Pathological Modification of TDP-43 in Amyotrophic Lateral Sclerosis with SOD1 Mutations

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1559-1182

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Pathological Modification of TDP-43 in Amyotrophic Lateral Sclerosis with SOD1 Mutations ; day:7 ; month:7 ; year:2018 ; pages:1-15
Molecular neurobiology ; (7.7.2018), 1-15

Creator: Jeon, Gye Sun

Contributor: Shim, Yu-Mi
Lee, Do-Yeon
Kim, Jun-Soon
Kang, MinJin
Ahn, So Hyun
Shin, Je-Young
Geum, Dongho
Hong, Yoon Ho
Sung, Jung-Joon
SpringerLink (Online service)

DOI: 10.1007/s12035-018-1218-2

URN: urn:nbn:de:101:1-2018081710140328927324

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:37 AM CEST

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Associated

Jeon, Gye Sun
Shim, Yu-Mi
Lee, Do-Yeon
Kim, Jun-Soon
Kang, MinJin
Ahn, So Hyun
Shin, Je-Young
Geum, Dongho
Hong, Yoon Ho
Sung, Jung-Joon
SpringerLink (Online service)

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The role of TDP-43 mislocalization in amyotrophic lateral sclerosis

TDP-43 protein variants as biomarkers in amyotrophic lateral sclerosis

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Systemic dysregulation of TDP-43 binding microRNAs in amyotrophic lateral sclerosis

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Misfolded SOD1 pathology in sporadic Amyotrophic Lateral Sclerosis

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TDP-43 protein variants as biomarkers in amyotrophic lateral sclerosis

Proteomics elucidating physiological and pathological functions of TDP‐43

TDP-43 dysregulation and neuromuscular junction disruption in amyotrophic lateral sclerosis

Pathological TDP-43 changes in Betz cells differ from those in bulbar and spinal α-motoneurons in sporadic amyotrophic lateral sclerosis

Widespread CNS pathology in amyotrophic lateral sclerosis homozygous for the D90A SOD1 mutation

Systemic dysregulation of TDP-43 binding microRNAs in amyotrophic lateral sclerosis

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Misfolded SOD1 pathology in sporadic Amyotrophic Lateral Sclerosis

Pathological hydrogen peroxide triggers the fibrillization of wild-type SOD1 via sulfenic acid modification of Cys-111

Amyotrophic lateral sclerosis with SOD1 mutations shows distinct brain metabolic changes

Aggregation-prone TDP-43 sequesters and drives pathological transitions of free nuclear TDP-43

The role of TDP-43 mislocalization in amyotrophic lateral sclerosis

TDP-43 protein variants as biomarkers in amyotrophic lateral sclerosis

Proteomics elucidating physiological and pathological functions of TDP‐43

TDP-43 dysregulation and neuromuscular junction disruption in amyotrophic lateral sclerosis

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Systemic dysregulation of TDP-43 binding microRNAs in amyotrophic lateral sclerosis

Heterogeneity of cortical pTDP-43 inclusion morphologies in amyotrophic lateral sclerosis

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Pathological Modification of TDP-43 in Amyotrophic Lateral Sclerosis with SOD1 Mutations

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Other Objects (12)

Misfolded SOD1 pathology in sporadic Amyotrophic Lateral Sclerosis

Pathological hydrogen peroxide triggers the fibrillization of wild-type SOD1 via sulfenic acid modification of Cys-111

Amyotrophic lateral sclerosis with SOD1 mutations shows distinct brain metabolic changes

Aggregation-prone TDP-43 sequesters and drives pathological transitions of free nuclear TDP-43

The role of TDP-43 mislocalization in amyotrophic lateral sclerosis

TDP-43 protein variants as biomarkers in amyotrophic lateral sclerosis

Proteomics elucidating physiological and pathological functions of TDP‐43

TDP-43 dysregulation and neuromuscular junction disruption in amyotrophic lateral sclerosis

Pathological TDP-43 changes in Betz cells differ from those in bulbar and spinal α-motoneurons in sporadic amyotrophic lateral sclerosis

Widespread CNS pathology in amyotrophic lateral sclerosis homozygous for the D90A SOD1 mutation

Systemic dysregulation of TDP-43 binding microRNAs in amyotrophic lateral sclerosis

Heterogeneity of cortical pTDP-43 inclusion morphologies in amyotrophic lateral sclerosis

Misfolded SOD1 pathology in sporadic Amyotrophic Lateral Sclerosis

Pathological hydrogen peroxide triggers the fibrillization of wild-type SOD1 via sulfenic acid modification of Cys-111

Amyotrophic lateral sclerosis with SOD1 mutations shows distinct brain metabolic changes

Aggregation-prone TDP-43 sequesters and drives pathological transitions of free nuclear TDP-43

The role of TDP-43 mislocalization in amyotrophic lateral sclerosis

TDP-43 protein variants as biomarkers in amyotrophic lateral sclerosis

Proteomics elucidating physiological and pathological functions of TDP‐43

TDP-43 dysregulation and neuromuscular junction disruption in amyotrophic lateral sclerosis

Pathological TDP-43 changes in Betz cells differ from those in bulbar and spinal α-motoneurons in sporadic amyotrophic lateral sclerosis

Widespread CNS pathology in amyotrophic lateral sclerosis homozygous for the D90A SOD1 mutation

Systemic dysregulation of TDP-43 binding microRNAs in amyotrophic lateral sclerosis

Heterogeneity of cortical pTDP-43 inclusion morphologies in amyotrophic lateral sclerosis

Misfolded SOD1 pathology in sporadic Amyotrophic Lateral Sclerosis

Pathological hydrogen peroxide triggers the fibrillization of wild-type SOD1 via sulfenic acid modification of Cys-111

Amyotrophic lateral sclerosis with SOD1 mutations shows distinct brain metabolic changes

Aggregation-prone TDP-43 sequesters and drives pathological transitions of free nuclear TDP-43

The role of TDP-43 mislocalization in amyotrophic lateral sclerosis

TDP-43 protein variants as biomarkers in amyotrophic lateral sclerosis

Proteomics elucidating physiological and pathological functions of TDP‐43

TDP-43 dysregulation and neuromuscular junction disruption in amyotrophic lateral sclerosis

Pathological TDP-43 changes in Betz cells differ from those in bulbar and spinal α-motoneurons in sporadic amyotrophic lateral sclerosis

Widespread CNS pathology in amyotrophic lateral sclerosis homozygous for the D90A SOD1 mutation

Systemic dysregulation of TDP-43 binding microRNAs in amyotrophic lateral sclerosis

Heterogeneity of cortical pTDP-43 inclusion morphologies in amyotrophic lateral sclerosis

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