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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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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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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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Role of primary afferents in the developmental regulation of motor axon synapse numbers on Renshaw cells

Journal of comparative neurology (1911), 2016-06, Vol.524 (9), p.1892-1919

2016

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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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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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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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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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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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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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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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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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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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NOS1AP is a novel molecular target and critical factor in TDP-43 pathology

Brain communications, 2022-09, Vol.4 (5), p.fcac242

2022

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Mechanisms regulating the specificity and strength of muscle afferent inputs in the spinal cord

Annals of the New York Academy of Sciences, 2010-06, Vol.1198 (1), p.220-230

2010

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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 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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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

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

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

Role of primary afferents in the developmental regulation of motor axon synapse numbers on Renshaw cells

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

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

Amyotrophic Lateral Sclerosis

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

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

Clonally expanded CD8 T cells characterize amyotrophic lateral sclerosis-4

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

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

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

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

NOS1AP is a novel molecular target and critical factor in TDP-43 pathology

Mechanisms regulating the specificity and strength of muscle afferent inputs in the spinal cord

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

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

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