threonine has been researched along with Thyroid Diseases in 1 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Bianco, AC; Deng, Y; Egri, P; Farkas, E; Fekete, C; Gereben, B; Jo, S; Li, Y; Mash, DC; McAninch, EA; Mohácsik, P; Patti, ME; Peeters, RP; Preite, NZ; Zevenbergen, C | 1 |
1 other study(ies) available for threonine and Thyroid Diseases
Article | Year |
---|---|
Prevalent polymorphism in thyroid hormone-activating enzyme leaves a genetic fingerprint that underlies associated clinical syndromes.
Topics: Adult; Alanine; Amino Acid Substitution; Case-Control Studies; Cerebral Cortex; Gene Frequency; HEK293 Cells; HeLa Cells; Humans; Iodide Peroxidase; Iodothyronine Deiodinase Type II; Male; Microarray Analysis; Nervous System Diseases; Oxidative Stress; Polymorphism, Single Nucleotide; Syndrome; Threonine; Thyroid Diseases; Transcriptome | 2015 |