A Comprehensive Resource for Induced Pluripotent Stem Cells from Patients with Primary Tauopathies
Primary (astronomy)
DOI:
10.1016/j.stemcr.2019.09.006
Publication Date:
2019-10-17T14:42:33Z
AUTHORS (55)
ABSTRACT
Primary tauopathies are characterized neuropathologically by inclusions containing abnormal forms of the microtubule-associated protein tau (MAPT) and clinically diverse neuropsychiatric, cognitive, motor impairments. Autosomal dominant mutations in MAPT gene cause heterogeneous frontotemporal lobar degeneration with tauopathy (FTLD-Tau). Common rare variants increase risk for sporadic FTLD-Tau, including progressive supranuclear palsy (PSP) corticobasal (CBD). We generated a collection fibroblasts from 140 mutation/risk variant carriers, PSP, CBD, cognitively normal controls; 31 induced pluripotent stem cell (iPSC) lines mutation non-carrier family members, autopsy-confirmed PSP patients; 33 genome engineered iPSCs that were corrected or mutagenized; forebrain neural progenitor cells (NPCs). Here, we present resource fibroblasts, iPSCs, NPCs comprehensive clinical histories can be accessed scientific community disease modeling development novel therapeutics tauopathies.
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