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Molecular and clinicopathologic features of gliomas harboring NTRK fusions

Molecular and clinicopathologic features of gliomas harboring NTRK fusions

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_a13bf05804df41039d210cc899efdb56

Molecular and clinicopathologic features of gliomas harboring NTRK fusions

About this item

Full title

Molecular and clinicopathologic features of gliomas harboring NTRK fusions

Publisher

England: BioMed Central

Journal title

Acta neuropathologica communications, 2020-07, Vol.8 (1), p.107-14, Article 107

Language

English

Formats

Publication information

Publisher

England: BioMed Central

More information

Scope and Contents

Contents

Fusions involving neurotrophic tyrosine receptor kinase (
NTRK
) genes are detected in ≤2% of gliomas and can promote gliomagenesis. The remarkable therapeutic efficacy of TRK inhibitors, which are among the first Food and Drug Administration-approved targeted therapies for
NTRK
-fused gliomas, has generated significant clinical interes...

Alternative Titles

Full title

Molecular and clinicopathologic features of gliomas harboring NTRK fusions

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_a13bf05804df41039d210cc899efdb56

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_a13bf05804df41039d210cc899efdb56

Other Identifiers

ISSN

2051-5960

E-ISSN

2051-5960

DOI

10.1186/s40478-020-00980-z

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