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Reagents, Molecular Assay, Gene Anomaly, Mutation, RET

Definition : Molecular assay reagents intended to identify mutations in the rearranged during transfection (RET) gene, located at chromosome 10q11.2, which encodes for a receptor tyrosine kinase that transduces signals for cell growth and differentiation. It is essential for the development of several kinds of nerve cells, kidney development, and sperm production. These genetic mutations have been identified in patients with several diseases, including multiple endocrine neoplasia type 2 (MEN2), both type II A (MEN 2A, Sipple's syndrome) and type II B (MEN 2B), and Hirschsprung's disease1.

Entry Terms : "Multiple Endocrine Neoplasia Gene Mutation Reagents" , "Multiple Endocrine Neoplasia Type IIA (MEN 2A) Gene Mutation Reagents" , "MEM2 Syndrome Gene Mutation Reagents" , "Multiple Endocrine Neoplasia Type II (MEM2) Gene Mutation Reagents" , "Familial Medullary thyroid Carcinoma (FMTC) Gene Mutation Reagents" , "Medullary Thyroid Carcinoma Gene Mutation Reagents" , "Aganglionic Megacolon Gene Mutation Reagents" , "Congenital Intestinal Aganglionosis Gene Mutation Reagents" , "Hirschspring Disease (HSCR) Gene Mutation Reagents" , "Reagents, Molecular Assay, Tumor Markers, Gene Mutation, ret" , "Hirschsprung Disease Gene Mutation Reagents" , "Sipple Disease Gene Mutation Reagents" , "Multiple Endocrine Neoplasia Type 2 (MEN2) Gene Mutation Reagents" , "RET Gene Mutation Detection Reagents" , "Reagents, Molecular Assay, Tumor Marker, Gene Mutation, ret" , "ret Gene Mutation Determination Reagents" , "Multiple Endocrine Neoplasia Determination Reagents"

UMDC code : 19622

   

1-1 of 1 Match(es).

Roche Diagnostics Corp

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1-1 of 1 Match(es).

 

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