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Drosophila screen connects nuclear transport genes to DPR pathology in c9ALS/FTD

Drosophila screen connects nuclear transport genes to DPR pathology in c9ALS/FTD

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4751451

Drosophila screen connects nuclear transport genes to DPR pathology in c9ALS/FTD

About this item

Full title

Drosophila screen connects nuclear transport genes to DPR pathology in c9ALS/FTD

Publisher

London: Nature Publishing Group UK

Journal title

Scientific reports, 2016-02, Vol.6 (1), p.20877-20877, Article 20877

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Hexanucleotide repeat expansions in
C9orf72
are the most common cause of amyotrophic lateral sclerosis (ALS) and frontotemporal degeneration (FTD) (c9ALS/FTD). Unconventional translation of these repeats produces dipeptide repeat proteins (DPRs) that may cause neurodegeneration. We performed a modifier screen in
Drosophila
and discovere...

Alternative Titles

Full title

Drosophila screen connects nuclear transport genes to DPR pathology in c9ALS/FTD

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4751451

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4751451

Other Identifiers

ISSN

2045-2322

E-ISSN

2045-2322

DOI

10.1038/srep20877

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