Vascular tumors in livers with targeted inactivation of the von Hippel–Lindau tumor suppressor
von Hippel–Lindau (VHL) disease is a pleomorphic familial tumor syndrome that is characterized by the development of highly vascularized tumors. Homozygous disruption of the VHL gene in mice results in embryonic lethality. To investigate VHL function in the adult we have generated a conditional VHL...
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| Vydáno v: | Proc Natl Acad Sci U S A |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
National Academy of Sciences
2001
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC29300/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/11171994/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.98.4.1583 |
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