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Fibrillogenesis of tau: Insights from Tau missense mutations in FTDP-17
Shu Hui Yen
, Michael Hutton
, Michael DeTure
, Li Wen Ko
, Parimala Nacharaju
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peer-review
44
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Keyphrases
Missense mutation
100%
Fibrillogenesis
100%
FTDP-17
100%
5′ Splice Site
50%
Tau Filaments
50%
Exon 10
50%
Tau Gene
50%
Neurological Disorders
25%
Transfected Cells
25%
Tau Pathology
25%
Frontotemporal Dementia
25%
Elongation Phase
25%
Heparin
25%
Chromosome 17
25%
Gene mutation
25%
Polymerized
25%
COS-7 Cells
25%
Parkinsonism
25%
Filament Formation
25%
Phosphorylation
25%
Cell Surface Display
25%
4R tau
25%
Tau mutation
25%
Tau Isoforms
25%
Tau Deposits
25%
Exon 9
25%
Cultured Cells
25%
3R tau
25%
Arachidonic Acid
25%
Extent of Reduction
25%
Cell Changes
25%
Tubulin
25%
Inducing Agents
25%
Alternative Splicing
25%
Nucleation Phase
25%
Phosphorylated tau
25%
Microtubule Assembly
25%
Number of mutations
25%
R406W
25%
Splice Site mutation
25%
Neuroscience
Missense Mutation
100%
Exon
100%
Microtubule Assembly
33%
In Vitro
33%
Heparin
33%
Frontotemporal Dementia
33%
Parkinsonism
33%
Tubulin
33%
Arachidonic Acid
33%
Gene Mutation
33%
Alternative Splicing
33%
Chromosome 17
33%
Nervous System Disorder
33%
phosphorylation
33%
Biochemistry, Genetics and Molecular Biology
Missense Mutation
100%
Tau
100%
Fibrillogenesis
100%
Exon
16%
Tubulin
5%
Chromosome 17
5%
Isoform
5%
Heparin
5%
Wild Type
5%
Microtubule Assembly
5%
Alternative Splicing
5%
Gene Mutation
5%
Splice Site Mutation
5%
Arachidonic Acid
5%
phosphorylation
5%