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

hSNF5/INI1‐deficient tumours and rhabdoid tumours are convergent but not fully overlapping entities

6 Dec 2006

Abstract excerpt

Rhabdoid tumours (RTs) are rare but highly aggressive tumours of childhood. Their rarity and their miscellaneous locations make the diagnosis particularly challenging for pathologists. Central nervous system and peripheral RTs have been associated with biallelic inactivation of the hSNF5/INI1/SMARCB1 (hSNF5/INI1) tumour suppressor gene. Immunohistochemistry (IHC) with a monoclonal anti-hSNF5/INI1 antibody has...

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 interferon and immune responses

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 17152049
DOI: 10.1002/path.2103

Provenance

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

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

hSNF5/INI1‐deficient tumours and rhabdoid tumours are convergent but not fully overlapping entitiesPMID 17152049Read ↗

Mutations of the INI1 rhabdoid tumor suppressor gene in medulloblastomas and primitive neuroectodermal tumors of the central nervous system.Semantic proximity Read ↗

Immunohistochemical analysis of hSNF5/INI1 in pediatric CNS neoplasms.Semantic proximity Read ↗

SMARCB1/INI1-deficient tumors of adulthoodSemantic proximity Read ↗

Molecular genetics of atypical teratoid/rhabdoid tumor.Semantic proximity Read ↗

SMARCB1/INI1-deficient tumors of adulthoodSemantic proximity Read ↗

Alterations of the hSNF5/INI1 gene in central nervous system atypical teratoid/rhabdoid tumors and renal and extrarenal rhabdoid tumors.Semantic proximity Read ↗

INI1-Deficient TumorsSemantic proximity Read ↗

[Infant rhabdoid tumors: a diagnostic emergency].Semantic proximity Read ↗

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

Rhabdoid tumour: a malignancy of early childhood with variable primary site, histology and clinical behaviour.Semantic proximity Read ↗

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

Spectrum of hSNF5/INI1 somatic mutations in human cancer and genotype-phenotype correlations.Semantic proximity Read ↗

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