| 1 | CTRCT34, FOXE3
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| Association of FOXE3-p.Ala170Ala and PITX3-p.Ile95Ile Polymorphisms with Congenital Cataract and Microphthalmia.
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| Vidya NG, Ganatra D, Vasavada AR, Rajkumar S.
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| J Ophthalmic Vis Res 13(4):397-402. doi: 10.4103/jovr.jovr_193_17.
2018
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| 2 | APKC, FOXE3
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| Sclerocornea-Microphthalmia-Aphakia Complex: Description of Two Additional Cases Associated With Novel FOXE3 Mutations and Review of the Literature.
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| Quiroz-Casian N, Chacon-Camacho OF, Barragan-Arevalo T, Nava-Valdez J, Lieberman E, Salgado-Medina A, Navas A, Graue-Hernandez EO, Zenteno JC.
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| Cornea 37(9):1178-1181. doi: 10.1097/ICO.0000000000001655. Review.
2018
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| 3 | APKC, FOXE3
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| FOXE3 mutations: genotype-phenotype correlations.
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| Plaisancié J, Ragge NK, Dollfus H, Kaplan J, Lehalle D, Francannet C, Morin G, Colineaux H, Calvas P, Chassaing N.
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| Clin Genet 93(4):837-845. doi: 10.1111/cge.13177.
2018
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| 4 | APKC, ASMD5, FOXE3
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| Sclerocornea-Microphthalmia-Aphakia Complex: Description of Two Additional Cases Associated With Novel FOXE3 Mutations and Review of the Literature.
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| Quiroz-Casian N, Chacon-Camacho OF, Barragan-Arevalo T, Nava-Valdez J, Lieberman E, Salgado-Medina A, Navas A, Graue-Hernandez EO, Zenteno JC.
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| Cornea 37(9):1178-1181. doi: 10.1097/ICO.0000000000001655. Review.
2018
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| 5 | DNAJB1, FOXE3
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| FOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1.
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| Khan SY, Vasanth S, Kabir F, Gottsch JD, Khan AO, Chaerkady R, Lee MC, Leitch CC, Ma Z, Laux J, Villasmil R, Khan SN, Riazuddin S, Akram J, Cole RN, Talbot CC, Pourmand N, Zaghloul NA, Hejtmancik JF, Riazuddin SA.
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| Nat Commun 7:10953. doi: 10.1038/ncomms10953.
2016
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| 6 | ASMD5, FOXE3
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| Functional analysis of FOXE3 mutations causing dominant and recessive ocular anterior segment disease.
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| Islam L, Kelberman D, Williamson L, Lewis N, Glindzicz MB, Nischal KK, Sowden JC.
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| Hum Mutat 36(3):296-300. doi: 10.1002/humu.22741.
2015
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| 7 | FOXE3, PITX3
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| Pitx3 directly regulates Foxe3 during early lens development.
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| Ahmad N, Aslam M, Muenster D, Horsch M, Khan MA, Carlsson P, Beckers J, Graw J.
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| Int J Dev Biol 57(9-10):741-51. doi: 10.1387/ijdb.130193jg.
2013
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| 8 | FOXE3
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| Activation of the hedgehog signaling pathway in the developing lens stimulates ectopic FoxE3 expression and disruption in fiber cell differentiation.
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| Kerr CL, Huang J, Williams T, West-Mays JA.
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| Invest Ophthalmol Vis Sci 53(7):3316-30. doi: 10.1167/iovs.12-9595.
2012
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| 9 | ASMD5, FOXE3
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| A novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variable anterior segment dysgenesis including Peters anomaly.
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| Doucette L, Green J, Fernandez B, Johnson GJ, Parfrey P, Young TL.
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| Eur J Hum Genet 19(3):293-9. doi: 10.1038/ejhg.2010.210. Epub 2010 Dec 8.
2011
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| 10 | APKC, FOXE3
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| FOXE3 plays a significant role in autosomal recessive microphthalmia.
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| Reis LM, Tyler RC, Schneider A, Bardakjian T, Stoler JM, Melancon SB, Semina EV.
