Holoprosencephaly phenotypes in LRP2 deficient mouse models are strongly modified by genetic background
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DOI: 10.1016/j.mod.2017.04.289
Abstract: spite of sequence divergence. We are currently identifying functional transcription factor binding sites in endodermal enhancers in both species to identify conserved upstream regulators shared between Phallusia and Ciona. Taken together our results suggest that… read more here.
Keywords: mouse models; lrp2 deficient; deficient mouse; holoprosencephaly phenotypes ... See more keywords