proline has been researched along with Spherocytosis, Hereditary 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 |
|---|---|
| Bhasin, N; Discher, DE; Gaetani, M; Gallagher, PG; Harper, S; Johnson, CP; Ortiz, V; Speicher, DW | 1 |
| Beth, AH; Brandon, S; Cobb, CE; DeSensi, SC; Hustedt, EJ; Song, L; Stein, RA; Zhou, Z | 1 |
2 other study(ies) available for proline and Spherocytosis, Hereditary
| Article | Year |
|---|---|
Pathogenic proline mutation in the linker between spectrin repeats: disease caused by spectrin unfolding.
Topics: Elliptocytosis, Hereditary; Humans; Mutation, Missense; Proline; Protein Folding; Spectrin; Spherocytosis, Hereditary | 2007 |
Structure of the cytoplasmic domain of erythrocyte band 3 hereditary spherocytosis variant P327R: band 3 Tuscaloosa.
Topics: Anion Exchange Protein 1, Erythrocyte; Arginine; Cytoplasm; Dimerization; Edetic Acid; Electron Spin Resonance Spectroscopy; Humans; Models, Molecular; Mutant Proteins; Mutation; Normal Distribution; Proline; Protein Structure, Secondary; Protein Structure, Tertiary; Spectrum Analysis; Spherocytosis, Hereditary; Spin Labels | 2007 |