A comparative study of Eya1 and Eya4 protein function and its implication in branchio-oto-renal syndrome and DFNA10 (Q41742284)

8 October 2017

A comparative study of Eya1 and Eya4 protein function and its implication in branchio-oto-renal syndrome and DFNA10 (English)

1 reference

8 October 2017

Yuzhou Zhang

1

1 reference

8 October 2017

Boyd M Knosp

2

1 reference

8 October 2017

Mark Maconochie

3

1 reference

8 October 2017

Rick A Friedman

4

1 reference

8 October 2017

Richard J H Smith

5

1 reference

8 October 2017

language of work or name

1 reference

24 June 2004

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8 October 2017

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8 October 2017

5

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8 October 2017

3

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8 October 2017

295-304

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https://scigraph.springernature.com/pub.10.1007/s10162-004-4044-3

8 October 2017

0 references

cites work

A 4-bp insertion in the eya-homologous region (eyaHR) of EYA4 causes hearing impairment in a Hungarian family linked to DFNA10

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504552

Impaired interactions between mouse Eyal harboring mutations found in patients with branchio-oto-renal syndrome and Six, Dach, and G proteins

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504552

Molecular effects of Eya1 domain mutations causing organ defects in BOR syndrome

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504552

Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504552

Synergistic regulation of vertebrate muscle development by Dach2, Eya2, and Six1, homologs of genes required for Drosophila eye formation

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504552

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

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504552

Detoxification of environmental mutagens and carcinogens: structure, mechanism, and evolution of liver epoxide hydrolase

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504552

EYA4, a novel vertebrate gene related to Drosophila eyes absent

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504552

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

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504552

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

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504552

Cloning and characterization of two vertebrate homologs of the Drosophila eyes absent gene

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504552

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

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504552

Mouse Eya homologues of the Drosophila eyes absent gene require Pax6 for expression in lens and nasal placode

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504552

The mutational spectrum in Waardenburg syndrome.

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504552

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

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504552

The molecular basis of genetic dominance

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504552

A method for plasmid purification directly from yeast.

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504552

18 August 2018

The DFNA10 phenotype.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504552

The Drosophila eyes absent gene directs ectopic eye formation in a pathway conserved between flies and vertebrates.

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504552

Phenotypic manifestations of branchio-oto-renal syndrome.

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504552

Loss of DNA-dependent dimerization of the transcription factor SOX9 as a cause for campomelic dysplasia

18 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15492887

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Dachshund and eyes absent proteins form a complex and function synergistically to induce ectopic eye development in Drosophila

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15492887

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S10162-004-4044-3

1 reference

8 October 2017

1 reference

8 October 2017

PubMed publication ID

15492887

1 reference