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| Am J Med Genet A m J Med Genet A. 2010 Feb 5. [Epub ahead of print]PMID: 20140963 2010
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| 11 | APKC, FOXE3
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| Homozygous FOXE3 mutations cause non-syndromic, bilateral, total sclerocornea, aphakia, microphthalmia and optic disc coloboma.
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| 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.
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| Mol Vis 16:1162-8.
2010
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| 12 | APKC, FOXE3
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| Seeing clearly: the dominant and recessive nature of FOXE3 in eye developmental anomalies.
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| 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.
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| Hum Mutat 30(10):1378-86.PMID: 19708017 2009
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| 13 | FOXE3
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| Persistent FoxE3 expression blocks cytoskeletal remodeling and organelle degradation during lens fiber differentiation.
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| Landgren H, Blixt A, Carlsson P.
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| Invest Ophthalmol Vis Sci 49(10):4269-77. Epub 2008 Jun 6.PMID: 18539941 2008
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| 14 | FOXE3
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| Regulation and function of foxe3 during early zebrafish development.
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| Swindell EC, Zilinski CA, Hashimoto R, Shah R, Lane ME, Jamrich M.
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| Genesis 46(3):177-83.PMID: 18327772 2008
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| 15 | CTRCT34, FOXE3
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| Localization of autosomal recessive congenital cataracts in consanguineous Pakistani families to a new locus on chromosome 1p.
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| Butt T, Yao W, Kaul H, Xiaodong J, Gradstein L, Zhang Y, Husnain T, Riazuddin S, Hejtmancik JF, Riazuddin SA.
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| Mol Vis 13:1635-40.
2007
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| 16 | FOXE3, APKC
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| Homozygous nonsense mutation in the FOXE3 gene as a cause of congenital primary aphakia in humans.
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| Valleix S, Niel F, Nedelec B, Algros MP, Schwartz C, Delbosc B, Delpech M, Kantelip B.
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| Am J Hum Genet 79(2):358-64. Epub 2006 Jun 8. 2006
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| 17 | FOXC2, LPDD,FOXC1, FOXE1, FOXE3, FOXL2, FOXN1, FOXP2, FOXP3, YNS
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| The establishment of a predictive mutational model of the forkhead domain through the analyses of FOXC2 missense mutations identified in patients with hereditary lymphedema with distichiasis.
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| Berry FB, Tamimi Y, Carle MV, Lehmann OJ, Walter MA.
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| Hum Mol Genet 14(18):2619-27. Epub 2005 Aug 4. 2005
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| 18 | ASMD5, FOXE3
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| Mutations in the human forkhead transcription factor FOXE3 associated with anterior segment ocular dysgenesis and cataracts.
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| Semina EV, Brownell I, Mintz-Hittner HA, Murray JC, Jamrich M.
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| Hum Mol Genet 10(3):231-6. 2001
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| 19 | FOXE3
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| A forkhead gene, FoxE3, is essential for lens epithelial proliferation and closure of the lens vesicle.
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| Blixt A, Mahlapuu M, Aitola M, Pelto-Huikko M, Enerback S, Carlsson P.
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| Genes Dev 14(2):245-54. 2000
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| 20 | FOXF1, FOXC1, FOXD1, FOXD4, FOXI1, FOXE3
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| Chromosomal localization of six human forkhead genes, freac-1 (FKHL5), -3 (FKHL7), -4 (FKHL8), -5 (FKHL9), -6 (FKHL10), and -8 (FKHL12).
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| Larsson C, Hellqvist M, Pierrou S, White I, Enerback S, Carlsson P.
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| Genomics 30(3):464-9. 1995
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| 21 | FOXC1, FOXD1, FOXD4, FOXE3, FOXF1, FOXI1, FOXL1
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| Cloning and characterization of seven human forkhead proteins: binding site specificity and DNA bending.
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| Pierrou S, Hellqvist M, Samuelsson L, Enerback S, Carlsson P.
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| EMBO J 13(20) : 5002-12. 1994
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