Characterization of Ret-Shc-Grb2 Complex Induced by GDNF, MEN 2A, and MEN 2B Mutations
- 1 August 1997
- journal article
- Published by Elsevier BV in Biochemical and Biophysical Research Communications
- Vol. 237 (3), 747-751
- https://doi.org/10.1006/bbrc.1997.7225
Abstract
No abstract availableKeywords
Funding Information
- Ministry of Education, Culture, Sports, Science and Technology
This publication has 19 references indexed in Scilit:
- Mechanism of ret dysfunction by Hirschsprung mutations affecting its extracellular domainHuman Molecular Genetics, 1996
- Molecular heterogeneity of RET loss of function in Hirschsprung's disease.The EMBO Journal, 1996
- RET mutations in human diseaseTrends in Genetics, 1996
- Detection of Ret Homodimers in MEN 2A-Associated PheochromocytomasBiochemical and Biophysical Research Communications, 1996
- The Men II Syndromes and the Role of the ret Proto-oncogeneAdvances in Cancer Research, 1996
- Loss of function effect of RET mutations causing Hirschsprung diseaseNature Genetics, 1995
- Mechanism of Activation of the ret Proto-oncogene by Multiple Endocrine Neoplasia 2A MutationsMolecular and Cellular Biology, 1995
- Activation of RET as a Dominant Transforming Gene by Germline Mutations of MEN2A and MEN2BScience, 1995
- Oncogenic Activation of the ret Protooncogene in Thyroid CancerCritical Reviews™ in Oncogenesis, 1995
- Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor RetNature, 1994