Identification of novelFUSmutations in sporadic cases of amyotrophic lateral sclerosis-Reference-Cited by-同舟云学术

Identification of novelFUSmutations in sporadic cases of amyotrophic lateral sclerosis

Published:2011-01-24 Issue:2 Volume:12 Page:113-117
ISSN:1748-2968
Container-title:Amyotrophic Lateral Sclerosis
language:en
Short-container-title:Amyotrophic Lateral Sclerosis

Author:

Belzil Veronique V.,Daoud Hussein,St-Onge Judith,Desjarlais Anne,Bouchard Jean-Pierre,Dupre Nicolas,Lacomblez Lucette,Salachas François,Pradat Pierre-François,Meininger Vincent,Camu William,Dion Patrick A.,Rouleau Guy A.

Publisher

Informa UK Limited

Subject

Neurology (clinical),Neurology,General Medicine

Link

http://www.tandfonline.com/doi/pdf/10.3109/17482968.2010.536840

Reference8 articles.

1. Familial amyotrophic lateral sclerosis: Molecular pathology of a patient with a SOD1 mutation

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

3. TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

4. Ubiquitinated TDP-43 in Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis

5. Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis

Cited by 29 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Stress granules in the spinal muscular atrophy and amyotrophic lateral sclerosis: The correlation and promising therapy;Neurobiology of Disease;2022-08

2. Frameshift peptides alter the properties of truncated FUS proteins in ALS-FUS;Molecular Brain;2020-05-13

3. Stress granule mediated protein aggregation and underlying gene defects in the FTD-ALS spectrum;Neurobiology of Disease;2020-02

4. ALS/FTD-Linked Mutation in FUS Suppresses Intra-axonal Protein Synthesis and Drives Disease Without Nuclear Loss-of-Function of FUS;Neuron;2018-11

5. Phenotypic and genotypic studies of ALS cases in ALS-SMA families;Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration;2018-03-01