Recapitulation of Pathological TDP-43 Features in Immortalized Lymphocytes from Sporadic ALS Patients-Reference-Cited by-同舟云学术

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Recapitulation of Pathological TDP-43 Features in Immortalized Lymphocytes from Sporadic ALS Patients

Published:2018-07-20 Issue:4 Volume:56 Page:2424-2432
ISSN:0893-7648
Container-title:Molecular Neurobiology
language:en
Short-container-title:Mol Neurobiol

Author:

Posa Diana,Martínez-González Loreto,Bartolomé Fernando,Nagaraj Siranjeevi,Porras Gracia,Martínez Ana,Martín-Requero Ángeles^ORCID

Funder

Secretaría de Estado de Investigación, Desarrollo e Innovación

Consejería de Educación, Juventud y Deporte, Comunidad de Madrid

Publisher

Springer Science and Business Media LLC

Subject

Neuroscience (miscellaneous),Cellular and Molecular Neuroscience,Neurology

Link

http://link.springer.com/content/pdf/10.1007/s12035-018-1249-8.pdf

Reference45 articles.

1. Rosen DR, Siddique T, Patterson D, Figlewicz DA, Sapp P, Hentati A, Donaldson D, Goto J et al (1993) Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Nature 362(6415):59–62. https://doi.org/10.1038/362059a0

2. Arai T, Hasegawa M, Akiyama H, Ikeda K, Nonaka T, Mori H, Mann D, Tsuchiya K et al (2006) TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Biochem Biophys Res Commun 351(3):602–611. https://doi.org/10.1016/j.bbrc.2006.10.093

3. Groen EJ, Fumoto K, Blokhuis AM, Engelen-Lee J, Zhou Y, van den Heuvel DM, Koppers M, van Diggelen F et al (2013) ALS-associated mutations in FUS disrupt the axonal distribution and function of SMN. Hum Mol Genet 22(18):3690–3704. https://doi.org/10.1093/hmg/ddt222

4. Johnson JO, Mandrioli J, Benatar M, Abramzon Y, Van Deerlin VM, Trojanowski JQ, Gibbs JR, Brunetti M et al (2010) Exome sequencing reveals VCP mutations as a cause of familial ALS. Neuron 68(5):857–864. https://doi.org/10.1016/j.neuron.2010.11.036

5. Kwiatkowski TJ Jr, Bosco DA, Leclerc AL, Tamrazian E, Vanderburg CR, Russ C, Davis A, Gilchrist J et al (2009) Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis. Science 323(5918):1205–1208. https://doi.org/10.1126/science.1166066

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2. Casein kinase 1 inhibitor avoids TDP-43 pathology propagation in a patient-derived cellular model of amyotrophic lateral sclerosis;Neurobiology of Disease;2024-03

3. The new missense G376V-TDP-43 variant induces late-onset distal myopathy but not amyotrophic lateral sclerosis;Brain;2023-12-11

4. The key role of TDP-43 in amyotrophic lateral sclerosis propagation and the disease-modifying profile of CK-1 inhibitors;2023-09-15

5. Functional Characterization of a Familial ALS-Associated Missense TBK1 (p-Arg573Gly) Mutation in Patient-Derived Lymphoblasts;International Journal of Molecular Sciences;2023-02-02

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