Keyphrases
Atypical Hemolytic Uremic Syndrome (aHUS)
100%
Complement Factors
100%
Genetic Variants
66%
Calcium Binding
66%
Protein Folding
33%
Low-density Lipoprotein Receptor
33%
Complement Proteins
33%
Site-directed mutagenesis
33%
Functional Role
33%
Serine Protease
33%
Calcium Binding Site
33%
Calcium Ion
33%
Thrombotic Microangiopathy
33%
Structural Role
33%
Multi-domain
33%
Calcium-binding Domain
33%
Biochemistry, Genetics and Molecular Biology
Calcium Binding
100%
Complement Factor I
100%
Fibrinogen
100%
Genetic Divergence
50%
Binding Site
25%
Crystal Structure
25%
Protein Folding
25%
Binding Domain
25%
C3b
25%
Site-Directed Mutagenesis
25%
LDL Receptor
25%
Serine Protease
25%
Calcium Ion
25%
Thrombotic Thrombocytopenic Purpura
25%
Thrombotic Microangiopathy
25%
Alanine
25%