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PML nuclear bodies: new players in familial amyotrophic lateral sclerosis-frontotemporal dementia?

Neural regeneration research, 2024-09, Vol.19 (9), p.1875-1876

2024

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NLRP3 inflammasome is expressed by astrocytes in the SOD1 mouse model of ALS and in human sporadic ALS patients

Glia, 2015-12, Vol.63 (12), p.2260-2273

2015

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Inhibition of Proteasomal Function by Curcumin Induces Apoptosis through Mitochondrial Pathway

The Journal of biological chemistry, 2004-03, Vol.279 (12), p.11680-11685

2004

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Pathomechanisms of ALS8: altered autophagy and defective RNA binding protein (RBP) homeostasis due to the VAPB P56S mutation

Cell death & disease, 2021-05, Vol.12 (5), p.466-466, Article 466

2021

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Phenotypes and malignancy risk of different FUS mutations in genetic amyotrophic lateral sclerosis

Annals of clinical and translational neurology, 2019-12, Vol.6 (12), p.2384-2394

2019

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Lipopolysaccharide triggers exacerbated microglial activation, excessive cytokine release and behavioural disturbances in mice with truncated Fused-in-Sarcoma Protein (FUS)

Brain, behavior, & immunity. Health, 2023-11, Vol.33, p.100686, Article 100686

2023

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Loss of PML nuclear bodies in familial amyotrophic lateral sclerosis-frontotemporal dementia

Cell death discovery, 2023-07, Vol.9 (1), p.248-248, Article 248

2023

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Oxidative stress promotes mutant huntingtin aggregation and mutant huntingtin-dependent cell death by mimicking proteasomal malfunction

Biochemical and biophysical research communications, 2006-03, Vol.342 (1), p.184-190

2006

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Cetuximab Induces Eme1-Mediated DNA Repair: a Novel Mechanism for Cetuximab Resistance

Neoplasia (New York, N.Y.), 2014-03, Vol.16 (3), p.207-220.e4

2014

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Abl kinase-mediated FUS Tyr526 phosphorylation alters nucleocytoplasmic FUS localization in FTLD-FUS

Brain (London, England : 1878), 2023-10, Vol.146 (10), p.4088-4104

2023

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The Mono-ADP-Ribosyltransferase ARTD10 Regulates KV1.1 through PKCD

Biophysical journal, 2018-02, Vol.114 (3), p.295a-295a

2018

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Hsp90‐mediated regulation of DYRK3 couples stress granule disassembly and growth via mTORC1 signaling

EMBO reports, 2021-05, Vol.22 (5), p.e51740-n/a

2021

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Interactome screening of C9orf72 dipeptide repeats reveals VCP sequestration and functional impairment by polyGA

Brain (London, England : 1878), 2022-04, Vol.145 (2), p.684-699

2022

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PI Controller Based Power Factor Correction Circuit for Plug-in Hybrid Electric Vehicle Using Solar Charging Module

Electric power components and systems, 2023-11, p.1-15

2023

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An Updated Review on Gastro Retentive Drug Delivery System

International journal of pharmaceutical sciences review and research, 2020-11, Vol.65 (1), p.45-51

2020

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Cuprizone‐induced graded oligodendrocyte vulnerability is regulated by the transcription factor DNA damage‐inducible transcript 3

Glia, 2019-02, Vol.67 (2), p.263-276

2019

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Early Alterations of RNA Binding Protein

Cells (Basel, Switzerland), 2023-04, Vol.12 (7)

2023

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An Optimized PV-Based Multi-Port Plug-In EV Charger Using Improved Particle Swarm Optimization Algorithm

Electric power components and systems, 2023-10, p.1-12

2023

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A serum microRNA sequence reveals fragile X protein pathology in amyotrophic lateral sclerosis

Brain (London, England : 1878), 2021-05, Vol.144 (4), p.1214-1229

2021

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Autosomal dominant spinal muscular atrophy with lower extremity predominance: A recognizable phenotype of BICD2 mutations

Muscle & nerve, 2016-09, Vol.54 (3), p.496-500

2016

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NLRP3 inflammasome is expressed by astrocytes in the SOD1 mouse model of ALS and in human sporadic ALS patients: NLRP3 Inflammasome Expression in ALS

Glia, 2015-12, Vol.63 (12), p.2260-2273

2015

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Aberrant association of misfolded SOD1 with Na^sup +^/K^sup +^ATPase-[alpha]3 impairs its activity and contributes to motor neuron vulnerability in ALS

Acta neuropathologica, 2016-03, Vol.131 (3), p.427

2016

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PML nuclear bodies: new players in familial amyotrophic lateral sclerosis-frontotemporal dementia?

NLRP3 inflammasome is expressed by astrocytes in the SOD1 mouse model of ALS and in human sporadic ALS patients

Impaired DNA damage response signaling by FUS-NLS mutations leads to neurodegeneration and FUS aggregate formation

FUS pathology in ALS is linked to alterations in multiple ALS-associated proteins and rescued by drugs stimulating autophagy

Inhibition of Proteasomal Function by Curcumin Induces Apoptosis through Mitochondrial Pathway

Pathomechanisms of ALS8: altered autophagy and defective RNA binding protein (RBP) homeostasis due to the VAPB P56S mutation

Phenotypes and malignancy risk of different FUS mutations in genetic amyotrophic lateral sclerosis

Lipopolysaccharide triggers exacerbated microglial activation, excessive cytokine release and behavioural disturbances in mice with truncated Fused-in-Sarcoma Protein (FUS)

Loss of PML nuclear bodies in familial amyotrophic lateral sclerosis-frontotemporal dementia

Oxidative stress promotes mutant huntingtin aggregation and mutant huntingtin-dependent cell death by mimicking proteasomal malfunction

Cetuximab Induces Eme1-Mediated DNA Repair: a Novel Mechanism for Cetuximab Resistance

Abl kinase-mediated FUS Tyr526 phosphorylation alters nucleocytoplasmic FUS localization in FTLD-FUS

The Mono-ADP-Ribosyltransferase ARTD10 Regulates KV1.1 through PKCD

Hsp90‐mediated regulation of DYRK3 couples stress granule disassembly and growth via mTORC1 signaling

Interactome screening of C9orf72 dipeptide repeats reveals VCP sequestration and functional impairment by polyGA

PI Controller Based Power Factor Correction Circuit for Plug-in Hybrid Electric Vehicle Using Solar Charging Module

An Updated Review on Gastro Retentive Drug Delivery System

Cuprizone‐induced graded oligodendrocyte vulnerability is regulated by the transcription factor DNA damage‐inducible transcript 3

PolyGA targets the ER stress-adaptive response by impairing GRP75 function at the MAM in C9ORF72-ALS/FTD

Early Alterations of RNA Binding Protein

An Optimized PV-Based Multi-Port Plug-In EV Charger Using Improved Particle Swarm Optimization Algorithm

A serum microRNA sequence reveals fragile X protein pathology in amyotrophic lateral sclerosis

Autosomal dominant spinal muscular atrophy with lower extremity predominance: A recognizable phenotype of BICD2 mutations

NLRP3 inflammasome is expressed by astrocytes in the SOD1 mouse model of ALS and in human sporadic ALS patients: NLRP3 Inflammasome Expression in ALS

Aberrant association of misfolded SOD1 with Na^sup +^/K^sup +^ATPase-[alpha]3 impairs its activity and contributes to motor neuron vulnerability in ALS

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