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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… 
National Institutes of Health

Papers overview

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Highly Cited
2017
Highly Cited
2017
Human WNT10A mutations are associated with developmental tooth abnormalities and adolescent onset of a broad range of ectodermal… 
Highly Cited
2012
Highly Cited
2012
Background Dental agenesis is the most common, often heritable, developmental anomaly in humans. Mutations in MSX1, PAX9, AXIN2… 
Highly Cited
2012
Highly Cited
2012
Renal cell carcinoma (RCC) is a malignancy with poor prognosis. WNT/β-catenin signaling dysregulation, especially β-catenin… 
Highly Cited
2011
Highly Cited
2011
Hypohidrotic and anhidrotic ectodermal dysplasia (HED/EDA) is a rare genodermatosis characterized by abnormal development of… 
Highly Cited
2011
Highly Cited
2011
WNT10A has been associated with various syndromes with ectodermal dysplasia from severe autosomal recessive SchÖpf–Schulz… 
Highly Cited
2009
Highly Cited
2009
Wnt signalling is one of a few pathways that are crucial for controlling genetic programs during embryonic development as well as… 
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… 
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…