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

Recent insights into the molecular pathogenesis of pheochromocytoma and paraganglioma.

Endocrine pathology - 1 Jan 2006

Nakamura Eijiro, Kaelin William G

Abstract excerpt

Pheochromocytomas and paragangliomas are rare tumors derived from chromaffin cells. These tumors can arise in the context of hereditary cancer syndromes such as von Hippel- Lindau disease, multiple endocrine neoplasia type 2, and neurofibromatosis 1. Recent studies indicate that germ line mutations of genes encoding specific succinate dehydrogenase (SDH) subunits also predispose individuals to pheochromocytomas...

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 Apoptosis
Share to Fetal Development

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Germ-Line Mutation

Share to Nerve Growth Factor

Share to Paraganglioma

Share to Pheochromocytoma

Share to Succinate Dehydrogenase

Source

Identifiers

PMID: 17159241
DOI: 10.1385/ep:17:2:97

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Recent insights into the molecular pathogenesis of pheochromocytoma and paraganglioma.PMID 17159241Read ↗

Evolving concepts in pheochromocytoma and paraganglioma.Semantic proximity Read ↗

Succinate Dehydrogenase-deficient TumorsSemantic proximity Read ↗

New Insights into the Genetics of Familial Chromaffin Cell TumorsSemantic proximity Read ↗

Hereditary pheochromocytoma and paraganglioma.Semantic proximity Read ↗

Back to Biochemistry: Evaluation for and Prognostic Significance of SDH Mutations in Paragangliomas and Pheochromocytomas.Semantic proximity Read ↗

Back to Biochemistry: Evaluation for and Prognostic Significance of SDH Mutations in Paragangliomas and Pheochromocytomas.Semantic proximity Read ↗

15 YEARS OF PARAGANGLIOMA: Genetics and mechanism of pheochromocytoma–paraganglioma syndromes characterized by germline SDHB and SDHD mutationsSemantic proximity Read ↗

Pheochromocytomas: from genetic diversity to new paradigms.Semantic proximity Read ↗

Pheochromocytoma: The Expanding Genetic Differential DiagnosisSemantic proximity Read ↗

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

Clinical and molecular progress in hereditary paraganglioma: Figure 1Semantic proximity Read ↗

SDH mutations in tumorigenesis and inherited endocrine tumours: lesson from the phaeochromocytoma-paraganglioma syndromes.Semantic proximity Read ↗

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