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Tyrosine kinase inhibitors in Ewing’s sarcoma: a systematic review

Tyrosine kinase inhibitors in Ewing’s sarcoma: a systematic review

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_7cf355562ef444929a290cac02cca5bb

Tyrosine kinase inhibitors in Ewing’s sarcoma: a systematic review

About this item

Full title

Tyrosine kinase inhibitors in Ewing’s sarcoma: a systematic review

Publisher

England: BioMed Central Ltd

Journal title

BMC cancer, 2025-04, Vol.25 (1), p.735-14, Article 735

Language

English

Formats

Publication information

Publisher

England: BioMed Central Ltd

More information

Scope and Contents

Contents

Ewing's sarcoma (ES) is a highly aggressive primary bone malignancy that primarily affects children and adolescents. Several tyrosine kinase receptors (RTKs) have been found to be overexpressed in ES samples, and it was demonstrated that some play significant roles in driving the malignant phenotype of ES. Specifically, ES with insulin-like growth...

Alternative Titles

Full title

Tyrosine kinase inhibitors in Ewing’s sarcoma: a systematic review

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_7cf355562ef444929a290cac02cca5bb

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_7cf355562ef444929a290cac02cca5bb

Other Identifiers

ISSN

1471-2407

E-ISSN

1471-2407

DOI

10.1186/s12885-025-14130-y

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