Associated Papers
Mutational scanning reveals substrate-assisted autoregulation of the WNT destruction complex.
Padmanarayana M et al.
Biorxiv : the Preprint Server for Biology, 2025
41278994 (PubMed )
Supplement: media-1.xlsx › WNT_DC_CBE_Screen
Low adenoma burden in unselected patients with a pathogenic APC variant.
Schwiter R et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2023
Genetic Variants in the Wingless Antagonist Genes (sFRP, DKK, and Axin2) Predict the Overall Survival and Prognosis of North Indian Lung Cancer Patients Treated with Platinum-Based Doublet Chemotherapy.
Bahl C et al.
Cancer Biotherapy & Radiopharmaceuticals, 2018
A Specific Mutational Signature Associated with DNA 8-Oxoguanine Persistence in MUTYH-defective Colorectal Cancer.
Viel A et al.
Ebiomedicine, 2017
28551381 (PubMed )
Supplement: mmc7.pdf
Identification of genetic contribution to ischemic stroke by screening of single nucleotide polymorphisms in stroke patients by using a case control study design.
Kumar A et al.
Bmc Neurology, 2013
Epigenetic and genetic analysis of WNT signaling pathway in sporadic colorectal cancer patients from Iran.
Naghibalhossaini F et al.
Molecular Biology Reports, 2012
AXIN2 polymorphism and its association with prostate cancer in a Turkish population.
Pinarbasi E et al.
Medical Oncology (northwood, London, England), 2011
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