MSX1, Hypodontia, Orofacial Clefting, and the Witkop Syndrome
Msx1 and Msx2 are functional interacting partners of T-box factors in the regulation of Connexin43
MSX1 and TGF-β3 are novel target genes functionally regulated by FOXE1
YY1 activates Msx2 gene independent of bone morphogenetic protein signaling
Expression and regulation of the Msx1 natural antisense transcript during development
A novel non-stop mutation in MSX1 causing autosomal dominant non-syndromic oligodontia
Molecular Evolution of the Primate Developmental Genes MSX1 and PAX9
Conserved Cis-Regulatory Modules Control Robustness in Msx1 Expression at Single-Cell Resolution
Influence of promoter potency on the transcriptional effects of YY1, SRF and Msx-1 in transient transfection analysis
Mutational analysis of MSX1 and PAX9 genes in Portuguese families with maxillary lateral incisor agenesis
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a homeobox protein.
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