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 *

204 related articles for article (PubMed ID: 37589570)

  • 1. The loop-tail mouse model displays open and closed caudal neural tube defects.
    Fernández-Santos B; Reyes-Corral M; Caro-Vega JM; Lao-Pérez M; Vallejo-Grijalba C; Mesa-Cruz C; Morón FJ; Ybot-González P
    Dis Model Mech; 2023 Aug; 16(8):. PubMed ID: 37589570
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Increased expression of Grainyhead-like-3 rescues spina bifida in a folate-resistant mouse model.
    Gustavsson P; Greene ND; Lad D; Pauws E; de Castro SC; Stanier P; Copp AJ
    Hum Mol Genet; 2007 Nov; 16(21):2640-6. PubMed ID: 17720888
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Loop-tail phenotype in heterozygous mice and neural tube defects in homozygous mice result from a nonsense mutation in the Vangl2 gene.
    Chen B; Mao HH; Chen L; Zhang FL; Li K; Xue ZF
    Genet Mol Res; 2013 Jan; 12(3):3157-65. PubMed ID: 23359061
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mini-review: toward understanding mechanisms of genetic neural tube defects in mice.
    Harris MJ; Juriloff DM
    Teratology; 1999 Nov; 60(5):292-305. PubMed ID: 10525207
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Overexpression of Grainyhead-like 3 causes spina bifida and interacts genetically with mutant alleles of Grhl2 and Vangl2 in mice.
    De Castro SCP; Gustavsson P; Marshall AR; Gordon WM; Galea G; Nikolopoulou E; Savery D; Rolo A; Stanier P; Andersen B; Copp AJ; Greene NDE
    Hum Mol Genet; 2018 Dec; 27(24):4218-4230. PubMed ID: 30189017
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Developmental basis of severe neural tube defects in the loop-tail (Lp) mutant mouse: use of microsatellite DNA markers to identify embryonic genotype.
    Copp AJ; Checiu I; Henson JN
    Dev Biol; 1994 Sep; 165(1):20-9. PubMed ID: 8088438
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Inositol- and folate-resistant neural tube defects in mice lacking the epithelial-specific factor Grhl-3.
    Ting SB; Wilanowski T; Auden A; Hall M; Voss AK; Thomas T; Parekh V; Cunningham JM; Jane SM
    Nat Med; 2003 Dec; 9(12):1513-9. PubMed ID: 14608380
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Syndecan 4 interacts genetically with Vangl2 to regulate neural tube closure and planar cell polarity.
    Escobedo N; Contreras O; Muñoz R; Farías M; Carrasco H; Hill C; Tran U; Pryor SE; Wessely O; Copp AJ; Larraín J
    Development; 2013 Jul; 140(14):3008-17. PubMed ID: 23760952
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Neural tube closure depends on expression of Grainyhead-like 3 in multiple tissues.
    De Castro SCP; Hirst CS; Savery D; Rolo A; Lickert H; Andersen B; Copp AJ; Greene NDE
    Dev Biol; 2018 Mar; 435(2):130-137. PubMed ID: 29397878
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetics and development of neural tube defects.
    Copp AJ; Greene ND
    J Pathol; 2010 Jan; 220(2):217-30. PubMed ID: 19918803
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Vangl2 disruption alters the biomechanics of late spinal neurulation leading to spina bifida in mouse embryos.
    Galea GL; Nychyk O; Mole MA; Moulding D; Savery D; Nikolopoulou E; Henderson DJ; Greene NDE; Copp AJ
    Dis Model Mech; 2018 Mar; 11(3):. PubMed ID: 29590636
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Insights into prevention of human neural tube defects by folic acid arising from consideration of mouse mutants.
    Harris MJ
    Birth Defects Res A Clin Mol Teratol; 2009 Apr; 85(4):331-9. PubMed ID: 19117321
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Spina bifida and other neural tube defects.
    Northrup H; Volcik KA
    Curr Probl Pediatr; 2000; 30(10):313-32. PubMed ID: 11147289
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Analysis of Gut Characteristics and Microbiota Changes with Maternal Supplementation in a Neural Tube Defect Mouse Model.
    Cordero-Varela JA; Reyes-Corral M; Lao-Pérez M; Fernández-Santos B; Montenegro-Elvira F; Sempere L; Ybot-González P
    Nutrients; 2023 Nov; 15(23):. PubMed ID: 38068802
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Ltap, a mammalian homolog of Drosophila Strabismus/Van Gogh, is altered in the mouse neural tube mutant Loop-tail.
    Kibar Z; Vogan KJ; Groulx N; Justice MJ; Underhill DA; Gros P
    Nat Genet; 2001 Jul; 28(3):251-5. PubMed ID: 11431695
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.