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1
A Liquid-to-Solid Phase Transition of the ALS Protein FUS Accelerated by Disease Mutation
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A Liquid-to-Solid Phase Transition of the ALS Protein FUS Accelerated by Disease Mutation

Cell, 2015-08, Vol.162 (5), p.1066-1077 [Peer Reviewed Journal]

2015 Elsevier Inc. ;Copyright © 2015 Elsevier Inc. All rights reserved. ;ISSN: 0092-8674 ;EISSN: 1097-4172 ;DOI: 10.1016/j.cell.2015.07.047 ;PMID: 26317470

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2
Decoding ALS: from genes to mechanism
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Decoding ALS: from genes to mechanism

Nature (London), 2016-11, Vol.539 (7628), p.197-206 [Peer Reviewed Journal]

COPYRIGHT 2016 Nature Publishing Group ;COPYRIGHT 2016 Nature Publishing Group ;Copyright Nature Publishing Group Nov 10, 2016 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/nature20413 ;PMID: 27830784 ;CODEN: NATUAS

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3
Amyloid Oligomers: A Joint Experimental/Computational Perspective on Alzheimer’s Disease, Parkinson’s Disease, Type II Diabetes, and Amyotrophic Lateral Sclerosis
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Amyloid Oligomers: A Joint Experimental/Computational Perspective on Alzheimer’s Disease, Parkinson’s Disease, Type II Diabetes, and Amyotrophic Lateral Sclerosis

Chemical reviews, 2021-02, Vol.121 (4), p.2545-2647 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0009-2665 ;EISSN: 1520-6890 ;DOI: 10.1021/acs.chemrev.0c01122

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4
Unconventional Translation of C9ORF72 GGGGCC Expansion Generates Insoluble Polypeptides Specific to c9FTD/ALS
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Unconventional Translation of C9ORF72 GGGGCC Expansion Generates Insoluble Polypeptides Specific to c9FTD/ALS

Neuron (Cambridge, Mass.), 2013-02, Vol.77 (4), p.639-646 [Peer Reviewed Journal]

2013 Elsevier Inc. ;Copyright © 2013 Elsevier Inc. All rights reserved. ;Copyright Elsevier Limited Feb 20, 2013 ;2013 Elsevier Inc. All rights reserved. 2013 ;ISSN: 0896-6273 ;EISSN: 1097-4199 ;DOI: 10.1016/j.neuron.2013.02.004 ;PMID: 23415312

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5
ALS Mutations Disrupt Phase Separation Mediated by α-Helical Structure in the TDP-43 Low-Complexity C-Terminal Domain
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ALS Mutations Disrupt Phase Separation Mediated by α-Helical Structure in the TDP-43 Low-Complexity C-Terminal Domain

Structure (London), 2016-09, Vol.24 (9), p.1537-1549 [Peer Reviewed Journal]

2016 Elsevier Ltd ;Copyright © 2016 Elsevier Ltd. All rights reserved. ;ISSN: 0969-2126 ;EISSN: 1878-4186 ;DOI: 10.1016/j.str.2016.07.007 ;PMID: 27545621

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6
Phase Separation of C9orf72 Dipeptide Repeats Perturbs Stress Granule Dynamics
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Phase Separation of C9orf72 Dipeptide Repeats Perturbs Stress Granule Dynamics

Molecular cell, 2017-03, Vol.65 (6), p.1044-1055.e5 [Peer Reviewed Journal]

2017 The Authors ;Copyright © 2017 The Authors. Published by Elsevier Inc. All rights reserved. ;2017 The Authors 2017 ;ISSN: 1097-2765 ;EISSN: 1097-4164 ;DOI: 10.1016/j.molcel.2017.02.013 ;PMID: 28306503

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7
In Situ Structure of Neuronal C9orf72 Poly-GA Aggregates Reveals Proteasome Recruitment
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In Situ Structure of Neuronal C9orf72 Poly-GA Aggregates Reveals Proteasome Recruitment

Cell, 2018-02, Vol.172 (4), p.696-705.e12 [Peer Reviewed Journal]

2018 Elsevier Inc. ;Copyright © 2018 Elsevier Inc. All rights reserved. ;ISSN: 0092-8674 ;EISSN: 1097-4172 ;DOI: 10.1016/j.cell.2017.12.030 ;PMID: 29398115

