threonine has been researched along with Kidney Diseases in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 5 (83.33) | 29.6817 |
| 2010's | 1 (16.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Hiepe, F; Radbruch, A | 1 |
| Cranston, T; Gaynor, KU; Gomes, T; Gortner, L; Grigorieva, IV; Nesbit, MA; Thakker, RV | 1 |
| Kawakami, J; Sugino, N; Suzuki, Y | 1 |
| Gejyo, F; Goto, S; Kondo, D; Narita, I; Omori, K; Saito, N; Sakatsume, M; Song, J | 1 |
| Al-Lamki, RS; Bradley, JA; Bradley, JR; Luo, D; Min, W; Pober, JS; Thiru, S; Vandenabeele, P; Wang, J | 1 |
| Buyan, N; Gönen, S; Hasanoğlu, E; Kalman, S; Misirlioğlu, M; Ozkaya, O; Söylemezoğlu, O; Tuncer, S | 1 |
1 review(s) available for threonine and Kidney Diseases
| Article | Year |
|---|---|
Plasma cells as an innovative target in autoimmune disease with renal manifestations.
Topics: Autoantibodies; Autoimmune Diseases; B-Lymphocytes; Boronic Acids; Bortezomib; Glomerulonephritis; Humans; Immunologic Memory; Immunosuppressive Agents; Kidney Diseases; Lupus Nephritis; Oligopeptides; Peptides; Plasma Cells; Proteasome Inhibitors; Threonine | 2016 |
5 other study(ies) available for threonine and Kidney Diseases
| Article | Year |
|---|---|
A missense GATA3 mutation, Thr272Ile, causes the hypoparathyroidism, deafness, and renal dysplasia syndrome.
Topics: Amino Acid Sequence; Blotting, Western; Deafness; DNA Mutational Analysis; Electrophoretic Mobility Shift Assay; Fluorescent Antibody Technique; GATA3 Transcription Factor; Humans; Hypoparathyroidism; Immunohistochemistry; Infant; Isoleucine; Kidney; Kidney Diseases; Male; Molecular Sequence Data; Mutation, Missense; Syndrome; Threonine | 2009 |
Evaluation of amino acid patterns in recipes for kidney disease patients.
Topics: Amino Acids; Amino Acids, Essential; Animals; Cooking; Diet, Protein-Restricted; Energy Intake; Humans; Kidney Diseases; Nutrition Disorders; Threonine; Valine | 2003 |
Angiotensinogen gene variation and renoprotective efficacy of renin-angiotensin system blockade in IgA nephropathy.
Topics: Adenine; Adult; Alleles; Angiotensin Receptor Antagonists; Angiotensin-Converting Enzyme Inhibitors; Angiotensinogen; Cytoprotection; Female; Gene Frequency; Genetic Variation; Genotype; Glomerulonephritis, IGA; Guanine; Haplotypes; Humans; Kidney; Kidney Diseases; Male; Methionine; Middle Aged; Polymorphism, Genetic; Renin-Angiotensin System; Risk Factors; Threonine | 2003 |
TNFR1- and TNFR2-mediated signaling pathways in human kidney are cell type-specific and differentially contribute to renal injury.
Topics: Apoptosis; Biological Assay; Biopsy; Cell Proliferation; Down-Regulation; Enzyme Activation; Humans; In Situ Hybridization; In Situ Nick-End Labeling; Kidney; Kidney Diseases; Kidney Neoplasms; Kidney Transplantation; Kidney Tubules; MAP Kinase Kinase Kinase 5; Microscopy, Confocal; Models, Biological; Organ Culture Techniques; Phosphorylation; Protein-Tyrosine Kinases; Receptors, Tumor Necrosis Factor, Type I; Receptors, Tumor Necrosis Factor, Type II; Signal Transduction; Threonine; Up-Regulation | 2005 |
Renin-angiotensin system gene polymorphisms: association with susceptibility to Henoch-Schonlein purpura and renal involvement.
Topics: Adolescent; Alanine; Angiotensinogen; Child; Child, Preschool; Cysteine; DNA Transposable Elements; Female; Gene Deletion; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; IgA Vasculitis; Kidney Diseases; Male; Methionine; Nephrotic Syndrome; Peptidyl-Dipeptidase A; Polymorphism, Genetic; Proteinuria; Receptor, Angiotensin, Type 1; Renin-Angiotensin System; Severity of Illness Index; Threonine | 2006 |