EYA1 gene

Known as: EYA transcriptional coactivator and phosphatase 1, Eyes Absent Homolog 1 (Drosophila) Gene, EYA1 
This gene may play a role in organ development.
National Institutes of Health

Papers overview

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Highly Cited
2007
Highly Cited
2007
In mammals, Pax3, Six4, Six1 and Six5 genes are co-expressed with Eya1, Eya2 and Eya4 genes during mouse somitogenesis. To… (More)
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Highly Cited
2006
Highly Cited
2006
Renal hypodysplasia (RHD) is characterized by a reduced nephron number, small kidney size, and disorganized renal tissue. A… (More)
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Highly Cited
2004
Highly Cited
2004
Urinary tract malformations constitute the most frequent cause of chronic renal failure in the first two decades of life… (More)
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Highly Cited
2004
Highly Cited
2004
Eya1 encodes a transcriptional co-activator and is expressed in cranial sensory placodes. It interacts with and functions… (More)
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Highly Cited
2002
Highly Cited
2002
Eyes absent (Eya) genes regulate organogenesis in both vertebrates and invertebrates. Mutations in human EYA1 cause congenital… (More)
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Highly Cited
2000
Highly Cited
2000
The Drosophila eyes absent gene ( eya ) is involved in the formation of compound eyes. Flies with loss-of-function mutations of… (More)
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Highly Cited
1999
Highly Cited
1999
Haploinsufficiency for human EYA1, a homologue of the Drosophila melanogaster gene eyes absent (eya), results in the dominantly… (More)
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Highly Cited
1999
Highly Cited
1999
 The eyes absent-like genes encode a group of putative transcriptional coactivators with a sole representative in Drosophila and… (More)
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Highly Cited
1997
Highly Cited
1997
Branchio-oto-renal (BOR) syndrome is an autosomal dominant disorder, characterised by the association of branchial, otic and… (More)
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Highly Cited
1997
Highly Cited
1997
A candidate gene for Branchio-Oto-Renal (BOR) syndrome was identified at chromosome 8q13.3 by positional cloning and shown to… (More)
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