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Article

Genetic imprinting suggested by maternal DNA methylation in CNS hemangioblastoma with clinical phenotypes of VHL disease.

Journal of neuro-oncology - 1 Sept 2015

Ma Dexuan, Wang Ying, Zhou Liangfu

Abstract excerpt

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Topics

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Share to Antigens, CD34
Share to Cerebellar Neoplasms
Share to DNA Methylation
Share to Family Health

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Genomic Imprinting

Share to Hemangioblastoma

Share to Magnetic Resonance Imaging

Share to Von Hippel-Lindau Tumor Suppressor Protein

Source

Identifiers

PMID: 26093619
DOI: 10.1007/s11060-015-1852-8

Genes

VHL

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 9 Sept 2026.

Related research

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Genetic imprinting suggested by maternal DNA methylation in CNS hemangioblastoma with clinical phenotypes of VHL disease.PMID 26093619Read ↗

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Identification of genomic aberrations in hemangioblastoma by droplet digital PCR and SNP microarray highlights novel candidate genes and pathways for pathogenesis.Semantic proximity Read ↗

Sporadic hemangioblastomas are characterized by cryptic VHL inactivation.Semantic proximity Read ↗

An 11-bp duplication in the promoter region of the VHL gene in a patient with cerebellar hemangioblastoma and renal oncocytoma.Semantic proximity Read ↗

Intronic mutation of the VHL gene associated with central nervous system hemangioblastomas in two Chinese families with Von Hippel-Lindau disease: case report.Semantic proximity Read ↗

Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndromeSemantic proximity Read ↗

Masked malignant phenotype with a benign appearance: beat-up copy number profile may be the key for hemangioblastoma dissemination.Semantic proximity Read ↗

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