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pro vyhledávání: '"Sabrina Brunk"'
Autor:
Sven Geissler, Martin Textor, Sabine Stumpp, Sebastian Seitz, Anja Lekaj, Sabrina Brunk, Sabine Klaassen, Thorsten Schinke, Christoph Klein, Stefan Mundlos, Uwe Kornak, Jirko Kühnisch
Publikováno v:
PLoS ONE, Vol 13, Iss 6, p e0198510 (2018)
Gfi1 is a key molecule in hematopoietic lineage development and mutations in GFI1 cause severe congenital neutropenia (SCN). Neutropenia is associated with low bone mass, but the underlying mechanisms are poorly characterized. Using Gfi1 knock-out mi
Externí odkaz:
https://doaj.org/article/264bdb4617e641ed968c635764215b6f