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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
WNT10A variants in relation to nonsyndromic hypodontia in eastern Slovak population
Nonsyndromic hypodontia is a congenital absence of less than six permanent teeth, with a most common subtype maxillary lateral… 
2018
2018
Schöpf‐Schulz‐Passarge‐Syndrom assoziiert mit zwei neuen Missense‐Mutationen des WNT10A‐Gens
2016
2016
WNT10A polymorphism may be a risk factor for non-syndromic hypodontia.
This study was designed to determine whether polymorphisms in the gene wingless-type MMTV integration site family, member 10A… 
2015
2015
WNT10A coding variants and maxillary lateral incisor agenesis with associated dental anomalies.
Congenital maxillary lateral incisor agenesis (MLIA) is one of the most common subtypes of dental agenesis. Because little is… 
2013
2013
Wnt-related genes and large-joint osteoarthritis: association study and replication
Osteoarthritis (OA) has a strong genetic component, and experimental evidence suggests the involvement of the Wnt pathway in its… 
2011
2011
Two families confirm Schöpf‐Schulz‐Passarge syndrome as a discrete entity within the WNT10A phenotypic spectrum
To the Editor : Schöpf-Schulz-Passarge syndrome (SSPS; OM IM 224750) is a rare ectodermal dysplasia which combines classical… 
2010
2010
Phenotypic variability associated with WNT10A nonsense mutations
elevated (IL-17A: clopidogrel, 237Æ8 pg mL; control, not detected; and IL-17F: clopidogrel, 187Æ3 pg mL; control, not detected… 
2005
2005
Identification and characterization of rat Wnt6 and Wnt10a genes in silico.
WNT and Hedgehog signaling pathways are implicated in various types of human cancer, such as gastric and pancreatic cancer. WNT1… 
2002
2002
Expression of ST7R (ST7-like, ST7L) in normal tissues and cancer.
We have recently cloned and characterized ST7R (ST7-like, ST7L), WNT3, WNT3A, WNT5B, WNT6, WNT7B, WNT8A, WNT8B, WNT10A, WNT10B… 
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