Código QR

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...

Descripción completa

Guardado en:
Detalles Bibliográficos
Publicado en:Proc Natl Acad Sci U S A
Autores principales: Haase, Volker H., Glickman, Jonathan N., Socolovsky, Merav, Jaenisch, Rudolf
Formato: Artigo
Lenguaje:Inglês
Publicado: National Academy of Sciences 2001
Materias:
Acceso en línea: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
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!