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

[Advances in genes and molecular markers of pheochromocytoma].

Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences - 1 Mar 2014

Gong Shi-kun, Liu Zhong

Abstract excerpt

Pheochromocytoma is a tumor derived from chromaffin tissue in the adrenergic system with excessive secretion of catecholamine.Pheochromocytoma occurs at any age of patients,commonly in 40-60 years,and the incidence is slightly higher in women than in men.In recent years,studies have shown that the mutations of von Hippel-Lindau gene (VHL),rearranged during transfection gene (RET),neurofibromatosis type 1 gene...

Read the complete abstract on PubMed

Topics

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

Share to Adrenal Gland Neoplasms
Share to Biomarkers, Tumor
Share to MAX gene

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to RET gene

Share to VHL gene

Share to Mutation

Share to Pheochromocytoma

Source

Identifiers

PMID: 24782382
DOI: 10.3785/j.issn.1008-9292.2014.01.016

Genes

MAX
RET
VHL

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Advances in genes and molecular markers of pheochromocytoma].PMID 24782382Read ↗

[Genetics of paragangliomas and pheochromocytomas].Semantic proximity Read ↗

Pheochromocytoma and paraganglioma: understanding the complexities of the genetic background.Semantic proximity Read ↗

Pheochromocytomas and Paragangliomas: An Update on Recent Molecular Genetic Advances and Criteria for Malignancy.Semantic proximity Read ↗

Pheochromocytoma: an update on genetics and management.Semantic proximity Read ↗

Pheochromocytoma and paraganglioma syndromes: genetics and management updateSemantic proximity Read ↗

[Genetics of pheochromocytoma].Semantic proximity Read ↗

Clinical Syndromes and Genetic Screening Strategies of Pheochromocytoma and ParagangliomaSemantic proximity Read ↗

An update on the genetics of pheochromocytoma.Semantic proximity Read ↗

An update on the genetics of paraganglioma, pheochromocytoma, and associated hereditary syndromes.Semantic proximity Read ↗

Molecular markers of paragangliomas/pheochromocytomas.Semantic proximity Read ↗

Genetics and molecular pathogenesis of pheochromocytoma and paraganglioma.Semantic proximity Read ↗

New Insights on the Genetics of Pheochromocytoma and Paraganglioma and Its Clinical ImplicationsSemantic proximity Read ↗

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