TDP-43 neuropathology is similar in sporadic amyotrophic lateral sclerosis with or withoutTDP-43mutations
Author:
Publisher
Wiley
Subject
Physiology (medical),Clinical Neurology,Neurology,Histology,Pathology and Forensic Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2990.2008.00982.x/fullpdf
Reference11 articles.
1. TDP-43 immunoreactivity in neuronal inclusions in familial amyotrophic lateral sclerosis with or without SOD1 gene mutation;Tan;Acta Neuropathol,2007
2. Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations;Mackenzie;Ann Neurol,2007
3. TDP-43 A315T mutation in familial motor neuron disease;Gitcho;Ann Neurol,2008
4. TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis;Sreedharan;Science,2008
5. TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis;Van Deerlin;Lancet Neurol,2008
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1. Neuromuscular junction denervation and terminal Schwann cell loss in the hTDP‐43 overexpression mouse model of amyotrophic lateral sclerosis;Neuropathology and Applied Neurobiology;2023-08
2. SQSTM1L341V variant that is linked to sporadic ALS exhibits impaired association with MAP1LC3 in cultured cells;eNeurologicalSci;2021-03
3. Aggresome formation and liquid–liquid phase separation independently induce cytoplasmic aggregation of TAR DNA-binding protein 43;Cell Death & Disease;2020-10
4. TDP-1/TDP-43 potentiates human α-Synuclein (HASN) neurodegeneration in Caenorhabditis elegans;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;2020-10
5. The role of TDP-43 mislocalization in amyotrophic lateral sclerosis;Molecular Neurodegeneration;2020-08-15
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