isomethyleugenol 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 | 2 (100.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| D'Angelo, S; Galletti, P; Ingrosso, D; Iolascon, A; Miraglia del Giudice, E; Perna, AF; Perrotta, S; Zappia, V | 1 |
| D'Angelo, S; d'Urzo, G; Galletti, P; Ingrosso, D; Iolascon, A; Miraglia del Giudice, E; Perna, AF; Perrotta, S; Zappia, V | 1 |
2 other study(ies) available for isomethyleugenol and Spherocytosis, Hereditary
| Article | Year |
|---|---|
Increased membrane-protein methylation in hereditary spherocytosis. A marker of cytoskeletal disarray.
Topics: Cytoskeleton; Erythrocyte Membrane; Esterification; Humans; Membrane Proteins; Methylation; Protein Methyltransferases; S-Adenosylhomocysteine; S-Adenosylmethionine; Spectrin; Spherocytosis, Hereditary | 1995 |
Cytoskeletal behaviour in spectrin and in band 3 deficient spherocytic red cells: evidence for differentiated splenic conditioning role.
Topics: Adolescent; Adult; Anion Exchange Protein 1, Erythrocyte; Child; Child, Preschool; Cytoskeleton; Erythrocytes; Female; Humans; Male; Membrane Proteins; Methylation; Spectrin; Spherocytosis, Hereditary; Splenectomy | 1996 |