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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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Gamma motor neurons survive and exacerbate alpha motor neuron degeneration in ALS

Proceedings of the National Academy of Sciences - PNAS, 2016-12, Vol.113 (51), p.E8316-E8325

2016

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Mutant TDP-43 Causes Early-Stage Dose-Dependent Motor Neuron Degeneration in a TARDBP Knockin Mouse Model of ALS

Cell reports (Cambridge), 2019-01, Vol.26 (2), p.364-373.e4

2019

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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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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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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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Hypoexcitability precedes denervation in the large fast-contracting motor units in two unrelated mouse models of ALS

eLife, 2018-03, Vol.7

2018

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Monitoring peripheral nerve degeneration in ALS by label-free stimulated Raman scattering imaging

Nature communications, 2016-10, Vol.7 (1), p.13283-13283, Article 13283

2016

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A Regulatory Circuitry Between Gria2, miR-409, and miR-495 Is Affected by ALS FUS Mutation in ESC-Derived Motor Neurons

Molecular neurobiology, 2018-10, Vol.55 (10), p.7635-7651

2018

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A new approach for rare variation collapsing on functional protein domains implicates specific genic regions in ALS

Genome research, 2019-05, Vol.29 (5), p.809-818

2019

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Unexpected similarities between C9ORF72 and sporadic forms of ALS/FTD suggest a common disease mechanism

eLife, 2018-07, Vol.7

2018

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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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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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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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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

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

2001

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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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Imaging the spatiotemporal organization of neural activity in the developing spinal cord

Developmental neurobiology (Hoboken, N.J.), 2008-05, Vol.68 (6), p.788-803

2008

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Preclinical evaluation of a microtubule PET ligand [11C]MPC-6827 in tau and amyotrophic lateral sclerosis animal models

Pharmacological reports, 2022-06, Vol.74 (3), p.539-544

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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Wnt7A identifies embryonic γ-motor neurons and reveals early postnatal dependence of γ-motor neurons on a muscle spindle-derived signal

The Journal of neuroscience, 2012-06, Vol.32 (25), p.8725-8731

2012

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Primary lateral sclerosis natural history study - planning, designing, and early enrollment

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2023-07, Vol.24 (5-6), p.394-404

2023

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Multiple System Atrophy With Predominant Striatonigral Degeneration and TAR DNA‐Binding Protein of 43 kDa Pathology: An Unusual Variant of Multiple System Atrophy

Movement disorders clinical practice (Hoboken, N.J.), 2019-11, Vol.6 (8), p.661-666

2019

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Postmortem Cortex Samples Identify Distinct Molecular Subtypes of ALS: Retrotransposon Activation, Oxidative Stress, and Activated Glia

Cell reports (Cambridge), 2019-10, Vol.29 (5), p.1164-1177.e5

2019

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

Gamma motor neurons survive and exacerbate alpha motor neuron degeneration in ALS

Mutant TDP-43 Causes Early-Stage Dose-Dependent Motor Neuron Degeneration in a TARDBP Knockin Mouse Model of ALS

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

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

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

Hypoexcitability precedes denervation in the large fast-contracting motor units in two unrelated mouse models of ALS

Monitoring peripheral nerve degeneration in ALS by label-free stimulated Raman scattering imaging

A Regulatory Circuitry Between Gria2, miR-409, and miR-495 Is Affected by ALS FUS Mutation in ESC-Derived Motor Neurons

A new approach for rare variation collapsing on functional protein domains implicates specific genic regions in ALS

Unexpected similarities between C9ORF72 and sporadic forms of ALS/FTD suggest a common disease mechanism

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

Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways

Clonally expanded CD8 T cells characterize amyotrophic lateral sclerosis-4

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

Amyotrophic Lateral Sclerosis

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

Imaging the spatiotemporal organization of neural activity in the developing spinal cord

Preclinical evaluation of a microtubule PET ligand [11C]MPC-6827 in tau and amyotrophic lateral sclerosis animal models

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

Wnt7A identifies embryonic γ-motor neurons and reveals early postnatal dependence of γ-motor neurons on a muscle spindle-derived signal

Primary lateral sclerosis natural history study - planning, designing, and early enrollment

Multiple System Atrophy With Predominant Striatonigral Degeneration and TAR DNA‐Binding Protein of 43 kDa Pathology: An Unusual Variant of Multiple System Atrophy

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

Postmortem Cortex Samples Identify Distinct Molecular Subtypes of ALS: Retrotransposon Activation, Oxidative Stress, and Activated Glia

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