Stepwise acquirement of hallmark neuropathology in FUS-ALS iPSC models depends on mutation type and neuronal aging

Erstveröffentlichung

2015

Authors

Japtok, Julia

Lojewski, Xenia

Naumann, Marcel

Klingenstein, Moritz

Reinhardt, Peter

et al.

Wissenschaftlicher Artikel

Published in

Neurobiology of Disease ; 82 (2015). - S. 420-429. - ISSN 0969-9961. - eISSN 1095-953X

Link to publication

https://dx.doi.org/10.1016/j.nbd.2015.07.017

Faculties

Medizinische Fakultät

Institutions

Institut für Anatomie und Zellbiologie
UKU. Klinik für Neurologie

Subject headings

[Free subject headings]: Amyotrophic lateral sclerosis | Frontotemporal dementia | Fused in sarcoma | Translated in sarcoma | RNA granules | Stress granules | Aggregate prone disease | Disease spreading | Cortical neurodegeneration | Motor neuron disease | FUS-FTLD | iPSC | Human cell models | amyotrophic-lateral-sclerosis | frontotemporal lobar degeneration | nuclear-localization signal | pluripotent stem-cells | wild-type fus | sarcoma fus | mutant fus | fet proteins | rna
[DDC subject group]: DDC 610 / Medicine & health

Metadata

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