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TDP-43 represses cryptic exon inclusion in the FTD–ALS gene UNC13A

TDP-43 represses cryptic exon inclusion in the FTD–ALS gene UNC13A

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8891019

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

A hallmark pathological feature of the neurodegenerative diseases amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) is the depletion of RNA-binding protein TDP-43 from the nucleus of neurons in the brain and spinal cord
1
. A major function of TDP-43 is as a repressor of cryptic exon inclusion during RNA splicing
2
–...

Alternative Titles

Full title

TDP-43 represses cryptic exon inclusion in the FTD–ALS gene UNC13A

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8891019

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8891019

Other Identifiers

ISSN

0028-0836

E-ISSN

1476-4687

DOI

10.1038/s41586-022-04424-7

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