Relation of neurological marker expression and EWS gene fusion types in MIC2/CD99-positive tumors of the Ewing family. (Q50756966)

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31 October 2019

title

Relation of neurological marker expression and EWS gene fusion types in MIC2/CD99-positive tumors of the Ewing family (English)

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31 October 2019

5

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31 October 2019

Reinhard Windhager

4

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31 October 2019

author name string

G Amann

1

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31 October 2019

A Zoubek

2

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31 October 2019

M Salzer-Kuntschik

3

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31 October 2019

language of work or name

English

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publication date

1 September 1999

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31 October 2019

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31 October 2019

volume

30

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31 October 2019

issue

9

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31 October 2019

page(s)

1058-1064

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MIC2 is a specific marker for ewing's sarcoma and peripheral primitive neuroectodermal tumors. Evidence for a common histogenesis of ewing's sarcoma and peripheral primitive neuroectodermal tumors from MIC2 expression and specific chromosome aberrati

31 October 2019

cites work

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The Ewing Family of Tumors -- A Subgroup of Small-Round-Cell Tumors Defined by Specific Chimeric Transcripts

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Combinatorial generation of variable fusion proteins in the Ewing family of tumours.

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Malignant peripheral neuroectodermal tumor and its necessary distinction from Ewing's sarcoma. A report from the Kiel Pediatric Tumor Registry

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Prognostic value of histopathology in Ewing's sarcoma. Long-term follow-up of distal extremity primary tumors

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7 January 2021

Neuron-specific enolase and Leu-7 immunoreactive small round-cell neoplasm. The relationship to Ewing's sarcoma in bone and soft tissue

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Neural differentiation in small round cell tumors of bone and soft tissue with the translocation t(11;22)(q24;q12): an immunohistochemical study of 11 cases

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The immunophenotype of Ewing's sarcoma. An immunohistochemical analysis

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Exacerbation of psoriasis with meclofenamate

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Chromosome translocation in peripheral neuroepithelioma

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Ewing's sarcoma of bone: clinicopathologic aspects of 303 cases from the Intergroup Ewing's Sarcoma Study

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Histopathological predictive factors in Ewing's sarcoma of bone and clinicopathological correlations. A retrospective study of 261 cases

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Pathologic features of extraosseous Ewing's sarcoma: a report from the Intergroup Rhabdomyosarcoma Study

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Cytogenetic and pathologic aspects of Ewing's sarcoma and neuroectodermal tumors

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Fusion of an ETS-family gene, EIAF, to EWS by t(17;22)(q12;q12) chromosome translocation in an undifferentiated sarcoma of infancy

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7 January 2021

A new member of the ETS family fused to EWS in Ewing tumors

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7 January 2021

Does expression of different EWS chimeric transcripts define clinically distinct risk groups of Ewing tumor patients?

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7 January 2021

Variability of EWS chimaeric transcripts in Ewing tumours: a comparison of clinical and molecular data.

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7 January 2021

Neuron-specific enolase in the diagnosis of neuroblastoma and other small, round-cell tumors in children

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A novel effector domain from the RNA-binding protein TLS or EWS is required for oncogenic transformation by CHOP

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7 January 2021

Xl-fli, the Xenopus homologue of the fli-1 gene, is expressed during embryogenesis in a restricted pattern evocative of neural crest cell distribution

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7 January 2021

EWS-FLI1 fusion transcript structure is an independent determinant of prognosis in Ewing's sarcoma

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7 January 2021

Among genes involved in the RB dependent cell cycle regulatory cascade, the p16 tumor suppressor gene is frequently lost in the Ewing family of tumors.

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7 January 2021

EWS-FLI1 fusion transcripts identified in patients with typical neuroblastoma.

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7 January 2021

Progress in the molecular biology of ewing tumors.

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7 January 2021

10.1016/S0046-8177(99)90223-X

Identifiers

DOI

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31 October 2019

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