aspartic acid has been researched along with Apolipoprotein B-100, Familial Defective in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (50.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Betteridge, J; Gudnason, V; Humphries, S; Mak, YT; McCarthy, SN | 1 |
Blacklow, SC; North, CL | 1 |
2 other study(ies) available for aspartic acid and Apolipoprotein B-100, Familial Defective
Article | Year |
---|---|
Use of the single-strand conformational polymorphism method to detect recurrent and novel mutations in the low-density lipoprotein receptor gene in patients with familial hypercholesterolaemia: detection of a novel mutation Asp200-->Gly.
Topics: Aspartic Acid; Base Sequence; Deoxyribonuclease HpaII; Deoxyribonucleases, Type II Site-Specific; DNA Mutational Analysis; DNA, Single-Stranded; Electrophoresis, Agar Gel; Gene Deletion; Genetic Carrier Screening; Glycine; Humans; Hyperlipoproteinemia Type II; Molecular Sequence Data; Nucleic Acid Conformation; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Receptors, LDL | 1993 |
Solution structure of the sixth LDL-A module of the LDL receptor.
Topics: Amino Acid Sequence; Aspartic Acid; Calcium; Crystallography, X-Ray; Glutamic Acid; Humans; Hyperlipoproteinemia Type II; Lysine; Molecular Sequence Data; Mutagenesis, Site-Directed; Nuclear Magnetic Resonance, Biomolecular; Protein Binding; Protein Conformation; Protein Folding; Receptors, LDL; Solutions | 2000 |