BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

289 related articles for article (PubMed ID: 29573971)

  • 1. 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; 124(1):94-100. PubMed ID: 29573971
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Rare copy number variations of planar cell polarity genes are associated with human neural tube defects.
    Tian T; Lei Y; Chen Y; Guo Y; Jin L; Finnell RH; Wang L; Ren A
    Neurogenetics; 2020 Jul; 21(3):217-225. PubMed ID: 32388773
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Expanding the mutational spectrum associated to neural tube defects: literature revision and description of novel VANGL1 mutations.
    Merello E; Mascelli S; Raso A; Piatelli G; Consales A; Cama A; Kibar Z; Capra V; Marco PD
    Birth Defects Res A Clin Mol Teratol; 2015 Jan; 103(1):51-61. PubMed ID: 25208524
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 7(10):1153-63. PubMed ID: 25128525
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 94(10):824-40. PubMed ID: 23024041
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Role of the planar cell polarity gene Protein tyrosine kinase 7 in neural tube defects in humans.
    Wang M; De Marco P; Merello E; Drapeau P; Capra V; Kibar Z
    Birth Defects Res A Clin Mol Teratol; 2015 Dec; 103(12):1021-7. PubMed ID: 26368655
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 11(1):38. PubMed ID: 29618362
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutations in the planar cell polarity genes CELSR1 and SCRIB are associated with the severe neural tube defect craniorachischisis.
    Robinson A; Escuin S; Doudney K; Vekemans M; Stevenson RE; Greene ND; Copp AJ; Stanier P
    Hum Mutat; 2012 Feb; 33(2):440-7. PubMed ID: 22095531
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Role of the planar cell polarity gene CELSR1 in neural tube defects and caudal agenesis.
    Allache R; De Marco P; Merello E; Capra V; Kibar Z
    Birth Defects Res A Clin Mol Teratol; 2012 Mar; 94(3):176-81. PubMed ID: 22371354
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutations associated with human neural tube defects display disrupted planar cell polarity in
    Humphries AC; Narang S; Mlodzik M
    Elife; 2020 Apr; 9():. PubMed ID: 32234212
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Somatic mutations in planar cell polarity genes in neural tissue from human fetuses with neural tube defects.
    Tian T; Lei Y; Chen Y; Karki M; Jin L; Finnell RH; Wang L; Ren A
    Hum Genet; 2020 Oct; 139(10):1299-1314. PubMed ID: 32356230
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Mutations in planar cell polarity gene SCRIB are associated with spina bifida.
    Lei Y; Zhu H; Duhon C; Yang W; Ross ME; Shaw GM; Finnell RH
    PLoS One; 2013; 8(7):e69262. PubMed ID: 23922697
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. Association between rare variants in specific functional pathways and human neural tube defects multiple subphenotypes.
    Zou J; Wang F; Yang X; Wang H; Niswander L; Zhang T; Li H
    Neural Dev; 2020 Jul; 15(1):8. PubMed ID: 32650820
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of novel CELSR1 mutations in spina bifida.
    Lei Y; Zhu H; Yang W; Ross ME; Shaw GM; Finnell RH
    PLoS One; 2014; 9(3):e92207. PubMed ID: 24632739
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Planar cell polarity gene mutations contribute to the etiology of human neural tube defects in our population.
    De Marco P; Merello E; Piatelli G; Cama A; Kibar Z; Capra V
    Birth Defects Res A Clin Mol Teratol; 2014 Aug; 100(8):633-41. PubMed ID: 24838524
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.