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Article

Absence of mutations at codon 768 of the RET proto-oncogene in sporadic and hereditary pheochromocytomas.

Endocrine journal - 1 Feb 1996

Yoshimoto K, Kimura T, Tanaka C, Moritani M, Iwahana H, Itakura M

Abstract excerpt

Sixteen sporadic pheochromocytomas, 3 pheochromocytomas in neurofibromatosis 1, and 4 pheochromocytomas in multiple endocrine neoplasia (MEN) 2A or 2B were screened for mutations at codon 768 of the RET proto-oncogene by AluI digestion of polymerase chain reaction PCR products and mutations in exon 13 by PCR-single strand conformation polymorphism (SSCP) analysis. Although mutations at codon 768 (GAG --> GAC; Glu...

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Identifiers

PMID: 8732460
DOI: 10.1507/endocrj.43.109

Genes

RET

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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.

Related research

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Absence of mutations at codon 768 of the RET proto-oncogene in sporadic and hereditary pheochromocytomas.PMID 8732460Read ↗

Tumor-specific mutations in the tyrosine kinase domain of the RET proto-oncogene in pheochromocytomas of sporadic type.Semantic proximity Read ↗

A single missense mutation in codon 918 of the RET proto-oncogene in sporadic medullary thyroid carcinomas.Semantic proximity Read ↗

Somatic mutations in the RET protooncogene in Japanese and Chinese sporadic medullary thyroid carcinomas.Semantic proximity Read ↗

Mutations in the cysteine-rich region of the RET proto-oncogene in patients diagnosed as having sporadic medullary thyroid carcinoma.Semantic proximity Read ↗

Mutations in the RET protooncogene in sporadic pheochromocytomas.Semantic proximity Read ↗

Infrequent detectable somatic mutations of the RET and glial cell line-derived neurotrophic factor (GDNF) genes in human pituitary adenomas.Semantic proximity Read ↗

Frequent RET protooncogene mutations in multiple endocrine neoplasia type 2A.Semantic proximity Read ↗

Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours.Semantic proximity Read ↗

RET protooncogene mutations in patients with apparently sporadic medullary thyroid carcinoma.Semantic proximity Read ↗

No correlation between RET immunostaining and the codon 918 mutation in sporadic medullary thyroid carcinoma.Semantic proximity Read ↗

Mutation of RET codon 768 is associated with the FMTC phenotype.Semantic proximity Read ↗

Genetic alterations of the RET proto-oncogene in familial and sporadic pheochromocytomas.Semantic proximity Read ↗

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