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Article

Molecular profiling in primary hyperparathyroidism.

Head & neck - 1 Feb 2015

Segiet Oliwia Anna, Deska Mariusz, Michalski Marek, Gawrychowski Jacek, Wojnicz Romuald

Abstract excerpt

BACKGROUND: Primary hyperparathyroidism (HPT) is one of the most common endocrine disorders, defined by hypersecretion of parathormone. Primary HPT can be caused by adenoma, hyperplasia, and carcinoma. A great amount of mechanisms contribute to the pathogenesis of this disease, such as genetic predispositions because of the germline-inactivating mutations in the multiple endocrine neoplasia type 1 (MEN1) and...

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Share to Comparative Genomic Hybridization
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Intercellular Signaling Peptides and Proteins

Share to Loss of Heterozygosity

Share to Multiple Endocrine Neoplasia Type 1

Share to Multiple Endocrine Neoplasia Type 2a

Share to Proto-Oncogene Proteins c-ret

Share to Receptors, Calcium-Sensing

Source

Identifiers

PMID: 24595969
DOI: 10.1002/hed.23656

Genes

MEN1

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.

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