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

<i>SMARCB1/INI1</i> Tumor Suppressor Gene Is Frequently Inactivated in Epithelioid Sarcomas

15 May 2005

Abstract excerpt

Epithelioid sarcoma is a rare soft tissue neoplasm of uncertain lineage that usually arises in the distal extremities of adults, presents a high rate of recurrences and metastases and frequently poses diagnostic dilemmas. The recently reported large-cell "proximal-type" variant is characterized by increased aggressiveness, deep location, preferential occurrence in proximal/axial regions of older patients, and...

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 Sarcoma Diagnosis and Treatment

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 15899790
DOI: 10.1158/0008-5472.can-04-3050

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

<i>SMARCB1/INI1</i> Tumor Suppressor Gene Is Frequently Inactivated in Epithelioid SarcomasPMID 15899790Read ↗

Consistent <i>SMARCB1</i> homozygous deletions in epithelioid sarcoma and in a subset of myoepithelial carcinomas can be reliably detected by FISH in archival materialSemantic proximity Read ↗

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

INI1-Deficient TumorsSemantic proximity Read ↗

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

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

SMARCB1/INI1-deficient tumors of adulthoodSemantic proximity Read ↗

SMARCB1/INI1-deficient tumors of adulthoodSemantic proximity Read ↗

Infrequent SMARCB1/INI1 gene alteration in epithelioid sarcoma: a useful tool in distinguishing epithelioid sarcoma from malignant rhabdoid tumor.Semantic proximity Read ↗

SMARCB1 / INI1 Genetic Inactivation Is Responsible for Tumorigenic Properties of Epithelioid Sarcoma Cell Line VAESBJSemantic proximity Read ↗

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

Epithelioid sarcoma is associated with a high percentage of SMARCB1 deletions.Semantic proximity Read ↗

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

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