Single-cell RNA-sequencing reveals early mitochondrial dysfunction unique to motor neurons shared across FUS- and TARDBP-ALS
Abstract Mutations in FUS and TARDBP cause amyotrophic lateral sclerosis (ALS), but the precise mechanisms of selective motor neuron degeneration remain unresolved. To address if pathomechanisms are shared across mutations and related to either gain- or loss-of-function, we performed single-cell RNA...
Saved in:
| Main Authors: | Christoph Schweingruber, Jik Nijssen, Jonas Mechtersheimer, Stefan Reber, Mélanie Lebœuf, Niamh L. O’Brien, Irene Mei, Erin Hedges, Michaela Keuper, Julio Aguila Benitez, Vlad Radoi, Martin Jastroch, Marc-David Ruepp, Eva Hedlund |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Nature Portfolio
2025-05-01
|
| Series: | Nature Communications |
| Online Access: | https://doi.org/10.1038/s41467-025-59679-1 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
FUS and TARDBP but not SOD1 interact in genetic models of amyotrophic lateral sclerosis.
by: Edor Kabashi, et al.
Published: (2011-08-01) -
Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis.
by: Nicola J Rutherford, et al.
Published: (2008-09-01) -
Initial outcomes and safety of MR guided focused ultrasound (MRgFUS) thalamotomy for essential tremor of the first FUS Medical Unit in Portugal
by: Nuno Vila-Chã, et al.
Published: (2024-08-01) -
Transcriptome-based screening in TARDBP/TDP-43 knock-in motor neurons identifies the NEDD8-activating enzyme inhibitor MLN4924
by: Sarah Lépine, et al.
Published: (2025-08-01) -
A nonsense mutation in mouse Tardbp affects TDP43 alternative splicing activity and causes limb-clasping and body tone defects.
by: Thomas Ricketts, et al.
Published: (2014-01-01)