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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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Bibliografiset tiedot
Julkaisussa:Proc Natl Acad Sci U S A
Päätekijät: Haase, Volker H., Glickman, Jonathan N., Socolovsky, Merav, Jaenisch, Rudolf
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: National Academy of Sciences 2001
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Linkit: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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