tryptophan has been researched along with Diseases in Twins in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (40.00) | 18.7374 |
| 1990's | 1 (20.00) | 18.2507 |
| 2000's | 1 (20.00) | 29.6817 |
| 2010's | 1 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Freidin, MB; Livshits, G; Menni, C; Potter, T; Wells, HRR; Williams, FMK | 1 |
| ALLEGRI, G; BENASSI, CA; BENASSI, P; RABASSINI, A | 1 |
| Cao, WH; Guo, XX; Hu, YH; Li, LM; Li, QN; Lv, J; Qin, Y; Zhan, SY | 1 |
| Hirano, M; Mori, T; Nagai, Y; Takakura, Y; Tamai, S; Ueno, S | 1 |
| Deacon-Smith, RA; Kamuzora, H; Lee-Potter, JP; Lehmann, H; Simpkiss, MJ | 1 |
5 other study(ies) available for tryptophan and Diseases in Twins
| Article | Year |
|---|---|
Metabolomic markers of fatigue: Association between circulating metabolome and fatigue in women with chronic widespread pain.
Topics: Adult; Aged; Area Under Curve; Biomarkers; C-Reactive Protein; Chronic Pain; Cohort Studies; Diseases in Twins; Eicosapentaenoic Acid; Fatigue; Fatty Acids, Omega-3; Female; Furans; Glycosylation; Humans; Inflammation; Linear Models; Metabolome; Middle Aged; Musculoskeletal Pain; Propionates; Risk Factors; ROC Curve; Tryptophan; United Kingdom | 2018 |
TRYPTOPHAN METABOLISM IN SPECIAL PAIRS OF TWINS.
Topics: Chromatography; Diseases in Twins; Genetics, Medical; Kynurenic Acid; Kynurenine; Metabolic Diseases; ortho-Aminobenzoates; Proteins; Schizophrenia; Spectrophotometry; Tryptophan; Urine; Xanthurenates | 1964 |
[A twin study of association of beta3AR Trp64Arg polymorphisms with insulin sensitivity].
Topics: Arginine; Diseases in Twins; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Insulin; Insulin Resistance; Polymorphism, Genetic; Receptors, Adrenergic, beta-3; Tryptophan; Twins, Dizygotic | 2004 |
Japanese triplets with cerebrotendinous xanthomatosis are homozygous for a mutant gene coding for the sterol 27-hydroxylase (Arg441Trp).
Topics: Adult; Amino Acid Sequence; Arginine; Base Sequence; Blotting, Northern; Cholestanetriol 26-Monooxygenase; Cytochrome P-450 Enzyme System; Diseases in Twins; DNA Primers; Exons; Female; Genetic Carrier Screening; Homozygote; Humans; Japan; Male; Molecular Sequence Data; Pedigree; Point Mutation; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Restriction Mapping; RNA, Messenger; Steroid Hydroxylases; Triplets; Tryptophan; Xanthomatosis | 1996 |
A new cause of haemolytic anaemia in the newborn. A description of an unstable fetal haemoglobin: F Poole, alpha2-G-gamma2 130 trptophan yeilds glycine.
Topics: Amino Acid Sequence; Anemia, Hemolytic; Diseases in Twins; Fetal Hemoglobin; Glycine; Hemoglobins, Abnormal; Humans; Infant, Newborn; Infant, Newborn, Diseases; Male; Tryptophan | 1975 |