glutamine has been researched along with Diseases in Twins in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Barrios, C; Beaumont, M; Bell, JT; Clark, A; Goodrich, JK; Ley, RE; Menni, C; Pallister, T; Pascual, J; Spector, TD; Villar, J | 1 |
| Banshodani, A; Hattori, M; Kosaki, K; Kozai, K; Moriyama, K; Suda, N; Tanimoto, K | 1 |
| Harper, PS | 1 |
3 other study(ies) available for glutamine and Diseases in Twins
| Article | Year |
|---|---|
Gut-Microbiota-Metabolite Axis in Early Renal Function Decline.
Topics: Adult; Aged; Aged, 80 and over; Body Mass Index; Clostridiales; Cresols; Cross-Sectional Studies; Diabetes Mellitus, Type 2; Diabetic Nephropathies; Diseases in Twins; Feces; Female; Fermentation; Gastrointestinal Microbiome; Glomerular Filtration Rate; Glutamine; Humans; Indican; Kidney Diseases; Male; Metabolome; Microbiota; Middle Aged; Ribotyping; Sulfuric Acid Esters | 2015 |
Correlation between genotype and supernumerary tooth formation in cleidocranial dysplasia.
Topics: Adenine; Adolescent; Adult; Arginine; Child; Cleidocranial Dysplasia; Core Binding Factor Alpha 1 Subunit; Diseases in Twins; DNA Copy Number Variations; Epigenesis, Genetic; Female; Frameshift Mutation; Genetic Heterogeneity; Genetic Variation; Genotype; Glutamine; Humans; Male; Middle Aged; Mutagenesis, Insertional; Mutation; Mutation, Missense; Point Mutation; Proline; Serine; Thymine; Tooth, Supernumerary; Twins, Monozygotic | 2010 |
Inborn errors of metabolism-the relationship of clinical and biochemical abnormalities.
Topics: Cystathionine; Diseases in Twins; Glutamine; Homocystinuria; Humans; Infant, Newborn; Intellectual Disability; Lesch-Nyhan Syndrome; Metabolism, Inborn Errors; NADH, NADPH Oxidoreductases; Phenotype; Phenylalanine; Phenylalanine Hydroxylase; Phenylketonurias | 1973 |