Back to search

Article

Loss of heterozygosity and absence of MAX immunostaining in a prolactinoma associated with multiple endocrine neoplasia type 5 (MEN5)

2025-10-07

Abstract excerpt

<title>Abstract</title> <p> Multiple endocrine neoplasia type 5 (MEN5) is an emerging syndrome caused by germline pathogenic variants involving the <italic>MYC Associated Factor X</italic> ( <italic>MAX</italic> ) gene. Affected individuals typically have pheochromocytomas, often bilateral, at a relatively early age. In <italic>MAX</italic> pheochromocytoma cohorts, pituitary adenomas are rarely reported....

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
44534aa1-941c-5491-b678-ba1f24192698
DOI
10.21203/rs.3.rs-7760856/v1
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Loss of heterozygosity and absence of MAX immunostaining in a prolactinoma associated with multiple endocrine neoplasia type 5 (MEN5)DOI 10.21203/rs.3.rs-7760856/v1
Select a neighboring publication to make it the new centre.