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1
Rilmenidine promotes MTOR-independent autophagy in the mutant SOD1 mouse model of amyotrophic lateral sclerosis without slowing disease progression
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Rilmenidine promotes MTOR-independent autophagy in the mutant SOD1 mouse model of amyotrophic lateral sclerosis without slowing disease progression

Autophagy, 2018-03, Vol.14 (3), p.534-551 [Peer Reviewed Journal]

2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group 2017 ;2017 The Author(s). Published with license by Taylor & Francis. 2017 The Author(s) ;ISSN: 1554-8627 ;EISSN: 1554-8635 ;DOI: 10.1080/15548627.2017.1385674 ;PMID: 28980850

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2
The bone morphogenetic protein axis is a positive regulator of skeletal muscle mass
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The bone morphogenetic protein axis is a positive regulator of skeletal muscle mass

The Journal of cell biology, 2013-10, Vol.203 (2), p.345-357 [Peer Reviewed Journal]

2013 Winbanks et al. 2013 ;ISSN: 0021-9525 ;ISSN: 1540-8140 ;EISSN: 1540-8140 ;DOI: 10.1083/jcb.201211134 ;PMID: 24145169 ;CODEN: JCLBA3

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3
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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4
Amyotrophic Lateral Sclerosis and Autophagy: Dysfunction and Therapeutic Targeting
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Amyotrophic Lateral Sclerosis and Autophagy: Dysfunction and Therapeutic Targeting

Cells (Basel, Switzerland), 2020-11, Vol.9 (11), p.2413 [Peer Reviewed Journal]

COPYRIGHT 2020 MDPI AG ;2020 by the authors. 2020 ;ISSN: 2073-4409 ;EISSN: 2073-4409 ;DOI: 10.3390/cells9112413 ;PMID: 33158177

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5
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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6
Androgen receptor antagonism accelerates disease onset in the SOD1G93A mouse model of amyotrophic lateral sclerosis
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Androgen receptor antagonism accelerates disease onset in the SOD1G93A mouse model of amyotrophic lateral sclerosis

British journal of pharmacology, 2019-07, Vol.176 (13), p.2111-2130 [Peer Reviewed Journal]

2019 The British Pharmacological Society ;ISSN: 0007-1188 ;EISSN: 1476-5381 ;DOI: 10.1111/bph.14657 ;PMID: 30849180

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7
Induction of the Unfolded Protein Response in Familial Amyotrophic Lateral Sclerosis and Association of Protein-disulfide Isomerase with Superoxide Dismutase 1
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Induction of the Unfolded Protein Response in Familial Amyotrophic Lateral Sclerosis and Association of Protein-disulfide Isomerase with Superoxide Dismutase 1

The Journal of biological chemistry, 2006-10, Vol.281 (40), p.30152-30165 [Peer Reviewed Journal]

2006 © 2006 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology. ;ISSN: 0021-9258 ;EISSN: 1083-351X ;DOI: 10.1074/jbc.M603393200 ;PMID: 16847061

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8
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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9
Diacetylbis(N(4)-methylthiosemicarbazonato) Copper(II) (CuII(atsm)) Protects against Peroxynitrite-induced Nitrosative Damage and Prolongs Survival in Amyotrophic Lateral Sclerosis Mouse Model
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Diacetylbis(N(4)-methylthiosemicarbazonato) Copper(II) (CuII(atsm)) Protects against Peroxynitrite-induced Nitrosative Damage and Prolongs Survival in Amyotrophic Lateral Sclerosis Mouse Model

The Journal of biological chemistry, 2011-12, Vol.286 (51), p.44035-44044 [Peer Reviewed Journal]

2011 © 2011 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology. ;2011 by The American Society for Biochemistry and Molecular Biology, Inc. 2011 ;ISSN: 0021-9258 ;EISSN: 1083-351X ;DOI: 10.1074/jbc.M111.274407 ;PMID: 22033929

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10
Altered Blood-Brain Barrier Dynamics in the C9orf72 Hexanucleotide Repeat Expansion Mouse Model of Amyotrophic Lateral Sclerosis
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Altered Blood-Brain Barrier Dynamics in the C9orf72 Hexanucleotide Repeat Expansion Mouse Model of Amyotrophic Lateral Sclerosis

