BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

262 related articles for article (PubMed ID: 15971254)

  • 1. Using genomewide mutagenesis screens to identify the genes required for neural tube closure in the mouse.
    Zohn IE; Anderson KV; Niswander L
    Birth Defects Res A Clin Mol Teratol; 2005 Sep; 73(9):583-90. PubMed ID: 15971254
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. Toward understanding the genetic basis of neural tube defects.
    Kibar Z; Capra V; Gros P
    Clin Genet; 2007 Apr; 71(4):295-310. PubMed ID: 17470131
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. Multisite neural tube closure in humans.
    Van Allen MI
    Birth Defects Orig Artic Ser; 1996; 30(1):203-25. PubMed ID: 9125329
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Testing for genetic associations in a spina bifida population: analysis of the HOX gene family and human candidate gene regions implicated by mouse models of neural tube defects.
    Volcik KA; Blanton SH; Kruzel MC; Townsend IT; Tyerman GH; Mier RJ; Northrup H
    Am J Med Genet; 2002 Jul; 110(3):203-7. PubMed ID: 12116226
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Genetic basis of neural tube defects. I. Regulatory genes for the neurulation process.
    Gos M; Szpecht-Potocka A
    J Appl Genet; 2002; 43(3):343-50. PubMed ID: 12177524
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mouse Fkbp8 activity is required to inhibit cell death and establish dorso-ventral patterning in the posterior neural tube.
    Wong RL; Wlodarczyk BJ; Min KS; Scott ML; Kartiko S; Yu W; Merriweather MY; Vogel P; Zambrowicz BP; Finnell RH
    Hum Mol Genet; 2008 Feb; 17(4):587-601. PubMed ID: 18003640
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Further characterization of the genetic defect of the Bent tail mouse, a mouse model for human neural tube defects.
    Klootwijk R; Schijvenaars MM; Mariman EC; Franke B
    Birth Defects Res A Clin Mol Teratol; 2004 Nov; 70(11):880-4. PubMed ID: 15526289
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic basis of neural tube defects.
    Bassuk AG; Kibar Z
    Semin Pediatr Neurol; 2009 Sep; 16(3):101-10. PubMed ID: 19778707
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Ribonucleotide reductase subunit R1: a gene conferring sensitivity to valproic acid-induced neural tube defects in mice.
    Craig JC; Bennett GD; Miranda RC; Mackler SA; Finnell RH
    Teratology; 2000 Apr; 61(4):305-13. PubMed ID: 10716750
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Modeling neural tube defects in the mouse.
    Zohn IE; Sarkar AA
    Curr Top Dev Biol; 2008; 84():1-35. PubMed ID: 19186242
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetically determined absence of an initiation site of cranial neural tube closure is causally related to exencephaly in SELH/Bc mouse embryos.
    Gunn TM; Juriloff DM; Harris MJ
    Teratology; 1995 Aug; 52(2):101-8. PubMed ID: 8588181
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Quantitative trait loci affecting phenotypic variation in the vacuolated lens mouse mutant, a multigenic mouse model of neural tube defects.
    Korstanje R; Desai J; Lazar G; King B; Rollins J; Spurr M; Joseph J; Kadambi S; Li Y; Cherry A; Matteson PG; Paigen B; Millonig JH
    Physiol Genomics; 2008 Nov; 35(3):296-304. PubMed ID: 18796533
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The genetic basis of mammalian neurulation.
    Copp AJ; Greene ND; Murdoch JN
    Nat Rev Genet; 2003 Oct; 4(10):784-93. PubMed ID: 13679871
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Epithelial cell polarity genes are required for neural tube closure.
    Doudney K; Stanier P
    Am J Med Genet C Semin Med Genet; 2005 May; 135C(1):42-7. PubMed ID: 15800847
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Evidence for multi-site closure of the neural tube in humans.
    Van Allen MI; Kalousek DK; Chernoff GF; Juriloff D; Harris M; McGillivray BC; Yong SL; Langlois S; MacLeod PM; Chitayat D
    Am J Med Genet; 1993 Oct; 47(5):723-43. PubMed ID: 8267004
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.