Multiple endocrine neoplasia type 2 and the RET protooncogene: From bedside to bench to bedside

Author:

Machens Andreas,Dralle Henning

Publisher

Elsevier BV

Subject

Endocrinology,Molecular Biology,Biochemistry

Reference58 articles.

1. Multiple endocrine neoplasia type 2B mutation in human RET oncogene induces medullary thyroid carcinoma in transgenic mice;Acton;Oncogene,2000

2. A RET double mutation in the germline of a kindred with FMTC;Bartsch;Exp. Clin. Endocrinol. Diabetes,2000

3. Sporadic and familial pheochromocytomas are associated with loss of at least two discrete intervals on chromosome 1p;Benn;Cancer Res.,2000

4. A new hot spot for mutations in the ret protooncogene causing familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2A;Berndt;J. Clin. Endocrinol. Metab.,1998

5. RET mutations in exons 13 and 14 of FMTC patients;Bolino;Oncogene,1995

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