These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


129 related items for PubMed ID: 33096676

  • 1. Significant Associations between AXIN1 rs1805105, rs12921862, rs370681 Haplotypes and Variant Genotypes of AXIN2 rs2240308 with Risk of Congenital Heart Defects.
    Crauciuc GA, Iancu M, Olah P, Tripon F, Anciuc M, Gozar L, Togănel R, Bănescu C.
    Int J Environ Res Public Health; 2020 Oct 21; 17(20):. PubMed ID: 33096676
    [Abstract] [Full Text] [Related]

  • 2. Association of AXIN1 rs12921862 C/A and rs1805105 G/A and CTSB rs12898 G/A polymorphisms with papillary thyroid carcinoma: A case-control study.
    Saljooghi S, Heidari Z, Saravani M, Rezaei M, Salimi S.
    J Clin Lab Anal; 2023 Jan 21; 37(1):e24804. PubMed ID: 36510340
    [Abstract] [Full Text] [Related]

  • 3. Association between polymorphisms in AXIN1 gene and atrial septal defect.
    Pu Y, Chen P, Zhou B, Wang Y, Song Y, Peng Y, Rao L, Zhang L.
    Biomarkers; 2014 Dec 21; 19(8):674-8. PubMed ID: 25355064
    [Abstract] [Full Text] [Related]

  • 4. Association between AXIN1 Gene Polymorphisms and Bladder Cancer in Chinese Han Population.
    Li Q, Zhang P, Wang Y, Zhang Y, Li K, Song Y, Su M, Zhou B, Zhang L.
    Dis Markers; 2019 Dec 21; 2019():3949343. PubMed ID: 31143301
    [Abstract] [Full Text] [Related]

  • 5. Genetic Variants at the rs4720169 Locus of TBX20 and the rs12921862 Locus of AXIN1 May Increase the Risk of Congenital Heart Defects in the Mexican Population: A Pilot Study.
    Hernández-Almaguer MD, Calvo-Anguiano G, Cerda-Flores RM, Salinas-Torres VM, Orozco-Galicia F, Glenn E, García-Guerra J, Sánchez-Cortés G, Lugo-Trampe J, Martínez-Garza LE.
    Genet Test Mol Biomarkers; 2019 Sep 21; 23(9):664-670. PubMed ID: 31524541
    [Abstract] [Full Text] [Related]

  • 6. Investigating AXIN1 gene polymorphisms in Turkish children with cryptorchidism: A pilot study.
    Doğan G, Yılmaz A, İpek H, Metin M, Peltek Kendirci HN, Afşarlar ÇE.
    J Pediatr Urol; 2024 Aug 21; 20(4):748.e1-748.e7. PubMed ID: 38880668
    [Abstract] [Full Text] [Related]

  • 7. The variations in the AXIN1 gene and susceptibility to cryptorchidism.
    Zhou B, Tang T, Chen P, Pu Y, Ma M, Zhang D, Li L, Zhang P, Song Y, Zhang L.
    J Pediatr Urol; 2015 Jun 21; 11(3):132.e1-5. PubMed ID: 25802106
    [Abstract] [Full Text] [Related]

  • 8. Association between AXIN1 gene polymorphisms and epithelial ovarian cancer in Chinese population.
    Zhang Y, Wang Y, Huang X, Li Q, Li K, You D, Song Y, Su M, Zhou B, Wang W.
    Biomark Med; 2019 Apr 21; 13(6):445-455. PubMed ID: 30929455
    [Abstract] [Full Text] [Related]

  • 9. Association Between AXIN1 Gene Polymorphisms and Dilated Cardiomyopathy in a Chinese Han Population.
    Li K, Zhong Y, Peng Y, Zhou B, Wang Y, Li Q, Zhang Y, Song H, Rao L.
    DNA Cell Biol; 2019 May 21; 38(5):436-442. PubMed ID: 30810360
    [Abstract] [Full Text] [Related]

  • 10. New concept of the Axin2 rs2240308 polymorphism and cancer risk: an updated meta-analysis.
    Yu Y, Tao Y, Liu L, Yang J, Wang L, Li X, Zhuang X, Chu M.
    Neoplasma; 2017 May 21; 64(2):269-277. PubMed ID: 28043155
    [Abstract] [Full Text] [Related]

  • 11. Quantitative assessment of the association between AXIN2 rs2240308 polymorphism and cancer risk.
    Gong J, Jiang Y, Hao N, Zhu B, Li Y.
    Sci Rep; 2015 May 14; 5():10111. PubMed ID: 25974148
    [Abstract] [Full Text] [Related]

