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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

210 related articles for article (PubMed ID: 27543293)

  • 1. Mutations in the Motile Cilia Gene DNAAF1 Are Associated with Neural Tube Defects in Humans.
    Miao C; Jiang Q; Li H; Zhang Q; Bai B; Bao Y; Zhang T
    G3 (Bethesda); 2016 Oct; 6(10):3307-3316. PubMed ID: 27543293
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutations in Dnaaf1 and Lrrc48 Cause Hydrocephalus, Laterality Defects, and Sinusitis in Mice.
    Ha S; Lindsay AM; Timms AE; Beier DR
    G3 (Bethesda); 2016 Aug; 6(8):2479-87. PubMed ID: 27261005
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Detection of copy number variants reveals association of cilia genes with neural tube defects.
    Chen X; Shen Y; Gao Y; Zhao H; Sheng X; Zou J; Lip V; Xie H; Guo J; Shao H; Bao Y; Shen J; Niu B; Gusella JF; Wu BL; Zhang T
    PLoS One; 2013; 8(1):e54492. PubMed ID: 23349908
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 34(8):1094-101. PubMed ID: 23592378
    [TBL] [Abstract][Full Text] [Related]  

  • 5. DNAAF1 links heart laterality with the AAA+ ATPase RUVBL1 and ciliary intraflagellar transport.
    Hartill VL; van de Hoek G; Patel MP; Little R; Watson CM; Berry IR; Shoemark A; Abdelmottaleb D; Parkes E; Bacchelli C; Szymanska K; Knoers NV; Scambler PJ; Ueffing M; Boldt K; Yates R; Winyard PJ; Adler B; Moya E; Hattingh L; Shenoy A; Hogg C; Sheridan E; Roepman R; Norris D; Mitchison HM; Giles RH; Johnson CA
    Hum Mol Genet; 2018 Feb; 27(3):529-545. PubMed ID: 29228333
    [TBL] [Abstract][Full Text] [Related]  

  • 6. G-protein-coupled receptor signaling and neural tube closure defects.
    Shimada IS; Mukhopadhyay S
    Birth Defects Res; 2017 Jan; 109(2):129-139. PubMed ID: 27731925
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An update to the list of mouse mutants with neural tube closure defects and advances toward a complete genetic perspective of neural tube closure.
    Harris MJ; Juriloff DM
    Birth Defects Res A Clin Mol Teratol; 2010 Aug; 88(8):653-69. PubMed ID: 20740593
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. Network correlation analysis revealed potential new mechanisms for neural tube defects beyond folic acid.
    Gao X; Finnell RH; Wang H; Zheng Y
    Birth Defects Res; 2018 Jul; 110(12):982-993. PubMed ID: 29732722
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Toward understanding the genetic basis of neural tube defects.
    Kibar Z; Capra V; Gros P
    Clin Genet; 2007 Apr; 71(4):295-310. PubMed ID: 17470131
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mouse mutants with neural tube closure defects and their role in understanding human neural tube defects.
    Harris MJ; Juriloff DM
    Birth Defects Res A Clin Mol Teratol; 2007 Mar; 79(3):187-210. PubMed ID: 17177317
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Genetic screening and functional analysis of CASP9 mutations in a Chinese cohort with neural tube defects.
    Liu XZ; Zhang Q; Jiang Q; Bai BL; Du XJ; Wang F; Wu LH; Lu XL; Bao YH; Li HL; Zhang T
    CNS Neurosci Ther; 2018 May; 24(5):394-403. PubMed ID: 29365368
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A unique missense allele of BAF155, a core BAF chromatin remodeling complex protein, causes neural tube closure defects in mice.
    Harmacek L; Watkins-Chow DE; Chen J; Jones KL; Pavan WJ; Salbaum JM; Niswander L
    Dev Neurobiol; 2014 May; 74(5):483-97. PubMed ID: 24170322
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A screen for mutations in human homologues of mice exencephaly genes Tfap2alpha and Msx2 in patients with neural tube defects.
    Stegmann K; Boecker J; Richter B; Capra V; Finnell RH; Ngo ET; Strehl E; Ermert A; Koch MC
    Teratology; 2001 May; 63(5):167-75. PubMed ID: 11320527
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Folate-mediated one-carbon metabolism and neural tube defects: balancing genome synthesis and gene expression.
    Beaudin AE; Stover PJ
    Birth Defects Res C Embryo Today; 2007 Sep; 81(3):183-203. PubMed ID: 17963270
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Polymorphisms of 5,10-methylenetetrahydrofolate reductase and cystathionine beta-synthase genes as a risk factor for neural tube defects in Sétif, Algeria.
    Houcher B; Bourouba R; Djabi F; Yilmaz E; Eğin Y; Akar N
    Pediatr Neurosurg; 2009; 45(6):472-7. PubMed ID: 20160465
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.