EYA1 expression in the developing inner ear.

Item

http://www.wikidata.org/entity/Q46854275

description

2005 nî lūn-bûn

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2005年の論文

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2005年学术文章

@wuu

2005年学术文章

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2005年学术文章

@zh-cn

2005年学术文章

@zh-hans

2005年学术文章

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2005年学术文章

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2005年學術文章

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2005年學術文章

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name

EYA1 expression in the developing inner ear.

@en

EYA1 expression in the developing inner ear.

@nl

type

Item

label

EYA1 expression in the developing inner ear.

@en

EYA1 expression in the developing inner ear.

@nl

prefLabel

EYA1 expression in the developing inner ear.

@en

EYA1 expression in the developing inner ear.

@nl

P1476

EYA1 expression in the developing inner ear.

@en

P2093

Brian C Bane

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Daniel L Weeks

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Jana M Van Rybroek

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Jose M Manaligod

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Sandra J Kolker

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P2860

Molecular interaction and synergistic activation of a promoter by Six, Eya, and Dach proteins mediated through CREB binding protein

Cooperation of six and eya in activation of their target genes through nuclear translocation of Eya

Mutations of a human homologue of the Drosophila eyes absent gene (EYA1) detected in patients with congenital cataracts and ocular anterior segment anomalies

Eya protein phosphatase activity regulates Six1-Dach-Eya transcriptional effects in mammalian organogenesis

Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1

Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia

Congenital cholesteatoma and malformations of the facial nerve: rare manifestations of the BOR syndrome.

The presence of a widened vestibular aqueduct and progressive sensorineural hearing loss in the branchio-oto-renal syndrome. A family study.

The eyes absent gene: genetic control of cell survival and differentiation in the developing Drosophila eye.

Genetic aspects of the BOR syndrome--branchial fistulas, ear pits, hearing loss, and renal anomalies.

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853-858

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scholarly article

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10.1177/000348940511401108

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P478

114

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2005-11-01T00:00:00Z

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16358604

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