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1
Stimulation of mTOR-independent autophagy and mitophagy by rilmenidine exacerbates the phenotype of transgenic TDP-43 mice
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Stimulation of mTOR-independent autophagy and mitophagy by rilmenidine exacerbates the phenotype of transgenic TDP-43 mice

Neurobiology of disease, 2021-07, Vol.154, p.105359-105359, Article 105359 [Peer Reviewed Journal]

2021 The Authors ;Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved. ;ISSN: 0969-9961 ;EISSN: 1095-953X ;DOI: 10.1016/j.nbd.2021.105359 ;PMID: 33798740

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2
Mutant SOD1 inhibits ER‐Golgi transport in amyotrophic lateral sclerosis
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Mutant SOD1 inhibits ER‐Golgi transport in amyotrophic lateral sclerosis

Journal of neurochemistry, 2014-04, Vol.129 (1), p.190-204 [Peer Reviewed Journal]

2013 International Society for Neurochemistry ;2013 International Society for Neurochemistry. ;Copyright © 2014 International Society for Neurochemistry ;ISSN: 0022-3042 ;EISSN: 1471-4159 ;DOI: 10.1111/jnc.12493 ;PMID: 24134191

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3
Application of Urine-Derived Stem Cells to Cellular Modeling in Neuromuscular and Neurodegenerative Diseases
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Application of Urine-Derived Stem Cells to Cellular Modeling in Neuromuscular and Neurodegenerative Diseases

Frontiers in molecular neuroscience, 2019-12, Vol.12, p.297-297 [Peer Reviewed Journal]

Copyright © 2019 Sato, Takizawa, Nakamura, Turner, Shabanpoor and Aoki. ;2019. This work is licensed under http://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. ;Copyright © 2019 Sato, Takizawa, Nakamura, Turner, Shabanpoor and Aoki. 2019 Sato, Takizawa, Nakamura, Turner, Shabanpoor and Aoki ;ISSN: 1662-5099 ;EISSN: 1662-5099 ;DOI: 10.3389/fnmol.2019.00297 ;PMID: 31920531

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4
Advances in Gene Delivery Methods to Label and Modulate Activity of Upper Motor Neurons: Implications for Amyotrophic Lateral Sclerosis
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Advances in Gene Delivery Methods to Label and Modulate Activity of Upper Motor Neurons: Implications for Amyotrophic Lateral Sclerosis

Brain sciences, 2021-08, Vol.11 (9), p.1112 [Peer Reviewed Journal]

2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2021 by the authors. 2021 ;ISSN: 2076-3425 ;EISSN: 2076-3425 ;DOI: 10.3390/brainsci11091112 ;PMID: 34573134

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5
Could an Impairment in Local Translation of mRNAs in Glia be Contributing to Pathogenesis in ALS?
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Could an Impairment in Local Translation of mRNAs in Glia be Contributing to Pathogenesis in ALS?

Frontiers in molecular neuroscience, 2019-05, Vol.12, p.124-124 [Peer Reviewed Journal]

2019. This work is licensed under http://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. ;Copyright © 2019 Barton, Gregory, Chandran and Turner. 2019 Barton, Gregory, Chandran and Turner ;ISSN: 1662-5099 ;EISSN: 1662-5099 ;DOI: 10.3389/fnmol.2019.00124 ;PMID: 31164803

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6
Survival motor neuron deficiency enhances progression in an amyotrophic lateral sclerosis mouse model
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Survival motor neuron deficiency enhances progression in an amyotrophic lateral sclerosis mouse model

Neurobiology of disease, 2009-06, Vol.34 (3), p.511-517 [Peer Reviewed Journal]

EISSN: 1095-953X ;DOI: 10.1016/j.nbd.2009.03.005

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7
TDP-43 expression in mouse models of amyotrophic lateral sclerosis and spinal muscular atrophy
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TDP-43 expression in mouse models of amyotrophic lateral sclerosis and spinal muscular atrophy

BMC neuroscience, 2008-10, Vol.9 (1), p.104-104, Article 104 [Peer Reviewed Journal]

COPYRIGHT 2008 BioMed Central Ltd. ;Copyright © 2008 Turner et al; licensee BioMed Central Ltd. 2008 Turner et al; licensee BioMed Central Ltd. ;ISSN: 1471-2202 ;EISSN: 1471-2202 ;DOI: 10.1186/1471-2202-9-104 ;PMID: 18957104

