Splicing factor proline and glutamine rich intron retention, reduced expression and aggregate formation are pathological features of amyotrophic lateral sclerosis-Reference-Cited by-同舟云学术

Splicing factor proline and glutamine rich intron retention, reduced expression and aggregate formation are pathological features of amyotrophic lateral sclerosis

Published:2021-08-02 Issue:7 Volume:47 Page:990-1003
ISSN:0305-1846
Container-title:Neuropathology and Applied Neurobiology
language:en
Short-container-title:Neuropathol Appl Neurobiol

Author:

Hogan Alison L.¹^ORCID,Grima Natalie¹,Fifita Jennifer A.¹,McCann Emily P.¹,Heng Benjamin¹,Fat Sandrine Chan Moi¹,Wu Sharlynn¹,Maharjan Ram²,Cain Amy K.²,Henden Lyndal¹,Rayner Stephanie¹,Tarr Ingrid¹,Zhang Katharine Y.¹,Zhao Qiongyi³,Zhang Zong‐Hong⁴,Wright Amanda¹,Lee Albert¹,Morsch Marco¹,Yang Shu¹,Williams Kelly L.¹,Blair Ian P.¹

Affiliation:

1. Centre for Motor Neuron Disease Research, Department of Biomedical Sciences, Faculty of Medicine, Health and Human Sciences Macquarie University Sydney New South Wales Australia

2. ARC Centre of Excellence in Synthetic Biology, Department of Molecular Sciences, Faculty of Science and Engineering Macquarie University Sydney New South Wales Australia

3. Queensland Brain Institute University of Queensland Brisbane Queensland Australia

4. School of Medicine, IMPACT, Bioinformatics Core Research Facility Deakin University Geelong Victoria Australia

Funder

Motor Neurone Disease Research Institute of Australia

National Health and Medical Research Council

Publisher

Wiley

Subject

Physiology (medical),Clinical Neurology,Neurology,Histology,Pathology and Forensic Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/nan.12749

Reference60 articles.

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4. TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

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

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