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Related Articles
Diminished Ret expression compromises neuronal survival in the colon and causes intestinal aganglionosis in mice.(Research article)
May 01, 2008;
Introduction Hirschsprung disease (HSCR), or intestinal aganglionosis, is one of the most common congenital disorders affecting...
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Novel RET Mutation Produces a Truncated RET Receptor Lacking the Intracellular Signaling Domain in a 3-Generation Family with Hirschsprung Disease
Aug 01, 2005;
The RET gene encodes a transmembrane receptor tyrosine kinase, RET (1,2), which is produced by enteric nervous system progenitors...
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Activation of RET as a dominant transforming gene by germline mutations of MEN2A and MEN2B.
Jan 20, 1995;
MEN2A, MEN2B, and familial medullary thyroid carcinoma (FMTC) are dominantly inherited cancer syndromes. MEN2A is defined by the...
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Prevalence of RET/PTC expression in papillary thyroid carcinoma and its correlation with prognostic factors in a north Indian population
Jul 01, 2009;
Papillary thyroid carcinoma (PTC) is the most common malignancy affecting the thyroid gland. [1] Gene arrangements activating the...
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Mutation Scanning of the RET Protooncogene Using High-Resolution Melting Analysis
Jan 01, 2006;
Background: Single-base pair missense mutations in exons 10, 11, 13, 14, 15, and 16 of the RET protooncogene are associated with...
Read more with a free trial on HighBeam.com »
HighBeam Research, Inc. © Copyright 2009.
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