(Q54603571)

1 June 2018

title

High-resolution array CGH identifies common mechanisms that drive embryonal rhabdomyosarcoma pathogenesis. (English)

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1 June 2018

embryonal rhabdomyosarcoma

main subject

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Vera Paulson

1

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1 June 2018

Garvin Chandler

2

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1 June 2018

Dinesh Rakheja

3

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1 June 2018

Rene L Galindo

4

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1 June 2018

Kathleen Wilson

5

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1 June 2018

James F Amatruda

6

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1 June 2018

Scott Cameron

7

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1 June 2018

publication date

15 March 2011

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1 June 2018

Genes, Chromosomes and Cancer

published in

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1 June 2018

volume

50

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1 June 2018

page(s)

397-408

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1 June 2018

issue

6

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1 June 2018

Replication stress induces genome-wide copy number changes in human cells that resemble polymorphic and pathogenic variants

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Analysis of the PTCH coding region in human rhabdomyosarcoma

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Genome-wide identification of PAX3-FKHR binding sites in rhabdomyosarcoma reveals candidate target genes important for development and cancer

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Effects of RAS on the genesis of embryonal rhabdomyosarcoma.

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Application of comparative genomic hybridization, spectral karyotyping, and microarray analysis in the identification of subtype-specific patterns of genomic changes in rhabdomyosarcoma

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Neurofibromin 1 (NF1) defects are common in human ovarian serous carcinomas and co-occur with TP53 mutations

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Silencing of SPRY1 triggers complete regression of rhabdomyosarcoma tumors carrying a mutated RAS gene

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21 January 2018

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21 January 2018

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Deregulation of the hedgehog signalling pathway: a possible role for the PTCH and SUFU genes in human rhabdomyoma and rhabdomyosarcoma development

21 January 2018

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Fusion gene-negative alveolar rhabdomyosarcoma is clinically and molecularly indistinguishable from embryonal rhabdomyosarcoma.

21 January 2018

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Molecular pathogenesis of rhabdomyosarcoma

21 January 2018

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Activation of the hedgehog pathway confers a poor prognosis in embryonal and fusion gene-negative alveolar rhabdomyosarcoma

21 January 2018

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Leukemia-associated NF1 inactivation in patients with pediatric T-ALL and AML lacking evidence for neurofibromatosis

21 January 2018

1 reference

7 January 2021

Novel genomic imbalances in embryonal rhabdomyosarcoma revealed by comparative genomic hybridization and fluorescence in situ hybridization: an intergroup rhabdomyosarcoma study

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7 January 2021

Genomic gains and losses are similar in genetic and histologic subsets of rhabdomyosarcoma, whereas amplification predominates in embryonal with anaplasia and alveolar subtypes

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7 January 2021

Analysis of cyclin-dependent kinase inhibitor genes (CDKN2A, CDKN2B, andCDKN2C) in childhood rhabdomyosarcoma

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7 January 2021

Identifiers

DOI

10.1002/GCC.20864

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1 June 2018

PubMed ID

21412928

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1 June 2018