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1
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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2
Compromised MAPK signaling in human diseases: an update
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Compromised MAPK signaling in human diseases: an update

Archives of toxicology, 2015-06, Vol.89 (6), p.867-882 [Peer Reviewed Journal]

Springer-Verlag Berlin Heidelberg 2015 ;ISSN: 0340-5761 ;EISSN: 1432-0738 ;DOI: 10.1007/s00204-015-1472-2 ;PMID: 25690731

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3
Childhood amyotrophic lateral sclerosis caused by excess sphingolipid synthesis
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Childhood amyotrophic lateral sclerosis caused by excess sphingolipid synthesis

Nature medicine, 2021-07, Vol.27 (7), p.1197-1204 [Peer Reviewed Journal]

2021. This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply. ;This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 2021. ;ISSN: 1078-8956 ;EISSN: 1546-170X ;DOI: 10.1038/s41591-021-01346-1 ;PMID: 34059824

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4
SOD1 mutations associated with amyotrophic lateral sclerosis analysis of variant severity
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SOD1 mutations associated with amyotrophic lateral sclerosis analysis of variant severity

Scientific reports, 2022-01, Vol.12 (1), p.103-103, Article 103 [Peer Reviewed Journal]

2022. The Author(s). ;The Author(s) 2022. This work is published 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. ;The Author(s) 2022 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-021-03891-8 ;PMID: 34996976

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5
The biophysics of superoxide dismutase-1 and amyotrophic lateral sclerosis
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The biophysics of superoxide dismutase-1 and amyotrophic lateral sclerosis

Quarterly reviews of biophysics, 2019-11, Vol.52, p.e12, Article e12 [Peer Reviewed Journal]

ISSN: 0033-5835 ;EISSN: 1469-8994 ;DOI: 10.1017/s003358351900012x ;PMID: 31760962

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6
Non-cell autonomous toxicity in neurodegenerative disorders: ALS and beyond
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Non-cell autonomous toxicity in neurodegenerative disorders: ALS and beyond

The Journal of cell biology, 2009-12, Vol.187 (6), p.761-772 [Peer Reviewed Journal]

2009 Ilieva et al. 2009 ;ISSN: 0021-9525 ;EISSN: 1540-8140 ;DOI: 10.1083/jcb.200908164 ;PMID: 19951898

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7
Mutant copper-zinc superoxide dismutase (SOD1) induces protein secretion pathway alterations and exosome release in astrocytes: implications for disease spreading and motor neuron pathology in amyotrophic lateral sclerosis
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Mutant copper-zinc superoxide dismutase (SOD1) induces protein secretion pathway alterations and exosome release in astrocytes: implications for disease spreading and motor neuron pathology in amyotrophic lateral sclerosis

The Journal of biological chemistry, 2013-05, Vol.288 (22), p.15699-15711 [Peer Reviewed Journal]

2013 by The American Society for Biochemistry and Molecular Biology, Inc. 2013 ;ISSN: 0021-9258 ;EISSN: 1083-351X ;DOI: 10.1074/jbc.M112.425066 ;PMID: 23592792

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8
Amyotrophic lateral sclerosis-associated mutant SOD1 inhibits anterograde axonal transport of mitochondria by reducing Miro1 levels
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Amyotrophic lateral sclerosis-associated mutant SOD1 inhibits anterograde axonal transport of mitochondria by reducing Miro1 levels

Human molecular genetics, 2017-12, Vol.26 (23), p.4668-4679 [Peer Reviewed Journal]

The Author 2017. Published by Oxford University Press. ;The Author 2017. Published by Oxford University Press. 2017 ;ISSN: 0964-6906 ;EISSN: 1460-2083 ;DOI: 10.1093/hmg/ddx348 ;PMID: 28973175

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9
Current hypotheses for the underlying biology of amyotrophic lateral sclerosis
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Current hypotheses for the underlying biology of amyotrophic lateral sclerosis

Annals of neurology, 2009-01, Vol.65 (S1), p.S3-S9 [Peer Reviewed Journal]

Copyright © 2009 American Neurological Association ;ISSN: 0364-5134 ;EISSN: 1531-8249 ;DOI: 10.1002/ana.21543 ;PMID: 19191304

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10
TBK1: a new player in ALS linking autophagy and neuroinflammation
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TBK1: a new player in ALS linking autophagy and neuroinflammation

Molecular brain, 2017-02, Vol.10 (1), p.5-5, Article 5 [Peer Reviewed Journal]

COPYRIGHT 2017 BioMed Central Ltd. ;Copyright BioMed Central 2017 ;The Author(s). 2017 ;ISSN: 1756-6606 ;EISSN: 1756-6606 ;DOI: 10.1186/s13041-017-0287-x ;PMID: 28148298

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11
Synaptic restoration by cAMP/PKA drives activity-dependent neuroprotection to motoneurons in ALS
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Synaptic restoration by cAMP/PKA drives activity-dependent neuroprotection to motoneurons in ALS

The Journal of experimental medicine, 2020-08, Vol.217 (8) [Peer Reviewed Journal]

