Structured Summary
Abstract
Receptor protein-tyrosine kinases involved in the signaling of GLIAL CELL-LINE DERIVED NEUROTROPHIC FACTOR ligands. They contain an extracellular cadherin domain and form a receptor complexes with GDNF RECEPTORS. Mutations in ret protein are responsible for HIRSCHSPRUNG DISEASE and MULTIPLE ENDOCRINE NEOPLASIA TYPE 2.
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Synonyms
13 entry terms
- Proto-Oncogene Protein Ret
- Proto-Oncogene Protein c-ret
- Receptor Tyrosine Kinase RET
- c-ret Protein
- ret Proto-Oncogene Proteins
- Proto Oncogene Protein Ret
- Proto Oncogene Protein c ret
- Proto Oncogene Proteins c ret
- Proto-Oncogene Proteins, ret
- Ret, Proto-Oncogene Protein
- c-ret, Proto-Oncogene Protein
- c-ret, Proto-Oncogene Proteins
- ret Proto Oncogene Proteins
MeSH Record
Aspects Covered
30 allowable subheadings
Indexed with the subheadings administration & dosage, adverse effects, agonists, analysis, antagonists & inhibitors, biosynthesis, blood, cerebrospinal fluid, chemical synthesis, chemistry, classification, deficiency, drug effects, economics, genetics, history, immunology, isolation & purification, metabolism, pharmacokinetics, pharmacology, physiology, poisoning, radiation effects, standards, supply & distribution, therapeutic use, toxicity, ultrastructure, urine.
MeSH Record
History Note
2006(1999)
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AMA Style
References
- National Library of Medicine. Proto-Oncogene Proteins c-ret. Medical Subject Headings (MeSH). 2026. Unique ID D051096. http://id.nlm.nih.gov/mesh/2026/D051096
- Proto-Oncogene Proteins c-ret. In: Wikipedia. https://en.wikipedia.org/wiki/RET_proto-oncogene
- Proto-Oncogene Proteins c-ret. In: Wikidata. https://www.wikidata.org/wiki/Q415976