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Significance of Oligomeric and Fibrillar Species in Amyloidosis: Insights into Pathophysiology and Treatment

Molecules (Basel, Switzerland), 2021-08, Vol.26 (16), p.5091

2021

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Exosome secretion is a key pathway for clearance of pathological TDP-43

Brain (London, England : 1878), 2016-12, Vol.139 (Pt 12), p.3187-3201

2016

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Aggresome formation and liquid-liquid phase separation independently induce cytoplasmic aggregation of TAR DNA-binding protein 43

Cell death & disease, 2020-10, Vol.11 (10), p.909-909, Article 909

2020

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Preclinical progression of neurodegenerative diseases

Nagoya journal of medical science, 2018-08, Vol.80 (3), p.289-298

2018

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Position-dependent FUS-RNA interactions regulate alternative splicing events and transcriptions

Scientific reports, 2012-07, Vol.2 (1), p.529-529, Article 529

2012

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Loss of TDP-43 causes age-dependent progressive motor neuron degeneration

Brain (London, England : 1878), 2013-05, Vol.136 (5), p.1371-1382

2013

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Therapeutic monoclonal antibody targeting of neuronal pentraxin receptor to control metastasis in gastric cancer

Molecular cancer, 2020-08, Vol.19 (1), p.1-131, Article 131

2020

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Neutrophil extracellular traps: from antimicrobial innate immunity to the development of chemotherapy-induced peripheral neuropathy

EBioMedicine, 2023-04, Vol.90, p.104526-104526, Article 104526

2023

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Blockade of CHRNB2 signaling with a therapeutic monoclonal antibody attenuates the aggressiveness of gastric cancer cells

Oncogene, 2021-09, Vol.40 (36), p.5495-5504

2021

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Exploring the factors underlying remyelination arrest by studying the post‐transcriptional regulatory mechanisms of cystatin F gene

Journal of neurochemistry, 2021-06, Vol.157 (6), p.2070-2090

2021

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Pathway from TDP-43-Related Pathology to Neuronal Dysfunction in Amyotrophic Lateral Sclerosis and Frontotemporal Lobar Degeneration

International journal of molecular sciences, 2021-04, Vol.22 (8), p.3843

2021

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Characteristic Features of FUS Inclusions in Spinal Motor Neurons of Sporadic Amyotrophic Lateral Sclerosis

Journal of neuropathology and experimental neurology, 2020-04, Vol.79 (4), p.370-377

2020

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Altered Tau Isoform Ratio Caused by Loss of FUS and SFPQ Function Leads to FTLD-like Phenotypes

Cell reports (Cambridge), 2017-01, Vol.18 (5), p.1118-1131

2017

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Amyotrophic lateral sclerosis: an update on recent genetic insights

Journal of neurology, 2013-11, Vol.260 (11), p.2917-2927

2013

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Spliceosome integrity is defective in the motor neuron diseases ALS and SMA

EMBO molecular medicine, 2013-02, Vol.5 (2), p.221-234

2013

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Alterations in the blood–spinal cord barrier in TDP-43 conditional knockout mice

Neuroscience letters, 2015-06, Vol.598, p.1-5

2015

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TDP-43 regulates early-phase insulin secretion via CaV1.2-mediated exocytosis in islets

The Journal of clinical investigation, 2019-09, Vol.130 (9), p.3578-3593

2019

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Oxidative stress induced by glutathione depletion reproduces pathological modifications of TDP-43 linked to TDP-43 proteinopathies

Neurobiology of disease, 2012-03, Vol.45 (3), p.862-870

2012

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Negative Effects of Diffuse Idiopathic Skeletal Hyperostosis on Bone Fusion after Transforaminal Lumbar Interbody Fusion

Asian Spine Journal, 2023, 17(5), , pp.818-825

2023

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The potential of GPNMB as novel neuroprotective factor in amyotrophic lateral sclerosis

Scientific reports, 2012-08, Vol.2 (1), p.573, Article 573

2012

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dnc-1/dynactin 1 knockdown disrupts transport of autophagosomes and induces motor neuron degeneration

PloS one, 2013-02, Vol.8 (2), p.e54511-e54511

2013

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TDP-43 Depletion Induces Neuronal Cell Damage through Dysregulation of Rho Family GTPases

The Journal of biological chemistry, 2009-08, Vol.284 (33), p.22059-22066

2009

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Gene Expression Profile of Inflammatory Myopathy with Malignancy is Similar to that of Dermatomyositis rather than Polymyositis

Internal Medicine, 2016/09/15, Vol.55(18), pp.2571-2580

2016

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The ALS/FTLD-related RNA-binding proteins TDP-43 and FUS have common downstream RNA targets in cortical neurons

FEBS open bio, 2014-01, Vol.4 (1), p.1-10

2014

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Significance of Oligomeric and Fibrillar Species in Amyloidosis: Insights into Pathophysiology and Treatment

Exosome secretion is a key pathway for clearance of pathological TDP-43

Aggresome formation and liquid-liquid phase separation independently induce cytoplasmic aggregation of TAR DNA-binding protein 43

Preclinical progression of neurodegenerative diseases

Position-dependent FUS-RNA interactions regulate alternative splicing events and transcriptions

Loss of TDP-43 causes age-dependent progressive motor neuron degeneration

Therapeutic monoclonal antibody targeting of neuronal pentraxin receptor to control metastasis in gastric cancer

Neutrophil extracellular traps: from antimicrobial innate immunity to the development of chemotherapy-induced peripheral neuropathy

Blockade of CHRNB2 signaling with a therapeutic monoclonal antibody attenuates the aggressiveness of gastric cancer cells

Exploring the factors underlying remyelination arrest by studying the post‐transcriptional regulatory mechanisms of cystatin F gene

Pathway from TDP-43-Related Pathology to Neuronal Dysfunction in Amyotrophic Lateral Sclerosis and Frontotemporal Lobar Degeneration

Characteristic Features of FUS Inclusions in Spinal Motor Neurons of Sporadic Amyotrophic Lateral Sclerosis

Altered Tau Isoform Ratio Caused by Loss of FUS and SFPQ Function Leads to FTLD-like Phenotypes

Amyotrophic lateral sclerosis: an update on recent genetic insights

Spliceosome integrity is defective in the motor neuron diseases ALS and SMA

Alterations in the blood–spinal cord barrier in TDP-43 conditional knockout mice

TDP-43 regulates early-phase insulin secretion via CaV1.2-mediated exocytosis in islets

Oxidative stress induced by glutathione depletion reproduces pathological modifications of TDP-43 linked to TDP-43 proteinopathies

Negative Effects of Diffuse Idiopathic Skeletal Hyperostosis on Bone Fusion after Transforaminal Lumbar Interbody Fusion

The potential of GPNMB as novel neuroprotective factor in amyotrophic lateral sclerosis

dnc-1/dynactin 1 knockdown disrupts transport of autophagosomes and induces motor neuron degeneration

TDP-43 Depletion Induces Neuronal Cell Damage through Dysregulation of Rho Family GTPases

Gene Expression Profile of Inflammatory Myopathy with Malignancy is Similar to that of Dermatomyositis rather than Polymyositis

Actin-binding protein filamin-A drives tau aggregation and contributes to progressive supranuclear palsy pathology

The ALS/FTLD-related RNA-binding proteins TDP-43 and FUS have common downstream RNA targets in cortical neurons

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