Page last updated: 2024-08-17

aspartic acid and Apolipoprotein B-100, Familial Defective

aspartic acid has been researched along with Apolipoprotein B-100, Familial Defective in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (50.00)18.2507
2000's1 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Betteridge, J; Gudnason, V; Humphries, S; Mak, YT; McCarthy, SN1
Blacklow, SC; North, CL1

Other Studies

2 other study(ies) available for aspartic acid and Apolipoprotein B-100, Familial Defective

ArticleYear
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.
    The Clinical investigator, 1993, Volume: 71, Issue:4

    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.
    Biochemistry, 2000, Mar-14, Volume: 39, Issue:10

    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