Wnt/β-Catenin Signaling: Components, Mechanisms, and Diseases
Author:
Publisher
Elsevier BV
Subject
Developmental Biology,Cell Biology,General Biochemistry, Genetics and Molecular Biology,Molecular Biology
Reference210 articles.
1. Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia;Adaimy;Am. J. Hum. Genet.,2007
2. Reduced affinity to and inhibition by DKK1 form a common mechanism by which high bone mass-associated missense mutations in LRP5 affect canonical Wnt signaling;Ai;Mol. Cell. Biol.,2005
3. The KLHL12-Cullin-3 ubiquitin ligase negatively regulates the Wnt-beta-catenin pathway by targeting Dishevelled for degradation;Angers;Nat. Cell Biol.,2006
4. Diversity of LEF/TCF action in development and disease;Arce;Oncogene,2006
5. A unique DNA binding domain converts T-cell factors into strong Wnt effectors;Atcha;Mol. Cell. Biol.,2007
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