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

SMARCB1 (INI1) Deficient Tumours of the Uterine Cervix: Report of Two Cases, Including One Associated With an NTRK Fusion

22 Jan 2024

Abstract excerpt

Pathogenic variants (mutations) and other molecular events involving subunits of the SWItch/Sucrose Non-Fermentable chromatin remodelling complex are common in a wide variety of malignancies. Many of these neoplasms are characterized by undifferentiated morphology. They arise at a variety of sites in the female genital tract but have rarely been reported in the uterine cervix. We report 2 primary cervical...

Read the complete abstract on PubMed

Topics

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

Share to Cancer Mechanisms and Therapy
Share to Chromatin Remodeling and Cancer
Share to Tumors and Oncological Cases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 38289183
DOI: 10.1097/pgp.0000000000001014

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

SMARCB1 (INI1) Deficient Tumours of the Uterine Cervix: Report of Two Cases, Including One Associated With an NTRK FusionPMID 38289183Read ↗

Molecular and immunophenotypic characterization of SMARCB1 (INI1) - deficient intrathoracic NeoplasmsSemantic proximity Read ↗

SMARCB1 -deficient Tumors of Childhood: A Practical GuideSemantic proximity Read ↗

[Molecular genetics and immunophenotype of INI1/SMARCB in epithelioid sarcoma].Semantic proximity Read ↗

Genetic basis of SMARCB1 protein loss in 22 sinonasal carcinomas.Semantic proximity Read ↗

The expanding family of SMARCB1(INI1)-deficient neoplasia: implications of phenotypic, biological, and molecular heterogeneity.Semantic proximity Read ↗

Gene of the month: <i>SMARCB1</i>Semantic proximity Read ↗

Primary adult sellar SMARCB1/INI1-deficient tumor represents a subtype of atypical teratoid/rhabdoid tumorSemantic proximity Read ↗

SWI/SNF-deficient Sinonasal CarcinomasSemantic proximity Read ↗

SMARCA4 and SMARCA2 co-deficiency: An uncommon molecular signature defining a subset of rare, aggressive and undifferentiated malignancies associated with defective chromatin remodelingSemantic proximity Read ↗

Elusive and Aggressive: Unraveling SMARCB1/INI1-Deficient Undifferentiated Carcinoma With Rhabdoid Features Arising From the Colon: A Case Report and Comprehensive Literature Review.Semantic proximity Read ↗

Switch/Sucrose Non-fermentable (SWI/SNF) Complex-Partial Loss in Sinonasal Squamous Cell Carcinoma. Impact in the Morphology and PrognosisSemantic proximity Read ↗

Hereditary SWI/SNF complex deficiency syndromes.Semantic proximity Read ↗

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