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WNT10A protein, human

Known as: WNT-10A Protein, WNT10A Protein, wingless-type MMTV integration site family, member 10A protein, human 
Encoded by human WNT10A Gene (WNT Family), 417-amino acid 46 kD (precursor) WNT10A Protein is a putative ligand for a member(s) of the frizzled… Expand
National Institutes of Health

Papers overview

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2015
2015
WNT10A is a signaling molecule involved in tooth development, and WNT10A defects are associated with tooth agenesis. We… Expand
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Highly Cited
2012
Highly Cited
2012
Wnt10b is an established regulator of mesenchymal stem cell (MSC) fate that inhibits adipogenesis and stimulates… Expand
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Highly Cited
2012
Highly Cited
2012
BACKGROUND Dental agenesis is the most common, often heritable, developmental anomaly in humans. Mutations in MSX1, PAX9, AXIN2… Expand
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2012
2012
Renal cell carcinoma (RCC) is a malignancy with poor prognosis. WNT/β-catenin signaling dysregulation, especially β-catenin… Expand
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Highly Cited
2011
Highly Cited
2011
Hypohidrotic and anhidrotic ectodermal dysplasia (HED/EDA) is a rare genodermatosis characterized by abnormal development of… Expand
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Highly Cited
2011
Highly Cited
2011
WNT10A has been associated with various syndromes with ectodermal dysplasia from severe autosomal recessive SchO?pf-Schulz… Expand
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Highly Cited
2009
Highly Cited
2009
Odonto-onycho-dermal dysplasia (OODD), a rare autosomal-recessive inherited form of ectodermal dysplasia including severe… Expand
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2009
2009
Wnt signalling is one of a few pathways that are crucial for controlling genetic programs during embryonic development as well as… Expand
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Highly Cited
2007
Highly Cited
2007
Odonto-onycho-dermal dysplasia is a rare autosomal recessive syndrome in which the presenting phenotype is dry hair, severe… Expand
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Highly Cited
2007
Highly Cited
2007
We have explored the role of Wnt signaling in dentinogenesis of mouse molar teeth. We found that Wnt10a was specifically… Expand
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