- Home
- Publications
- Publication Search
- Publication Details
Title
Molecular Dissection of TDP-43 Proteinopathies
Authors
Keywords
-
Journal
JOURNAL OF MOLECULAR NEUROSCIENCE
Volume 45, Issue 3, Pages 480-485
Publisher
Springer Nature
Online
2011-06-15
DOI
10.1007/s12031-011-9571-x
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Pathogenic TARDBP Mutations in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia: Disease-Associated Pathways
- (2011) Sami J. Barmada et al. REVIEWS IN THE NEUROSCIENCES
- Seeded Aggregation and Toxicity of α-Synuclein and Tau
- (2010) Takashi Nonaka et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Phosphorylated TDP-43 in Alzheimer’s disease and dementia with Lewy bodies
- (2009) Tetsuaki Arai et al. ACTA NEUROPATHOLOGICA
- TARDBPmutations in motoneuron disease with frontotemporal lobar degeneration
- (2009) Lina Benajiba et al. ANNALS OF NEUROLOGY
- Methylene blue and dimebon inhibit aggregation of TDP-43 in cellular models
- (2009) Makiko Yamashita et al. FEBS LETTERS
- Truncation and pathogenic mutations facilitate the formation of intracellular aggregates of TDP-43
- (2009) Takashi Nonaka et al. HUMAN MOLECULAR GENETICS
- Mutations in TDP-43 link glycine-rich domain functions to amyotrophic lateral sclerosis
- (2009) G. S. Pesiridis et al. HUMAN MOLECULAR GENETICS
- Mutation withinTARDBPleads to Frontotemporal Dementia without motor neuron disease
- (2009) B. Borroni et al. HUMAN MUTATION
- Conversion of Wild-type α-Synuclein into Mutant-type Fibrils and Its Propagation in the Presence of A30P Mutant
- (2009) Motokuni Yonetani et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Accumulation of phosphorylated TDP-43 in brains of patients with argyrophilic grain disease
- (2008) Hiroshige Fujishiro et al. ACTA NEUROPATHOLOGICA
- Sporadic amyotrophic lateral sclerosis of long duration is associated with relatively mild TDP-43 pathology
- (2008) Yasushi Nishihira et al. ACTA NEUROPATHOLOGICA
- Ultrastructural localization of TDP-43 in filamentous neuronal inclusions in various neurodegenerative diseases
- (2008) Wen-Lang Lin et al. ACTA NEUROPATHOLOGICA
- TDP-43mutation in familial amyotrophic lateral sclerosis
- (2008) Akio Yokoseki et al. ANNALS OF NEUROLOGY
- TDP-43A315T mutation in familial motor neuron disease
- (2008) Michael A. Gitcho et al. ANNALS OF NEUROLOGY
- Phosphorylated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
- (2008) Masato Hasegawa et al. ANNALS OF NEUROLOGY
- Evidence of Multisystem Disorder in Whole-Brain Map of Pathological TDP-43 in Amyotrophic Lateral Sclerosis
- (2008) Felix Geser et al. ARCHIVES OF NEUROLOGY
- Phosphorylated and ubiquitinated TDP-43 pathological inclusions in ALS and FTLD-U are recapitulated in SH-SY5Y cells
- (2008) Takashi Nonaka et al. FEBS LETTERS
- TDP-43 Overexpression Enhances Exon 7 Inclusion during the Survival of Motor Neuron Pre-mRNA Splicing
- (2008) Jayarama Krishnan Bose et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Concomitant TAR-DNA-Binding Protein 43 Pathology Is Present in Alzheimer Disease and Corticobasal Degeneration but Not in Other Tauopathies
- (2008) Kunihiro Uryu et al. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
- TAR-DNA Binding Protein 43 in Pick Disease
- (2008) Stefanie H. Freeman et al. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
- TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis
- (2008) Vivianna M Van Deerlin et al. LANCET NEUROLOGY
- TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
- (2008) Edor Kabashi et al. NATURE GENETICS
- TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis
- (2008) J. Sreedharan et al. SCIENCE
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started