(Q24317065)

GOA release 2020-03-11

SIX homeobox 1

1 reference

GOA release 2020-03-11

author name string

Aaron N Patrick

1

0 references

Barbara J Schiemann

2

0 references

Kui Yang

3

0 references

Rui Zhao

4

0 references

Heide L Ford

Journal of Biological Chemistry

5

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language of work or name

English

0 references

publication date

31 July 2009

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published in

0 references

volume

284

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issue

31

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page(s)

20781-90

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cites work

Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2742842

SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2742842

A gene locus for branchio-otic syndrome maps to chromosome 14q21.3-q24.3

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2742842

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2742842

Structure, function and expression of a murine homeobox protein AREC3, a homologue of Drosophila sine oculis gene product, and implication in development

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2742842

Eyes absent represents a class of protein tyrosine phosphatases

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2742842

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2742842

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2742842

Expression of myogenin during embryogenesis is controlled by Six/sine oculis homeoproteins through a conserved MEF3 binding site

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2742842

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2742842

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2742842

Cell cycle regulation of the human Six1 homeoprotein is mediated by APC(Cdh1).

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2742842

Using Drosophila to decipher how mutations associated with human branchio-oto-renal syndrome and optical defects compromise the protein tyrosine phosphatase and transcriptional functions of eyes absent

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2742842

Six family genes--structure and function as transcription factors and their roles in development

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2742842

Molecular analysis of Drosophila eyes absent mutants reveals features of the conserved Eya domain

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2742842

Mouse Eya genes are expressed during limb tendon development and encode a transcriptional activation function

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2742842

Differential DNA-binding specificity of the engrailed homeodomain: the role of residue 50.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2742842

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

27 September 2017

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M109.016832

Branchio-oto-renal syndrome: the mutation spectrum in EYA1 and its phenotypic consequences.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M109.016832

The transcription factor Eyes absent is a protein tyrosine phosphatase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M109.016832

SIX1 mutation screening in 247 branchio-oto-renal syndrome families: a recurrent missense mutation associated with BOR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M109.016832

DNA-binding and regulation mechanisms of the SIX family of retinal determination proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M109.016832

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

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2742842

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

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19497856

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Branchio-oto-renal syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19497856