis, TM | 1 |
| Hokken-Koelega, AC | 1 |
| Del Blanco, DG | 1 |
| Rangasami, JJ | 1 |
| Ruivenkamp, CA | 1 |
| Laros, JF | 1 |
| Kriek, M | 1 |
| Kant, SG | 1 |
| Bosch, CA | 1 |
| Biermasz, NR | 1 |
| Appelman-Dijkstra, NM | 1 |
| Corssmit, EP | 1 |
| Hovens, GC | 1 |
| Pereira, AM | 1 |
| den Dunnen, JT | 1 |
| Wade, MG | 1 |
| Breuning, MH | 1 |
| Hennekam, RC | 1 |
| Chatterjee, K | 1 |
| Dattani, MT | 1 |
| Wit, JM | 1 |
| Bernard, DJ | 1 |
| Bhatkar, SV | 1 |
| Rajan, MG | 1 |
| Velumani, A | 1 |
| Samuel, AM | 1 |
| Maranduba, CM | 1 |
| Friesema, EC | 2 |
| Kok, F | 1 |
| Kester, MH | 2 |
| Jansen, J | 2 |
| Sertié, AL | 1 |
| Passos-Bueno, MR | 1 |
| Visser, TJ | 2 |
| Milici, C | 1 |
| Reeser, M | 1 |
| Grüters, A | 1 |
| Barrett, TG | 1 |
| Mancilla, EE | 1 |
| Svensson, J | 1 |
| Wemeau, JL | 1 |
| Busi da Silva Canalli, MH | 1 |
| Lundgren, J | 1 |
| McEntagart, ME | 1 |
| Hopper, N | 1 |
| Arts, WF | 1 |
1 review available for triiodothyronine and Genetic Diseases, X-Chromosome Linked
| Article | Year |
|---|---|
[MCT8-specific thyroid hormone cell transporter deficiency: a case report and review of the literature].
Topics: Amino Acid Substitution; Anticonvulsants; Biological Transport; Brain; Child, Preschool; Cord Blood | 2013 |
4 other studies available for triiodothyronine and Genetic Diseases, X-Chromosome Linked
| Article | Year |
|---|---|
Loss-of-function mutations in IGSF1 cause an X-linked syndrome of central hypothyroidism and testicular enlargement.
Topics: Adolescent; Adult; Aged; Animals; Base Sequence; Child; Child, Preschool; Congenital Hypothyroidism; | 2012 |
Thyroid hormone binding protein abnormalities in patients referred for thyroid disorders.
Topics: Autoradiography; Electrophoresis, Polyacrylamide Gel; Genetic Diseases, X-Linked; Humans; India; Ped | 2004 |
Decreased cellular uptake and metabolism in Allan-Herndon-Dudley syndrome (AHDS) due to a novel mutation in the MCT8 thyroid hormone transporter.
Topics: Adult; Aged; Biological Transport; DNA Mutational Analysis; Female; Frameshift Mutation; Genetic Dis | 2006 |
Functional analysis of monocarboxylate transporter 8 mutations identified in patients with X-linked psychomotor retardation and elevated serum triiodothyronine.
Topics: Cell Line, Tumor; Codon, Nonsense; Gene Deletion; Genetic Diseases, X-Linked; Humans; Intellectual D | 2007 |