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ALS-associated mutant FUS induces selective motor neuron degeneration through toxic gain of function

Nature communications, 2016-02, Vol.7 (1), p.10465-14, Article 10465

2016

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The ALS-associated proteins FUS and TDP-43 function together to affect Drosophila locomotion and life span

The Journal of clinical investigation, 2011-10, Vol.121 (10), p.4118-4126

2011

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ALS/FTD-associated protein FUS induces mitochondrial dysfunction by preferentially sequestering respiratory chain complex mRNAs

Genes & development, 2020-06, Vol.34 (11-12), p.785-805

2020

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Alternative Splicing Generates Functionally Distinct N-Methyl-D-Aspartate Receptors

Proceedings of the National Academy of Sciences - PNAS, 1992-09, Vol.89 (18), p.8552-8556

1992

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Amyotrophic Lateral Sclerosis

The New England journal of medicine, 2001-10, Vol.345 (15), p.1131-1132

2001

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Amyotrophic Lateral Sclerosis

The New England journal of medicine, 2001-05, Vol.344 (22), p.1688-1700

2001

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Amyotrophic Lateral Sclerosis Modifiers in Drosophila Reveal the Phospholipase D Pathway as a Potential Therapeutic Target

Genetics (Austin), 2020-07, Vol.215 (3), p.747-766

2020

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Amyotrophic Lateral Sclerosis Patients Regain Head-Neck Control Using a Powered Neck Exoskeleton

2022 9th IEEE RAS/EMBS International Conference for Biomedical Robotics and Biomechatronics (BioRob), 2022, p.01-06

2022

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Antisense oligonucleotide silencing of FUS expression as a therapeutic approach in amyotrophic lateral sclerosis

Nature medicine, 2022-01, Vol.28 (1), p.104-116

2022

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Author Correction: Clonally expanded CD8 T cells characterize amyotrophic lateral sclerosis-4

Nature (London), 2022-08, Vol.608 (7924), p.E34-E34

2022

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Body mass index is lower in asymptomatic C9orf72 expansion carriers but not in SOD1 pathogenic variant carriers compared to gene negatives

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2024-08, p.1-8

2024

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The C9ORF72 GGGGCC expansion forms RNA G-quadruplex inclusions and sequesters hnRNP H to disrupt splicing in ALS brains

eLife, 2016-09, Vol.5

2016

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Central Nervous System (CNS)-Derived Extracellular Vesicles (EVs) as Novel Biomarkers for Environmental Exposure and Disease Progression in ALS

Environmental health perspectives. Supplements, 2021-08, Vol.2021 (1)

2021

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Clonally expanded CD8 T cells characterize amyotrophic lateral sclerosis-4

Nature (London), 2022-06, Vol.606 (7916), p.945-952

2022

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The cycad genotoxin methylazoxymethanol, linked to Guam ALS/PDC, induces transcriptional mutagenesis

Acta neuropathologica communications, 2024-02, Vol.12 (1), p.30-5, Article 30

2024

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Deletion of Ripk3 Prevents Motor Neuron Death In Vitro but not In Vivo

eNeuro, 2019-01, Vol.6 (1), p.ENEURO.0308-18.2018

2019

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Engineered Nuclear Import Receptor Karyopherin‐β2 Chaperones Aberrant Phase Transitions of Disease‐Associated Cargo

The FASEB journal, 2022-05, Vol.36 (S1), p.n/a

2022

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Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways

Science (American Association for the Advancement of Science), 2015-03, Vol.347 (6229), p.1436-1441

2015

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A framework for sharing of clinical and genetic data for precision medicine applications

Nature medicine, 2024-09

2024

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Functionally Reduced Sensorimotor Connections Form with Normal Specificity Despite Abnormal Muscle Spindle Development: The Role of Spindle-Derived Neurotrophin 3

The Journal of neuroscience, 2009-04, Vol.29 (15), p.4719-4735

2009

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FUS affects circular RNA expression in murine embryonic stem cell-derived motor neurons

Nature communications, 2017-03, Vol.8 (1), p.14741-11, Article 14741

2017

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FUS-SMN Protein Interactions Link the Motor Neuron Diseases ALS and SMA

Cell reports (Cambridge), 2012-10, Vol.2 (4), p.799-806

2012

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Gamma motor neurons express distinct genetic markers at birth and require muscle spindle-derived GDNF for postnatal survival

Neural development, 2009-12, Vol.4 (1), p.42-42

2009

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Access for ALL in ALS: A large-scale, inclusive, collaborative consortium to unlock the molecular and genetic mechanisms of amyotrophic lateral sclerosis

ALS-associated mutant FUS induces selective motor neuron degeneration through toxic gain of function

The ALS-associated proteins FUS and TDP-43 function together to affect Drosophila locomotion and life span

ALS/FTD-associated protein FUS induces mitochondrial dysfunction by preferentially sequestering respiratory chain complex mRNAs

Alternative Splicing Generates Functionally Distinct N-Methyl-D-Aspartate Receptors

Amyotrophic Lateral Sclerosis

Amyotrophic Lateral Sclerosis

Amyotrophic Lateral Sclerosis Modifiers in Drosophila Reveal the Phospholipase D Pathway as a Potential Therapeutic Target

Amyotrophic Lateral Sclerosis Patients Regain Head-Neck Control Using a Powered Neck Exoskeleton

Antisense oligonucleotide silencing of FUS expression as a therapeutic approach in amyotrophic lateral sclerosis

Author Correction: Clonally expanded CD8 T cells characterize amyotrophic lateral sclerosis-4

Author Correction: TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13A

Body mass index is lower in asymptomatic C9orf72 expansion carriers but not in SOD1 pathogenic variant carriers compared to gene negatives

The C9ORF72 GGGGCC expansion forms RNA G-quadruplex inclusions and sequesters hnRNP H to disrupt splicing in ALS brains

Central Nervous System (CNS)-Derived Extracellular Vesicles (EVs) as Novel Biomarkers for Environmental Exposure and Disease Progression in ALS

Clonally expanded CD8 T cells characterize amyotrophic lateral sclerosis-4

The cycad genotoxin methylazoxymethanol, linked to Guam ALS/PDC, induces transcriptional mutagenesis

Deletion of Ripk3 Prevents Motor Neuron Death In Vitro but not In Vivo

Engineered Nuclear Import Receptor Karyopherin‐β2 Chaperones Aberrant Phase Transitions of Disease‐Associated Cargo

Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways

A framework for sharing of clinical and genetic data for precision medicine applications

Functionally Reduced Sensorimotor Connections Form with Normal Specificity Despite Abnormal Muscle Spindle Development: The Role of Spindle-Derived Neurotrophin 3

FUS affects circular RNA expression in murine embryonic stem cell-derived motor neurons

FUS-SMN Protein Interactions Link the Motor Neuron Diseases ALS and SMA

Gamma motor neurons express distinct genetic markers at birth and require muscle spindle-derived GDNF for postnatal survival

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