isoleucine has been researched along with Kidney Diseases in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cranston, T; Gaynor, KU; Gomes, T; Gortner, L; Grigorieva, IV; Nesbit, MA; Thakker, RV | 1 |
| Baranowicz-Gaszczyk, I; Bednarek-Skublewska, A; Ksiazek, A; Swatowski, A; Wawrzycki, S | 1 |
1 trial(s) available for isoleucine and Kidney Diseases
| Article | Year |
|---|---|
Concentrations of branched amino acids: isoleucine, valine, leucine in serum of hemodialysis patients during one-year observation.
Topics: Adult; Aged; Amino Acids, Branched-Chain; Female; Humans; Isoleucine; Kidney Diseases; Leucine; Male; Malnutrition; Middle Aged; Renal Dialysis; Serum Albumin; Valine | 2002 |
1 other study(ies) available for isoleucine 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 |