phosphatidylcholines has been researched along with Elliptocytosis, Hereditary in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (66.67) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Fowler, PW; Reithmeier, RA; Sansom, MS | 1 |
| Weed, RI | 1 |
| Mannoji, M; Sugihra, T; Yawata, Y | 1 |
1 review(s) available for phosphatidylcholines and Elliptocytosis, Hereditary
| Article | Year |
|---|---|
Membrane structure and its relation to haemolysis.
Topics: Abetalipoproteinemia; Anemia, Sickle Cell; Cell Membrane; Cell Membrane Permeability; Elliptocytosis, Hereditary; Erythrocytes; Erythrocytes, Abnormal; Heinz Bodies; Hematologic Diseases; Hemolysis; Humans; Lecithin Cholesterol Acyltransferase Deficiency; Liver Cirrhosis, Biliary; Phosphatidylcholines; Spherocytosis, Hereditary | 1975 |
2 other study(ies) available for phosphatidylcholines and Elliptocytosis, Hereditary
| Article | Year |
|---|---|
Effect of the Southeast Asian Ovalocytosis Deletion on the Conformational Dynamics of Signal-Anchor Transmembrane Segment 1 of Red Cell Anion Exchanger 1 (AE1, Band 3, or SLC4A1).
Topics: Amino Acid Sequence; Anion Exchange Protein 1, Erythrocyte; Base Sequence; Elliptocytosis, Hereditary; Erythrocytes; Gene Expression; Humans; Hydrophobic and Hydrophilic Interactions; Membranes, Artificial; Molecular Dynamics Simulation; Phosphatidylcholines; Proline; Protein Domains; Protein Folding; Protein Structure, Secondary; Sequence Deletion | 2017 |
Heinz body formation in red cell membrane disorders: its acceleration in membrane lipid abnormalities.
Topics: Anemia, Hemolytic; Cholesterol; Elliptocytosis, Hereditary; Erythrocyte Membrane; Erythrocytes, Abnormal; Heinz Bodies; Hemoglobin E; Hemoglobin M; Humans; Membrane Lipids; Phosphatidylcholines; Phospholipids; Sodium; Spherocytosis, Hereditary; Thalassemia | 1985 |