(Q46973585)

27 December 2017

title

Mutations in the tyrosine kinase domain of the EGFR gene are rare in synovial sarcoma (English)

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27 December 2017

7

Holger Moch

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27 December 2017

author name string

Beata Bode

1

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27 December 2017

Simona Frigerio

2

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27 December 2017

Silvia Behnke

3

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27 December 2017

Belinda Senn

4

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27 December 2017

Bernhard Odermatt

5

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27 December 2017

Dieter R Zimmermann

6

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27 December 2017

publication date

1 April 2006

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27 December 2017

published in

Modern Pathology

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27 December 2017

volume

19

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27 December 2017

issue

4

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27 December 2017

page(s)

541-547

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27 December 2017

https://scigraph.springernature.com/pub.10.1038/modpathol.3800560

exact match

0 references

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Tissue microarray validation of epidermal growth factor receptor and SALL2 in synovial sarcoma with comparison to tumors of similar histology

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Expression of receptor tyrosine kinases epidermal growth factor receptor and HER-2/neu in synovial sarcoma

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SYT, a partner of SYT-SSX oncoprotein in synovial sarcomas, interacts with mSin3A, a component of histone deacetylase complex

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SYT associates with human SNF/SWI complexes and the C-terminal region of its fusion partner SSX1 targets histones

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Epidermal growth factor receptor mutations, small-molecule kinase inhibitors, and non-small-cell lung cancer: current knowledge and future directions

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Variability in organ-specific EGFR mutational spectra in tumour epithelium and stroma may be the biological basis for differential responses to tyrosine kinase inhibitors.

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Detection of response-predicting mutations in the kinase domain of the epidermal growth factor receptor gene in cholangiocarcinomas

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EGF receptor gene mutations are common in lung cancers from "never smokers" and are associated with sensitivity of tumors to gefitinib and erlotinib

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Clinical and biological features associated with epidermal growth factor receptor gene mutations in lung cancers

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Oncoproteins and proliferation markers in synovial sarcomas: a clinicopathologic study of 19 cases

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Patterns of p53, erbB-2, and EGF-r expression in premalignant lesions of the urinary bladder

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Identifiers

DOI

1 reference

27 December 2017

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27 December 2017