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RET wt Allele

Known as: CDHF12, RET, Gene Rearranged During Transfection 
Human RET wild-type allele is located in the vicinity of 10q11.2 and is approximately 53 kb in length. This allele, which encodes proto-oncogene… Expand
National Institutes of Health

Papers overview

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2010
2010
The receptor tyrosine kinase ret protooncogene (RET) is implicated in the pathogenesis of several diseases and in several… Expand
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2009
2009
CONTEXT RET is a tyrosine kinase transmembrane receptor expressed in two main alternative isoforms: RET9 and RET51. RET… Expand
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Highly Cited
2006
Highly Cited
2006
Molecular mechanisms that lead to congenital anomalies of kidneys and the lower urinary tract (CAKUT) are poorly understood. To… Expand
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Highly Cited
2005
Highly Cited
2005
ABSTRACT The receptor tyrosine kinase Ret plays a critical role in the development of the mammalian excretory and enteric nervous… Expand
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Highly Cited
2005
Highly Cited
2005
Alternative splicing of transcripts encoding the RET kinase receptor leads to isoforms differing in their cytoplasmic tail… Expand
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Highly Cited
2002
Highly Cited
2002
Ret, the receptor tyrosine kinase for the glial cell line-derived neurotrophic factor family ligands (GFLs), is alternatively… Expand
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Highly Cited
2001
Highly Cited
2001
The RET receptor tyrosine kinase has a critical role in kidney organogenesis and the development of the enteric nervous system… Expand
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Highly Cited
2001
Highly Cited
2001
Gain-of-function mutations in the gene encoding the receptor tyrosine kinase RET have been identified as the aetiological factor… Expand
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Highly Cited
1998
Highly Cited
1998
Hirschsprung's disease (HSCR) is a common congenital malformation characterized by the absence of intramural ganglion cells of… Expand
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1998
1998
The mature mammalian kidney arises through a series of reciprocal inductive interactions between two different cell groups, the… Expand
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