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Delineation of the Core Aggregation Sequences of TDP-43 C-Terminal Fragment

Chembiochem : a European journal of chemical biology, 2011-11, Vol.12 (16), p.2495-2501

2011

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Quantitative assessment of the degradation of aggregated TDP‐43 mediated by the ubiquitin proteasome system and macroautophagy

The FASEB journal, 2017-12, Vol.31 (12), p.5609-5624

2017

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Proteolytic processing of TAR DNA binding protein‐43 by caspases produces C‐terminal fragments with disease defining properties independent of progranulin

Journal of neurochemistry, 2009-08, Vol.110 (3), p.1082-1094

2009

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Progranulin: a new avenue towards the understanding and treatment of neurodegenerative disease

Brain (London, England : 1878), 2017-12, Vol.140 (12), p.3081-3104

2017

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Reappraisal of TDP-43 pathology in FTLD-U subtypes

Acta neuropathologica, 2017-07, Vol.134 (1), p.79-96

2017

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Progranulin: normal function and role in neurodegeneration

Journal of neurochemistry, 2008-01, Vol.104 (2), p.287-297

2008

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Restoring functional TDP-43 oligomers in ALS and laminopathic cellular models through baicalein-induced reconfiguration of TDP-43 aggregates

Scientific reports, 2024-02, Vol.14 (1), p.4620-4620, Article 4620

2024

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TDP-43 toxicity is mediated by the unfolded protein response-unrelated induction of C/EBP homologous protein expression

Journal of neuroscience research, 2012-03, Vol.90 (3), p.641-647

2012

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Frontotemporal lobar degeneration with TAR DNA-binding protein 43 (TDP-43): its journey of more than 100 years

Journal of neurology, 2022-08, Vol.269 (8), p.4030-4054

2022

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Autophagy activation ameliorates neuronal pathogenesis of FTLD-U mice: A new light for treatment of TARDBP/TDP-43 proteinopathies

Autophagy, 2013-02, Vol.9 (2), p.239-240

2013

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Znf179 E3 ligase-mediated TDP-43 polyubiquitination is involved in TDP-43- ubiquitinated inclusions (UBI) (+)-related neurodegenerative pathology

Journal of biomedical science, 2018-11, Vol.25 (1), p.76-76, Article 76

2018

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Atypical frontotemporal lobar degeneration with ubiquitin-positive, TDP-43-negative neuronal inclusions

Brain (London, England : 1878), 2008-05, Vol.131 (5), p.1282-1293

2008

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Temporal lobar predominance of TDP-43 neuronal cytoplasmic inclusions in Alzheimer disease

Acta neuropathologica, 2008-08, Vol.116 (2), p.215-220

2008

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A90V TDP-43 variant results in the aberrant localization of TDP-43 in vitro

FEBS letters, 2008-06, Vol.582 (15), p.2252-2256

2008

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Phosphorylated and ubiquitinated TDP-43 pathological inclusions in ALS and FTLD-U are recapitulated in SH-SY5Y cells

FEBS letters, 2009-01, Vol.583 (2), p.394-400

2009

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Hippocampal sclerosis dementia: a reappraisal

Acta neuropathologica, 2007-10, Vol.114 (4), p.335-345

2007

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RNA-binding proteins with prion-like domains in ALS and FTLD-U

Prion, 2011-07, Vol.5 (3), p.179-187

2011

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TDP-43 Variants of Frontotemporal Lobar Degeneration

Journal of molecular neuroscience, 2011-11, Vol.45 (3), p.390-401

Bigio, Eileen H.

2011

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Inositol Hexakisphosphate Kinase 2 Promotes Cell Death in Cells with Cytoplasmic TDP-43 Aggregation

Molecular neurobiology, 2016-10, Vol.53 (8), p.5377-5383

2016

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TDP-43 in differential diagnosis of motor neuron disorders

Acta neuropathologica, 2007-07, Vol.114 (1), p.71-79

2007

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Making Connections: Pathology and Genetics Link Amyotrophic Lateral Sclerosis with Frontotemporal Lobe Dementia

Journal of molecular neuroscience, 2011-11, Vol.45 (3), p.663-675

2011

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Mutations in progranulin explain atypical phenotypes with variants in MAPT

Brain (London, England : 1878), 2006-11, Vol.129 (11), p.3124-3126

2006

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Progranulin deficiency leads to enhanced cell vulnerability and TDP-43 translocation in primary neuronal cultures

Brain research, 2010-12, Vol.1366, p.1-8

2010

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Laminar distribution of the pathological changes in sporadic frontotemporal lobar degeneration with transactive response (TAR) DNA-binding protein of 43 kDa (TDP-43) proteinopathy: a quantitative study using polynomial curve fitting

Neuropathology and applied neurobiology, 2013-06, Vol.39 (4), p.335-347

2013

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The JNK/c-Jun signaling axis contributes to the TDP-43-induced cell death

Molecular and cellular biochemistry, 2013-01, Vol.372 (1-2), p.241-248

2013

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Delineation of the Core Aggregation Sequences of TDP-43 C-Terminal Fragment

Quantitative assessment of the degradation of aggregated TDP‐43 mediated by the ubiquitin proteasome system and macroautophagy

Proteolytic processing of TAR DNA binding protein‐43 by caspases produces C‐terminal fragments with disease defining properties independent of progranulin

Progranulin: a new avenue towards the understanding and treatment of neurodegenerative disease

Reappraisal of TDP-43 pathology in FTLD-U subtypes

Progranulin: normal function and role in neurodegeneration

Restoring functional TDP-43 oligomers in ALS and laminopathic cellular models through baicalein-induced reconfiguration of TDP-43 aggregates

TDP-43 toxicity is mediated by the unfolded protein response-unrelated induction of C/EBP homologous protein expression

Frontotemporal lobar degeneration with TAR DNA-binding protein 43 (TDP-43): its journey of more than 100 years

Autophagy activation ameliorates neuronal pathogenesis of FTLD-U mice: A new light for treatment of TARDBP/TDP-43 proteinopathies

Znf179 E3 ligase-mediated TDP-43 polyubiquitination is involved in TDP-43- ubiquitinated inclusions (UBI) (+)-related neurodegenerative pathology

Atypical frontotemporal lobar degeneration with ubiquitin-positive, TDP-43-negative neuronal inclusions

Temporal lobar predominance of TDP-43 neuronal cytoplasmic inclusions in Alzheimer disease

A90V TDP-43 variant results in the aberrant localization of TDP-43 in vitro

Phosphorylated and ubiquitinated TDP-43 pathological inclusions in ALS and FTLD-U are recapitulated in SH-SY5Y cells

Hippocampal sclerosis dementia: a reappraisal

RNA-binding proteins with prion-like domains in ALS and FTLD-U

TDP-43 Variants of Frontotemporal Lobar Degeneration

Inositol Hexakisphosphate Kinase 2 Promotes Cell Death in Cells with Cytoplasmic TDP-43 Aggregation

TDP-43 in differential diagnosis of motor neuron disorders

Making Connections: Pathology and Genetics Link Amyotrophic Lateral Sclerosis with Frontotemporal Lobe Dementia

Mutations in progranulin explain atypical phenotypes with variants in MAPT

Progranulin deficiency leads to enhanced cell vulnerability and TDP-43 translocation in primary neuronal cultures

Laminar distribution of the pathological changes in sporadic frontotemporal lobar degeneration with transactive response (TAR) DNA-binding protein of 43 kDa (TDP-43) proteinopathy: a quantitative study using polynomial curve fitting

The JNK/c-Jun signaling axis contributes to the TDP-43-induced cell death

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