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MSX1 protein, human

Known as: HOX7, msh homeo box homolog 1 (Drosophila) protein, human, MSH Homeo Box Homolog 1 
Homeobox protein MSX-1 (297 aa, ~31 kDa) is encoded by the human MSX1 gene. This protein plays a role in transcriptional modulation and odontogenesis… 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
2006
Highly Cited
2006
Can kindreds with tooth agenesis caused by MSX1 or PAX9 mutations be distinguished by their phenotypes? We have identified an… 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
2002
Highly Cited
2002
Cleft palate, the most frequent congenital craniofacial birth defects in humans, arises from genetic or environmental… Expand
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Highly Cited
2001
Highly Cited
2001
Witkop syndrome, also known as tooth and nail syndrome (TNS), is a rare autosomal dominant disorder. Affected individuals have… Expand
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Highly Cited
2000
Highly Cited
2000
The process of cellular differentiation culminating in terminally differentiated mammalian cells is thought to be irreversible… Expand
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Highly Cited
1997
Highly Cited
1997
Epidermal fate in Xenopus ectoderm has been shown to be induced by a secreted growth factor, Bone Morphogenetic Protein 4 (BMP4… Expand
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Highly Cited
1996
Highly Cited
1996
Members of the Msx homeobox family are thought to play important roles in inductive tissue interactions during vertebrate… Expand
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Highly Cited
1994
Highly Cited
1994
The Msx1 homeobox gene is expressed at diverse sites of epithelial–mesenchymal interaction during vertebrate embryogenesis, and… Expand
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