Effect of the D178N mutation and the codon 129 polymorphism on the metabolism of the prion protein

Biochemistry, Genetics and Molecular Biology

• Metabolic Pathway 100%
• Mutation 100%
• Codon 100%
• Prion 100%
• Fatal Familial Insomnia 80%
• Phenotype 40%
• Creutzfeldt-Jakob Disease 40%
• Age 40%
• Mutant 40%
• Nested Gene 20%
• Conformation 20%
• Glycosylation 20%
• Genotyping 20%
• Methionine 20%
• Valine 20%
• Gerstmann-Sträussler-Scheinker Syndrome 20%
• Surface Property 20%
• Protein 20%
• Protease 20%

Neuroscience

• Prion Protein 100%
• Polymorphism 100%
• Fatal Familial Insomnia 100%
• Phenotype 50%
• Transmissible Spongiform Encephalopathies 50%
• Creutzfeldt Jakob Disease 50%
• Proteinase 25%
• Gerstmann Straussler Scheinker Syndrome 25%
• Methionine 25%
• Valine 25%
• Brain 25%
• Gene 25%
• Protein 25%
• Glycosylation 25%
• Genotype 25%