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 *

222 related articles for article (PubMed ID: 23874236)

  • 41. Over-expression of Grhl2 causes spina bifida in the Axial defects mutant mouse.
    Brouns MR; De Castro SC; Terwindt-Rouwenhorst EA; Massa V; Hekking JW; Hirst CS; Savery D; Munts C; Partridge D; Lamers W; Köhler E; van Straaten HW; Copp AJ; Greene ND
    Hum Mol Genet; 2011 Apr; 20(8):1536-46. PubMed ID: 21262862
    [TBL] [Abstract][Full Text] [Related]  

  • 42. 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]  

  • 43. Genetic landmarks for defects in mouse neural tube closure.
    Harris MJ; Juriloff DM
    Teratology; 1997 Sep; 56(3):177-87. PubMed ID: 9358605
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Genetic and functional analysis of the NKX2-5 gene promoter in patients with ventricular septal defects.
    Pang S; Shan J; Qiao Y; Ma L; Qin X; Wanyan H; Xing Q; Wu G; Yan B
    Pediatr Cardiol; 2012 Dec; 33(8):1355-61. PubMed ID: 22576768
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Evaluation of common genetic variants in 82 candidate genes as risk factors for neural tube defects.
    Pangilinan F; Molloy AM; Mills JL; Troendle JF; Parle-McDermott A; Signore C; O'Leary VB; Chines P; Seay JM; Geiler-Samerotte K; Mitchell A; VanderMeer JE; Krebs KM; Sanchez A; Cornman-Homonoff J; Stone N; Conley M; Kirke PN; Shane B; Scott JM; Brody LC
    BMC Med Genet; 2012 Aug; 13():62. PubMed ID: 22856873
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Maternal one-carbon metabolism, MTHFR and TCN2 genotypes and neural tube defects in India.
    Godbole K; Gayathri P; Ghule S; Sasirekha BV; Kanitkar-Damle A; Memane N; Suresh S; Sheth J; Chandak GR; Yajnik CS
    Birth Defects Res A Clin Mol Teratol; 2011 Sep; 91(9):848-56. PubMed ID: 21770021
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Genetics of neural tube defects.
    Gelineau-van Waes J; Finnell RH
    Semin Pediatr Neurol; 2001 Sep; 8(3):160-4. PubMed ID: 11575845
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Interaction between Maternal and Paternal SHMT1 C1420T Predisposes to Neural Tube Defects in the Fetus: Evidence from Case-Control and Family-Based Triad Approaches.
    K Rebekah P; Tella S; Buragadda S; Tiruvatturu MK; Akka J
    Birth Defects Res; 2017 Jul; 109(13):1020-1029. PubMed ID: 28762673
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Concepts in the neurosurgical care of patients with spinal neural tube defects: An embryologic approach.
    Blount JP; George TM; Koueik J; Iskandar BJ
    Birth Defects Res; 2019 Nov; 111(19):1564-1576. PubMed ID: 31576681
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Association of FOLH1, DHFR, and MTHFR gene polymorphisms with susceptibility of Neural Tube Defects: A case control study from Eastern India.
    Paul S; Sadhukhan S; Munian D; Bankura B; Das M
    Birth Defects Res; 2018 Aug; 110(14):1129-1138. PubMed ID: 30120883
    [TBL] [Abstract][Full Text] [Related]  

  • 51. TRIM4 is associated with neural tube defects based on genome-wide DNA methylation analysis.
    Zhang H; Guo Y; Gu H; Wei X; Ma W; Liu D; Yu K; Luo W; Ma L; Liu Y; Xue J; Huang J; Wang Y; Jia S; Dong N; Wang H; Yuan Z
    Clin Epigenetics; 2019 Feb; 11(1):17. PubMed ID: 30709423
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Alx3-deficient mice exhibit folic acid-resistant craniofacial midline and neural tube closure defects.
    Lakhwani S; García-Sanz P; Vallejo M
    Dev Biol; 2010 Aug; 344(2):869-80. PubMed ID: 20534379
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Methylome analysis for spina bifida shows
    Rochtus A; Winand R; Laenen G; Vangeel E; Izzi B; Wittevrongel C; Moreau Y; Verpoorten C; Jansen K; Van Geet C; Freson K
    Clin Epigenetics; 2016; 8():108. PubMed ID: 27757173
    [TBL] [Abstract][Full Text] [Related]  

  • 54. 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]  

  • 55. CIC missense variants contribute to susceptibility for spina bifida.
    Han X; Cao X; Aguiar-Pulido V; Yang W; Karki M; Ramirez PAP; Cabrera RM; Lin YL; Wlodarczyk BJ; Shaw GM; Ross ME; Zhang C; Finnell RH; Lei Y
    Hum Mutat; 2022 Dec; 43(12):2021-2032. PubMed ID: 36054333
    [TBL] [Abstract][Full Text] [Related]  

  • 56. 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]  

  • 57. Association of main folate metabolic pathway gene polymorphisms with neural tube defects in Han population of Northern China.
    Fang Y; Zhang R; Zhi X; Zhao L; Cao L; Wang Y; Cai C
    Childs Nerv Syst; 2018 Apr; 34(4):725-729. PubMed ID: 29392422
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Comparison of inherited neural tube defects in companion animals and livestock.
    Zarzycki A; Thomas ZM; Mazrier H
    Birth Defects Res; 2021 Mar; 113(4):319-348. PubMed ID: 33615733
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Mouse models for neural tube closure defects.
    Juriloff DM; Harris MJ
    Hum Mol Genet; 2000 Apr; 9(6):993-1000. PubMed ID: 10767323
    [TBL] [Abstract][Full Text] [Related]  

  • 60. The folate metabolic enzyme ALDH1L1 is restricted to the midline of the early CNS, suggesting a role in human neural tube defects.
    Anthony TE; Heintz N
    J Comp Neurol; 2007 Jan; 500(2):368-83. PubMed ID: 17111379
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.