Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Comprehensive genetic analysis of a paediatric pleomorphic myxoid liposarcoma reveals near‐haploidization and loss of the RB 1 gene

9 Dec 2015

Abstract excerpt

AIMS: Pleomorphic myxoid liposarcoma (PML) is an exceptionally rare and poorly studied subtype of liposarcoma, occurring typically in children and adolescents. The few previous genetic studies have shown that PML lacks the gene fusions and amplifications that characterize myxoid liposarcoma, atypical lipomatous tumour and de-differentiated liposarcoma. To learn more about its pathogenesis, we performed a...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Bone Tumor Diagnosis and Treatments
Share to Cardiac tumors and thrombi
Share to Sarcoma Diagnosis and Treatment

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 26647907
DOI: 10.1111/his.12913

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Comprehensive genetic analysis of a paediatric pleomorphic myxoid liposarcoma reveals near‐haploidization and loss of the RB 1 genePMID 26647907Read ↗

New molecular insights into the pathogenesis of lipoblastomas: clinicopathologic, immunohistochemical, and molecular analysis in pediatric cases.Semantic proximity Read ↗

Liposarcoma: Molecular Genetics and TherapeuticsSemantic proximity Read ↗

Liposarcoma in children and young adults: a clinicopathologic and molecular study of 23 cases in one of the largest institutions of China.Semantic proximity Read ↗

Genomic profiling of pleomorphic rhabdomyosarcoma reveals a genomic signature distinct from that of embryonal rhabdomyosarcoma.Semantic proximity Read ↗

Undifferentiated myxoid lipoblastoma with PLAG1–HAS2 fusion in an infant; morphologically mimicking primitive myxoid mesenchymal tumor of infancy (PMMTI)—diagnostic importance of cytogenetic and molecular testing and literature reviewSemantic proximity Read ↗

Genomic landscape of liposarcoma.Semantic proximity Read ↗

Diagnostic utility of molecular and cytogenetic analysis in lipoblastoma: a study of two cases and review of the literatureSemantic proximity Read ↗

Cytogenetics and Molecular Genetics of Myxoid Soft-Tissue SarcomasSemantic proximity Read ↗

Structural Variants in the SMC1A Gene Associated With Near-Haploidy in Undifferentiated Pleomorphic Sarcomas.Semantic proximity Read ↗

Inflammatory leiomyosarcoma is a distinct tumor characterized by near-haploidization, few somatic mutations, and a primitive myogenic gene expression signature.Semantic proximity Read ↗

Pleomorphic myxoid liposarcoma in an adolescent with Li–Fraumeni syndromeSemantic proximity Read ↗

Liposarcomas: diagnostic pitfalls and new insightsSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.