aspartic acid has been researched along with Angiohemophilia 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 |
|---|---|
| Rabinowitz, I; Randi, AM; Rustagi, PK; Sadler, JE; Shindler, KS; Tuley, EA | 1 |
| Gaucher, C; Goudemand, J; Jorieux, S; Mazurier, C | 1 |
2 other study(ies) available for aspartic acid and Angiohemophilia
| Article | Year |
|---|---|
Type IIB mutation His-505-->Asp implicates a new segment in the control of von Willebrand factor binding to platelet glycoprotein Ib.
Topics: Alleles; Amino Acid Sequence; Aspartic Acid; Base Sequence; Binding Sites; Blood Platelets; Crotalid Venoms; DNA; Electrophoresis, Agar Gel; Female; Hemagglutinins; Histidine; Humans; Kinetics; Middle Aged; Molecular Sequence Data; Oligodeoxyribonucleotides; Plasmids; Platelet Membrane Glycoproteins; Point Mutation; Polymerase Chain Reaction; Recombinant Proteins; Ristocetin; von Willebrand Diseases; von Willebrand Factor | 1993 |
A novel mutation in the D3 domain of von Willebrand factor markedly decreases its ability to bind factor VIII and affects its multimerization.
Topics: Amino Acid Substitution; Asparagine; Aspartic Acid; Base Sequence; DNA Mutational Analysis; Electrophoresis, Polyacrylamide Gel; Factor VIII; Heterozygote; Humans; Leukocytes; Male; Middle Aged; Mutation; Protein Binding; Protein Structure, Tertiary; von Willebrand Diseases; von Willebrand Factor | 1998 |