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8
Mechanistic View of hnRNPA2 Low-Complexity Domain Structure, Interactions, and Phase Separation Altered by Mutation and Arginine Methylation
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Mechanistic View of hnRNPA2 Low-Complexity Domain Structure, Interactions, and Phase Separation Altered by Mutation and Arginine Methylation

Molecular cell, 2018-02, Vol.69 (3), p.465-479.e7 [Peer Reviewed Journal]

2018 Elsevier Inc. ;Copyright © 2018 Elsevier Inc. All rights reserved. ;ISSN: 1097-2765 ;EISSN: 1097-4164 ;DOI: 10.1016/j.molcel.2017.12.022 ;PMID: 29358076

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9
Modeling sporadic ALS in iPSC-derived motor neurons identifies a potential therapeutic agent
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Modeling sporadic ALS in iPSC-derived motor neurons identifies a potential therapeutic agent

Nature medicine, 2018-10, Vol.24 (10), p.1579-1589 [Peer Reviewed Journal]

COPYRIGHT 2018 Nature Publishing Group ;COPYRIGHT 2018 Nature Publishing Group ;Copyright Nature Publishing Group Oct 2018 ;ISSN: 1078-8956 ;EISSN: 1546-170X ;DOI: 10.1038/s41591-018-0140-5 ;PMID: 30127392

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10
Haploinsufficiency leads to neurodegeneration in C9ORF72 ALS/FTD human induced motor neurons
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Haploinsufficiency leads to neurodegeneration in C9ORF72 ALS/FTD human induced motor neurons

Nature medicine, 2018-03, Vol.24 (3), p.313-325 [Peer Reviewed Journal]

COPYRIGHT 2018 Nature Publishing Group ;COPYRIGHT 2018 Nature Publishing Group ;Copyright Nature Publishing Group Mar 2018 ;ISSN: 1078-8956 ;EISSN: 1546-170X ;DOI: 10.1038/nm.4490 ;PMID: 29400714

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11
A single N‐terminal phosphomimic disrupts TDP‐43 polymerization, phase separation, and RNA splicing
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A single N‐terminal phosphomimic disrupts TDP‐43 polymerization, phase separation, and RNA splicing

The EMBO journal, 2018-03, Vol.37 (5), p.n/a [Peer Reviewed Journal]

2018 The Authors. Published under the terms of the CC BY 4.0 license ;2018 The Authors. Published under the terms of the CC BY 4.0 license. ;2018 EMBO ;ISSN: 0261-4189 ;EISSN: 1460-2075 ;DOI: 10.15252/embj.201797452 ;PMID: 29438978

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12
Antisense Proline-Arginine RAN Dipeptides Linked to C9ORF72-ALS/FTD Form Toxic Nuclear Aggregates that Initiate In Vitro and In Vivo Neuronal Death
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Antisense Proline-Arginine RAN Dipeptides Linked to C9ORF72-ALS/FTD Form Toxic Nuclear Aggregates that Initiate In Vitro and In Vivo Neuronal Death

Neuron (Cambridge, Mass.), 2014-12, Vol.84 (6), p.1213-1225 [Peer Reviewed Journal]

2014 Elsevier Inc. ;Copyright © 2014 Elsevier Inc. All rights reserved. ;ISSN: 0896-6273 ;EISSN: 1097-4199 ;DOI: 10.1016/j.neuron.2014.12.010 ;PMID: 25521377

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13
Drosophila as an In Vivo Model for Human Neurodegenerative Disease
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Drosophila as an In Vivo Model for Human Neurodegenerative Disease

Genetics (Austin), 2015-10, Vol.201 (2), p.377-402 [Peer Reviewed Journal]

Copyright © 2015 by the Genetics Society of America. ;Copyright Genetics Society of America Oct 2015 ;Copyright © 2015 by the Genetics Society of America 2015 ;ISSN: 1943-2631 ;ISSN: 0016-6731 ;EISSN: 1943-2631 ;DOI: 10.1534/genetics.115.179457 ;PMID: 26447127 ;CODEN: GENTAE

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14
TIA1 Mutations in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Promote Phase Separation and Alter Stress Granule Dynamics
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TIA1 Mutations in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Promote Phase Separation and Alter Stress Granule Dynamics

