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Journal Abstract Search

243 related items for PubMed ID: 29618362

  • 1. Genetic analysis of Wnt/PCP genes in neural tube defects.
    Chen Z, Lei Y, Cao X, Zheng Y, Wang F, Bao Y, Peng R, Finnell RH, Zhang T, Wang H.
    BMC Med Genomics; 2018 Apr 04; 11(1):38. PubMed ID: 29618362
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  • 2. Digenic variants of planar cell polarity genes in human neural tube defect patients.
    Wang L, Xiao Y, Tian T, Jin L, Lei Y, Finnell RH, Ren A.
    Mol Genet Metab; 2018 May 04; 124(1):94-100. PubMed ID: 29573971
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  • 4. Novel Mutation of LRP6 Identified in Chinese Han Population Links Canonical WNT Signaling to Neural Tube Defects.
    Shi Z, Yang X, Li BB, Chen S, Yang L, Cheng L, Zhang T, Wang H, Zheng Y.
    Birth Defects Res; 2018 Jan 15; 110(1):63-71. PubMed ID: 28960852
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  • 5. Genetic interactions between planar cell polarity genes cause diverse neural tube defects in mice.
    Murdoch JN, Damrau C, Paudyal A, Bogani D, Wells S, Greene ND, Stanier P, Copp AJ.
    Dis Model Mech; 2014 Oct 15; 7(10):1153-63. PubMed ID: 25128525
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  • 7. A consideration of the evidence that genetic defects in planar cell polarity contribute to the etiology of human neural tube defects.
    Juriloff DM, Harris MJ.
    Birth Defects Res A Clin Mol Teratol; 2012 Oct 15; 94(10):824-40. PubMed ID: 23024041
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  • 16. DVL mutations identified from human neural tube defects and Dandy-Walker malformation obstruct the Wnt signaling pathway.
    Liu L, Liu W, Shi Y, Li L, Gao Y, Lei Y, Finnell R, Zhang T, Zhang F, Jin L, Li H, Tao W, Wang H.
    J Genet Genomics; 2020 Jun 20; 47(6):301-310. PubMed ID: 32900645
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  • 17. Mutations in the COPII vesicle component gene SEC24B are associated with human neural tube defects.
    Yang XY, Zhou XY, Wang QQ, Li H, Chen Y, Lei YP, Ma XH, Kong P, Shi Y, Jin L, Zhang T, Wang HY.
    Hum Mutat; 2013 Aug 20; 34(8):1094-101. PubMed ID: 23592378
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