A comparative clinical, pathological, biochemical and genetic study of fused in sarcoma proteinopathies
出版年份 2011 全文链接
标题
A comparative clinical, pathological, biochemical and genetic study of fused in sarcoma proteinopathies
作者
关键词
-
出版物
BRAIN
Volume 134, Issue 9, Pages 2548-2564
出版商
Oxford University Press (OUP)
发表日期
2011-07-14
DOI
10.1093/brain/awr160
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Sustained Expression of TDP-43 and FUS in Motor Neurons in Rodent's Lifetime
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- The spectrum and severity of FUS-immunoreactive inclusions in the frontal and temporal lobes of ten cases of neuronal intermediate filament inclusion disease
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- FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration
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- Very early-onset frontotemporal dementia with no family history predicts underlying fused in sarcoma pathology
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- Fused in sarcoma/translocated in liposarcoma: A multifunctional DNA/RNA binding protein
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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
- (2009) T. J. Kwiatkowski et al. SCIENCE
- TDP-43-negative FTLD-U is a significant new clinico-pathological subtype of FTLD
- (2008) Sigrun Roeber et al. ACTA NEUROPATHOLOGICA
- Maturation process of TDP-43-positive neuronal cytoplasmic inclusions in amyotrophic lateral sclerosis with and without dementia
- (2008) Fumiaki Mori et al. ACTA NEUROPATHOLOGICA
- 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
- Multiple roles of TDP-43 in gene expression, splicing regulation, and human disease
- (2007) Emanuele Buratti Frontiers in Bioscience-Landmark
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