Pharmaceutics, 2022-12, Vol.14 (12), p.2803 [Peer Reviewed Journal]

COPYRIGHT 2022 MDPI AG ;2022 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. ;2022 by the authors. 2022 ;ISSN: 1999-4923 ;EISSN: 1999-4923 ;DOI: 10.3390/pharmaceutics14122803 ;PMID: 36559296

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11
Enhancing survival motor neuron expression extends lifespan and attenuates neurodegeneration in mutant TDP-43 mice
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Enhancing survival motor neuron expression extends lifespan and attenuates neurodegeneration in mutant TDP-43 mice

Human molecular genetics, 2016-09, Vol.25 (18), p.4080-4093 [Peer Reviewed Journal]

The Author 2016. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com. ;ISSN: 0964-6906 ;EISSN: 1460-2083 ;DOI: 10.1093/hmg/ddw247 ;PMID: 27466204

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12
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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13
Phosphorylation of hnRNP K by cyclin-dependent kinase 2 controls cytosolic accumulation of TDP-43
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Phosphorylation of hnRNP K by cyclin-dependent kinase 2 controls cytosolic accumulation of TDP-43

Human molecular genetics, 2015-03, Vol.24 (6), p.1655-1669 [Peer Reviewed Journal]

The Author 2014. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com. ;ISSN: 0964-6906 ;EISSN: 1460-2083 ;DOI: 10.1093/hmg/ddu578 ;PMID: 25410660

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14
Mapping Motor Neuron Vulnerability in the Neuraxis of Male SOD1G93A Mice Reveals Widespread Loss of Androgen Receptor Occurring Early in Spinal Motor Neurons
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Mapping Motor Neuron Vulnerability in the Neuraxis of Male SOD1G93A Mice Reveals Widespread Loss of Androgen Receptor Occurring Early in Spinal Motor Neurons

Frontiers in endocrinology (Lausanne), 2022-02, Vol.13, p.808479-808479 [Peer Reviewed Journal]

Copyright © 2022 McLeod, Chiam, Perera, Lau, Boon and Turner 2022 McLeod, Chiam, Perera, Lau, Boon and Turner ;ISSN: 1664-2392 ;EISSN: 1664-2392 ;DOI: 10.3389/fendo.2022.808479 ;PMID: 35273564

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15
Inhibition of motor neuron death in vitro and in vivo by a p75 neurotrophin receptor intracellular domain fragment
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Inhibition of motor neuron death in vitro and in vivo by a p75 neurotrophin receptor intracellular domain fragment

Journal of cell science, 2016-02, Vol.129 (3), p.517-530 [Peer Reviewed Journal]

2016. Published by The Company of Biologists Ltd. ;ISSN: 0021-9533 ;EISSN: 1477-9137 ;DOI: 10.1242/jcs.173864 ;PMID: 26503157

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16
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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17
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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18
Lipid Metabolism Is Dysregulated in the Motor Cortex White Matter in Amyotrophic Lateral Sclerosis
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Lipid Metabolism Is Dysregulated in the Motor Cortex White Matter in Amyotrophic Lateral Sclerosis

Metabolites, 2022-06, Vol.12 (6), p.554 [Peer Reviewed Journal]

2022 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. ;2022 by the authors. 2022 ;ISSN: 2218-1989 ;EISSN: 2218-1989 ;DOI: 10.3390/metabo12060554 ;PMID: 35736487

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19
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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20
Ferroptosis mediates selective motor neuron death in amyotrophic lateral sclerosis
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Ferroptosis mediates selective motor neuron death in amyotrophic lateral sclerosis

Cell death and differentiation, 2022-06, Vol.29 (6), p.1187-1198 [Peer Reviewed Journal]

2021. The Author(s), under exclusive licence to ADMC Associazione Differenziamento e Morte Cellulare. ;The Author(s), under exclusive licence to ADMC Associazione Differenziamento e Morte Cellulare 2021. ;The Author(s), under exclusive licence to ADMC Associazione Differenziamento e Morte Cellulare 2021 ;ISSN: 1350-9047 ;EISSN: 1476-5403 ;DOI: 10.1038/s41418-021-00910-z ;PMID: 34857917

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