Associated Papers
Shared and divergent contribution of vitamin A and oxytocin to the aetiology of autism spectrum disorder.
Wang T et al.
Computational and Structural Biotechnology Journal, 2023
38213898 (PubMed )
Supplement: mmc2.xlsx › RIVs_in_VARGs
A Novel Homozygous Nonsense Mutation p.Cys366* in the WNT10B Gene Underlying Split-Hand/Split Foot Malformation in a Consanguineous Pakistani Family.
Khan A et al.
Frontiers in Pediatrics, 2019
An association study between USP34 and polycystic ovary syndrome.
Zhao S et al.
Journal of Ovarian Research, 2015
Disulfide bond requirements for active Wnt ligands.
MacDonald BT et al.
The Journal of Biological Chemistry, 2014
Mutation analysis of WNT10B in obese children, adolescents and adults.
Van Camp JK et al.
Endocrine, 2013
Genetic association between WNT10B polymorphisms and obesity in a Belgian case-control population is restricted to males.
Van Camp JK et al.
Molecular Genetics and Metabolism, 2012
A functional promoter polymorphism -607G>C of WNT10B is associated with abdominal fat in Korean female subjects.
Kim IC et al.
The Journal of Nutritional Biochemistry, 2011
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