aspartic acid has been researched along with Amyloidosis, Hereditary in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Benson, MD; Connors, LH; Skinner, M; Yamashita, T; Yazaki, M | 1 |
| Baert-Desurmont, S; Cabot, A; Chastan, N; Dérumeaux, G; Frébourg, T; Hannequin, D; Saugier-Veber, P | 1 |
| An, C; Buckle, A; Daggett, V; Fersht, AR; Isaacson, RL; Johnson, CM; Kazmirski, SL | 1 |
3 other study(ies) available for aspartic acid and Amyloidosis, Hereditary
| Article | Year |
|---|---|
A rare transthyretin mutation (Asp18Glu) associated with cardiomyopathy.
Topics: Amino Acid Substitution; Amyloidosis, Familial; Aspartic Acid; Cardiomyopathies; Exons; Glutamic Acid; Humans; Male; Mass Spectrometry; Middle Aged; Polymorphism, Restriction Fragment Length; Polymorphism, Single-Stranded Conformational; Prealbumin | 2004 |
Cardiac conduction alterations in a French family with amyloidosis of the Finnish type with the p.Asp187Tyr mutation in the GSN gene.
Topics: Aged; Amyloidosis, Familial; Arrhythmias, Cardiac; Aspartic Acid; Facies; France; Gelsolin; Heart Conduction System; Humans; Male; Middle Aged; Pedigree; Point Mutation; Tongue; Tyrosine | 2006 |
Loss of a metal-binding site in gelsolin leads to familial amyloidosis-Finnish type.
Topics: Amino Acid Substitution; Amyloidosis, Familial; Aspartic Acid; Binding Sites; Cadmium; Calcium; Calorimetry, Differential Scanning; Computer Simulation; Crystallography, X-Ray; Finland; Gelsolin; Humans; Models, Molecular; Mutation; Protein Binding; Protein Structure, Secondary; Protein Structure, Tertiary; Thermodynamics | 2002 |