Related references
Note: Only part of the references are listed.TDP-43 pathology in sporadic ALS occurs in motor neurons lacking the RNA editing enzyme ADAR2
Hitoshi Aizawa et al.
ACTA NEUROPATHOLOGICA (2010)
TDP-43 Redistribution is an Early Event in Sporadic Amyotrophic Lateral Sclerosis
Maria Teresa Giordana et al.
BRAIN PATHOLOGY (2010)
TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration
Clotilde Lagier-Tourenne et al.
HUMAN MOLECULAR GENETICS (2010)
Global Analysis of TDP-43 Interacting Proteins Reveals Strong Association with RNA Splicing and Translation Machinery
Brian D. Freibaum et al.
JOURNAL OF PROTEOME RESEARCH (2010)
Nuclear networking fashions pre-messenger RNA and primary microRNA transcripts for function
Jan M. Pawlicki et al.
TRENDS IN CELL BIOLOGY (2010)
Phosphorylated and ubiquitinated TDP-43 pathological inclusions in ALS and FTLD-U are recapitulated in SH-SY5Y cells
Takashi Nonaka et al.
FEBS LETTERS (2009)
Truncation and pathogenic mutations facilitate the formation of intracellular aggregates of TDP-43
Takashi Nonaka et al.
HUMAN MOLECULAR GENETICS (2009)
Mutations in TDP-43 link glycine-rich domain functions to amyotrophic lateral sclerosis
G. Scott Pesiridis et al.
HUMAN MOLECULAR GENETICS (2009)
Potentiation of Amyotrophic Lateral Sclerosis (ALS)-associated TDP-43 Aggregation by the Proteasome-targeting Factor, Ubiquilin 1
Sang Hwa Kim et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2009)
TDP-43 localizes in mRNA transcription and processing sites in mammalian neurons
Inigo Casafont et al.
JOURNAL OF STRUCTURAL BIOLOGY (2009)
The NF90-NF45 Complex Functions as a Negative Regulator in the MicroRNA Processing Pathway
Shuji Sakamoto et al.
MOLECULAR AND CELLULAR BIOLOGY (2009)
An RNA code for the FOX2 splicing regulator revealed by mapping RNA-protein interactions in stem cells
Gene W. Yeo et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2009)
TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degeneration
Iga Wegorzewska et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
Aberrant cleavage of TDP-43 enhances aggregation and cellular toxicity
Yong-Jie Zhang et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6
Caroline Vance et al.
SCIENCE (2009)
Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis
T. J. Kwiatkowski et al.
SCIENCE (2009)
Enrichment of C-terminal fragments in TAR DNA-binding protein-43 cytoplasmic inclusions in brain but not in spinal cord of frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Lionel M. Igaz et al.
AMERICAN JOURNAL OF PATHOLOGY (2008)
Phosphorylated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Masato Hasegawa et al.
ANNALS OF NEUROLOGY (2008)
TDP-43 Overexpression Enhances Exon 7 Inclusion during the Survival of Motor Neuron Pre-mRNA Splicing
Jayarama Krishnan Bose et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
Identifying specific protein interaction partners using quantitative mass spectrometry and bead proteomes
Laura Trinkle-Mulcahy et al.
JOURNAL OF CELL BIOLOGY (2008)
TDP-43, the signature protein of FTLD-U, is a neuronal activity-responsive factor
I. -Fan Wang et al.
JOURNAL OF NEUROCHEMISTRY (2008)
TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology:: a genetic and histopathological analysis
Vivianna M. Van Deerlin et al.
LANCET NEUROLOGY (2008)
TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
Edor Kabashi et al.
NATURE GENETICS (2008)
TDP-43 regulates retinoblastoma protein phosphorylation through the repression of cyclin-dependent kinase 6 expression
Youhna M. Ayala et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
A yeast TDP-43 proteinopathy model: Exploring the molecular determinants of TDR-43 aggregation and cellular toxicity
Brian S. Johnson et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis
Jemeen Sreedharan et al.
SCIENCE (2008)
Functional multivesicular bodies are required for autophagic clearance of protein aggregates associated with neurodegenerative disease
Maria Filimonenko et al.
JOURNAL OF CELL BIOLOGY (2007)
TDP-43: a novel neurodegenerative proteinopathy
Mark S. Forman et al.
CURRENT OPINION IN NEUROBIOLOGY (2007)
TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Tetsuaki Arai et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2006)
Functional and quantitative proteomics using SILAC
Matthias Mann
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2006)
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Manuela Neumann et al.
SCIENCE (2006)
cis-requirement for the maintenance of round spermatid-specific transcription
Kshitish K. Acharya et al.
DEVELOPMENTAL BIOLOGY (2006)
A practical recipe for stable isotope labeling by amino acids in cell culture (SILAC)
Shao-En Ong et al.
NATURE PROTOCOLS (2006)
Modulation of microRNA processing and expression through RNA editing by ADAR deaminases
WD Yang et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2006)
TDP-43 binds heterogeneous nuclear ribonucleoprotein A/B through its C-terminal tail - An important region for the inhibition of cystic fibrosis transmembrane conductance regulator exon 9 splicing
E Buratti et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
Transgenic mice expressing CUG-BP1 reproduce splicing mis-regulation observed in myotonic dystrophy
TH Ho et al.
HUMAN MOLECULAR GENETICS (2005)
Depletion of TDP 43 overrides the need for exonic and intronic splicing enhancers in the human apoA-II gene
PA Mercado et al.
NUCLEIC ACIDS RESEARCH (2005)
Bub1 is required for kinetochore localization of BubR1, Cenp-E, Cenp-F and Mad2, and chromosome congression
VL Johnson et al.
JOURNAL OF CELL SCIENCE (2004)
Stabilization of α-synuclein protein with aging and familial Parkinson's disease-linked A53T mutation
WX Li et al.
JOURNAL OF NEUROSCIENCE (2004)
Protein aggregation and neurodegenerative disease
CA Ross et al.
NATURE MEDICINE (2004)
A protein interaction framework for human mRNA degradation
B Lehner et al.
GENOME RESEARCH (2004)
The Microprocessor complex mediates the genesis of microRNAs
RI Gregory et al.
NATURE (2004)
Evidence for reassociation of RNA-binding proteins after cell lysis: Implications for the interpretation of immunoprecipitation analyses
S Mili et al.
RNA (2004)
Higher order arrangement of the eukaryotic nuclear bodies
IF Wang et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)
An extensive network of coupling among gene expression machines
T Maniatis et al.
NATURE (2002)
Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping
E Buratti et al.
EMBO JOURNAL (2001)