Skip to search formSkip to main contentSkip to account menu

WNT10A gene

Known as: WINGLESS-TYPE MMTV INTEGRATION SITE FAMILY, MEMBER 10A, Wnt family member 10A, Wingless-Type MMTV Integration Site Family, Member 10A Gene 
This gene plays a role in signal transduction and intercellular communication. It is involved in the regulation of cell fate and pattern formation… 
National Institutes of Health

Related topics

Related topics

8 relations
Cell Differentiation processCell Fate ControlCervix carcinomaIntercellular Communication Process

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… 
2018
2018
Identification of the rs121908120 polymorphism of the WNT10A gene as a risk factor for developing Keratoconus in a Mexican population sample
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… 
2015
2015
WNT 3 involvement in human bladder exstrophy and cloaca development in zebra fi sh
Bladder exstrophy, a severe congenital urological malformation when a child is born with an open urinary bladder, is the most… 
2014
2014
Role of DNA Methylation in Adipogenesis
The increase in the prevalence of obesity and obesity-related diseases has caused greater attention to be placed on the molecular… 
2014
2014
[WNT 10A-mutations as explanation for tooth agenesis].
In the literature many different mutations of the WNT10A-gene have been described in relation to the prevalence of tooth agenesis…