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8
AMPK Signalling and Defective Energy Metabolism in Amyotrophic Lateral Sclerosis
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AMPK Signalling and Defective Energy Metabolism in Amyotrophic Lateral Sclerosis

Neurochemical research, 2016-03, Vol.41 (3), p.544-553 [Peer Reviewed Journal]

Springer Science+Business Media New York 2015 ;Springer Science+Business Media New York 2016 ;ISSN: 0364-3190 ;EISSN: 1573-6903 ;DOI: 10.1007/s11064-015-1665-3 ;PMID: 26202426

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9
Antisense peptide nucleic acid‐mediated knockdown of the p75 neurotrophin receptor delays motor neuron disease in mutant SOD1 transgenic mice
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Antisense peptide nucleic acid‐mediated knockdown of the p75 neurotrophin receptor delays motor neuron disease in mutant SOD1 transgenic mice

Journal of neurochemistry, 2003-11, Vol.87 (3), p.752-763 [Peer Reviewed Journal]

2004 INIST-CNRS ;ISSN: 0022-3042 ;EISSN: 1471-4159 ;DOI: 10.1046/j.1471-4159.2003.02053.x ;PMID: 14535957 ;CODEN: JONRA9

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10
Synapse Dysfunction of Layer V Pyramidal Neurons Precedes Neurodegeneration in a Mouse Model of TDP-43 Proteinopathies
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Synapse Dysfunction of Layer V Pyramidal Neurons Precedes Neurodegeneration in a Mouse Model of TDP-43 Proteinopathies

Cerebral cortex (New York, N.Y. 1991), 2017-07, Vol.27 (7), p.3630-3647 [Peer Reviewed Journal]

The Author 2016. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com. ;ISSN: 1047-3211 ;EISSN: 1460-2199 ;DOI: 10.1093/cercor/bhw185 ;PMID: 27496536

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11
SYT1-associated neurodevelopmental disorder: a case series
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SYT1-associated neurodevelopmental disorder: a case series

Brain (London, England : 1878), 2018-09, Vol.141 (9), p.2576-2591 [Peer Reviewed Journal]

The Author(s) (2018). Published by Oxford University Press on behalf of the Guarantors of Brain. 2018 ;ISSN: 0006-8950 ;EISSN: 1460-2156 ;DOI: 10.1093/brain/awy209 ;PMID: 30107533

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12
Antisense peptide nucleic acid targeting GluR3 delays disease onset and progression in the SOD1 G93A mouse model of familial ALS
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Antisense peptide nucleic acid targeting GluR3 delays disease onset and progression in the SOD1 G93A mouse model of familial ALS

Journal of neuroscience research, 2004-08, Vol.77 (4), p.573-582 [Peer Reviewed Journal]

Copyright © 2004 Wiley‐Liss, Inc. ;Copyright 2004 Wiley-Liss, Inc. ;ISSN: 0360-4012 ;EISSN: 1097-4547 ;DOI: 10.1002/jnr.20191 ;PMID: 15264227

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13
Effect of p75 neurotrophin receptor antagonist on disease progression in transgenic amyotrophic lateral sclerosis mice
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Effect of p75 neurotrophin receptor antagonist on disease progression in transgenic amyotrophic lateral sclerosis mice

Journal of neuroscience research, 2004-10, Vol.78 (2), p.193-199 [Peer Reviewed Journal]

Copyright © 2004 Wiley‐Liss, Inc. ;Copyright 2004 Wiley-Liss, Inc. ;ISSN: 0360-4012 ;EISSN: 1097-4547 ;DOI: 10.1002/jnr.20256 ;PMID: 15378612

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14
Transactive Response DNA-Binding Protein 43 Abnormalities after Traumatic Brain Injury
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Transactive Response DNA-Binding Protein 43 Abnormalities after Traumatic Brain Injury

Journal of neurotrauma, 2019-01, Vol.36 (1), p.87-99 [Peer Reviewed Journal]

Copyright 2019, Mary Ann Liebert, Inc., publishers ;ISSN: 0897-7151 ;EISSN: 1557-9042 ;DOI: 10.1089/neu.2017.5491 ;PMID: 29901412

