Associated Papers
A rare deleterious missense mutation in the AXIN2 gene in Chinese women with polycystic ovary syndrome.
Zhang Y et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology, 2025
Clinical and genomic features of Lynch syndrome differ by tumor site and disease spectrum.
Li S et al.
Nature Communications, 2025
Tumor DNA from tumor in situ fluid was used to track evolution of glioma under first-line treatment.
Yu J et al.
Frontiers in Oncology, 2025
AXIN2 germline testing in a French cohort validates pathogenic variants as a rare cause of predisposition to colorectal polyposis and cancer.
Leclerc J et al.
Genes, Chromosomes & Cancer, 2023
Responses to the Tepotinib in Gastric Cancers with MET Amplification or MET Exon 14 Skipping Mutations and High Expression of Both PD-L1 and CD44.
Sohn SH et al.
Cancers, 2022
Genotypes and Haplotypes in the AXIN2 and TCF7L2 Genes are Associated With Susceptibility and With Clinicopathological Characteristics in Breast Cancer Patients.
Rosales-Reynoso MA et al.
British Journal of Biomedical Science, 2022
Association of AXIN2 s2240308 C>T, rs1133683 C>T, rs7224837 A>G Polymorphisms with Susceptibility to Breast Cancer.
Sayad S et al.
Asian Pacific Journal of Cancer Prevention : Apjcp, 2021
Identification of New Tumor-Related Gene Mutations in Chinese Gastrointestinal Stromal Tumors.
Feng Y et al.
Frontiers in Cell and Developmental Biology, 2021
The association between three AXIN2 variants and cancer risk.
Dai F et al.
Journal of Cellular Biochemistry, 2019
Association study between genetic variations in Axin2 gene and lung cancer risk in North Indian population: A multiple interaction analysis.
Bahl C et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine, 2017
AXIN2 Polymorphisms and Their Association with Colorectal Cancer in Mexican Patients.
Rosales-Reynoso MA et al.
Genetic Testing and Molecular Biomarkers, 2016
A Novel Inherited Mutation in PRKAR1A Abrogates PreRNA Splicing in a Carney Complex Family.
Sun Y et al.
The Canadian Journal of Cardiology, 2015
Mutational analysis of AXIN2, MSX1, and PAX9 in two Mexican oligodontia families.
Mu YD et al.
Genetics and Molecular Research : Gmr, 2013
PAX9 polymorphism and susceptibility to sporadic non-syndromic severe anodontia: a case-control study in southwest China.
Wang J et al.
Journal of Applied Oral Science : Revista Fob, 2013
AXIN2 polymorphism and its association with prostate cancer in a Turkish population.
Pinarbasi E et al.
Medical Oncology (northwood, London, England), 2011
Axis inhibition protein 2 (AXIN2) polymorphisms may be a risk factor for selective tooth agenesis.
Mostowska A et al.
Journal of Human Genetics, 2006
AXIN2 polymorphism and its association with astrocytoma in a Turkish population.
Gunes EG et al.
Molecular Medicine Reports, 0