| [Association between RET proto-oncogene polymorphisms and Hirschsprung disease in Chinese Han population of Hubei district]. | None |
| [Characterization of RET proto-oncogene C634Y mutation in a Moroccan family with multiple endocrine neoplasia type 2A]. | None |
| Double germline mutations in the RET Proto-oncogene in MEN 2A and MEN 2B kindreds. | None |
| strong propensity to self-association in the RET-transmembrane underlies - and may be required for - dimer formation and oncogenic activation of juxtamembrane cysteine mutants of RET | None |
| The identification of ganglion cells in Hirschsprung disease by the immunohistochemical detection of ret oncoprotein. | None |
| Some patients with apparently sporadic pheochromacytoma were carrier of mutations in RET proto-oncogene. | None |
| Isolated intestinal ganglioneuromatosis with a new mutation of RET proto-oncogene. | None |
| An STS in the human PTC oncogene located at 10q11.2. | None |
| Tight linkage of the ret proto-oncogene with the multiple endocrine neoplasia type 2A locus. | None |
| A rare extracellular D631Y germline mutation of the RET proto-oncogene in two Korean families with multiple endocrine neoplasia 2A. | None |
| Video-assisted central compartment lymphadenectomy in a patient with a positive RET oncogene: initial experience. | None |
| Allele dosage-dependent penetrance of RET proto-oncogene in an Israeli-Arab inbred family segregating Hirschsprung disease. | None |
| The identification of ganglion cells in Hirschsprung disease by the immunohistochemical detection of ret oncoprotein. | None |
| RET proto-oncogene in Sardinia: V804M is the most frequent mutation and may be associated with FMTC/MEN-2A phenotype. | None |
| C620R mutation of the murine ret proto-oncogene: loss of function effect in homozygotes and possible gain of function effect in heterozygotes. | None |
| RET proto-oncogene mutations are restricted to codons 634 and 918 in mainland Chinese families with MEN2A and MEN2B. | None |
| RET proto-oncogene mutations were restricted to codon 634 and 918 in Chinese families with MEN2A and MEN2B. | None |
| A heterozygous M918T mutation of the RET proto-oncogene was found in MEN 2B patients. | None |
| Orolabial signs are important clues for diagnosis of the rare endocrine syndrome MEN 2B. Presentation of two unrelated cases. | None |
| oncogenic precursor of RET(MEN 2B) is phosphorylated, interacts with adapter proteins and induces downstream signalling from the ER. | None |