| 27-bp deletion in the ret proto-oncogene as a somatic mutation associated with medullary thyroid carcinoma. | thyroid, |
| Germline and somatic mutations of the RET proto-oncogene in apparently sporadic medullary thyroid carcinomas. | thyroid, |
| Mutational analysis of the RET proto-oncogene in 71 Japanese patients with medullary thyroid carcinoma. | thyroid, |
| Novel point mutation in exon 10 of the RET proto-oncogene in a family with medullary thyroid carcinoma. | thyroid, |
| Analysis of RET proto-oncogene abnormalities in patients with MEN 2A, MEN 2B, familial or sporadic medullary thyroid carcinoma. | thyroid, |
| Alterations of RET oncogene in human adrenal tumors. | kidney, |
| Multiple endocrine neoplasia type 2-associated RET proto-oncogene mutations do not contribute to the pathogenesis of sporadic parathyroid tumors. | thyroid, |
| [A new inherited RET proto-oncogene mutation associated with familial medullary thyroid carcinoma and polymorphisms in adjacent regions]. | thyroid, |
| Papillary thyroid carcinoma oncogene (RET/PTC) alters the nuclear envelope and chromatin structure. | thyroid, |
| The RET/PTC3 oncogene: metastatic solid-type papillary carcinomas in murine thyroids. | thyroid, |
| Mutation of the RET proto-oncogene is correlated with RET immunostaining in subpopulations of cells in sporadic medullary thyroid carcinoma. | thyroid, |
| RET proto-oncogene: role in kidney development and molecular pathology. | kidney, |
| Two germline missense mutations at codons 804 and 806 of the RET proto-oncogene in the same allele in a patient with multiple endocrine neoplasia type 2B without codon 918 mutation. | None |
| FISH mapping of the mouse Ret oncogene to the junction of G-bands E3/F1 on chromosome 6 indicates a need for reassessment of the physical and consensus maps. | None |
| RET proto-oncogene in the development of human cancer. | None |
| Point nucleotidic changes in both the RET proto-oncogene and the endothelin-B receptor gene in a Hirschsprung disease patient associated with Down syndrome. | None |
| Specific polymorphisms in the RET proto-oncogene are over-represented in patients with Hirschsprung disease and may represent loci modifying phenotypic expression. | None |
| Mutational analysis of the RET proto-oncogene in a kindred with multiple endocrine neoplasia type 2A and Hirschsprung s disease. | None |
| De novo RET proto-oncogene mutation in a patient with multiple endocrine neoplasia type 2B. | None |
| Expression of RET proto-oncogene and GDNF deficit in Hirschsprung s disease. | None |