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The RET proto-oncogene induces apoptosis: a novel mechanism for Hirschsprung disease
The RET (rearranged during transfection) proto-oncogene encodes a tyrosine kinase receptor involved in both multiple endocrine neoplasia type 2 (MEN 2), an inherited cancer syndrome, and Hirschsprung disease (HSCR), a developmental defect of enteric neurons. We report here that the expression of RET...
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| Autors principals: | , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2000
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC306592/ https://ncbi.nlm.nih.gov/pubmed/10921886 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/emboj/19.15.4056 |
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