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Items: 1 to 20 of 101

1.

Transcriptional analyses of two mouse models of spina bifida.

Cabrera RM, Finnell RH, Zhu H, Shaw GM, Wlodarczyk BJ.

Birth Defects Res A Clin Mol Teratol. 2012 Oct;94(10):782-9. doi: 10.1002/bdra.23081. Epub 2012 Sep 28.

2.

Effect of arsenite, maternal age, and embryonic sex on spina bifida, exencephaly, and resorption rates in the splotch mouse.

Martin LJ, Machado AF, Loza MA, Mao GE, Lee GS, Hovland DN Jr, Cantor RM, Collins MD.

Birth Defects Res A Clin Mol Teratol. 2003 Apr;67(4):231-9.

PMID:
12854658
3.

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 15;17(4):587-601. Epub 2007 Nov 13.

PMID:
18003640
4.

Transgenic rescue of congenital heart disease and spina bifida in Splotch mice.

Li J, Liu KC, Jin F, Lu MM, Epstein JA.

Development. 1999 Jun;126(11):2495-503.

5.

Screening for novel PAX3 polymorphisms and risks of spina bifida.

Lu W, Zhu H, Wen S, Laurent C, Shaw GM, Lammer EJ, Finnell RH.

Birth Defects Res A Clin Mol Teratol. 2007 Jan;79(1):45-9.

PMID:
17149730
6.

Fetal neural tube stem cells from Pax3 mutant mice proliferate, differentiate, and form synaptic connections when stimulated with folic acid.

Ichi S, Nakazaki H, Boshnjaku V, Singh RM, Mania-Farnell B, Xi G, McLone DG, Tomita T, Mayanil CS.

Stem Cells Dev. 2012 Jan 20;21(2):321-30. doi: 10.1089/scd.2011.0100. Epub 2011 Jun 9.

PMID:
21521032
7.

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. doi: 10.1242/dev.101550. Epub 2013 Nov 27.

8.

Neurofibromin deficiency in mice causes exencephaly and is a modifier for Splotch neural tube defects.

Lakkis MM, Golden JA, O'Shea KS, Epstein JA.

Dev Biol. 1999 Aug 1;212(1):80-92.

9.

Over-expression of Grhl2 causes spina bifida in the Axial defects mutant mouse.

Brouns MR, De Castro SC, Terwindt-Rouwenhorst EA, Massa V, Hekking JW, Hirst CS, Savery D, Munts C, Partridge D, Lamers W, Köhler E, van Straaten HW, Copp AJ, Greene ND.

Hum Mol Genet. 2011 Apr 15;20(8):1536-46. doi: 10.1093/hmg/ddr031. Epub 2011 Jan 24.

10.

Transgenic mice expressing PAX3-FKHR have multiple defects in muscle development, including ectopic skeletal myogenesis in the developing neural tube.

Finckenstein FG, Davicioni E, Osborn KG, Cavenee WK, Arden KC, Anderson MJ.

Transgenic Res. 2006 Oct;15(5):595-614. Epub 2006 Sep 2.

PMID:
16952014
11.

Understanding the causes and prevention of neural tube defects: Insights from the splotch mouse model.

Greene ND, Massa V, Copp AJ.

Birth Defects Res A Clin Mol Teratol. 2009 Apr;85(4):322-30. doi: 10.1002/bdra.20539. Review.

PMID:
19180568
12.

Exon sequencing of PAX3 and T (brachyury) in cases with spina bifida.

Agopian AJ, Bhalla AD, Boerwinkle E, Finnell RH, Grove ML, Hixson JE, Shimmin LC, Sewda A, Stuart C, Zhong Y, Zhu H, Mitchell LE.

Birth Defects Res A Clin Mol Teratol. 2013 Sep;97(9):597-601. doi: 10.1002/bdra.23163. Epub 2013 Aug 2.

13.

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 1;16(21):2640-6. Epub 2007 Aug 24.

PMID:
17720888
14.
15.

Mechanisms of mutant genes in spina bifida: a review of implications from animal models.

George TM, McLone DG.

Pediatr Neurosurg. 1995;23(5):236-45. Review.

PMID:
8688348
16.

Spontaneous neural tube defects in splotch mice supplemented with selected micronutrients.

Wlodarczyk BJ, Tang LS, Triplett A, Aleman F, Finnell RH.

Toxicol Appl Pharmacol. 2006 May 15;213(1):55-63. Epub 2005 Oct 14.

PMID:
16226775
17.

Increased thymus- and decreased parathyroid-fated organ domains in Splotch mutant embryos.

Griffith AV, Cardenas K, Carter C, Gordon J, Iberg A, Engleka K, Epstein JA, Manley NR, Richie ER.

Dev Biol. 2009 Mar 1;327(1):216-27. doi: 10.1016/j.ydbio.2008.12.019. Epub 2008 Dec 25.

18.

Disruption of PDGFRalpha-initiated PI3K activation and migration of somite derivatives leads to spina bifida.

Pickett EA, Olsen GS, Tallquist MD.

Development. 2008 Feb;135(3):589-98. doi: 10.1242/dev.013763.

19.

De novo 2q36.1q36.3 interstitial deletion involving the PAX3 and EPHA4 genes in a fetus with spina bifida and cleft palate.

Goumy C, Gay-Bellile M, Eymard-Pierre E, Kemeny S, Gouas L, Déchelotte P, Gallot D, Véronèse L, Tchirkov A, Pebrel-Richard C, Vago P.

Birth Defects Res A Clin Mol Teratol. 2014 Jun;100(6):507-11. doi: 10.1002/bdra.23246. Epub 2014 Apr 18.

PMID:
24753315
20.

Interaction between undulated and Patch leads to an extreme form of spina bifida in double-mutant mice.

Helwig U, Imai K, Schmahl W, Thomas BE, Varnum DS, Nadeau JH, Balling R.

Nat Genet. 1995 Sep;11(1):60-3.

PMID:
7550316

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