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 *

190 related articles for article (PubMed ID: 21674647)

  • 21. 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]  

  • 22. SEC14 and spectrin domains 1 (Sestd1) and Dapper antagonist of catenin 1 (Dact1) scaffold proteins cooperatively regulate the Van Gogh-like 2 (Vangl2) four-pass transmembrane protein and planar cell polarity (PCP) pathway during embryonic development in mice.
    Yang X; Cheyette BN
    J Biol Chem; 2013 Jul; 288(28):20111-20. PubMed ID: 23696638
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Novel Mutation of LRP6 Identified in Chinese Han Population Links Canonical WNT Signaling to Neural Tube Defects.
    Shi Z; Yang X; Li BB; Chen S; Yang L; Cheng L; Zhang T; Wang H; Zheng Y
    Birth Defects Res; 2018 Jan; 110(1):63-71. PubMed ID: 28960852
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Planar cell polarity genes and neural tube closure.
    Ueno N; Greene ND
    Birth Defects Res C Embryo Today; 2003 Nov; 69(4):318-24. PubMed ID: 14745972
    [TBL] [Abstract][Full Text] [Related]  

  • 26. An expanding role of Vangl proteins in embryonic development.
    Torban E; Iliescu A; Gros P
    Curr Top Dev Biol; 2012; 101():237-61. PubMed ID: 23140632
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. 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]  

  • 29. Vangl2-environment interaction causes severe neural tube defects, without abnormal neuroepithelial convergent extension.
    Nychyk O; Galea GL; Molè M; Savery D; Greene NDE; Stanier P; Copp AJ
    Dis Model Mech; 2022 Jan; 15(1):. PubMed ID: 34842271
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Update on the Role of the Non-Canonical Wnt/Planar Cell Polarity Pathway in Neural Tube Defects.
    Wang M; Marco P; Capra V; Kibar Z
    Cells; 2019 Oct; 8(10):. PubMed ID: 31590237
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Novel mutations in VANGL1 in neural tube defects.
    Kibar Z; Bosoi CM; Kooistra M; Salem S; Finnell RH; De Marco P; Merello E; Bassuk AG; Capra V; Gros P
    Hum Mutat; 2009 Jul; 30(7):E706-15. PubMed ID: 19319979
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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; 49(16):3445-55. PubMed ID: 20329788
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

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

  • 35. Genetic studies of ANKRD6 as a molecular switch between Wnt signaling pathways in human neural tube defects.
    Allache R; Wang M; De Marco P; Merello E; Capra V; Kibar Z
    Birth Defects Res A Clin Mol Teratol; 2015 Jan; 103(1):20-6. PubMed ID: 25200652
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. 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]  

  • 38. Bimodal regulation of Dishevelled function by Vangl2 during morphogenesis.
    Seo HS; Habas R; Chang C; Wang J
    Hum Mol Genet; 2017 Jun; 26(11):2053-2061. PubMed ID: 28334810
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A Van Gogh/Vangl tyrosine phosphorylation switch regulates its interaction with core Planar Cell Polarity factors Prickle and Dishevelled.
    Humphries AC; Molina-Pelayo C; Sil P; Hazelett CC; Devenport D; Mlodzik M
    PLoS Genet; 2023 Jul; 19(7):e1010849. PubMed ID: 37463168
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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; 7(9):e46213. PubMed ID: 23029439
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.