Related references
Note: Only part of the references are listed.ALS-Associated Ataxin 2 PolyQ Expansions Enhance Stress-Induced Caspase 3 Activation and Increase TDP-43 Pathological Modifications
Michael P. Hart et al.
JOURNAL OF NEUROSCIENCE (2012)
Nuclear Transport Impairment of Amyotrophic Lateral Sclerosis-Linked Mutations in FUS/TLS
Daisuke Ito et al.
ANNALS OF NEUROLOGY (2011)
ATXN-2 CAG repeat expansions are interrupted in ALS patients
Lucia Corrado et al.
HUMAN GENETICS (2011)
Dysregulation of the ALS-associated gene TDP-43 leads to neuronal death and degeneration in mice
Lionel M. Igaz et al.
JOURNAL OF CLINICAL INVESTIGATION (2011)
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)
Expanded ATXN2 CAG repeat size in ALS identifies genetic overlap between ALS and SCA2
P. Van Damme et al.
NEUROLOGY (2011)
Evaluating the prevalence of polyglutamine repeat expansions in amyotrophic lateral sclerosis
T. Lee et al.
NEUROLOGY (2011)
Conjoint pathologic cascades mediated by ALS/FTLD-U linked RNA-binding proteins TDP-43 and FUS
Daisuke Ito et al.
NEUROLOGY (2011)
Primary Central Nervous System Lymphoma
Elizabeth R. Gerstner et al.
ARCHIVES OF NEUROLOGY (2010)
Nuclear import impairment causes cytoplasmic trans-activation response DNA-binding protein accumulation and is associated with frontotemporal lobar degeneration
Agnes L. Nishimura et al.
BRAIN (2010)
ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import
Dorothee Dormann et al.
EMBO JOURNAL (2010)
TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration
Clotilde Lagier-Tourenne et al.
HUMAN MOLECULAR GENETICS (2010)
Characterization of Alternative Isoforms and Inclusion Body of the TAR DNA-binding Protein-43
Yoshinori Nishimoto et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2010)
Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS
Andrew C. Elden et al.
NATURE (2010)
Localization to, and Effects of Pbp1, Pbp4, Lsm12, Dhh1, and Pab1 on Stress Granules in Saccharomyces cerevisiae
Kylie D. Swisher et al.
PLOS ONE (2010)
Tar DNA Binding Protein-43 (TDP-43) Associates with Stress Granules: Analysis of Cultured Cells and Pathological Brain Tissue
Liqun Liu-Yesucevitz et al.
PLOS ONE (2010)
Eukaryotic Stress Granules: The Ins and Outs of Translation
J. Ross Buchan et al.
MOLECULAR CELL (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)
Immunohistochemical identification of messenger RNA-related proteins in basophilic inclusions of adult-onset atypical motor neuron disease
Kengo Fujita et al.
ACTA NEUROPATHOLOGICA (2008)
P bodies promote stress granule assembly in Saccharomyces cerevisiae
J. Ross Buchan et al.
JOURNAL OF CELL BIOLOGY (2008)
TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis
Jemeen Sreedharan et al.
SCIENCE (2008)
Molecular pathogenesis of seipin/BSCL2-related motor neuron diseases
Daisuke Ito et al.
ANNALS OF NEUROLOGY (2007)
Ataxin-2 interacts with the DEAD/H-box RNA helicase DDX6 and interferes with P-bodies and stress granules
Ute Nonhoff et al.
MOLECULAR BIOLOGY OF THE CELL (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)
Ataxin-2 and its Drosophila homolog, ATX2, physically assemble with polyribosomes
Terrence F. Satterfield et al.
HUMAN MOLECULAR GENETICS (2006)
Stress granules and processing bodies are dynamically linked sites of mRNP remodeling
N Kedersha et al.
JOURNAL OF CELL BIOLOGY (2005)
Global impairment of the ubiquitin-proteasome system by nuclear or cytoplasmic protein aggregates precedes inclusion body formation
EJ Bennett et al.
MOLECULAR CELL (2005)
Structural and functional analysis of ataxin-2 and ataxin-3
M Albrecht et al.
EUROPEAN JOURNAL OF BIOCHEMISTRY (2004)
Characterization of stanniocalcin 2, a novel target of the mammalian unfolded protein response with cytoprotective properties
D Ito et al.
MOLECULAR AND CELLULAR BIOLOGY (2004)
Inclusion body formation reduces levels of mutant huntingtin and the risk of neuronal death
M Arrasate et al.
NATURE (2004)
Aggresomes protect cells by enhancing the degradation of toxic polyglutamine-containing protein
JP Taylor et al.
HUMAN MOLECULAR GENETICS (2003)
Share Paper
