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Article

[Adrenocorticotropin receptor in familial glucocorticoid deficiency].

Nihon rinsho. Japanese journal of clinical medicine - 1 Oct 1993

Takayanagi R, Sakai Y, Nawata H, Nishiyama S, Ito T, Kodama M, Matsuda I, Matsuda H

Abstract excerpt

Recent studies have revealed the presence of four subtypes for the melanocortin receptor (MC-R). Among these MC-Rs, MC2-R is considered to be an adrenocorticotropin (ACTH) receptor because its expression is almost localized in the adrenal cortex. Five Japanese patients with ACTH unresponsiveness were examined as to whether they have mutations in the putative ACTH receptor. Among these patients, there are two...

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Source

Identifiers

PMID: 8254933

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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Research trail→

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[Adrenocorticotropin receptor in familial glucocorticoid deficiency].PMID 8254933Read ↗

[ACTH receptor, ACTH receptor anomaly, and familial glucocorticoid deficiency].Semantic proximity Read ↗

[Familial glucocorticoid deficiency due to the ACTH receptor gene mutations].Semantic proximity Read ↗

[Mutations of ACTH receptor gene and familial syndrome of glucocorticoid deficiency].Semantic proximity Read ↗

The genetics of ACTH resistance syndromes.Semantic proximity Read ↗

Familial glucocorticoid deficiency: advances in the molecular understanding of ACTH action.Semantic proximity Read ↗

[Familial glucocorticoid deficiency].Semantic proximity Read ↗

Genetic heterogeneity of adrenocorticotropin (ACTH) resistance syndromes: identification of a novel mutation of the ACTH receptor gene in hereditary glucocorticoid deficiency.Semantic proximity Read ↗

Clinical, genetic, and functional characterization of adrenocorticotropin receptor mutations using a novel receptor assay.Semantic proximity Read ↗

A rare homozygous variant of MC2R gene identified in a Chinese family with familial glucocorticoid deficiency type 1: A case report.Semantic proximity Read ↗

ACTH resistance syndromes.Semantic proximity Read ↗

Molecular identification of the human melanocortin-2 receptor responsible for ligand binding and signaling.Semantic proximity Read ↗

Adrenocorticotropin receptor gene mutations in familial glucocorticoid deficiency: relationships with clinical features in four families.Semantic proximity Read ↗

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