threonine has been researched along with Graves Disease in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (66.67) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Babenko, A; Bogdanova, M; Grineva, E; Kostareva, A; Larionova, V; Popcova, D; Vahrameeva, N | 1 |
| Behr, M; Bohr, UR; Loos, U | 1 |
| Bengtsson, M; Heldin, NE; Kinch, A; Schuppert, F; Simanainen, J; Westermark, B; Westermark, K; Winsa, B | 1 |
3 other study(ies) available for threonine and Graves Disease
| Article | Year |
|---|---|
Type 2 deiodinase Thr92Ala polymorphism impact on clinical course and myocardial remodeling in patients with Graves' disease.
Topics: Adult; Alanine; Echocardiography; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Graves Disease; Humans; Male; Polymorphism, Genetic; Threonine; Ventricular Remodeling; Young Adult | 2009 |
A heritable point mutation in an extracellular domain of the TSH receptor involved in the interaction with Graves' immunoglobulins.
Topics: Adult; Alleles; Amino Acid Sequence; Base Sequence; DNA; DNA Primers; Exons; Female; Graves Disease; Humans; Immunoglobulins; Male; Molecular Sequence Data; Pedigree; Point Mutation; Polymerase Chain Reaction; Proline; Protein Structure, Secondary; Receptors, Thyrotropin; Threonine; Thyroid Gland | 1993 |
Analysis of mutations in exon 1 of the human thyrotropin receptor gene: high frequency of the D36H and P52T polymorphic variants.
Topics: Alleles; Amino Acid Substitution; Aspartic Acid; Exons; Female; Gene Frequency; Genetic Testing; Graves Disease; Heterozygote; Histidine; Humans; Male; Mutation; Polymorphism, Single-Stranded Conformational; Proline; Receptors, Thyrotropin; Restriction Mapping; Threonine | 1999 |