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Elevated expression of TDP-43 in the forebrain of mice is sufficient to cause neurological and pathological phenotypes mimicking FTLD-U
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SF2/ASF autoregulation involves multiple layers of post-transcriptional and translational control
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ALS-associated mutations in TDP-43 increase its stability and promote TDP-43 complexes with FUS/TLS
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A Drosophila model for TDP-43 proteinopathy
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TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration
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PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
TARDBP 3'-UTR variant in autopsy-confirmed frontotemporal lobar degeneration with TDP-43 proteinopathy
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Depletion of TDP-43 affects Drosophila motoneurons terminal synapsis and locomotive behavior
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Mutations in TDP-43 link glycine-rich domain functions to amyotrophic lateral sclerosis
G. Scott Pesiridis et al.
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Auto- and Cross-Regulation of the hnRNP L Proteins by Alternative Splicing
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MOLECULAR AND CELLULAR BIOLOGY (2009)
An integrated workflow for charting the human interaction proteome: insights into the PP2A system
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CLIP: Construction of cDNA libraries for high-throughput sequencing from RNAs cross-linked to proteins in vivo
Zhen Wang et al.
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Functional mapping of the interaction between TDP-43 and hnRNP A2 in vivo
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Structural insights into TDP-43 in nucleic-acid binding and domain interactions
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TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degeneration
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Multiple roles of TDP-43 in gene expression, splicing regulation, and human disease
Emanuele Buratti et al.
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Concomitant TAR-DNA-binding in Alzheimer disease and protein 43 pathology is present corticobasal degeneration but not in other tauopathies
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Regulation of multiple core spliceosomal proteins by alternative splicing-coupled nonsense-mediated mRNA decay
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TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
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Pathological TDP-43 in parkinsonism-dementia complex and amyotrophic lateral sclerosis of Guam
Felix Geser et al.
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Concurrence of TDP-43, tau and α-synuclein pathology in brains of Alzheimer's disease and dementia with Lewy bodies
Shinji Higashi et al.
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Co-morbidity of TDP-43 proteinopathy in Lewy body related diseases
Hanae Nakashima-Yasuda et al.
ACTA NEUROPATHOLOGICA (2007)
TDP-43 immunoreactivity in hippocampal sclerosis and Alzheimer's disease
Catalina Amador-Ortiz et al.
ANNALS OF NEUROLOGY (2007)
Unproductive splicing of SR genes associated with highly conserved and ultraconserved DNA elements
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Ultraconserved elements are associated with homeostatic control of splicing regulators by alternative splicing and nonsense-mediated decay
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TDP-43 in the ubiquitin pathology of frontotemporal dementia with VCP gene mutations
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TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
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BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2006)
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
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Mammalian Staufen1 recruits Upf1 to specific mRNA 3'UTRs so as to elicit mRNA decay
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Autoregulation of polypyrimidine tract binding protein by alternative splicing leading to nonsense-mediated decay
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Nonsense-mediated mRNA decay in mammalian cells involves decapping, deadenylating, and exonucleolytic activities
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Regulated splicing of the fibronectin EDA exon is essential for proper skin wound healing and normal lifespan
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E Buratti et al.
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Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping
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SC35 autoregulates its expression by promoting splicing events that destabilize its mRNAs
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