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HIF-2α-pVHL complex reveals broad genotype-phenotype correlations in HIF-2α-driven disease

It is definitively established that mutations in transcription factor HIF-2α are causative of both neuroendocrine tumors (class 1 disease) and polycythemia (class 2 disease). However, the molecular mechanism that underlies this emergent genotype–phenotype relationship has remained unclear. Here, we...

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Detalles Bibliográficos
Autores principales: Tarade, Daniel, Robinson, Claire M., Lee, Jeffrey E., Ohh, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6105673/
https://www.ncbi.nlm.nih.gov/pubmed/30135421
http://dx.doi.org/10.1038/s41467-018-05554-1