PubMed (cited) for id: 601094

Year	Number of Results
1986	1
1995	1
2000	1
2001	1
2006	1
2007	1
2008	1
2010	2
2011	2
2016	2
2024	0

1

FOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1.

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. Khan SY, et al. Nat Commun. 2016 Apr 6;7:10953. doi: 10.1038/ncomms10953. Nat Commun. 2016. PMID: 27218149 Free PMC article.

2

FOXE3 mutations predispose to thoracic aortic aneurysms and dissections.

Kuang SQ, Medina-Martinez O, Guo DC, Gong L, Regalado ES, Reynolds CL, Boileau C, Jondeau G, Prakash SK, Kwartler CS, Zhu LY, Peters AM, Duan XY, Bamshad MJ, Shendure J, Nickerson DA, Santos-Cortez RL, Dong X, Leal SM, Majesky MW, Swindell EC, Jamrich M, Milewicz DM. Kuang SQ, et al. J Clin Invest. 2016 Mar 1;126(3):948-61. doi: 10.1172/JCI83778. Epub 2016 Feb 8. J Clin Invest. 2016. PMID: 26854927 Free PMC article.

3

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. Wada K, et al. Mamm Genome. 2011 Dec;22(11-12):693-702. doi: 10.1007/s00335-011-9358-y. Epub 2011 Oct 15. Mamm Genome. 2011. PMID: 22002806

4

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. Doucette L, et al. Eur J Hum Genet. 2011 Mar;19(3):293-9. doi: 10.1038/ejhg.2010.210. Epub 2010 Dec 8. Eur J Hum Genet. 2011. PMID: 21150893 Free PMC article.

5

A mutation in the FOXE3 gene causes congenital primary aphakia in an autosomal recessive consanguineous Pakistani family.

Anjum I, Eiberg H, Baig SM, Tommerup N, Hansen L. Anjum I, et al. Mol Vis. 2010 Mar 30;16:549-55. Mol Vis. 2010. PMID: 20361012 Free PMC article.

6

The orphan G protein-coupled receptor, Gpr161, encodes the vacuolated lens locus and controls neurulation and lens development.

Matteson PG, Desai J, Korstanje R, Lazar G, Borsuk TE, Rollins J, Kadambi S, Joseph J, Rahman T, Wink J, Benayed R, Paigen B, Millonig JH. Matteson PG, et al. Proc Natl Acad Sci U S A. 2008 Feb 12;105(6):2088-93. doi: 10.1073/pnas.0705657105. Epub 2008 Feb 4. Proc Natl Acad Sci U S A. 2008. PMID: 18250320 Free PMC article.

7

Localization of autosomal recessive congenital cataracts in consanguineous Pakistani families to a new locus on chromosome 1p.

Butt T, Yao W, Kaul H, Xiaodong J, Gradstein L, Zhang Y, Husnain T, Riazuddin S, Hejtmancik JF, Riazuddin SA. Butt T, et al. Mol Vis. 2007 Sep 10;13:1635-40. Mol Vis. 2007. PMID: 17893665

8

Homozygous nonsense mutation in the FOXE3 gene as a cause of congenital primary aphakia in humans.

Valleix S, Niel F, Nedelec B, Algros MP, Schwartz C, Delbosc B, Delpech M, Kantelip B. Valleix S, et al. Am J Hum Genet. 2006 Aug;79(2):358-64. doi: 10.1086/505654. Epub 2006 Jun 8. Am J Hum Genet. 2006. PMID: 16826526 Free PMC article.

9

Mutations in the human forkhead transcription factor FOXE3 associated with anterior segment ocular dysgenesis and cataracts.

Semina EV, Brownell I, Mintz-Hittner HA, Murray JC, Jamrich M. Semina EV, et al. Hum Mol Genet. 2001 Feb 1;10(3):231-6. doi: 10.1093/hmg/10.3.231. Hum Mol Genet. 2001. PMID: 11159941

10

A forkhead gene, FoxE3, is essential for lens epithelial proliferation and closure of the lens vesicle.

Blixt A, Mahlapuu M, Aitola M, Pelto-Huikko M, Enerbäck S, Carlsson P. Blixt A, et al. Genes Dev. 2000 Jan 15;14(2):245-54. Genes Dev. 2000. PMID: 10652278 Free PMC article.

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