Identification of CTNNB1 mutations, CTNNB1 amplifications, and an Axin2 splice variant in juvenile angiofibromas.
Wemmert, Silke; Willnecker, Vivienne; Kulas, Philipp; Weber, Stefanie; Lerner, Cornelia; Berndt, Sabrina; Wendler, Olaf; Schick, Bernhard.
; 37(4): 5539-49, 2016 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-26572152
Determination of Rate-Limiting Factor for Formation of Beta-Catenin Destruction Complexes Using Absolute Protein Quantification.
Functional analysis of a novel missense mutation in AXIN2 associated with non-syndromic tooth agenesis.
The SIAH E3 ubiquitin ligases promote Wnt/ß-catenin signaling through mediating Wnt-induced Axin degradation.
[Advance in research on the correlation between genotypes of susceptible mutations and clinical phenotype of familial adenomatous polyposis].
Dysregulation of the Wnt pathway in adult eosinophilic esophagitis.
Reversible modification of adenomatous polyposis coli (APC) with K63-linked polyubiquitin regulates the assembly and activity of the ß-catenin destruction complex.
Gtpbp2 is a positive regulator of Wnt signaling and maintains low levels of the Wnt negative regulator Axin.
Mutations in AXIN2 gene as a risk factor for tooth agenesis and cancer: A review.
GSK3ß/axin-1/ß-catenin complex is involved in semaphorin3A signaling.
CDK5 activator protein p25 preferentially binds and activates GSK3ß.