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Article

[Discovery of a new mutation in MYOD1 characterizes a subset of aggressive embryonal rhabdomyosarcoma partnering with mutations of the PI3K-AKT pathway].

Bulletin du cancer - 1 Sept 2014

Orbach Daniel

Abstract excerpt

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Topics

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Share to Chromosomes, Human, Pair 8
Share to MyoD Protein
Share to Oncogene Proteins, Fusion
Share to Paired Box Transcription Factors

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to PAX7 Transcription Factor

Share to Phosphatidylinositol 3-Kinases

Share to Proto-Oncogene Proteins c-akt

Share to Rhabdomyosarcoma, Embryonal

Source

Identifiers

PMID: 25295632
DOI: 10.1684/bdc.2014.2017

Genes

MYOD1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

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Research trail→

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[Discovery of a new mutation in MYOD1 characterizes a subset of aggressive embryonal rhabdomyosarcoma partnering with mutations of the PI3K-AKT pathway].PMID 25295632Read ↗

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

Biological Role and Clinical Implications of MYOD1L122R Mutation in RhabdomyosarcomaSemantic proximity Read ↗

Genomic analysis and preclinical xenograft model development identify potential therapeutic targets for MYOD1-mutant soft-tissue sarcoma of childhood.Semantic proximity Read ↗

MyoD-Cre driven alterations in K-Ras and p53 lead to a mouse model with histological and molecular characteristics of human rhabdomyosarcoma with direct translational applicationsSemantic proximity Read ↗

MyoD1 and Myogenin Expression in Human Neoplasia: A Review and UpdateSemantic proximity Read ↗

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

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

Transactivating mutation of the MYOD1 gene is a frequent event in adult spindle cell rhabdomyosarcoma.Semantic proximity Read ↗

Clinicopathological Analysis of a European Cohort of MYOD1 Mutant Rhabdomyosarcomas in Children and Young Adults.Semantic proximity Read ↗

[Function of Proto-oncogene Product PPM1D and Development of PPM1D Inhibitors for Cancer Chemotherapy].Semantic proximity Read ↗

Fusion of the Paired Box 3 (PAX3) and Myocardin (MYOCD) Genes in Pediatric RhabdomyosarcomaSemantic proximity Read ↗

Functional impact and targetability of PI3KCA, GNAS, and PTEN mutations in a spindle cell rhabdomyosarcoma with MYOD1 L122R mutation.Semantic proximity Read ↗

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