A proteomic network approach across the ALS‐FTD disease spectrum resolves clinical phenotypes and genetic vulnerability in human brain
Abstract Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are neurodegenerative diseases with overlap in clinical presentation, neuropathology, and genetic underpinnings. The molecular basis for the overlap of these disorders is not well established. We performed a comparative u...
Saved in:
| Main Authors: | Mfon E Umoh, Eric B Dammer, Jingting Dai, Duc M Duong, James J Lah, Allan I Levey, Marla Gearing, Jonathan D Glass, Nicholas T Seyfried |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Springer Nature
2017-11-01
|
| Series: | EMBO Molecular Medicine |
| Subjects: | |
| Online Access: | https://doi.org/10.15252/emmm.201708202 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
The Role of TDP-43 in SARS-CoV-2-Related Neurodegenerative Changes
by: Dong-Hwi Kim, et al.
Published: (2025-05-01) -
Active poly‐GA vaccination prevents microglia activation and motor deficits in a C9orf72 mouse model
by: Qihui Zhou, et al.
Published: (2019-12-01) -
G‐quadruplex‐binding small molecules ameliorate C9orf72 FTD/ALS pathology in vitro and in vivo
by: Roberto Simone, et al.
Published: (2017-11-01) -
Poly‐GP in cerebrospinal fluid links C9orf72‐associated dipeptide repeat expression to the asymptomatic phase of ALS/FTD
by: Carina Lehmer, et al.
Published: (2017-04-01) -
Molecular mechanisms and consequences of TDP-43 phosphorylation in neurodegeneration
by: Elise A. Kellett, et al.
Published: (2025-05-01)