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

MED12 exon 2 mutation is uncommon in intravenous leiomyomatosis: clinicopathologic features and molecular study.

Human pathology - 1 May 2020

Wang Lili, Hu Shasha, Xin Fangjie, Zhao Han, Li Guangqi, Ran Wenwen, Xing Xiaoming, Wang Jigang

Abstract excerpt

Intravenous leiomyomatosis (IVL) is a rare neoplasm that is characterized by smooth muscle cell proliferation within venous vessels. The aim of this study is to investigate the clinicopathological features, immunophenotypes, and MED12 gene mutations in IVL. Nine cases of IVL from the Affiliated Hospital of Qingdao University were collected, and the clinicopathological features were reviewed. The...

Read the complete abstract on PubMed

Topics

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

Share to Biomarkers, Tumor
Share to Cell Proliferation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Immunohistochemistry

Share to Leiomyomatosis

Share to Mediator Complex

Share to Uterine Neoplasms

Source

Identifiers

PMID: 32240666
DOI: 10.1016/j.humpath.2020.03.011

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

MED12 exon 2 mutation is uncommon in intravenous leiomyomatosis: clinicopathologic features and molecular study.PMID 32240666Read ↗

Intravenous leiomyomatosis: molecular analysis of 17 cases.Semantic proximity Read ↗

Intravenous leiomyomatosis is inclined to a solid entity different from uterine leiomyoma based on RNA‐seq analysis with RT‐qPCR validationSemantic proximity Read ↗

[Clinicopathological features and gene phenotypes of benign metastasizing leiomyoma].Semantic proximity Read ↗

Integrated genome analysis of uterine leiomyosarcoma to identify novel driver genes and targetable pathwaysSemantic proximity Read ↗

Prevalence of MED12 mutations in uterine and extrauterine smooth muscle tumours.Semantic proximity Read ↗

Mutational analysis of MED12 exon 2 in uterine leiomyoma and other common tumors.Semantic proximity Read ↗

Intramuscular hemangioma capillary type with HRAS mutation: Expanding the molecular genetic spectrum with an emphasis on overlap with arteriovenous malformations and distinct from infantile hemangioma.Semantic proximity Read ↗

Characterization of MED12, HMGA2, and FH alterations reveals molecular variability in uterine smooth muscle tumors.Semantic proximity Read ↗

The study of MED12 gene mutations in uterine leiomyomas from Iranian patients.Semantic proximity Read ↗

Analysis of MED12 Mutation in Multiple Uterine Leiomyomas in South Korean patients.Semantic proximity Read ↗

Frequency and Spectrum of MED12 Exon 2 Mutations in Multiple Versus Solitary Uterine Leiomyomas From Russian Patients.Semantic proximity Read ↗

MED12 mutations in leiomyosarcoma and extrauterine leiomyoma.Semantic proximity Read ↗

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