threonine has been researched along with Diseases, Metabolic in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (33.33) | 2.80 |
| Authors | Studies |
|---|---|
| An, J; Jia, X; Li, X; Liu, R; Liu, S; Mo, Y; Wei, X; Zhang, S; Zhang, Y; Zhou, L | 1 |
| Goebel, HH; Gross, M; Kölle, P; Lochmüller, H; Mahnke-Zizelman, DK; Mortier, W; Pongratz, D; Reichmann, H; Rötzer, E; Sabina, RL | 1 |
| Celotto, AM; Frank, AC; Palladino, MJ; Seigle, JL | 1 |
3 other study(ies) available for threonine and Diseases, Metabolic
| Article | Year |
|---|---|
Metabolic pathway analysis of hyperuricaemia patients with hyperlipidaemia based on high-throughput mass spectrometry: a case‒control study.
Topics: Alanine; Aspartic Acid; Biomarkers; Case-Control Studies; Glycine; Humans; Hyperlipidemias; Hyperuricemia; Linoleic Acid; Mass Spectrometry; Metabolic Diseases; Metabolic Networks and Pathways; Phenylalanine; Serine; Threonine; Tryptophan; Tyrosine | 2022 |
A G468-T AMPD1 mutant allele contributes to the high incidence of myoadenylate deaminase deficiency in the Caucasian population.
Topics: Alleles; AMP Deaminase; Blotting, Western; DNA Probes; DNA, Complementary; Electromyography; Genotype; Glycine; Humans; Metabolic Diseases; Muscle, Skeletal; Muscular Diseases; Mutation; Phenotype; Polymerase Chain Reaction; Threonine; White People | 2002 |
Drosophila model of human inherited triosephosphate isomerase deficiency glycolytic enzymopathy.
Topics: Amino Acid Sequence; Amino Acid Substitution; Animals; Disease Models, Animal; Drosophila; Gene Expression Regulation, Enzymologic; Humans; Longevity; Metabolic Diseases; Metabolism, Inborn Errors; Molecular Sequence Data; Mutation, Missense; Reverse Transcriptase Polymerase Chain Reaction; Sequence Homology, Amino Acid; Threonine; Transgenes; Triose-Phosphate Isomerase | 2006 |