serine has been researched along with Hyperthyroid in 5 studies
Serine: A non-essential amino acid occurring in natural form as the L-isomer. It is synthesized from GLYCINE or THREONINE. It is involved in the biosynthesis of PURINES; PYRIMIDINES; and other amino acids.
serine : An alpha-amino acid that is alanine substituted at position 3 by a hydroxy group.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Hyperthyroidism was difficult to treat in all of these patients and was complicated by premature craniosynostosis." | 1.31 | Constitutively activating TSH-receptor mutations as a molecular cause of non-autoimmune hyperthyroidism in childhood. ( Biebermann, H; Grüters, A; Gudermann, T; Krude, H; Schöneberg, T, 2000) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (40.00) | 18.7374 |
| 1990's | 2 (40.00) | 18.2507 |
| 2000's | 1 (20.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kopp, P | 1 |
| Muirhead, S | 1 |
| Jourdain, N | 1 |
| Gu, WX | 1 |
| Jameson, JL | 1 |
| Rodd, C | 1 |
| Holzapfel, HP | 1 |
| Wonerow, P | 1 |
| von Petrykowski, W | 1 |
| Henschen, M | 1 |
| Scherbaum, WA | 1 |
| Paschke, R | 1 |
| Biebermann, H | 1 |
| Schöneberg, T | 1 |
| Krude, H | 1 |
| Gudermann, T | 1 |
| Grüters, A | 1 |
| Björnesjö, KB | 1 |
| Ishii, J | 1 |
| Nakao, K | 1 |
5 other studies available for serine and Hyperthyroid
| Article | Year |
|---|---|
Congenital hyperthyroidism caused by a solitary toxic adenoma harboring a novel somatic mutation (serine281-->isoleucine) in the extracellular domain of the thyrotropin receptor.
Topics: Adenoma; Cells, Cultured; Cyclic AMP; Humans; Hyperthyroidism; Infant, Newborn; Isoleucine; Male; Mu | 1997 |
Sporadic congenital hyperthyroidism due to a spontaneous germline mutation in the thyrotropin receptor gene.
Topics: Animals; Asparagine; Cloning, Molecular; COS Cells; DNA; Gene Expression; Germ-Line Mutation; Humans | 1997 |
Constitutively activating TSH-receptor mutations as a molecular cause of non-autoimmune hyperthyroidism in childhood.
Topics: Child; Child, Preschool; Exons; Germ-Line Mutation; Glycine; Humans; Hyperthyroidism; Infant; Recept | 2000 |
The erythrocyte plasma distribution of amino acids in health and disease.
Topics: Acute Disease; Adolescent; Adult; Alanine; Amino Acids; Anemia, Hemolytic; Anemia, Pernicious; Bronc | 1968 |
Analysis of the human erythrocyte lipid in various functional conditions of the thyroid.
Topics: Centrifugation; Cerebrosides; Cholesterol; Chromatography, Thin Layer; Densitometry; Erythrocytes; H | 1968 |