Mechanism of Activation of the ret Proto-oncogene by Multiple Endocrine Neoplasia 2A Mutations
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References (29)
Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A
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Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret
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Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC
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A point mutation in the extracellular domain of the human CSF-1 receptor (c-fms proto-oncogene product) activates its transforming potential
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The ret proto-oncogene is consistently expressed in human pheochromocytomas and thyroid medullary carcinomas.
1990 • 233 citations
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1994 • 119 citations
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1990 • 93 citations
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1993 • 88 citations
Human trk Oncogenes Activated by Point Mutation, In-Frame Deletion, and Duplication of the Tyrosine Kinase Domain
1990 • 73 citations
The human protooncogene ret: a communicative cadherin?
1992 • 62 citations
Motifs of cadherin- and fibronectin type III-related sequences and evolution of the receptor-type-protein tyrosine kinases: sequence similarity between proto-oncogene ret and cadherin family.
1993 • 36 citations
Germ Line Mutations of the ret Proto‐oncogene in Japanese Patients with Multiple Endocrine Neoplasia Type 2A and Type 2B
1994 • 11 citations
Specific expression of the ret proto-oncogene in human neuroblastoma cell lines
1994 • 6 citations
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