Impaired NHEJ repair in amyotrophic lateral sclerosis is associated with TDP-43 mutations

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1750-1326

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Impaired NHEJ repair in amyotrophic lateral sclerosis is associated with TDP-43 mutations ; volume:15 ; number:1 ; day:9 ; month:9 ; year:2020 ; pages:1-28 ; date:12.2020
Molecular neurodegeneration ; 15, Heft 1 (9.9.2020), 1-28, 12.2020

Creator: Konopka, Anna
Whelan, Donna R.
Jamali, Md Shafi
Perri, Emma
Shahheydari, Hamideh
Toth, Reka P.
Parakh, Sonam
Robinson, Tina
Cheong, Alison
Mehta, Prachi
Vidal, Marta
Ragagnin, Audrey M. G.
Khizhnyak, Ivan
Jagaraj, Cyril J.
Galper, Jasmin
Grima, Natalie
Deva, Anand
Shadfar, Sina
Nicholson, Garth A.
Yang, Shu
Cutts, Suzanne M.
Horejsi, Zuzana
Bell, Toby D. M.
Walker, Adam K.
Blair, Ian P.
Atkin, Julie D.

Contributor: SpringerLink (Online service)

DOI: 10.1186/s13024-020-00386-4

URN: urn:nbn:de:101:1-2020102922500808898824

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:22 AM CEST

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Associated

Konopka, Anna
Whelan, Donna R.
Jamali, Md Shafi
Perri, Emma
Shahheydari, Hamideh
Toth, Reka P.
Parakh, Sonam
Robinson, Tina
Cheong, Alison
Mehta, Prachi
Vidal, Marta
Ragagnin, Audrey M. G.
Khizhnyak, Ivan
Jagaraj, Cyril J.
Galper, Jasmin
Grima, Natalie
Deva, Anand
Shadfar, Sina
Nicholson, Garth A.
Yang, Shu
Cutts, Suzanne M.
Horejsi, Zuzana
Bell, Toby D. M.
Walker, Adam K.
Blair, Ian P.
Atkin, Julie D.
SpringerLink (Online service)

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Impaired NHEJ repair in amyotrophic lateral sclerosis is associated with TDP-43 mutations

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Other Objects (12)

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

The role of TDP-43 mislocalization in amyotrophic lateral sclerosis

TDP-43 protein variants as biomarkers in amyotrophic lateral sclerosis

Mice with endogenous TDP ‐43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis

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

Impaired glymphatic function in the early stages of disease in a TDP-43 mouse model of amyotrophic lateral sclerosis

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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TDP-43 protein variants as biomarkers in amyotrophic lateral sclerosis

Mice with endogenous TDP ‐43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis

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

Impaired glymphatic function in the early stages of disease in a TDP-43 mouse model of amyotrophic lateral sclerosis

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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Frontotemporal dementia and amyotrophic lateral sclerosis-associated disease protein TDP-43 promotes dendritic branching

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

The role of TDP-43 mislocalization in amyotrophic lateral sclerosis

TDP-43 protein variants as biomarkers in amyotrophic lateral sclerosis

Mice with endogenous TDP ‐43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis

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

Impaired glymphatic function in the early stages of disease in a TDP-43 mouse model of amyotrophic lateral sclerosis

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

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