Related references
Note: Only part of the references are listed.TDP-43 and FUS RNA-binding Proteins Bind Distinct Sets of Cytoplasmic Messenger RNAs and Differently Regulate Their Post-transcriptional Fate in Motoneuron-like Cells
Claudia Colombrita et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2012)
Inhibition of RNA lariat debranching enzyme suppresses TDP-43 toxicity in ALS disease models
Maria Armakola et al.
NATURE GENETICS (2012)
TDP-43 regulates global translational yield by splicing of exon junction complex component SKAR
Fabienne C. Fiesel et al.
NUCLEIC ACIDS RESEARCH (2012)
Alteration of POLDIP3 Splicing Associated with Loss of Function of TDP-43 in Tissues Affected with ALS
Atsushi Shiga et al.
PLOS ONE (2012)
FUS-SMN Protein Interactions Link the Motor Neuron Diseases ALS and SMA
Tomohiro Yamazaki et al.
CELL REPORTS (2012)
Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43
Magdalini Polymenidou et al.
NATURE NEUROSCIENCE (2011)
Characterizing the RNA targets and position-dependent splicing regulation by TDP-43
James R. Tollervey et al.
NATURE NEUROSCIENCE (2011)
Association of TALS Developmental Disorder with Defect in Minor Splicing Component U4atac snRNA
Patrick Edery et al.
SCIENCE (2011)
Mutations in U4atac snRNA, a Component of the Minor Spliceosome, in the Developmental Disorder MOPD I
Huiling He et al.
SCIENCE (2011)
Biogenesis and function of nuclear bodies
Yuntao S. Mao et al.
TRENDS IN GENETICS (2011)
Sporadic ALS has compartment-specific aberrant exon splicing and altered cell-matrix adhesion biology
Stuart J. Rabin et al.
HUMAN MOLECULAR GENETICS (2010)
Gain and loss of function of ALS-related mutations of TARDBP (TDP-43) cause motor deficits in vivo
Edor Kabashi et al.
HUMAN MOLECULAR GENETICS (2010)
TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration
Clotilde Lagier-Tourenne et al.
HUMAN MOLECULAR GENETICS (2010)
TDP-43 Is a Developmentally Regulated Protein Essential for Early Embryonic Development
Chantelle F. Sephton et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (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)
Deletion of TDP-43 down-regulates Tbc1d1, a gene linked to obesity, and alters body fat metabolism
Po-Min Chiang et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Altered distributions of Gemini of coiled bodies and mitochondria in motor neurons of TDP-43 transgenic mice
Xiu Shan et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Biogenesis of Nuclear Bodies
Miroslav Dundr et al.
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY (2010)
The MIQE Guidelines: Minimum Information for Publication of Quantitative Real-Time PCR Experiments
Stephen A. Bustin et al.
CLINICAL CHEMISTRY (2009)
Spinal muscular atrophy: why do low levels of survival motor neuron protein make motor neurons sick?
Arthur H. M. Burghes et al.
NATURE REVIEWS NEUROSCIENCE (2009)
Rates of in situ transcription and splicing in large human genes
Jarnail Singh et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2009)
Structural insights into TDP-43 in nucleic-acid binding and domain interactions
Pan-Hsien Kuo et al.
NUCLEIC ACIDS RESEARCH (2009)
Sporadic amyotrophic lateral sclerosis: two pathological patterns shown by analysis of distribution of TDP-43-immunoreactive neuronal and glial cytoplasmic inclusions
Yasushi Nishihira et al.
ACTA NEUROPATHOLOGICA (2008)
Maturation process of TDP-43-positive neuronal cytoplasmic inclusions in amyotrophic lateral sclerosis with and without dementia
Fumiaki Mori et al.
ACTA NEUROPATHOLOGICA (2008)
TDP-43 mutation in familial amyotrophic lateral sclerosis
Akio Yokoseki et al.
ANNALS OF NEUROLOGY (2008)
The Cajal body
Glenn E. Morris
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2008)
SMN deficiency causes tissue-specific perturbations in the repertoire of snRNAs and widespread defects in splicing
Zhenxi Zhang et al.
CELL (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)
The U11-48K protein contacts the 5′ splice site of U12-type introns and the U11-59K protein
Janne J. Turunen et al.
MOLECULAR AND CELLULAR BIOLOGY (2008)
De Novo Formation of a Subnuclear Body
Trish E. Kaiser et al.
SCIENCE (2008)
TDP-43 proteinopathy in frontotemporal lobar degeneration and amyotrophic lateral sclerosis - Protein misfolding diseases without amyloidosis
Manuela Neumann et al.
ARCHIVES OF NEUROLOGY (2007)
Ribonucleoprotein Assembly Defects Correlate with Spinal Muscular Atrophy Severity and Preferentially Affect a Subset of Spliceosomal snRNPs
Francesca Gabanella et al.
PLOS ONE (2007)
TDP-43 immunoreactivity in neuronal inclusions in familial amyotrophic lateral sclerosis with or without SOD1 gene mutation
Chun-Feng Tan et al.
ACTA NEUROPATHOLOGICA (2007)
Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations
Ian R. A. Mackenzie et al.
ANNALS OF NEUROLOGY (2007)
Chaperoning ribonucleoprotein biogenesis in health and disease
Livio Pellizzoni
EMBO REPORTS (2007)
A comprehensive interaction map of the human survival of motor neuron (SMN) complex
Simon Otter et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2007)
U12DB: a database of orthologous U12-type spliceosomal introns
Tyler S. Alioto
NUCLEIC ACIDS RESEARCH (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)
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Manuela Neumann et al.
SCIENCE (2006)
The abundance of the spliceosomal snRNPs is not limiting the splicing of U12-type introns
Heli K. J. Pessa et al.
RNA (2006)
Splicing of a rare class of introns by the U12-dependent spliceosome
CL Will et al.
BIOLOGICAL CHEMISTRY (2005)
Gemins modulate the expression and activity of the SMN complex
WQ Feng et al.
HUMAN MOLECULAR GENETICS (2005)
Familial amyotrophic lateral sclerosis with bulbar onset and a novel Asp101Tyr Cu/Zn superoxide dismutase gene mutation
CF Tan et al.
ACTA NEUROPATHOLOGICA (2004)
Modification of Sm small nuclear RNAs occurs in the nucleoplasmic Cajal body following import from the cytoplasm
BE Jády et al.
EMBO JOURNAL (2003)
Splicing double: Insights from the second spliceosome
AA Patel et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2003)
The spliceosome: the most complex macromolecular machine in the cell?
TW Nilsen
BIOESSAYS (2003)
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)
A computational scan for U12-dependent introns in the human genome sequence
A Levine et al.
NUCLEIC ACIDS RESEARCH (2001)
Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping
E Buratti et al.
EMBO JOURNAL (2001)
Share Paper