  • 12. Genotypes and Haplotypes in the AXIN2 and TCF7L2 Genes are Associated With Susceptibility and With Clinicopathological Characteristics in Breast Cancer Patients.
    Rosales-Reynoso MA, Rosas-Enríquez V, Saucedo-Sariñana AM, Pérez-Coria M, Gallegos-Arreola MP, Salas-González E, Barros-Núñez P, Juárez-Vázquez CI, Flores-Martínez SE, Sánchez-Corona J.
    Br J Biomed Sci; 2022 May 14; 79():10211. PubMed ID: 35996498
    [Abstract] [Full Text] [Related]

  • 13. Association of AXIN2 s2240308 C>T, rs1133683 C>T, rs7224837 A>G Polymorphisms with Susceptibility to Breast Cancer.
    Sayad S, Abdi-Gamsae M, Jafari-Nedooshan J, Farbod M, Dastgheib SA, Karimi-Zarchi M, Asadian F, Neamatzadeh H.
    Asian Pac J Cancer Prev; 2021 Aug 01; 22(8):2717-2722. PubMed ID: 34452579
    [Abstract] [Full Text] [Related]

  • 14. Genetic association of polymorphisms in AXIN1 gene with clear cell renal cell carcinoma in a Chinese population.
    Pu Y, Mi X, Chen P, Zhou B, Zhang P, Wang Y, Song Y, Zhang L.
    Biomark Med; 2017 Nov 01; 11(11):947-955. PubMed ID: 29053018
    [Abstract] [Full Text] [Related]

  • 15. Genetic Polymorphisms in APC, DVL2, and AXIN1 Are Associated with Susceptibility, Advanced TNM Stage or Tumor Location in Colorectal Cancer.
    Rosales-Reynoso MA, Saucedo-Sariñana AM, Contreras-Díaz KB, Márquez-González RM, Barros-Núñez P, Pineda-Razo TD, Marin-Contreras ME, Durán-Anguiano Ó, Gallegos-Arreola MP, Flores-Martínez SE, Sánchez-Corona J.
    Tohoku J Exp Med; 2019 Nov 01; 249(3):173-183. PubMed ID: 31723073
    [Abstract] [Full Text] [Related]

  • 16. The Axin2 rs2240308 polymorphism and susceptibility to lung cancer in a Chinese population.
    Liu D, Li L, Yang Y, Liu W, Wu J.
    Tumour Biol; 2014 Nov 01; 35(11):10987-91. PubMed ID: 25091576
    [Abstract] [Full Text] [Related]

  • 17. Study of rs12532, rs8670 Polymorphism of Msh Homeobox 1 (MSX1), rs61754301, rs4904155 Polymorphism of Paired Box Gene 9 (PAX9), and rs2240308 Polymorphism of Axis Inhibitor Protein 2 (AXIN2) Genes in Nonsyndromic Hypodontia.
    Mártha K, Kerekes Máthé B, Moldovan VG, Bănescu C.
    Biomed Res Int; 2019 Nov 01; 2019():2183720. PubMed ID: 31781599
    [Abstract] [Full Text] [Related]

  • 18. The association between three AXIN2 variants and cancer risk.
    Dai F, Zhu LJ, Zhang W, Mi YY, Sun HY, Zhang LF, Yue C, Wu XY, Zuo L, Bai Y.
    J Cell Biochem; 2019 Sep 01; 120(9):15561-15571. PubMed ID: 31038806
    [Abstract] [Full Text] [Related]

  • 19. Association of Axis Inhibition Protein 2 Polymorphisms with Non-Syndromic Cleft Lip with or without Cleft Palate in Iranian Children.
    Noroozi N, Dastgheib SA, Lookzadeh MH, Mirjalili SR, Noorishadkam M, Akbarian-Bafghi MJ, Neamatzadeh H.
    Fetal Pediatr Pathol; 2020 Feb 01; 39(1):29-37. PubMed ID: 31268379
    [Abstract] [Full Text] [Related]

  • 20. [Association of single nucleotide polymorphisms of Axis inhibitor-2 gene rs224030, rs8081536, rs9913621 with Hirschsprung disease].
    Gao H, Zhang J, Wang W, Zhang Z, Huang Y, Zhang S.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Dec 01; 25(6):697-700. PubMed ID: 19065536
    [Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 7.