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Article

Point Mutation of the RetProto-oncogene in the TT Human Medullary Thyroid Carcinoma Cell Line

1 Feb 1995

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Share to Thyroid Cancer Diagnosis and Treatment

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 7864888
DOI: 10.1006/bbrc.1995.1287

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Point Mutation of the RetProto-oncogene in the TT Human Medullary Thyroid Carcinoma Cell LinePMID 7864888Read ↗

The RET proto-oncogene in medullary and papillary thyroid carcinoma. Molecular features, pathophysiology and clinical implications.Semantic proximity Read ↗

Mutational analysis of the RET proto-oncogene in 71 Japanese patients with medullary thyroid carcinomaSemantic proximity Read ↗

Molecular defects in thyroid carcinomas: role of the RET oncogene in thyroid neoplastic transformation.Semantic proximity Read ↗

Deletion-insertion mutation encompassing RET codon 634 is associated with medullary thyroid carcinoma.Semantic proximity Read ↗

A Mutation in the RET Protooncogene Associated with Multiple Endocrine Neoplasia Type 2B and Sporadic Medullary Thyroid CarcinomaSemantic proximity Read ↗

Mutation analysis of the RET proto-oncogene and early thyroidectomy: results of a Portuguese cancer centreSemantic proximity Read ↗

A New Hot Spot for Mutations in the ret Protooncogene Causing Familial Medullary Thyroid Carcinoma and Multiple Endocrine Neoplasia Type 2ASemantic proximity Read ↗

Germline polymorphisms on RET proto-oncogene involved in medullary thyroid carcinoma in a Druze family.Semantic proximity Read ↗

Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's diseaseSemantic proximity Read ↗

Analysis of Newly Identified and Rare Synonymous Genetic Variants in the RET Gene in Patients with Medullary Thyroid Carcinoma in Polish Population.Semantic proximity Read ↗

Malignant progression from C-cell hyperplasia to medullary thyroid carcinoma in 167 carriers of RET germline mutationsSemantic proximity Read ↗

A rare variant, I852M, of the RET proto-oncogene in a patient with medullary thyroid carcinoma at age 20 years.Semantic proximity Read ↗

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