Neuron (Cambridge, Mass.), 2017-08, Vol.95 (4), p.808-816.e9 [Peer Reviewed Journal]

2017 Elsevier Inc. ;Copyright © 2017 Elsevier Inc. All rights reserved. ;Copyright Elsevier Limited Aug 16, 2017 ;ISSN: 0896-6273 ;EISSN: 1097-4199 ;DOI: 10.1016/j.neuron.2017.07.025 ;PMID: 28817800

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15
Spatiotemporal Proteomic Analysis of Stress Granule Disassembly Using APEX Reveals Regulation by SUMOylation and Links to ALS Pathogenesis
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Article
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Spatiotemporal Proteomic Analysis of Stress Granule Disassembly Using APEX Reveals Regulation by SUMOylation and Links to ALS Pathogenesis

Molecular cell, 2020-12, Vol.80 (5), p.876-891.e6 [Peer Reviewed Journal]

2020 Elsevier Inc. ;Copyright © 2020 Elsevier Inc. All rights reserved. ;ISSN: 1097-2765 ;EISSN: 1097-4164 ;DOI: 10.1016/j.molcel.2020.10.032 ;PMID: 33217318

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16
TDP-43 pathology disrupts nuclear pore complexes and nucleocytoplasmic transport in ALS/FTD
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TDP-43 pathology disrupts nuclear pore complexes and nucleocytoplasmic transport in ALS/FTD

Nature neuroscience, 2018-02, Vol.21 (2), p.228-239 [Peer Reviewed Journal]

COPYRIGHT 2018 Nature Publishing Group ;COPYRIGHT 2018 Nature Publishing Group ;2017. This work is published under https://creativecommons.org/licenses/by/4.0 (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1097-6256 ;EISSN: 1546-1726 ;DOI: 10.1038/s41593-017-0047-3 ;PMID: 29311743

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17
Pathways Disrupted in Human ALS Motor Neurons Identified through Genetic Correction of Mutant SOD1
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Pathways Disrupted in Human ALS Motor Neurons Identified through Genetic Correction of Mutant SOD1

Cell stem cell, 2014-06, Vol.14 (6), p.781-795 [Peer Reviewed Journal]

2014 Elsevier Inc. ;Copyright © 2014 Elsevier Inc. All rights reserved. ;ISSN: 1934-5909 ;EISSN: 1875-9777 ;DOI: 10.1016/j.stem.2014.03.004 ;PMID: 24704492

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18
Reduced C9ORF72 function exacerbates gain of toxicity from ALS/FTD-causing repeat expansion in C9orf72
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Reduced C9ORF72 function exacerbates gain of toxicity from ALS/FTD-causing repeat expansion in C9orf72

Nature neuroscience, 2020-05, Vol.23 (5), p.615-624 [Peer Reviewed Journal]

COPYRIGHT 2020 Nature Publishing Group ;COPYRIGHT 2020 Nature Publishing Group ;The Author(s), under exclusive licence to Springer Nature America, Inc. 2020. ;ISSN: 1097-6256 ;EISSN: 1546-1726 ;DOI: 10.1038/s41593-020-0619-5 ;PMID: 32284607

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19
The C9orf72 repeat expansion disrupts nucleocytoplasmic transport
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The C9orf72 repeat expansion disrupts nucleocytoplasmic transport

Nature (London), 2015-09, Vol.525 (7567), p.56-61 [Peer Reviewed Journal]

COPYRIGHT 2015 Nature Publishing Group ;COPYRIGHT 2015 Nature Publishing Group ;Copyright Nature Publishing Group Sep 3, 2015 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/nature14973 ;PMID: 26308891 ;CODEN: NATUAS

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20
Intrinsic membrane hyperexcitability of amyotrophic lateral sclerosis patient-derived motor neurons
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Intrinsic membrane hyperexcitability of amyotrophic lateral sclerosis patient-derived motor neurons

Cell reports (Cambridge), 2014-04, Vol.7 (1), p.1-11 [Peer Reviewed Journal]

Copyright © 2014 The Authors. Published by Elsevier Inc. All rights reserved. ;ISSN: 2211-1247 ;EISSN: 2211-1247 ;DOI: 10.1016/j.celrep.2014.03.019 ;PMID: 24703839

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