(Q91289385)

English

MYOD1-mutant spindle cell and sclerosing rhabdomyosarcoma: an aggressive subtype irrespective of age. A reappraisal for molecular classification and risk stratification

scientific article published on 04 September 2018

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scholarly article

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30181563%20AND%20SRC:MED&resulttype=core&format=json

21 April 2020

MYOD1-mutant spindle cell and sclerosing rhabdomyosarcoma: an aggressive subtype irrespective of age. A reappraisal for molecular classification and risk stratification (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30181563%20AND%20SRC:MED&resulttype=core&format=json

21 April 2020

sclerosing rhabdomyosarcoma

1 reference

based on heuristic

inferred from title

Leonard H Wexler

7

object named as

Leonard H Wexler

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30181563%20AND%20SRC:MED&resulttype=core&format=json

21 April 2020

author name string

Narasimhan P Agaram

1

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21 April 2020

Michael P LaQuaglia

2

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21 April 2020

Rita Alaggio

3

1 reference

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21 April 2020

Lei Zhang

4

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21 April 2020

Yumi Fujisawa

5

1 reference

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21 April 2020

Marc Ladanyi

6

1 reference

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21 April 2020

Cristina R Antonescu

8

1 reference

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21 April 2020

publication date

4 September 2018

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21 April 2020

Modern Pathology

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21 April 2020

32

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21 April 2020

1

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21 April 2020

27-36

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21 April 2020

Trends in childhood rhabdomyosarcoma incidence and survival in the United States, 1975-2005

1 reference

https://api.crossref.org/works/10.1038%2FS41379-018-0120-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Prognostic factors in metastatic rhabdomyosarcomas: results of a pooled analysis from United States and European cooperative groups.

1 reference

https://api.crossref.org/works/10.1038%2FS41379-018-0120-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Spindle cell rhabdomyosarcoma. A prognostically favorable variant of rhabdomyosarcoma

1 reference

https://api.crossref.org/works/10.1038%2FS41379-018-0120-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Spindle cell variants of embryonal rhabdomyosarcoma in the paratesticular region. A report of the Intergroup Rhabdomyosarcoma Study

1 reference

https://api.crossref.org/works/10.1038%2FS41379-018-0120-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Sclerosing rhabdomyosarcoma in adults: report of four cases of a hyalinizing, matrix-rich variant of rhabdomyosarcoma that may be confused with osteosarcoma, chondrosarcoma, or angiosarcoma

1 reference

https://api.crossref.org/works/10.1038%2FS41379-018-0120-9

7 January 2021

based on heuristic

inferred from DOI database lookup

[Spindle cell rhabdomyosarcoma in adults: a new entity in the spectrum of malignant mesenchymal tumors of soft tissues]

1 reference

https://api.crossref.org/works/10.1038%2FS41379-018-0120-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Sclerosing, pseudovascular rhabdomyosarcoma in adults. Clinicopathological and immunohistochemical analysis of three cases

1 reference

https://api.crossref.org/works/10.1038%2FS41379-018-0120-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Spindle cell rhabdomyosarcoma in adults: clinicopathological and immunohistochemical analysis of seven new cases.

1 reference

https://api.crossref.org/works/10.1038%2FS41379-018-0120-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Transactivating mutation of theMYOD1gene is a frequent event in adult spindle cell rhabdomyosarcoma

1 reference

https://api.crossref.org/works/10.1038%2FS41379-018-0120-9

7 January 2021

based on heuristic

inferred from DOI database lookup

A recurrent neomorphic mutation in MYOD1 defines a clinically aggressive subset of embryonal rhabdomyosarcoma associated with PI3K-AKT pathway mutations

1 reference

https://api.crossref.org/works/10.1038%2FS41379-018-0120-9

7 January 2021

based on heuristic

inferred from DOI database lookup

A clinicopathologic study of head and neck rhabdomyosarcomas showing FOXO1 fusion-positive alveolar and MYOD1-mutant sclerosing are associated with unfavorable outcome

1 reference

https://api.crossref.org/works/10.1038%2FS41379-018-0120-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Recurrent MYOD1 mutations in pediatric and adult sclerosing and spindle cell rhabdomyosarcomas: evidence for a common pathogenesis

1 reference

https://api.crossref.org/works/10.1038%2FS41379-018-0120-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Clinical and molecular heterogeneity of head and neck spindle cell and sclerosing rhabdomyosarcoma

1 reference

https://api.crossref.org/works/10.1038%2FS41379-018-0120-9

7 January 2021

based on heuristic

inferred from DOI database lookup

MYOD1 (L122R) mutations are associated with spindle cell and sclerosing rhabdomyosarcomas with aggressive clinical outcomes.

1 reference

https://api.crossref.org/works/10.1038%2FS41379-018-0120-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Sclerosing rhabdomyosarcomas in children and adolescents: a clinicopathologic review of 13 cases from the Intergroup Rhabdomyosarcoma Study Group and Children's Oncology Group

1 reference

https://api.crossref.org/works/10.1038%2FS41379-018-0120-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Memorial Sloan Kettering-Integrated Mutation Profiling of Actionable Cancer Targets (MSK-IMPACT): A Hybridization Capture-Based Next-Generation Sequencing Clinical Assay for Solid Tumor Molecular Oncology

1 reference

https://api.crossref.org/works/10.1038%2FS41379-018-0120-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Recurrent NCOA2 gene rearrangements in congenital/infantile spindle cell rhabdomyosarcoma

1 reference

https://api.crossref.org/works/10.1038%2FS41379-018-0120-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Oncogene mutation profiling of pediatric solid tumors reveals significant subsets of embryonal rhabdomyosarcoma and neuroblastoma with mutated genes in growth signaling pathways

1 reference

https://api.crossref.org/works/10.1038%2FS41379-018-0120-9

7 January 2021

based on heuristic

inferred from DOI database lookup

A point mutation in the MyoD basic domain imparts c-Myc-like properties

1 reference

https://api.crossref.org/works/10.1038%2FS41379-018-0120-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/S41379-018-0120-9

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30181563%20AND%20SRC:MED&resulttype=core&format=json

21 April 2020

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30181563%20AND%20SRC:MED&resulttype=core&format=json

21 April 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30181563%20AND%20SRC:MED&resulttype=core&format=json

21 April 2020

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