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135 related items for PubMed ID: 25068569

  • 1. Independent mutations at Arg181 and Arg274 of Vangl proteins that are associated with neural tube defects in humans decrease protein stability and impair membrane targeting.
    Iliescu A, Gravel M, Horth C, Gros P.
    Biochemistry; 2014 Aug 19; 53(32):5356-64. PubMed ID: 25068569
    [Abstract] [Full Text] [Related]

  • 2. Loss of membrane targeting of Vangl proteins causes neural tube defects.
    Iliescu A, Gravel M, Horth C, Kibar Z, Gros P.
    Biochemistry; 2011 Feb 08; 50(5):795-804. PubMed ID: 21142127
    [Abstract] [Full Text] [Related]

  • 3. Molecular and cellular mechanisms underlying neural tube defects in the loop-tail mutant mouse.
    Gravel M, Iliescu A, Horth C, Apuzzo S, Gros P.
    Biochemistry; 2010 Apr 27; 49(16):3445-55. PubMed ID: 20329788
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  • 5. 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 27; 103(1):51-61. PubMed ID: 25208524
    [Abstract] [Full Text] [Related]

  • 6. Genetic interaction between members of the Vangl family causes neural tube defects in mice.
    Torban E, Patenaude AM, Leclerc S, Rakowiecki S, Gauthier S, Andelfinger G, Epstein DJ, Gros P.
    Proc Natl Acad Sci U S A; 2008 Mar 04; 105(9):3449-54. PubMed ID: 18296642
    [Abstract] [Full Text] [Related]

  • 7. Transmembrane topology of mammalian planar cell polarity protein Vangl1.
    Iliescu A, Gravel M, Horth C, Apuzzo S, Gros P.
    Biochemistry; 2011 Mar 29; 50(12):2274-82. PubMed ID: 21291170
    [Abstract] [Full Text] [Related]

  • 8. Independent mutations in mouse Vangl2 that cause neural tube defects in looptail mice impair interaction with members of the Dishevelled family.
    Torban E, Wang HJ, Groulx N, Gros P.
    J Biol Chem; 2004 Dec 10; 279(50):52703-13. PubMed ID: 15456783
    [Abstract] [Full Text] [Related]

  • 9. 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 15; 26(12):2307-2320. PubMed ID: 28369449
    [Abstract] [Full Text] [Related]

  • 10. Molecular characterisation of endogenous Vangl2/Vangl1 heteromeric protein complexes.
    Belotti E, Puvirajesinghe TM, Audebert S, Baudelet E, Camoin L, Pierres M, Lasvaux L, Ferracci G, Montcouquiol M, Borg JP.
    PLoS One; 2012 Jun 15; 7(9):e46213. PubMed ID: 23029439
    [Abstract] [Full Text] [Related]

  • 11. 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 15; 34(8):1094-101. PubMed ID: 23592378
    [Abstract] [Full Text] [Related]

  • 12. 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 01; 19(23):4663-76. PubMed ID: 20843830
    [Abstract] [Full Text] [Related]

  • 13. The intracellular carboxyl terminal domain of Vangl proteins contains plasma membrane targeting signals.
    Iliescu A, Gros P.
    Protein Sci; 2014 Apr 01; 23(4):337-43. PubMed ID: 24452931
    [Abstract] [Full Text] [Related]

  • 14. Human neural tube defects: genetic causes and prevention.
    De Marco P, Merello E, Cama A, Kibar Z, Capra V.
    Biofactors; 2011 Apr 01; 37(4):261-8. PubMed ID: 21674647
    [Abstract] [Full Text] [Related]

  • 15. VANGL1 rare variants associated with neural tube defects affect convergent extension in zebrafish.
    Reynolds A, McDearmid JR, Lachance S, De Marco P, Merello E, Capra V, Gros P, Drapeau P, Kibar Z.
    Mech Dev; 2010 Apr 01; 127(7-8):385-92. PubMed ID: 20043994
    [Abstract] [Full Text] [Related]

  • 16. 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 15; 20(22):4324-33. PubMed ID: 21840926
    [Abstract] [Full Text] [Related]

  • 17. Mutations in VANGL1 associated with neural-tube defects.
    Kibar Z, Torban E, McDearmid JR, Reynolds A, Berghout J, Mathieu M, Kirillova I, De Marco P, Merello E, Hayes JM, Wallingford JB, Drapeau P, Capra V, Gros P.
    N Engl J Med; 2007 Apr 05; 356(14):1432-7. PubMed ID: 17409324
    [Abstract] [Full Text] [Related]

  • 18. 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 05; 139(10):1299-1314. PubMed ID: 32356230
    [Abstract] [Full Text] [Related]

  • 19. Effects of retinoic acid on the expressions of Vangl1 and vangl2 in mouse fetuses.
    Liu J, Qi J, Zhu J, Zhang L, Liang Y, Ning Q, Luo X.
    J Neurogenet; 2008 Oct 05; 22(3):167-79. PubMed ID: 19012162
    [Abstract] [Full Text] [Related]

  • 20. Tissue, cellular and sub-cellular localization of the Vangl2 protein during embryonic development: effect of the Lp mutation.
    Torban E, Wang HJ, Patenaude AM, Riccomagno M, Daniels E, Epstein D, Gros P.
    Gene Expr Patterns; 2007 Jan 05; 7(3):346-54. PubMed ID: 16962386
    [Abstract] [Full Text] [Related]

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