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15
Mutant TDP-43 Expression Triggers TDP-43 Pathology and Cell Autonomous Effects on Primary Astrocytes: Implications for Non-cell Autonomous Pathology in ALS
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Mutant TDP-43 Expression Triggers TDP-43 Pathology and Cell Autonomous Effects on Primary Astrocytes: Implications for Non-cell Autonomous Pathology in ALS

Neurochemical research, 2020-06, Vol.45 (6), p.1451-1459 [Peer Reviewed Journal]

Springer Science+Business Media, LLC, part of Springer Nature 2020 ;Springer Science+Business Media, LLC, part of Springer Nature 2020. ;ISSN: 0364-3190 ;EISSN: 1573-6903 ;DOI: 10.1007/s11064-020-03048-5 ;PMID: 32410044

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16
Dysregulation of the complement cascade in the hSOD1G93A transgenic mouse model of amyotrophic lateral sclerosis
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Dysregulation of the complement cascade in the hSOD1G93A transgenic mouse model of amyotrophic lateral sclerosis

Journal of neuroinflammation, 2013-09, Vol.10, p.119-119 [Peer Reviewed Journal]

2013 Lee et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. ;Copyright © 2013 Lee et al.; licensee BioMed Central Ltd. 2013 Lee et al.; licensee BioMed Central Ltd. ;EISSN: 1742-2094 ;DOI: 10.1186/1742-2094-10-119 ;PMID: 24067070

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17
SOD1 protein aggregates stimulate macropinocytosis in neurons to facilitate their propagation
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SOD1 protein aggregates stimulate macropinocytosis in neurons to facilitate their propagation

Molecular neurodegeneration, 2015-10, Vol.10 (54), p.57-57, Article 57 [Peer Reviewed Journal]

COPYRIGHT 2015 BioMed Central Ltd. ;Copyright BioMed Central 2015 ;Zeineddine et al. 2015 ;ISSN: 1750-1326 ;EISSN: 1750-1326 ;DOI: 10.1186/s13024-015-0053-4 ;PMID: 26520394

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18
HspB8 mutation causing hereditary distal motor neuropathy impairs lysosomal delivery of autophagosomes
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HspB8 mutation causing hereditary distal motor neuropathy impairs lysosomal delivery of autophagosomes

Journal of neurochemistry, 2011-12, Vol.119 (6), p.1155-1161 [Peer Reviewed Journal]

2011 The Authors. Journal of Neurochemistry © 2011 International Society for Neurochemistry ;2015 INIST-CNRS ;2011 The Authors. Journal of Neurochemistry © 2011 International Society for Neurochemistry. ;ISSN: 0022-3042 ;EISSN: 1471-4159 ;DOI: 10.1111/j.1471-4159.2011.07521.x ;PMID: 21985219 ;CODEN: JONRA9

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19
α-Amino-3-hydroxyl-5-methyl-4-isoxazole-propionate receptor and RNA processing gene dysregulation are early determinants of selective motor neuron vulnerability in a mouse model of amyotrophic lateral sclerosis
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α-Amino-3-hydroxyl-5-methyl-4-isoxazole-propionate receptor and RNA processing gene dysregulation are early determinants of selective motor neuron vulnerability in a mouse model of amyotrophic lateral sclerosis

Brain communications, 2022, Vol.4 (2), p.fcac081-fcac081 [Peer Reviewed Journal]

The Author(s) 2022. Published by Oxford University Press on behalf of the Guarantors of Brain. 2022 ;The Author(s) 2022. Published by Oxford University Press on behalf of the Guarantors of Brain. ;ISSN: 2632-1297 ;EISSN: 2632-1297 ;DOI: 10.1093/braincomms/fcac081 ;PMID: 35445192

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20
Impaired extracellular secretion of mutant superoxide dismutase 1 associates with neurotoxicity in familial amyotrophic lateral sclerosis
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Impaired extracellular secretion of mutant superoxide dismutase 1 associates with neurotoxicity in familial amyotrophic lateral sclerosis

The Journal of neuroscience, 2005-01, Vol.25 (1), p.108-117 [Peer Reviewed Journal]

Copyright © 2005 Society for Neuroscience 0270-6474/05/25108-10.00/0 2005 ;ISSN: 0270-6474 ;EISSN: 1529-2401 ;DOI: 10.1523/JNEUROSCI.4253-04.2005 ;PMID: 15634772

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