2020 Bączyk et al. ;Distributed under a Creative Commons Attribution 4.0 International License ;2020 Bączyk et al. 2020 ;ISSN: 0022-1007 ;EISSN: 1540-9538 ;DOI: 10.1084/jem.20191734 ;PMID: 32484501

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12
Large SOD1 aggregates, unlike trimeric SOD1, do not impact cell viability in a model of amyotrophic lateral sclerosis
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Large SOD1 aggregates, unlike trimeric SOD1, do not impact cell viability in a model of amyotrophic lateral sclerosis

Proceedings of the National Academy of Sciences - PNAS, 2018-05, Vol.115 (18), p.4661-4665 [Peer Reviewed Journal]

Volumes 1–89 and 106–114, copyright as a collective work only; author(s) retains copyright to individual articles ;Copyright National Academy of Sciences May 1, 2018 ;2018 ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.1800187115 ;PMID: 29666246

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13
A Small Molecule Screen in Stem-Cell-Derived Motor Neurons Identifies a Kinase Inhibitor as a Candidate Therapeutic for ALS
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A Small Molecule Screen in Stem-Cell-Derived Motor Neurons Identifies a Kinase Inhibitor as a Candidate Therapeutic for ALS

Cell stem cell, 2013-06, Vol.12 (6), p.713-726 [Peer Reviewed Journal]

2013 Elsevier Inc. ;Copyright © 2013 Elsevier Inc. All rights reserved. ;2013 ll Press. All rights reserved. 2013 ;ISSN: 1934-5909 ;EISSN: 1875-9777 ;DOI: 10.1016/j.stem.2013.04.003 ;PMID: 23602540

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14
Inhibition of RNA lariat debranching enzyme suppresses TDP-43 toxicity in ALS disease models
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Inhibition of RNA lariat debranching enzyme suppresses TDP-43 toxicity in ALS disease models

Nature genetics, 2012-12, Vol.44 (12), p.1302-1309 [Peer Reviewed Journal]

2014 INIST-CNRS ;COPYRIGHT 2012 Nature Publishing Group ;COPYRIGHT 2012 Nature Publishing Group ;Copyright Nature Publishing Group Dec 2012 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/ng.2434 ;PMID: 23104007 ;CODEN: NGENEC

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15
Partially native intermediates mediate misfolding of SOD1 in single-molecule folding trajectories
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Partially native intermediates mediate misfolding of SOD1 in single-molecule folding trajectories

Nature communications, 2017-12, Vol.8 (1), p.1881-11, Article 1881 [Peer Reviewed Journal]

2017. This work is published 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. ;The Author(s) 2017 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-017-01996-1 ;PMID: 29192167

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16
Glycosphingolipids are modulators of disease pathogenesis in amyotrophic lateral sclerosis
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Glycosphingolipids are modulators of disease pathogenesis in amyotrophic lateral sclerosis

Proceedings of the National Academy of Sciences - PNAS, 2015-06, Vol.112 (26), p.8100-8105 [Peer Reviewed Journal]

Volumes 1–89 and 106–112, copyright as a collective work only; author(s) retains copyright to individual articles ;Copyright National Academy of Sciences Jun 30, 2015 ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.1508767112 ;PMID: 26056266

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17
A Zn‐dependent structural transition of SOD1 modulates its ability to undergo phase separation
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A Zn‐dependent structural transition of SOD1 modulates its ability to undergo phase separation

The EMBO journal, 2023-01, Vol.42 (2), p.e111185-n/a [Peer Reviewed Journal]

2022 The Authors ;2022 The Authors. ;2023 EMBO ;ISSN: 0261-4189 ;EISSN: 1460-2075 ;DOI: 10.15252/embj.2022111185 ;PMID: 36416085

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18
Oligodendrocyte dysfunction in the pathogenesis of amyotrophic lateral sclerosis
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Oligodendrocyte dysfunction in the pathogenesis of amyotrophic lateral sclerosis

Brain (London, England : 1878), 2013-02, Vol.136 (Pt 2), p.471-482 [Peer Reviewed Journal]

The Author (2013). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For Permissions, please email: journals.permissions@oup.com 2013 ;ISSN: 0006-8950 ;EISSN: 1460-2156 ;DOI: 10.1093/brain/aws339 ;PMID: 23378219

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19
Amyotrophic lateral sclerosis associated with mutations in the CuZn superoxide dismutase gene
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Amyotrophic lateral sclerosis associated with mutations in the CuZn superoxide dismutase gene

Current neurology and neuroscience reports, 2006-01, Vol.6 (1), p.37-46 [Peer Reviewed Journal]

Current Science Inc. 2006 ;ISSN: 1528-4042 ;EISSN: 1534-6293 ;DOI: 10.1007/s11910-996-0008-9 ;PMID: 16469270

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20
NADPH oxidases as drug targets and biomarkers in neurodegenerative diseases: What is the evidence?
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NADPH oxidases as drug targets and biomarkers in neurodegenerative diseases: What is the evidence?

Free radical biology & medicine, 2017-11, Vol.112, p.387 [Peer Reviewed Journal]

ISSN: 1873-4596 ;EISSN: 1873-4596 ;DOI: 10.1016/j.freeradbiomed.2017.08.006

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