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MSX1 wt Allele

Known as: HOX7, MSH Homeo Box Homolog 1 (Drosophila) wt Allele, MSX1 
Human MSX1 wild-type allele is located within 4p16.3-16.1 and is approximately 4 kb in length. This allele, which encodes homeobox protein MSX-1, is… Expand
National Institutes of Health

Papers overview

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Highly Cited
2010
Highly Cited
2010
Developmental abnormalities of craniofacial structures and teeth often occur sporadically and the underlying genetic defects are… Expand
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Highly Cited
2009
Highly Cited
2009
The ablation of Apc function or the constitutive activation ofβ -catenin in embryonic mouse oral epithelium results in… Expand
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Highly Cited
2009
Highly Cited
2009
Mammals have single-rowed dentitions, whereas many nonmammalian vertebrates have teeth in multiple rows. Neither the molecular… Expand
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Highly Cited
2005
Highly Cited
2005
FGF, WNT, and BMP signaling promote neural crest formation at the neural plate boundary in vertebrate embryos. To understand how… Expand
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Highly Cited
2003
Highly Cited
2003
There is evidence in Xenopus and zebrafish embryos that the neural crest/neural folds are specified at the border of the neural… Expand
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Highly Cited
2003
Highly Cited
2003
MSX1 and TGFB3 have been proposed as genes in which mutations may contribute to non-syndromic forms of oral clefts; however, an… Expand
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Highly Cited
2002
Highly Cited
2002
MSX1 has a critical role in craniofacial development, as indicated by expression assays and transgenic mouse phenotypes… Expand
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Highly Cited
2001
Highly Cited
2001
Mice deficient for FgfR2-IIIb were generated by placing translational stop codons and an IRES-LacZ cassette into exon IIIb of… Expand
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Highly Cited
2000
Highly Cited
2000
The development of many organs depends on sequential epithelial-mesenchymal interactions, and the developing tooth germ provides… Expand
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Highly Cited
1995
Highly Cited
1995
We report that during mouse fetal development transcripts of Msx1 and Msx2 become progressively restricted to cells that will… Expand
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