tryptophan has been researched along with Antibody Deficiency Syndrome in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (33.33) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (50.00) | 29.6817 |
| 2010's | 1 (16.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ferster, A; Le, PQ; Mascart, F; Schandené, L; Smet, J; van der Burg, M; van Dongen, JJ; van Zelm, MC | 1 |
| Brandacher, G; Fuchs, D; Margreiter, R; Schroecksnadel, K; Winkler, C | 1 |
| Carney, D; Champagne, KS; Cheung, P; Ciccone, DN; Gallardo, M; Gozani, O; Han, S; Ivanov, D; Kuo, AJ; Kutateladze, TG; Matthews, AG; Oettinger, MA; Ramón-Maiques, S; Shi, Y; Utz, PJ; Walter, KL; Yang, W | 1 |
| Baier-Bitterlich, G; Fuchs, D; Weiss, G; Widner, B; Wirleitner, B | 1 |
| Tabolin, VA | 1 |
3 review(s) available for tryptophan and Antibody Deficiency Syndrome
| Article | Year |
|---|---|
Antitumoral activity of interferon-gamma involved in impaired immune function in cancer patients.
Topics: Anemia; Cachexia; Cell Proliferation; Depression; Humans; Immunologic Deficiency Syndromes; Indoleamine-Pyrrole 2,3,-Dioxygenase; Interferon-gamma; Neoplasms; Neopterin; Tryptophan; Tumor Escape | 2006 |
Cellular immune activation, neopterin production, tryptophan degradation and the development of immunodeficiency.
Topics: Humans; Immune Tolerance; Immunologic Deficiency Syndromes; Interferon-gamma; Lymphocyte Activation; Neopterin; Respiratory Burst; Th1 Cells; Th2 Cells; Tryptophan | 2000 |
Metabolic changes in acrodermatitis enteropathica.
Topics: Acrodermatitis; Amino Acid Metabolism, Inborn Errors; Celiac Disease; Diarrhea, Infantile; Fatty Acids, Unsaturated; Humans; Immunity; Immunologic Deficiency Syndromes; Infant; Infant Nutritional Physiological Phenomena; Iodoquinol; Male; Metabolism, Inborn Errors; Nutrition Disorders; Tryptophan | 1974 |
3 other study(ies) available for tryptophan and Antibody Deficiency Syndrome
| Article | Year |
|---|---|
Antibody deficiency due to a missense mutation in CD19 demonstrates the importance of the conserved tryptophan 41 in immunoglobulin superfamily domain formation.
Topics: Amino Acid Sequence; Antigens, CD19; Case-Control Studies; Child; Female; Humans; Immunologic Deficiency Syndromes; Male; Molecular Sequence Data; Mutation, Missense; Protein Structure, Tertiary; T-Lymphocytes; Tryptophan | 2011 |
RAG2 PHD finger couples histone H3 lysine 4 trimethylation with V(D)J recombination.
Topics: Amino Acid Motifs; Animals; Binding Sites; DNA-Binding Proteins; Gene Rearrangement, B-Lymphocyte; Histones; Homeodomain Proteins; Humans; Immunologic Deficiency Syndromes; Lysine; Methylation; Mice; Models, Molecular; Protein Binding; Recombination, Genetic; Structure-Activity Relationship; Substrate Specificity; Tryptophan; VDJ Recombinases | 2007 |
[Metabolic disorders, their early diagnosis and therapy in newborn infants].
Topics: Adrenal Hyperplasia, Congenital; Amino Acid Metabolism, Inborn Errors; Carbohydrate Metabolism, Inborn Errors; Child, Preschool; Cystic Fibrosis; Fanconi Syndrome; Humans; Hyperbilirubinemia, Hereditary; Immunologic Deficiency Syndromes; Infant; Infant, Newborn; Jaundice, Neonatal; Malabsorption Syndromes; Neurologic Manifestations; Phenylketonurias; Tryptophan | 1973 |