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注意：仅列出部分参考文献，下载原文获取全部文献信息。PRO-MINE: A Bioinformatics Repository and Analytical Tool for TARDBP Mutations
Sofia Pinto et al.
HUMAN MUTATION (2011)
Identification of Neuronal RNA Targets of TDP-43-containing Ribonucleoprotein Complexes
Chantelle F. Sephton et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2011)
TDP-43 Redistribution is an Early Event in Sporadic Amyotrophic Lateral Sclerosis
Maria Teresa Giordana et al.
BRAIN PATHOLOGY (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)
Cytoplasmic Mislocalization of TDP-43 Is Toxic to Neurons and Enhanced by a Mutation Associated with Familial Amyotrophic Lateral Sclerosis
Sami J. Barmada et al.
JOURNAL OF NEUROSCIENCE (2010)
TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia
Ian R. A. Mackenzie et al.
LANCET NEUROLOGY (2010)
Progressive motor weakness in transgenic mice expressing human TDP-43
Nancy R. Stallings et al.
NEUROBIOLOGY OF DISEASE (2010)
TDP-43-Mediated Neuron Loss In Vivo Requires RNA-Binding Activity
Aaron Voigt et al.
PLOS ONE (2010)
ALS-associated mutations in TDP-43 increase its stability and promote TDP-43 complexes with FUS/TLS
Shuo-Chien Ling et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
A Drosophila model for TDP-43 proteinopathy
Yan Li et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
TARDBP Mutations in Frontotemporal Lobar Degeneration: Frequency, Clinical Features, and Disease Course
B. Borroni et al.
REJUVENATION RESEARCH (2010)
Letter from the Editor
Renee Schroeder et al.
RNA Biology (2010)
Transgenic Rat Model of Neurodegeneration Caused by Mutation in the TDP Gene
Hongxia Zhou et al.
PLOS GENETICS (2010)
Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations
Ian R. A. Mackenzie et al.
ACTA NEUROPATHOLOGICA (2009)
TARDBP 3'-UTR variant in autopsy-confirmed frontotemporal lobar degeneration with TDP-43 proteinopathy
Michael A. Gitcho et al.
ACTA NEUROPATHOLOGICA (2009)
Phosphorylation of S409/410 of TDP-43 is a consistent feature in all sporadic and familial forms of TDP-43 proteinopathies
Manuela Neumann et al.
ACTA NEUROPATHOLOGICA (2009)
TARDBP Mutations in Motoneuron Disease with Frontotemporal Lobar Degeneration
Lina Benajiba et al.
ANNALS OF NEUROLOGY (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)
Mutation within TARDBP Leads to Frontotemporal Dementia without Motor Neuron Disease
B. Borroni et al.
HUMAN MUTATION (2009)
TDP-43 Is Intrinsically Aggregation-prone, and Amyotrophic Lateral Sclerosis-linked Mutations Accelerate Aggregation and Increase Toxicity
Brian S. Johnson et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2009)
Frontotemporal dementia and motor neurone disease: Overlapping clinic-pathological disorders
Patricia Lillo et al.
JOURNAL OF CLINICAL NEUROSCIENCE (2009)
Amyotrophic lateral sclerosis, frontotemporal dementia and beyond: the TDP-43 diseases
Felix Geser et al.
JOURNAL OF NEUROLOGY (2009)
No Evidence for Cognitive Dysfunction or Depression in Patients with Mild Restless Legs Syndrome
Erika Driver-Dunckley et al.
MOVEMENT DISORDERS (2009)
Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS
Ilse Gijselinck et al.
NEUROBIOLOGY OF AGING (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)
Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis
T. J. Kwiatkowski et al.
SCIENCE (2009)
Frontotemporal dementia and amyotrophic lateral sclerosis-associated disease protein TDP-43 promotes dendritic branching
Yubing Lu et al.
MOLECULAR BRAIN (2009)
Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis
H. Daoud et al.
JOURNAL OF MEDICAL GENETICS (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)
Evidence of multisystem disorder in whole-brain map of pathological TDP-43 in amyotrophic lateral sclerosis
Felix Geser et al.
ARCHIVES OF NEUROLOGY (2008)
Multiple roles of TDP-43 in gene expression, splicing regulation, and human disease
Emanuele Buratti et al.
FRONTIERS IN BIOSCIENCE-LANDMARK (2008)
Disturbance of nuclear and cytoplasmic TAR DNA-binding protein (TDP-43) induces disease-like redistribution, sequestration, and aggregate formation
Matthew J. Winton et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
Edor Kabashi et al.
NATURE GENETICS (2008)
TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis
Jemeen Sreedharan et al.
SCIENCE (2008)
Amyotrophic lateral sclerosis
J. D. Mitchell et al.
LANCET (2007)
TDP43 is a human low molecular weight neurofilament (hNFL) mRNA-binding protein
Michael J. Strong et al.
MOLECULAR AND CELLULAR NEUROSCIENCE (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)
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)
ALS:: A disease of motor neurons and their nonneuronal neighbors
Sverine Boillee et al.
NEURON (2006)
Protein aggregation and neurodegenerative disease
CA Ross et al.
NATURE MEDICINE (2004)
Structural diversity and functional implications of the eukaryotic TDP gene family
HY Wang et al.
GENOMICS (2004)
Characterization and functional implications of the RNA binding properties of nuclear factor TDP-43, a novel splicing regulator of CFTR exon 9
E Buratti et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
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