Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia (Q28587212)

31 January 2017

title

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

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EYA transcriptional coactivator and phosphatase 1

31 January 2017

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GOA release 2020-03-11

P. X. Xu

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31 January 2017

J. Adams

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31 January 2017

H. Peters

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31 January 2017

M. C. Brown

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31 January 2017

S. Heaney

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31 January 2017

R. Maas

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31 January 2017

language of work or name

English

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publication date

1 September 1999

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31 January 2017

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31 January 2017

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31 January 2017

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31 January 2017

page(s)

113–117

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A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family

31 January 2017

cites work

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7 January 2021

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

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7 January 2021

GDNF signalling through the Ret receptor tyrosine kinase

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7 January 2021

Glial cell line-derived neurotrophic factor activates the receptor tyrosine kinase RET and promotes kidney morphogenesis

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7 January 2021

Glial cell line-derived neurotrophic factor-dependent RET activation can be mediated by two different cell-surface accessory proteins

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7 January 2021

Functional receptor for GDNF encoded by the c-ret proto-oncogene

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7 January 2021

The eye-specification proteins So and Eya form a complex and regulate multiple steps in Drosophila eye development

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7 January 2021

Frequency of the branchio-oto-renal (BOR) syndrome in children with profound hearing loss

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7 January 2021

Phenotypic manifestations of branchio-oto-renal syndrome.

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7 January 2021

Branchio-oto-renal syndrome: reduced penetrance and variable expressivity in four generations of a large kindred

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7 January 2021

Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus

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7 January 2021

Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux.

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7 January 2021

The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney

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7 January 2021

Pax9-deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities.

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7 January 2021

WT-1 is required for early kidney development

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7 January 2021

Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret

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7 January 2021

Inner ear and kidney anomalies caused by IAP insertion in an intron of the Eya1 gene in a mouse model of BOR syndrome

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7 January 2021

Identifiers

DOI

10.1038/12722

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Consolidated OpenCitations Corpus – April 2017

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Consolidated OpenCitations Corpus – April 2017

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Consolidated OpenCitations Corpus – April 2017