MFH1 | definition of MFH1 by Medical dictionary
FOXC2 (redirected from MFH1)
FOXC2 A gene on chromosome 16q24.1 that encodes a member of the forkhead family of transcription factors, which plays a role in development of mesenchymal tissues.
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References in periodicals archive
Noda, "Bone morphogenetic protein regulation of forkhead/winged helix transcription factor Foxc2 (Mfh1
) in a murine mesodermal cell line C1 and in skeletal precursor cells," Journal of Bone and Mineral Research, vol.
NC: control group A (distilled water only); UHG: spiking group (8 g/L [Fe.sub.2][O.sub.3], no radiation); MFH4: MHF group with 8 g/L [Fe.sub.2][O.sub.3]; mFh3: MHF group with 6 g/L [Fe.sub.2][O.sub.3]; PC: control group B (MCF-7 cell group only); MFH2: MHF group with 4 g/L [Fe.sub.2][O.sub.3]; MFH1
: MHF group with 2 g/L [Fe.sub.2][O.sub.3].