Associated Papers
Mutational scanning reveals substrate-assisted autoregulation of the WNT destruction complex.
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Biorxiv : the Preprint Server for Biology, 2025
41278994 (PubMed )
Supplement: media-1.xlsx › WNT_DC_CBE_Screen
Genotypic, functional, and phenotypic characterization in CTNNB1 neurodevelopmental syndrome.
Žakelj N et al.
Hgg Advances, 2025
40684264 (PubMed )
Supplement: mmc3.xlsx › Case_Variants
Clinical phenotypic spectrum of CTNNB1 neurodevelopmental disorder.
Sudnawa KK et al.
Clinical Genetics, 2024
Somatic mutations in CDH1 and CTNNB1 in primary carcinomas at 13 anatomic sites.
Busch EL et al.
Oncotarget, 2017
29156750 (PubMed )
Supplement: oncotarget-08-85680-s002.xlsx › CTNNB1
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