RUNX1:CBFB:MYL9 gene [nucleoplasm]

Stable Identifier
R-HSA-8938205
Type
Complex
Species
Homo sapiens
Compartment
Locations in the PathwayBrowser
Literature References
PubMed ID Title Journal Year
20876458 Regulation of platelet myosin light chain (MYL9) by RUNX1: implications for thrombocytopenia and platelet dysfunction in RUNX1 haplodeficiency

Jalagadugula, G, Mao, G, Kaur, G, Goldfinger, LE, Dhanasekaran, DN, Rao, AK

Blood 2010
Participants
Participant Of
This entity regulates
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