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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

Related topics

Related topics

7 relations
Biologic DevelopmentDephosphorylationEYA1 protein, humanHydrolysis

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Chondrogenic differentiation in vitro of hiPSCs activates pathways engaged in limb development.
2012
2012
Eya1 protein phosphatase regulates tight junction formation in lung distal epithelium
Summary Little is known about the regulatory mechanisms underlying lung epithelial tight junction (TJ) assembly, which is… 
2009
2009
A novel splice site mutation in the EYA1 gene in a Korean family with branchio-oto (BO) syndrome
Branchio-oto-renal (BOR) and branchio-oto (BO) syndromes are autosomal dominant hereditary disorders characterized by the… 
2009
2009
Familial transmission of oculoauriculovertebral spectrum (Goldenhar syndrome) is not due to mutations in either EYA1 or SALL1
Familial Transmission of Oculoauriculovertebral Spectrum (Goldenhar Syndrome) Is Not Due to Mutations in Either EYA1 or SALL1… 
2006
2006
Renal hypoplasia and dysplasia: starting to put the puzzle together.
The human metanephros is the direct precursor of the mature kidney: It begins to form in the fifth gestational week, when… 
Highly Cited
2006
Highly Cited
2006
Transcriptional Activation of the SALL1 by the Human SIX1 Homeodomain during Kidney Development*
SALL1 is a member of the SAL gene family that encodes a group of putative developmental transcription factors. SALL1 plays a… 
2005
2005
Eya1 acts upstream of Tbx1, Neurogenin 1, NeuroD and the neurotrophins BDNF and NT-3 during inner ear development
2004
2004
SIX 1 mutations cause branchio-oto-renal syndrome by disruption of EYA 1 – SIX 1 – DNA complexes
Rainer G. Rufa,b,c, Pin-Xian Xuc,d,e, Derek Silviusd, Edgar A. Ottoa, Frank Beekmanna, Ulla T. Muerba, Shrawan Kumarf, Thomas J… 
2001
2001
Genetic features of hearing loss associated with ear anomalies: PDS and EYA1 mutation analysis
AbstractMutation analysis of the PDS gene and the EYA1 gene, which are reported to be responsible for hearing loss associated… 
1999
1999
EYA1 nonsense mutation in a Japanese branchio-oto-renal syndrome family
AbstractAdvances in molecular genetics have recently revealed that mutations in the EYA1 gene are responsible for branchio-oto… 
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