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Correction to: A zebrafish model of foxe3 deficiency demonstrates lens and eye defects with dysregulation of key genes involved in cataract formation in humans.

Krall M, Htun S, Anand D, Hart D, Lachke SA, Slavotinek AM.

Hum Genet. 2018 May;137(5):427-428. doi: 10.1007/s00439-018-1890-3.


A zebrafish model of foxe3 deficiency demonstrates lens and eye defects with dysregulation of key genes involved in cataract formation in humans.

Krall M, Htun S, Anand D, Hart D, Lachke SA, Slavotinek AM.

Hum Genet. 2018 Apr;137(4):315-328. doi: 10.1007/s00439-018-1884-1. Epub 2018 Apr 30. Erratum in: Hum Genet. 2018 May 11;:.


Mutation update of transcription factor genes FOXE3, HSF4, MAF, and PITX3 causing cataracts and other developmental ocular defects.

Anand D, Agrawal SA, Slavotinek A, Lachke SA.

Hum Mutat. 2018 Apr;39(4):471-494. doi: 10.1002/humu.23395. Epub 2018 Jan 16. Review.


Zebrafish foxe3: roles in ocular lens morphogenesis through interaction with pitx3.

Shi X, Luo Y, Howley S, Dzialo A, Foley S, Hyde DR, Vihtelic TS.

Mech Dev. 2006 Oct;123(10):761-82. Epub 2006 Jul 16.


Molecular characterization of mouse lens epithelial cell lines and their suitability to study RNA granules and cataract associated genes.

Terrell AM, Anand D, Smith SF, Dang CA, Waters SM, Pathania M, Beebe DC, Lachke SA.

Exp Eye Res. 2015 Feb;131:42-55. doi: 10.1016/j.exer.2014.12.011. Epub 2014 Dec 19.


Identification of dominant FOXE3 and PAX6 mutations in patients with congenital cataract and aniridia.

Brémond-Gignac D, Bitoun P, Reis LM, Copin H, Murray JC, Semina EV.

Mol Vis. 2010 Aug 22;16:1705-11.


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.


FOXE3 plays a significant role in autosomal recessive microphthalmia.

Reis LM, Tyler RC, Schneider A, Bardakjian T, Stoler JM, Melancon SB, Semina EV.

Am J Med Genet A. 2010 Mar;152A(3):582-90. doi: 10.1002/ajmg.a.33257.


Seeing clearly: the dominant and recessive nature of FOXE3 in eye developmental anomalies.

Iseri SU, Osborne RJ, Farrall M, Wyatt AW, Mirza G, Nürnberg G, Kluck C, Herbert H, Martin A, Hussain MS, Collin JR, Lathrop M, Nürnberg P, Ragoussis J, Ragge NK.

Hum Mutat. 2009 Oct;30(10):1378-86. doi: 10.1002/humu.21079.


Foxe3 haploinsufficiency in mice: a model for Peters' anomaly.

Ormestad M, Blixt A, Churchill A, Martinsson T, Enerbäck S, Carlsson P.

Invest Ophthalmol Vis Sci. 2002 May;43(5):1350-7.


Overexpression of PAX6(5a) in lens fiber cells results in cataract and upregulation of (alpha)5(beta)1 integrin expression.

Duncan MK, Kozmik Z, Cveklova K, Piatigorsky J, Cvekl A.

J Cell Sci. 2000 Sep;113 ( Pt 18):3173-85.


A deletion in a cis element of Foxe3 causes cataracts and microphthalmia in rct mice.

Wada K, Maeda YY, Watanabe K, Oshio T, Ueda T, Takahashi G, Yokohama M, Saito J, Seki Y, Takahama S, Ishii R, Shitara H, Taya C, Yonekawa H, Kikkawa Y.

Mamm Genome. 2011 Dec;22(11-12):693-702. doi: 10.1007/s00335-011-9358-y. Epub 2011 Oct 15.


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.


Foxe3 is required for morphogenesis and differentiation of the anterior segment of the eye and is sensitive to Pax6 gene dosage.

Blixt A, Landgren H, Johansson BR, Carlsson P.

Dev Biol. 2007 Feb 1;302(1):218-29. Epub 2006 Sep 16.


Severe defects in proliferation and differentiation of lens cells in Foxe3 null mice.

Medina-Martinez O, Brownell I, Amaya-Manzanares F, Hu Q, Behringer RR, Jamrich M.

Mol Cell Biol. 2005 Oct;25(20):8854-63.


Activation of the hedgehog signaling pathway in the developing lens stimulates ectopic FoxE3 expression and disruption in fiber cell differentiation.

Kerr CL, Huang J, Williams T, West-Mays JA.

Invest Ophthalmol Vis Sci. 2012 Jun 5;53(7):3316-30. doi: 10.1167/iovs.12-9595.


Expression of FoxE4 and Rx visualizes the timing and dynamics of critical processes taking place during initial stages of vertebrate eye development.

Zilinski C, Brownell I, Hashimoto R, Medina-Martinez O, Swindell EC, Jamrich M.

Dev Neurosci. 2004;26(5-6):294-307. Review.


Growth inhibition of human lens epithelial cells by short hairpin RNA in transcription factor forkhead box E3 (FOXE3).

Wang Y, Li W, Wang Y, Huang Y.

Graefes Arch Clin Exp Ophthalmol. 2012 Jul;250(7):999-1007. doi: 10.1007/s00417-012-1944-5. Epub 2012 Apr 18.


Systems biology of lens development: A paradigm for disease gene discovery in the eye.

Anand D, Lachke SA.

Exp Eye Res. 2017 Mar;156:22-33. doi: 10.1016/j.exer.2016.03.010. Epub 2016 Mar 16. Review.

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