Genotype K14-Cre;Tgfbr2fl/fl Symbol (MGI) Tgfbr2tm1.2Hlm Known defects Submucosal cleft palate Known human diseases Histology P0 SEM P0 μCT P0: soft – hard 3D μCT P0: soft – hard μMRI P0: soft Gene expression analysis Protein expression analysis References Iwata J. et al., Development 2013…Continue Reading Craniofacial phenotype analysis: K14-Cre;Tgfbr2fl/fl
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Craniofacial phenotype analysis: Wnt1-Cre;Tgfbr2fl/fl
Genotype Wnt1-Cre;Tgfbr2fl/fl Symbol (MGI) Tgfbr2tm1.2Hlm Known defects Cleft palate, bone defects, small tongue Known human diseases Loeys-Dietz Syndrome Histology E18.5 SEM E18.5 μCT E18.5: soft – hard 3D μCT E18.5: soft – hard μMRI E18.5: soft Gene expression analysis E14.5 Protein expression analysis References Ito Y et al., Development 2003Sasaki T et al., Development 2006Oka K et al., Dev Biol…Continue Reading Craniofacial phenotype analysis: Wnt1-Cre;Tgfbr2fl/fl
Class III cleft palate
Class III: Palatal shelves fail to meet at the midline Complete cleft of secondary palate Ctgf-/- K14-Cre;Shhfl/fl Wnt1-Cre;Alk5fl/fl Wnt1-Cre;Tgfbr2fl/fl Partial cleft of secondary palate: anterior K14-Cre;Alk5fl/fl K14-Cre;Tgfbr2fl/fl Shox2-/- Wnt1-Cre;Shox2fl/fl Partial cleft of secondary palate: posterior / cleft soft palate K14-Cre;Alk5fl/fl K14-Cre;Tgfbr2fl/fl Tbx1-/-…Continue Reading Class III cleft palate