thyroxine has been researched along with Genetic Diseases in 4 studies
Thyroxine: The major hormone derived from the thyroid gland. Thyroxine is synthesized via the iodination of tyrosines (MONOIODOTYROSINE) and the coupling of iodotyrosines (DIIODOTYROSINE) in the THYROGLOBULIN. Thyroxine is released from thyroglobulin by proteolysis and secreted into the blood. Thyroxine is peripherally deiodinated to form TRIIODOTHYRONINE which exerts a broad spectrum of stimulatory effects on cell metabolism.
thyroxine : An iodothyronine compound having iodo substituents at the 3-, 3'-, 5- and 5'-positions.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (25.00) | 18.7374 |
| 1990's | 2 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Qiang, L | 1 |
| Guan, Y | 1 |
| Li, X | 1 |
| Liu, L | 1 |
| Mu, Y | 1 |
| Sugano, A | 1 |
| Takaoka, Y | 1 |
| Sakaeda, T | 1 |
| Imbimbo, BP | 1 |
| Yamamura, KI | 1 |
| Jin, S | 1 |
| Li, Z | 1 |
| Petersen, CE | 1 |
| Ha, CE | 1 |
| Mandel, M | 1 |
| Bhagavan, NV | 1 |
| Poitrineau, P | 1 |
| Malpuech, G | 1 |
| Nivelon, JL | 1 |
| Huet, F | 1 |
| Giraud, G | 1 |
| François, C | 1 |
| Carla, H | 1 |
| Loriette, Y | 1 |
| Bürgi, H | 1 |
| Zuppinger, K | 1 |
| Köchli, HP | 1 |
| Burger, A | 1 |
1 trial available for thyroxine and Genetic Diseases
| Article | Year |
|---|---|
CSP-1103 (CHF5074) stabilizes human transthyretin in healthy human subjects.
Topics: Amyloidosis; Cyclopropanes; Flurbiprofen; Genetic Diseases, Inborn; Humans; Prealbumin; Thyroxine | 2017 |
3 other studies available for thyroxine and Genetic Diseases
| Article | Year |
|---|---|
Expression of a human serum albumin variant with high affinity for thyroxine.
Topics: Amino Acid Sequence; Binding Sites; Cloning, Molecular; Gene Expression; Genetic Diseases, Inborn; G | 1995 |
[Discovery, in neonatal screening, of 2 families carrying a syndrome of generalized resistance to thyroid hormones].
Topics: Female; Genes, Dominant; Genetic Carrier Screening; Genetic Diseases, Inborn; Humans; Infant, Newbor | 1993 |
[Familial disorders of thyroxin-binding globulin as a cause of misleading serum thyroxin values. A study of 6 families].
Topics: Adolescent; Adult; Aged; Child; Diagnosis, Differential; Diagnostic Errors; Female; Genetic Diseases | 1974 |