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Title
Transportin1: a marker of FTLD-FUS
Authors
Keywords
-
Journal
ACTA NEUROPATHOLOGICA
Volume 122, Issue 5, Pages 591-600
Publisher
Springer Nature
Online
2011-08-17
DOI
10.1007/s00401-011-0863-6
References
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Related references
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- Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6
- (2009) C. Vance et al. SCIENCE
- Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis
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- The TET Family of Proteins: Functions and Roles in Disease
- (2009) A. Y. Tan et al. Journal of Molecular Cell Biology
- TDP-43-negative FTLD-U is a significant new clinico-pathological subtype of FTLD
- (2008) Sigrun Roeber et al. ACTA NEUROPATHOLOGICA
- Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations
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- The multifunctional FUS, EWS and TAF15 proto-oncoproteins show cell type-specific expression patterns and involvement in cell spreading and stress response
- (2008) Mattias K Andersson et al. BMC CELL BIOLOGY
- TDP-43: an emerging new player in neurodegenerative diseases
- (2008) I-Fan Wang et al. TRENDS IN MOLECULAR MEDICINE
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