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Items: 1 to 20 of 65

1.

A novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variable anterior segment dysgenesis including Peters anomaly.

Doucette L, Green J, Fernandez B, Johnson GJ, Parfrey P, Young TL.

Eur J Hum Genet. 2011 Mar;19(3):293-9. doi: 10.1038/ejhg.2010.210. Epub 2010 Dec 8.

2.

[Peter's anomaly, clinical and therapeutic aspects: case report].

Meyer I, Rolim H, Medeiros A, Paiva L, Galv√£o Filho R.

Arq Bras Oftalmol. 2010 Jul-Aug;73(4):367-9. Portuguese.

3.

Homozygous FOXE3 mutations cause non-syndromic, bilateral, total sclerocornea, aphakia, microphthalmia and optic disc coloboma.

Ali M, Buentello-Volante B, McKibbin M, Rocha-Medina JA, Fernandez-Fuentes N, Koga-Nakamura W, Ashiq A, Khan K, Booth AP, Williams G, Raashid Y, Jafri H, Rice A, Inglehearn CF, Zenteno JC.

Mol Vis. 2010 Jun 23;16:1162-8.

4.
5.

A novel mutation of PAX6 in Chinese patients with new clinical features of Peters' anomaly.

Jia X, Guo X, Jia X, Xiao X, Li S, Zhang Q.

Mol Vis. 2010 Apr 15;16:676-81.

6.

Analysis of Msx1 and Msx2 transactivation function in the context of the heat shock 70 (Hspa1b) gene promoter.

Zhuang F, Nguyen MP, Shuler C, Liu YH.

Biochem Biophys Res Commun. 2009 Apr 3;381(2):241-6. doi: 10.1016/j.bbrc.2009.02.016. Epub 2009 Feb 11.

7.

Pitx3 controls multiple aspects of lens development.

Medina-Martinez O, Shah R, Jamrich M.

Dev Dyn. 2009 Sep;238(9):2193-201. doi: 10.1002/dvdy.21924.

8.

Anterior segment mesenchymal dysgenesis in a large Australian family is associated with the recurrent 17 bp duplication in PITX3.

Summers KM, Withers SJ, Gole GA, Piras S, Taylor PJ.

Mol Vis. 2008;14:2010-5. Epub 2008 Nov 5.

9.

Functions of the type 1 BMP receptor Acvr1 (Alk2) in lens development: cell proliferation, terminal differentiation, and survival.

Rajagopal R, Dattilo LK, Kaartinen V, Deng CX, Umans L, Zwijsen A, Roberts AB, Bottinger EP, Beebe DC.

Invest Ophthalmol Vis Sci. 2008 Nov;49(11):4953-60. doi: 10.1167/iovs.08-2217. Epub 2008 Jun 19.

10.

Msx2 exerts bone anabolism via canonical Wnt signaling.

Cheng SL, Shao JS, Cai J, Sierra OL, Towler DA.

J Biol Chem. 2008 Jul 18;283(29):20505-22. doi: 10.1074/jbc.M800851200. Epub 2008 May 15.

11.

Anterior segment dysgenesis: Peters anomaly and sclerocornea.

Harissi-Dagher M, Colby K.

Int Ophthalmol Clin. 2008 Spring;48(2):35-42. doi: 10.1097/IIO.0b013e318169526c. Review. No abstract available.

PMID:
18427259
12.

Anterior segment dysgenesis in the eyes of mice deficient for the high-mobility-group transcription factor Sox11.

Wurm A, Sock E, Fuchshofer R, Wegner M, Tamm ER.

Exp Eye Res. 2008 Jun;86(6):895-907. doi: 10.1016/j.exer.2008.03.004. Epub 2008 Mar 12.

PMID:
18423449
13.

Crucial role of zebrafish prox1 in hypothalamic catecholaminergic neurons development.

Pistocchi A, Gaudenzi G, Carra S, Bresciani E, Del Giacco L, Cotelli F.

BMC Dev Biol. 2008 Mar 10;8:27. doi: 10.1186/1471-213X-8-27.

14.

Regulation and function of foxe3 during early zebrafish development.

Swindell EC, Zilinski CA, Hashimoto R, Shah R, Lane ME, Jamrich M.

Genesis. 2008 Mar;46(3):177-83. doi: 10.1002/dvg.20380.

PMID:
18327772
15.

Cell autonomous roles for AP-2alpha in lens vesicle separation and maintenance of the lens epithelial cell phenotype.

Pontoriero GF, Deschamps P, Ashery-Padan R, Wong R, Yang Y, Zavadil J, Cvekl A, Sullivan S, Williams T, West-Mays JA.

Dev Dyn. 2008 Mar;237(3):602-17. doi: 10.1002/dvdy.21445.

16.

Prox1 regulates a transitory state for interneuron neurogenesis in the spinal cord.

Misra K, Gui H, Matise MP.

Dev Dyn. 2008 Feb;237(2):393-402. doi: 10.1002/dvdy.21422. Erratum in: Dev Dyn. 2011 Feb;240(2):458. Dev Dyn. 2008 Apr;237(4):1214. Mishra, Kamana [corrected to Misra, Kamana].

17.

BMP signaling mediates stem/progenitor cell-induced retina regeneration.

Haynes T, Gutierrez C, Aycinena JC, Tsonis PA, Del Rio-Tsonis K.

Proc Natl Acad Sci U S A. 2007 Dec 18;104(51):20380-5.

18.

Convergence of a head-field selector Otx2 and Notch signaling: a mechanism for lens specification.

Ogino H, Fisher M, Grainger RM.

Development. 2008 Jan;135(2):249-58. Epub 2007 Dec 5.

19.

Anophthalmia and microphthalmia.

Verma AS, Fitzpatrick DR.

Orphanet J Rare Dis. 2007 Nov 26;2:47. Review.

20.

Molecular and developmental mechanisms of anterior segment dysgenesis.

Sowden JC.

Eye (Lond). 2007 Oct;21(10):1310-8. Review.

PMID:
17914434

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