threonine has been researched along with Recrudescence in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (25.00) | 18.2507 |
| 2000's | 2 (25.00) | 29.6817 |
| 2010's | 4 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Assies, J; Bockting, CL; Koeter, MW; Lok, A; Mocking, RJ; Ruhé, HG; Schene, AH; Visser, I | 1 |
| Pelcastre, EL; Villanueva-Mendoza, C; Zenteno, JC | 1 |
| How, GF; Lim, LC; Müller, MC | 1 |
| Djordjevic, V; Kovac, M; Mitic, G; Pruner, I; Radojkovic, D | 1 |
| Eberly, SW; Goldenberg, I; McNitt, S; Moss, AJ; Ryan, D; Zareba, W | 1 |
| Franz, P; Frey, UH; Grehl, S; Jahnke, K; Lang, S; Lehnerdt, GF; Schmid, KW; Schmitz, KJ; Siffert, W; Zaqoul, A | 1 |
| Choi, CR; Kim, HK; Kim, HS; Park, Q; Park, YS; Song, KS | 1 |
| Blench, I; Freyssinet, JM; Grunebaum, L; Ireland, H; Lane, DA; Morris, HR; Olds, R; Thein, SL; Thompson, E; Walker, ID | 1 |
8 other study(ies) available for threonine and Recrudescence
| Article | Year |
|---|---|
Ala54Thr fatty acid-binding protein 2 (FABP2) polymorphism in recurrent depression: associations with fatty acid concentrations and waist circumference.
Topics: Adult; Alanine; Arachidonic Acid; Depressive Disorder, Major; Eicosanoic Acids; Erythrocytes; Fatty Acid-Binding Proteins; Fatty Acids; Female; Genotype; Humans; Male; Middle Aged; Polymorphism, Genetic; Randomized Controlled Trials as Topic; Recurrence; Risk Factors; Threonine; Waist Circumference | 2013 |
Novel and recurrent NDP gene mutations in familial cases of Norrie disease and X-linked exudative vitreoretinopathy.
Topics: Adult; Arginine; Base Sequence; Child, Preschool; Exudates and Transudates; Eye Diseases; Eye Proteins; Genes, X-Linked; Haplotypes; Humans; Infant, Newborn; Male; Mutation, Missense; Nerve Tissue Proteins; Pedigree; Rare Diseases; Recurrence; Retinal Diseases; Threonine; Ultrasonography; Vitreous Body; Young Adult | 2010 |
Acquisition of the novel ABL kinase domain mutation T315L in a relapsed Philadelphia-positive acute lymphoblastic leukemia patient.
Topics: Amino Acid Substitution; Base Sequence; Catalytic Domain; Fusion Proteins, bcr-abl; Humans; Karyotype; Leucine; Male; Middle Aged; Mutation, Missense; Precursor Cell Lymphoblastic Leukemia-Lymphoma; Recurrence; Threonine | 2012 |
Are thrombophilia more multifactorial than we thought: report of mosaicism for FII G20210A and novel FII T20061C gene variants.
Topics: Alanine; Biomarkers; Cysteine; Female; Genotype; Glycine; Humans; Hypertension, Pulmonary; Middle Aged; Mosaicism; Phenotype; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide; Prothrombin; Pulmonary Embolism; Recurrence; Risk Factors; Threonine; Thrombophilia | 2012 |
Polymorphism in the angiotensinogen gene, hypertension, and ethnic differences in the risk of recurrent coronary events.
Topics: Aged; Angiotensin-Converting Enzyme Inhibitors; Angiotensinogen; Black People; Cardiovascular Diseases; Cohort Studies; Female; Gene Frequency; Genetic Predisposition to Disease; Homozygote; Humans; Hypertension; Male; Methionine; Middle Aged; Myocardial Infarction; Polymorphism, Genetic; Prospective Studies; Recurrence; Threonine; White People | 2006 |
Overall and relapse-free survival in oropharyngeal and hypopharyngeal squamous cell carcinoma are associated with genotypes of T393C polymorphism of the GNAS1 gene.
Topics: Adult; Aged; Amino Acid Substitution; Biomarkers, Tumor; Carcinoma, Squamous Cell; Chromogranins; Cysteine; Disease-Free Survival; Female; Genetic Predisposition to Disease; Genotype; GTP-Binding Protein alpha Subunits, Gs; Humans; Hypopharyngeal Neoplasms; Male; Middle Aged; Oropharyngeal Neoplasms; Polymorphism, Single Nucleotide; Prognosis; Recurrence; Survival Analysis; Threonine | 2008 |
Hereditary protein C deficiency with recurrent thrombosis: identification of a missense mutation (C6218T).
Topics: Adult; Cysteine; Female; Genetic Diseases, Inborn; Humans; Male; Pedigree; Point Mutation; Protein C; Protein C Deficiency; Recurrence; Threonine; Thrombosis | 1998 |
Antithrombin Glasgow II: alanine 382 to threonine mutation in the serpin P12 position, resulting in a substrate reaction with thrombin.
Topics: Adult; Alanine; Antithrombin III; Electrophoresis, Polyacrylamide Gel; Female; Humans; Male; Middle Aged; Mutation; Polymerase Chain Reaction; Recurrence; Serpins; Threonine; Thrombin; Thrombosis | 1991 |