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FOXE3 gene

Known as: FORKHEAD-RELATED ACTIVATOR 8, FOXE3, FORKHEAD BOX E3 
National Institutes of Health

Papers overview

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Review
2018
Review
2018
Mutations in the transcription factor genes FOXE3, HSF4, MAF, and PITX3 cause congenital lens defects including cataracts that… Expand
Highly Cited
2016
Highly Cited
2016
The ascending thoracic aorta is designed to withstand biomechanical forces from pulsatile blood. Thoracic aortic aneurysms and… Expand
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2010
2010
Purpose Aniridia and congenital cataract represent rare but severe developmental ocular conditions. We examined 33 probands from… Expand
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Highly Cited
2010
Highly Cited
2010
FOXE3 forkhead transcription factor is essential to lens development in vertebrates. The eyes of Foxe3/foxe3‐deficient mice and… Expand
Highly Cited
2009
Highly Cited
2009
FOXE3 is a lens‐specific transcription factor with a highly conserved forkhead domain previously implicated in congenital primary… Expand
Highly Cited
2007
Highly Cited
2007
The dysgenetic lens (dyl) mouse mutant has mutations in Foxe3, which inactivate DNA binding by the encoded forkhead transcription… Expand
Highly Cited
2002
Highly Cited
2002
PURPOSE To evaluate the importance in anterior segment dysgenesis of genetic variation in Foxe3, a gene encoding a forkhead… Expand
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Highly Cited
2001
Highly Cited
2001
Dysgenesis of the anterior segment of the eye delineates a spectrum of human developmental disorders that show wide phenotypic… Expand
Highly Cited
2000
Highly Cited
2000
Summary: Here we report the isolation of a novel forkhead gene, Foxe3, that plays an important role in lens formation. During… Expand
Highly Cited
1995
Highly Cited
1995
The forkhead family of transcription factors has been shown to be involved in the regulation of embryonic development in… Expand