disease 1,396 words KG: ent-dise-31ef2f82
Contents

FTD-17 (Frontotemporal Dementia with Parkinsonism Linked to Chromosome 17)

Disease Info
HyperphosphorylationAbnormal phosphorylation of tau protein reduces its ability to bind to microtubules, leading to microtubule destabilization and impaired axonal transport.
AggregationMutant tau proteins have an increased tendency to form insoluble aggregates, including neurofibrillary tangles (NFTs), which are hallmark pathological features of FTD-17.[^7]
Tau isoform imbalanceMutations affecting exon 10 splicing lead to an imbalance between 3R and 4R tau isoforms, disrupting normal tau function.
Early stageBehavioral changes and mild cognitive impairment
Middle stageProgressive dementia, motor symptoms become more prominent
Late stageSevere cognitive decline, complete motor impairment, and eventual death
DatabasesOMIMOrphanetClinicalTrialsPubMed

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Related Hypotheses (2)

Bacterial Enzyme-Mediated Dopamine Precursor Synthesis
Score: 0.38
Dual-Domain Antibodies with Engineered Fc-FcRn Affinity Modu
Score: 0.77

Related Analyses (10)

TDP-43 phase separation therapeutics for ALS-FTD
neurodegeneration · completed
RNA binding protein dysregulation across ALS FTD and AD
neurodegeneration · completed
RNA binding protein dysregulation across ALS FTD AD
neurodegeneration · archived
RNA binding protein dysregulation across ALS FTD and AD
neurodegeneration · archived
TDP-43 phase separation therapeutics for ALS-FTD
neurodegeneration · archived

Related Experiments (15)

Autophagy Enhancement Drug Screening for Neurodegeneration
clinical · proposed · Score: 0.40
Proposed experiment from debate on TDP-43 undergoes liquid-l
falsification · proposed · Score: 0.40
TMEM106B Haplotype as Genetic Modifier in FTD — Mechanism an
validation · proposed · Score: 0.40
Progranulin Replacement Therapy for FTD — Vector Development
clinical · proposed · Score: 0.40
Mechanism: Progranulin Loss and TDP-43 Pathology in FTD
validation · proposed · Score: 0.40

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