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Oncogene, RET

Known as: MEN2B, RET, ret oncogene 
Human Oncogene RET is a mutated variant of RET Gene, which encodes Tyrosine-Protein Kinase Receptor RET, a type I membrane protein receptor for Glial… Expand
National Institutes of Health

Papers overview

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Highly Cited
2013
Highly Cited
2013
The discovery of RET fusions in lung cancers has uncovered a new therapeutic target for patients whose tumors harbor these… Expand
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Review
2009
Review
2009
The RET (rearranged during transfection) protooncogene encodes a single pass transmembrane receptor that is expressed in cells… Expand
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Highly Cited
2006
Highly Cited
2006
BACKGROUND Medullary and papillary thyroid carcinomas are often associated with oncogenic activation of the RET tyrosine kinase… Expand
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Highly Cited
2006
Highly Cited
2006
CONTEXT RET/PTC rearrangements have been reported in papillary thyroid carcinomas with variable frequency in studies that used… Expand
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Highly Cited
2000
Highly Cited
2000
The RET (rearranged during transfection) proto-oncogene encodes a tyrosine kinase receptor involved in both multiple endocrine… Expand
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Highly Cited
1997
Highly Cited
1997
In this study, we compare the morphological and genetic characteristics of 38 post-Chernobyl thyroid papillary carcinomas from… Expand
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Highly Cited
1995
Highly Cited
1995
Multiple endocrine neoplasia types 2A and 2B (MEN2A and MEN2B) and familial medullary thyroid carcinoma are dominantly inherited… Expand
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Highly Cited
1994
Highly Cited
1994
We have analysed 118 families with inherited medullary thyroid carcinoma (MTC) for mutations of the RET proto–oncogene. These… Expand
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Highly Cited
1993
Highly Cited
1993
MULTIPLE endocrine neoplasia type 2A (MEN 2A) is a dominantly inherited cancer syndrome that affects tissues derived from neural… Expand
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Highly Cited
1993
Highly Cited
1993
Multiple endocrine neoplasia type 2A (MEN 2A) and familial medullary thyroid carcinoma (FMTC) are dominantly inherited conditions… Expand
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