BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

104 related articles for article (PubMed ID: 12906864)

  • 21. 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; 7(3):346-54. PubMed ID: 16962386
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Disruption of scribble (Scrb1) causes severe neural tube defects in the circletail mouse.
    Murdoch JN; Henderson DJ; Doudney K; Gaston-Massuet C; Phillips HM; Paternotte C; Arkell R; Stanier P; Copp AJ
    Hum Mol Genet; 2003 Jan; 12(2):87-98. PubMed ID: 12499390
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Identification and characterization of a novel chemically induced allele at the planar cell polarity gene Vangl2.
    El-Hassan AR; Leung V; Kharfallah F; Guyot MC; Allache R; Gros P; Kibar Z
    Mamm Genome; 2018 Apr; 29(3-4):229-244. PubMed ID: 29063958
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genetic basis of neural tube defects: the mouse gene loop-tail maps to a region of chromosome 1 syntenic with human 1q21-q23.
    Stanier P; Henson JN; Eddleston J; Moore GE; Copp AJ
    Genomics; 1995 Apr; 26(3):473-8. PubMed ID: 7607670
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Nhlh1, a basic helix-loop-helix transcription factor, is very tightly linked to the mouse looptail (Lp) mutation.
    Mullick A; Groulx N; Trasler D; Gros P
    Mamm Genome; 1995 Oct; 6(10):700-4. PubMed ID: 8563167
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. 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]  

  • 29. Mutations in Lyar and p53 are synergistically lethal in female mice.
    Wang G; Fulkerson CM; Malek R; Ghassemifar S; Snyder PW; Mendrysa SM
    Birth Defects Res A Clin Mol Teratol; 2012 Sep; 94(9):729-37. PubMed ID: 22815056
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Neural tube defects without neural crest defects in splotch mice.
    Franz T
    Teratology; 1992 Dec; 46(6):599-604. PubMed ID: 1290160
    [TBL] [Abstract][Full Text] [Related]  

  • 31. High-resolution linkage map in the vicinity of the Lp locus.
    Mullick A; Trasler D; Gros P
    Genomics; 1995 Apr; 26(3):479-88. PubMed ID: 7607671
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Analysis of the embryonic phenotype of Bent tail, a mouse model for X-linked neural tube defects.
    Franke B; Klootwijk R; Hekking JW; de Boer RT; ten Donkelaar HJ; Mariman EC; van Straaten HW
    Anat Embryol (Berl); 2003 Oct; 207(3):255-62. PubMed ID: 14523648
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Expression of the sonic hedgehog gene in human embryos with neural tube defects.
    Kirillova I; Novikova I; Augé J; Audollent S; Esnault D; Encha-Razavi F; Lazjuk G; Attié-Bitach T; Vekemans M
    Teratology; 2000 May; 61(5):347-54. PubMed ID: 10777830
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Abnormal elevation of the neural folds in the loop-tail mutant mouse.
    Wilson DB; Wyatt DP
    Acta Anat (Basel); 1992; 143(2):89-95. PubMed ID: 1598821
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Modifier locus for exencephaly in Cecr2 mutant mice is syntenic to the 10q25.3 region associated with neural tube defects in humans.
    Davidson CE; Li Q; Churchill GA; Osborne LR; McDermid HE
    Physiol Genomics; 2007 Oct; 31(2):244-51. PubMed ID: 17623803
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Genetic backgrounds and modifier genes of NTD mouse models: An opportunity for greater understanding of the multifactorial etiology of neural tube defects.
    Leduc RY; Singh P; McDermid HE
    Birth Defects Res; 2017 Jan; 109(2):140-152. PubMed ID: 27768235
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Cardiovascular defects associated with abnormalities in midline development in the Loop-tail mouse mutant.
    Henderson DJ; Conway SJ; Greene ND; Gerrelli D; Murdoch JN; Anderson RH; Copp AJ
    Circ Res; 2001 Jul; 89(1):6-12. PubMed ID: 11440971
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Phenotype of the neural tube defect mouse model bent tail is not sensitive to maternal folinic acid, myo-inositol, or zinc supplementation.
    Franke B; Klootwijk R; Lemmers B; de Kovel CG; Steegers-Theunissen RP; Mariman EC
    Birth Defects Res A Clin Mol Teratol; 2003 Dec; 67(12):979-84. PubMed ID: 14745918
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 6.