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The role of ATP in solubilizing RNA‐binding protein fused in sarcoma

Proteins, structure, function, and bioinformatics, 2022-08, Vol.90 (8), p.1606-1612

2022

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Utility of whole exome sequencing in evaluation of juvenile motor neuron disease

Muscle & nerve, 2016-04, Vol.53 (4), p.648-652

2016

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The Solution Structure of FUS Bound to RNA Reveals a Bipartite Mode of RNA Recognition with Both Sequence and Shape Specificity

Molecular cell, 2019-02, Vol.73 (3), p.490-504.e6

2019

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Phase Separation of FUS Is Suppressed by Its Nuclear Import Receptor and Arginine Methylation

Cell, 2018-04, Vol.173 (3), p.706-719.e13

2018

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The RNA-binding protein FUS is chaperoned and imported into the nucleus by a network of import receptors

The Journal of biological chemistry, 2021-01, Vol.296, p.100659-100659, Article 100659

2021

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Intrinsically disordered sequences enable modulation of protein phase separation through distributed tyrosine motifs

The Journal of biological chemistry, 2017-11, Vol.292 (46), p.19110-19120

2017

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Widespread FUS mislocalization is a molecular hallmark of amyotrophic lateral sclerosis

Brain (London, England : 1878), 2019-09, Vol.142 (9), p.2572-2580

2019

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ALS mutations of FUS suppress protein translation and disrupt the regulation of nonsense-mediated decay

Proceedings of the National Academy of Sciences - PNAS, 2018-12, Vol.115 (51), p.E11904-E11913

2018

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“Boundary residues” between the folded RNA recognition motif and disordered RGG domains are critical for FUS–RNA binding

The Journal of biological chemistry, 2023-12, Vol.299 (12), p.105392, Article 105392

2023

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LncRNA KCNQ1OT1 contributes to cardiomyocyte apoptosis by targeting FUS in heart failure

Experimental and molecular pathology, 2020-08, Vol.115, p.104480-104480, Article 104480

2020

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ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import

The EMBO journal, 2010-08, Vol.29 (16), p.2841-2857

2010

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ATP enhances at low concentrations but dissolves at high concentrations liquid-liquid phase separation (LLPS) of ALS/FTD-causing FUS

Biochemical and biophysical research communications, 2018-10, Vol.504 (2), p.545-551

2018

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Casein kinase 1δ/ε phosphorylates fused in sarcoma (FUS) and ameliorates FUS-mediated neurodegeneration

The Journal of biological chemistry, 2022-08, Vol.298 (8), p.102191-102191, Article 102191

2022

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Arginine methylation next to the PY-NLS modulates Transportin binding and nuclear import of FUS

The EMBO journal, 2012-11, Vol.31 (22), p.4258-4275

2012

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Pathological heterogeneity in amyotrophic lateral sclerosis with FUS mutations: two distinct patterns correlating with disease severity and mutation

Acta neuropathologica, 2011-07, Vol.122 (1), p.87-98

2011

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Mechanisms of FUS mutations in familial amyotrophic lateral sclerosis

Brain research, 2016-09, Vol.1647, p.65-78

2016

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ALS-linked FUS mutations dysregulate G-quadruplex-dependent liquid–liquid phase separation and liquid-to-solid transition

The Journal of biological chemistry, 2021-11, Vol.297 (5), p.101284-101284, Article 101284

2021

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A new subtype of frontotemporal lobar degeneration with FUS pathology

Brain (London, England : 1878), 2009-11, Vol.132 (11), p.2922-2931

2009

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The RNA-binding Protein Fused in Sarcoma (FUS) Functions Downstream of Poly(ADP-ribose) Polymerase (PARP) in Response to DNA Damage

The Journal of biological chemistry, 2013-08, Vol.288 (34), p.24731-24741

2013

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A de novo c.1509dupA:p.R503fs mutation of FUS : report of a girl with sporadic juvenile amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2020-11, Vol.21 (7-8), p.635-637

2020

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Post-translational modifications on RNA-binding proteins: accelerators, brakes, or passengers in neurodegeneration?

Trends in biochemical sciences (Amsterdam. Regular ed.), 2022-01, Vol.47 (1), p.6-22

2022

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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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Oocyte electroporation prior to in vitro fertilization is an efficient method to generate single, double, and multiple knockout porcine embryos of interest in biomedicine and animal production

Theriogenology, 2024-04, Vol.218, p.111-118

2024

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Random forest modelling demonstrates microglial and protein misfolding features to be key phenotypic markers in C9orf72‐ALS

The Journal of pathology, 2022-12, Vol.258 (4), p.366-381

2022

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Altered distributions of Gemini of coiled bodies and mitochondria in motor neurons of TDP-43 transgenic mice

Proceedings of the National Academy of Sciences - PNAS, 2010-09, Vol.107 (37), p.16325-16330

2010

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The role of ATP in solubilizing RNA‐binding protein fused in sarcoma

Utility of whole exome sequencing in evaluation of juvenile motor neuron disease

The Solution Structure of FUS Bound to RNA Reveals a Bipartite Mode of RNA Recognition with Both Sequence and Shape Specificity

Phase Separation of FUS Is Suppressed by Its Nuclear Import Receptor and Arginine Methylation

The RNA-binding protein FUS is chaperoned and imported into the nucleus by a network of import receptors

Intrinsically disordered sequences enable modulation of protein phase separation through distributed tyrosine motifs

Widespread FUS mislocalization is a molecular hallmark of amyotrophic lateral sclerosis

ALS mutations of FUS suppress protein translation and disrupt the regulation of nonsense-mediated decay

“Boundary residues” between the folded RNA recognition motif and disordered RGG domains are critical for FUS–RNA binding

LncRNA KCNQ1OT1 contributes to cardiomyocyte apoptosis by targeting FUS in heart failure

ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import

ATP enhances at low concentrations but dissolves at high concentrations liquid-liquid phase separation (LLPS) of ALS/FTD-causing FUS

Casein kinase 1δ/ε phosphorylates fused in sarcoma (FUS) and ameliorates FUS-mediated neurodegeneration

Arginine methylation next to the PY-NLS modulates Transportin binding and nuclear import of FUS

Pathological heterogeneity in amyotrophic lateral sclerosis with FUS mutations: two distinct patterns correlating with disease severity and mutation

Mechanisms of FUS mutations in familial amyotrophic lateral sclerosis

ALS-linked FUS mutations dysregulate G-quadruplex-dependent liquid–liquid phase separation and liquid-to-solid transition

A new subtype of frontotemporal lobar degeneration with FUS pathology

The RNA-binding Protein Fused in Sarcoma (FUS) Functions Downstream of Poly(ADP-ribose) Polymerase (PARP) in Response to DNA Damage

A de novo c.1509dupA:p.R503fs mutation of FUS : report of a girl with sporadic juvenile amyotrophic lateral sclerosis

Post-translational modifications on RNA-binding proteins: accelerators, brakes, or passengers in neurodegeneration?

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

Oocyte electroporation prior to in vitro fertilization is an efficient method to generate single, double, and multiple knockout porcine embryos of interest in biomedicine and animal production

Random forest modelling demonstrates microglial and protein misfolding features to be key phenotypic markers in C9orf72‐ALS

Altered distributions of Gemini of coiled bodies and mitochondria in motor neurons of TDP-43 transgenic mice

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