Loss of nuclear TDP-43 in amyotrophic lateral sclerosis (ALS) causes altered expression of splicing machinery and widespread dysregulation of RNA splicing in motor neurones-Reference-Cited by-同舟云学术

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Loss of nuclear TDP-43 in amyotrophic lateral sclerosis (ALS) causes altered expression of splicing machinery and widespread dysregulation of RNA splicing in motor neurones

Published:2014-09-25 Issue:6 Volume:40 Page:670-685
ISSN:0305-1846
Container-title:Neuropathology and Applied Neurobiology
language:en
Short-container-title:Neuropathol Appl Neurobiol

Author:

Highley J. Robin¹,Kirby Janine¹,Jansweijer Joeri A.²,Webb Philip S.¹,Hewamadduma Channa A.¹³,Heath Paul R.¹,Higginbottom Adrian¹,Raman Rohini¹,Ferraiuolo Laura¹,Cooper-Knock Johnathan¹,McDermott Christopher J.¹,Wharton Stephen B.¹,Shaw Pamela J.¹,Ince Paul G.¹

Affiliation:

1. Sheffield Institute for Translational Neuroscience (SITraN); University of Sheffield; Sheffield UK

2. MRC Centre for Developmental and Biomedical Genetics; Firth Court; University of Sheffield; Sheffield UK

3. Academisch Medisch Centrum; Amsterdam The Netherlands

Funder

Medical Research Council

Wellcome Trust

National Institute for Health Research

European Communitys Seventh Framework Programme (FP7/2007-2013)

Publisher

Wiley

Subject

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

Reference48 articles.

1. Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis;Neumann;Science,2006

2. Mutations in TDP-43 link glycine-rich domain functions to amyotrophic lateral sclerosis;Pesiridis;Hum Mol Genet,2009

3. TDP-43: gumming up neurons through protein-protein and protein-RNA interactions;Buratti;Trends Biochem Sci,2012

4. Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping;Buratti;EMBO J,2001

5. Depletion of TDP 43 overrides the need for exonic and intronic splicing enhancers in the human apoA-II gene;Mercado;Nucleic Acids Res,2005

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