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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

Related topics

Related topics

10 relations
Cell Differentiation processCell Fate ControlGlycoproteinsIntercellular Communication Process

Broader (1)

Wnt Proteins

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Hypermethylated WNT10A and its clinical significance in colorectal cancer.
Colorectal cancer (CRC) is a heterogeneous disease in which unique subtypes are characterized by distinct genetic and epigenetic… 
2017
2017
University of Groningen Mutations in WNT 10 A are present in more than half of isolated hypodontia cases
Background Dental agenesis is the most common, often heritable, developmental anomaly in humans. Mutations in MSX1, PAX9, AXIN2… 
2017
2017
Expression of WNT 10 A Gene in Oral Squamous Cell Carcinoma
Objective: Oral squamous cell carcinoma (OSCC) constitutes the most frequent malignant tumour of the oral cavity. Considering the… 
2016
2016
WNT10A and Odonto-Onycho-Dermal Dysplasia
2016
2016
Uticaj mutacija RUNX2 I WNT10A gena na broj i veličinu zuba
Review
2014
Review
2014
Exclusion of PAX 9 and MSX 1 mutation in six families affected by tooth agenesis . A genetic study and literature review
Objectives: In the present study, it is described the phenotypical analysis and the mutational screening, for genes PAX9 and MSX1… 
2010
2010
Mutations in WNT10A lead to the odonto-onycho-dermal dysplasia syndrome - the first Australian case