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

The connection between tricarboxylic acid cycle enzyme mutations and pseudohypoxic signaling in pheochromocytoma and paraganglioma.

Frontiers in endocrinology - 1 Jan 2023

Wang Yuxiong, Liu Bin, Li Faping, Zhang Yanghe, Gao Xin, Wang Yishu, Zhou Honglan

Abstract excerpt

Pheochromocytomas and paragangliomas (PPGLs) are rare neuroendocrine tumors originating from chromaffin cells, holding significant clinical importance due to their capacity for excessive catecholamine secretion and associated cardiovascular complications. Roughly 80% of cases are associated with genetic mutations. Based on the functionality of these mutated genes, PPGLs can be categorized into distinct molecular...

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 Citric Acid Cycle

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Fumarates

Share to Ketoglutaric Acids

Share to Paraganglioma

Share to Pheochromocytoma

Share to Succinates

Share to Succinic Acid

Source

Open in PubMed Open full text

Identifiers

PMID: 37867526
DOI: 10.3389/fendo.2023.1274239
PMCID: PMC10585109

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The connection between tricarboxylic acid cycle enzyme mutations and pseudohypoxic signaling in pheochromocytoma and paraganglioma.PMID 37867526Read ↗

New insights on the pathogenesis of paraganglioma and pheochromocytomaSemantic proximity Read ↗

The VHL/HIF Axis in the Development and Treatment of Pheochromocytoma/ParagangliomaSemantic proximity Read ↗

New Insights into the Nuclear Imaging Phenotypes of Cluster 1 Pheochromocytoma and Paraganglioma.Semantic proximity Read ↗

Epigenetic and metabolic reprogramming of SDH-deficient paragangliomasSemantic proximity Read ↗

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

Current Management of Pheochromocytoma/Paraganglioma: A Guide for the Practicing Clinician in the Era of Precision MedicineSemantic proximity Read ↗

MITOCHONDRIA: Succinate dehydrogenase subunit B-associated phaeochromocytoma and paraganglioma.Semantic proximity Read ↗

Current views on cell metabolism in SDHx-related pheochromocytoma and paraganglioma.Semantic proximity Read ↗

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

Tumour microenvironment in pheochromocytoma and paragangliomaSemantic proximity Read ↗

Genotype and tumor locus determine expression profile of pseudohypoxic pheochromocytomas and paragangliomas.Semantic proximity Read ↗

Hypoxia Pathway Mutations in Pheochromocytomas and Paragangliomas.Semantic proximity Read ↗

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