FET proteins TAF15 and EWS are selective markers that distinguish FTLD with FUS pathology from amyotrophic lateral sclerosis with FUS mutations
Published 2011 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
FET proteins TAF15 and EWS are selective markers that distinguish FTLD with FUS pathology from amyotrophic lateral sclerosis with FUS mutations
Authors
Keywords
-
Journal
BRAIN
Volume 134, Issue 9, Pages 2595-2609
Publisher
Oxford University Press (OUP)
Online
2011-08-20
DOI
10.1093/brain/awr201
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Pathological heterogeneity in amyotrophic lateral sclerosis with FUS mutations: two distinct patterns correlating with disease severity and mutation
- (2011) Ian R. A. Mackenzie et al. ACTA NEUROPATHOLOGICA
- The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene
- (2011) Julie S. Snowden et al. ACTA NEUROPATHOLOGICA
- Mutational analysis reveals the FUS homolog TAF15 as a candidate gene for familial amyotrophic lateral sclerosis
- (2011) N. Ticozzi et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
- FUS Immunogold Labeling TEM Analysis of the Neuronal Cytoplasmic Inclusions of Neuronal Intermediate Filament Inclusion Disease: A Frontotemporal Lobar Degeneration with FUS Proteinopathy
- (2011) Tristan Page et al. JOURNAL OF MOLECULAR NEUROSCIENCE
- TDP-43 and FUS: a nuclear affair
- (2011) Dorothee Dormann et al. TRENDS IN NEUROSCIENCES
- Distinct pathological subtypes of FTLD-FUS
- (2010) Ian R. A. Mackenzie et al. ACTA NEUROPATHOLOGICA
- FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration
- (2010) Hazel Urwin et al. ACTA NEUROPATHOLOGICA
- Nuclear transport impairment of amyotrophic lateral sclerosis-linked mutations in FUS/TLS
- (2010) Daisuke Ito et al. ANNALS OF NEUROLOGY
- FUS Mutations in Familial Amyotrophic Lateral Sclerosis in the Netherlands
- (2010) Ewout J. N. Groen et al. ARCHIVES OF NEUROLOGY
- Novel FUS/TLS Mutations and Pathology in Familial and Sporadic Amyotrophic Lateral Sclerosis
- (2010) Christopher Hewitt et al. ARCHIVES OF NEUROLOGY
- ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import
- (2010) Dorothee Dormann et al. EMBO JOURNAL
- TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia
- (2010) Ian RA Mackenzie et al. LANCET NEUROLOGY
- Fusgene mutations in familial and sporadic amyotrophic lateral sclerosis
- (2010) Rosa Rademakers et al. MUSCLE & NERVE
- Intracellular localization and splicing regulation of FUS/TLS are variably affected by amyotrophic lateral sclerosis-linked mutations
- (2010) Yoshihiro Kino et al. NUCLEIC ACIDS RESEARCH
- Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease
- (2009) Manuela Neumann et al. ACTA NEUROPATHOLOGICA
- FUS pathology in basophilic inclusion body disease
- (2009) David G. Munoz et al. ACTA NEUROPATHOLOGICA
- Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update
- (2009) Ian R. A. Mackenzie et al. ACTA NEUROPATHOLOGICA
- A new subtype of frontotemporal lobar degeneration with FUS pathology
- (2009) M. Neumann et al. BRAIN
- FUS-Immunoreactive Intranuclear Inclusions in Neurodegenerative Disease
- (2009) John Woulfe et al. BRAIN PATHOLOGY
- FUS mutations in amyotrophic lateral sclerosis: clinical, pathological, neurophysiological and genetic analysis
- (2009) I. P. Blair et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- The RNA-binding protein FUS/TLS is a common aggregate-interacting protein in polyglutamine diseases
- (2009) Hiroshi Doi et al. NEUROSCIENCE RESEARCH
- 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
- (2009) T. J. Kwiatkowski et al. SCIENCE
- The TET Family of Proteins: Functions and Roles in Disease
- (2009) A. Y. Tan et al. Journal of Molecular Cell Biology
- Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations
- (2008) Ian R. A. Mackenzie et al. ACTA NEUROPATHOLOGICA
- PRMT1 mediated methylation of TAF15 is required for its positive gene regulatory function
- (2008) Laure Jobert et al. EXPERIMENTAL CELL RESEARCH
- Identification of proteins interacting with protein arginine methyltransferase 8: The Ewing sarcoma (EWS) protein binds independent of its methylation state
- (2008) Steffen Pahlich et al. PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS
Find the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
SearchBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started