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.
242 related articles for article (PubMed ID: 29618362)
21. Loss-of-function or gain-of-function variations in VINCULIN (VCL) are risk factors of human neural tube defects. Wang Y; Qin Y; Peng R; Wang H Mol Genet Genomic Med; 2021 Feb; 9(2):e1563. PubMed ID: 33491343 [TBL] [Abstract][Full Text] [Related]
22. Epithelial cell polarity genes are required for neural tube closure. Doudney K; Stanier P Am J Med Genet C Semin Med Genet; 2005 May; 135C(1):42-7. PubMed ID: 15800847 [TBL] [Abstract][Full Text] [Related]
23. Rare Deleterious PARD3 Variants in the aPKC-Binding Region are Implicated in the Pathogenesis of Human Cranial Neural Tube Defects Via Disrupting Apical Tight Junction Formation. Chen X; An Y; Gao Y; Guo L; Rui L; Xie H; Sun M; Lam Hung S; Sheng X; Zou J; Bao Y; Guan H; Niu B; Li Z; Finnell RH; Gusella JF; Wu BL; Zhang T Hum Mutat; 2017 Apr; 38(4):378-389. PubMed ID: 27925688 [TBL] [Abstract][Full Text] [Related]
24. The planar cell polarity gene Vangl2 is required for mammalian kidney-branching morphogenesis and glomerular maturation. Yates LL; Papakrivopoulou J; Long DA; Goggolidou P; Connolly JO; Woolf AS; Dean CH Hum Mol Genet; 2010 Dec; 19(23):4663-76. PubMed ID: 20843830 [TBL] [Abstract][Full Text] [Related]
25. Contribution of VANGL2 mutations to isolated neural tube defects. Kibar Z; Salem S; Bosoi CM; Pauwels E; De Marco P; Merello E; Bassuk AG; Capra V; Gros P Clin Genet; 2011 Jul; 80(1):76-82. PubMed ID: 20738329 [TBL] [Abstract][Full Text] [Related]
26. Planar cell polarity genes and neural tube closure. Ueno N; Greene ND Birth Defects Res C Embryo Today; 2003 Nov; 69(4):318-24. PubMed ID: 14745972 [TBL] [Abstract][Full Text] [Related]
27. Genetic and functional analysis of SHROOM1-4 in a Chinese neural tube defect cohort. Chen Z; Kuang L; Finnell RH; Wang H Hum Genet; 2018 Mar; 137(3):195-202. PubMed ID: 29423651 [TBL] [Abstract][Full Text] [Related]
28. Roles of planar cell polarity pathways in the development of neural [correction of neutral] tube defects. Wu G; Huang X; Hua Y; Mu D J Biomed Sci; 2011 Aug; 18(1):66. PubMed ID: 21864354 [TBL] [Abstract][Full Text] [Related]
29. Comparative integromics on non-canonical WNT or planar cell polarity signaling molecules: transcriptional mechanism of PTK7 in colorectal cancer and that of SEMA6A in undifferentiated ES cells. Katoh M; Katoh M Int J Mol Med; 2007 Sep; 20(3):405-9. PubMed ID: 17671748 [TBL] [Abstract][Full Text] [Related]
30. β-catenin regulates Pax3 and Cdx2 for caudal neural tube closure and elongation. Zhao T; Gan Q; Stokes A; Lassiter RN; Wang Y; Chan J; Han JX; Pleasure DE; Epstein JA; Zhou CJ Development; 2014 Jan; 141(1):148-57. PubMed ID: 24284205 [TBL] [Abstract][Full Text] [Related]
31. Rare missense variants in DVL1, one of the human counterparts of the Drosophila dishevelled gene, do not confer increased risk for neural tube defects. Merello E; Kibar Z; Allache R; Piatelli G; Cama A; Capra V; De Marco P Birth Defects Res A Clin Mol Teratol; 2013 Jul; 97(7):452-5. PubMed ID: 23836490 [TBL] [Abstract][Full Text] [Related]
32. The role of Lrp6-mediated Wnt/β-catenin signaling in the development and intervention of spinal neural tube defects in mice. Zhao T; McMahon M; Reynolds K; Saha SK; Stokes A; Zhou CJ Dis Model Mech; 2022 Jun; 15(6):. PubMed ID: 35514236 [TBL] [Abstract][Full Text] [Related]
33. Genetic evidence in planar cell polarity signaling pathway in human neural tube defects. Cai C; Shi O Front Med; 2014 Mar; 8(1):68-78. PubMed ID: 24307374 [TBL] [Abstract][Full Text] [Related]
34. Mutations in the planar cell polarity gene, Fuzzy, are associated with neural tube defects in humans. Seo JH; Zilber Y; Babayeva S; Liu J; Kyriakopoulos P; De Marco P; Merello E; Capra V; Gros P; Torban E Hum Mol Genet; 2011 Nov; 20(22):4324-33. PubMed ID: 21840926 [TBL] [Abstract][Full Text] [Related]
35. Identification of novel rare mutations of DACT1 in human neural tube defects. Shi Y; Ding Y; Lei YP; Yang XY; Xie GM; Wen J; Cai CQ; Li H; Chen Y; Zhang T; Wu BL; Jin L; Chen YG; Wang HY Hum Mutat; 2012 Oct; 33(10):1450-5. PubMed ID: 22610794 [TBL] [Abstract][Full Text] [Related]
36. Wnt/planar cell polarity signaling controls morphogenetic movements of gastrulation and neural tube closure. Shi DL Cell Mol Life Sci; 2022 Nov; 79(12):586. PubMed ID: 36369349 [TBL] [Abstract][Full Text] [Related]
37. Targeted panel sequencing establishes the implication of planar cell polarity pathway and involves new candidate genes in neural tube defect disorders. Beaumont M; Akloul L; Carré W; Quélin C; Journel H; Pasquier L; Fradin M; Odent S; Hamdi-Rozé H; Watrin E; Dupé V; Dubourg C; David V Hum Genet; 2019 Apr; 138(4):363-374. PubMed ID: 30838450 [TBL] [Abstract][Full Text] [Related]
38. Genetic analysis of disheveled 2 and disheveled 3 in human neural tube defects. De Marco P; Merello E; Consales A; Piatelli G; Cama A; Kibar Z; Capra V J Mol Neurosci; 2013 Mar; 49(3):582-8. PubMed ID: 22892949 [TBL] [Abstract][Full Text] [Related]
39. Variants identified in PTK7 associated with neural tube defects. Lei Y; Kim SE; Chen Z; Cao X; Zhu H; Yang W; Shaw GM; Zheng Y; Zhang T; Wang HY; Finnell RH Mol Genet Genomic Med; 2019 Apr; 7(4):e00584. PubMed ID: 30689296 [TBL] [Abstract][Full Text] [Related]
40. Scribble1 plays an important role in the pathogenesis of neural tube defects through its mediating effect of Par-3 and Vangl1/2 localization. Kharfallah F; Guyot MC; El Hassan AR; Allache R; Merello E; De Marco P; Di Cristo G; Capra V; Kibar Z Hum Mol Genet; 2017 Jun; 26(12):2307-2320. PubMed ID: 28369449 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]