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

[Molecular characterisation of SMARCB1 and NF2 in familial and sporadic schwannomatosis: an evolving paradigm].

Annales de dermatologie et de venereologie - 1 Dec 2008

Dereure O

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Chromosomal Proteins, Non-Histone
Share to Chromosomes, Human, Pair 22
Share to Disease Models, Animal
Share to DNA-Binding Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Neurilemmoma

Share to Neurofibromatosis 2

Share to SMARCB1 Protein

Share to Transcription Factors

Source

Identifiers

PMID: 19084709
DOI: 10.1016/j.annder.2008.09.007

Genes

SMARCB1

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

[Molecular characterisation of SMARCB1 and NF2 in familial and sporadic schwannomatosis: an evolving paradigm].PMID 19084709Read ↗

Molecular characterisation of SMARCB1 and NF2 in familial and sporadic schwannomatosis.Semantic proximity Read ↗

Therapeutic advances for the tumors associated with neurofibromatosis type 1, type 2, and schwannomatosisSemantic proximity Read ↗

SMARCB1-related schwannomatosis and other SMARCB1-associated phenotypes: clinical spectrum and molecular pathogenesis.Semantic proximity Read ↗

Molecular pathogenesis of the schwannomatosis genes and genetic testing strategies.Semantic proximity Read ↗

[Record no. 34: hSNF5/INI1 (SMARCB1)].Semantic proximity Read ↗

The molecular pathogenesis of schwannomatosis, a paradigm for the co-involvement of multiple tumour suppressor genes in tumorigenesis.Semantic proximity Read ↗

SMARCA4-Associated SchwannomatosisSemantic proximity Read ↗

Novel susceptibility genes for non-NF2-/LZTR1-/SMARCB1-related hereditary schwannomatosis.Semantic proximity Read ↗

Frequency of SMARCB1 mutations in familial and sporadic schwannomatosis.Semantic proximity Read ↗

Update from the 2011 International Schwannomatosis Workshop: From genetics to diagnostic criteriaSemantic proximity Read ↗

Classification of schwannomas and the new naming convention for “neurofibromatosis-2”: Genetic updates and international consensus recommendationSemantic proximity Read ↗

CTF meeting 2012: Translation of the basic understanding of the biology and genetics of NF1, NF2, and schwannomatosis toward the development of effective therapiesSemantic proximity Read ↗

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