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A kinase-deficient NTRK2 splice variant predominates in glioma and amplifies several oncogenic signa...

A kinase-deficient NTRK2 splice variant predominates in glioma and amplifies several oncogenic signa...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_e76b737ec4c34d949cb32dc9395b4f44

A kinase-deficient NTRK2 splice variant predominates in glioma and amplifies several oncogenic signaling pathways

About this item

Full title

A kinase-deficient NTRK2 splice variant predominates in glioma and amplifies several oncogenic signaling pathways

Publisher

London: Nature Publishing Group UK

Journal title

Nature communications, 2020-06, Vol.11 (1), p.2977-14, Article 2977

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Independent scientific achievements have led to the discovery of aberrant splicing patterns in oncogenesis, while more recent advances have uncovered novel gene fusions involving neurotrophic tyrosine receptor kinases (NTRKs) in gliomas. The exploration of
NTRK
splice variants in normal and neoplastic brain provides an intersection of these t...

Alternative Titles

Full title

A kinase-deficient NTRK2 splice variant predominates in glioma and amplifies several oncogenic signaling pathways

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_e76b737ec4c34d949cb32dc9395b4f44

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_e76b737ec4c34d949cb32dc9395b4f44

Other Identifiers

ISSN

2041-1723

E-ISSN

2041-1723

DOI

10.1038/s41467-020-16786-5

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