(Q34127314)

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Multiple enhancers located in a 1-Mb region upstream of POU3F4 promote expression during inner ear development and may be required for hearing

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20668882%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

Multiple enhancers located in a 1-Mb region upstream of POU3F4 promote expression during inner ear development and may be required for hearing (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20668882%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

1

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8 February 2020

Elisa de la Calle-Mustienes

3

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8 February 2020

Àlex Robert-Moreno

4

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8 February 2020

8

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8 February 2020

José Luis Gómez-Skarmeta

14

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8 February 2020

13

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Hannie Kremer

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8 February 2020

author name string

Krysta Voesenek

2

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8 February 2020

Haris Kokotas

5

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8 February 2020

Maria Grigoriadou

6

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8 February 2020

John Economides

7

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8 February 2020

Nele Hilgert

9

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8 February 2020

Felipe Moreno

10

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8 February 2020

Berta Alsina

11

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8 February 2020

Michael B Petersen

12

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8 February 2020

publication date

29 July 2010

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8 February 2020

1 reference

Europe PubMed Central

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8 February 2020

128

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8 February 2020

4

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8 February 2020

411-419

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Europe PubMed Central

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8 February 2020

https://scigraph.springernature.com/pub.10.1007/s00439-010-0864-x

0 references

Phenotypic robustness conferred by apparently redundant transcriptional enhancers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2939330

5 July 2018

The colorectal cancer risk at 18q21 is caused by a novel variant altering SMAD7 expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2939330

5 July 2018

Understanding the regulatory genome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2939330

5 July 2018

Metrics of sequence constraint overlook regulatory sequences in an exhaustive analysis at phox2b

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2939330

5 July 2018

A functional survey of the enhancer activity of conserved non-coding sequences from vertebrate Iroquois cluster gene deserts.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2939330

5 July 2018

The role of Brn4/Pou3f4 and Pax6 in forming the pancreatic glucagon cell identity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2939330

5 July 2018

Regulatory regions from the Brn4 promoter direct LACZ expression to the developing forebrain and neural tube.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2939330

5 July 2018

The virtuoso of versatility: POU proteins that flex to fit

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2939330

5 July 2018

The sex-linked fidget mutation abolishes Brn4/Pou3f4 gene expression in the embryonic inner ear

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2939330

5 July 2018

Changes in the subcellular localization of the Brn4 gene product precede mesenchymal remodeling of the otic capsule

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2939330

5 July 2018

The molecular basis of X-linked deafness type 3 (DFN3) in two sporadic cases: identification of a somatic mosaicism for a POU3F4 missense mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2939330

5 July 2018

Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2939330

5 July 2018

Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2939330

5 July 2018

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2939330

5 July 2018

Appendix G: In Situ Hybridization: An Improved Whole-Mount Method for Xenopus Embryos

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2939330

5 July 2018

Otic mesenchyme expression of Cre recombinase directed by the inner ear enhancer of the Brn4/Pou3f4 gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2939330

28 October 2018

Odd-skipped genes encode repressors that control kidney development.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2939330

28 October 2018

A functional screen for sonic hedgehog regulatory elements across a 1 Mb interval identifies long-range ventral forebrain enhancers.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2939330

28 October 2018

Targeted mutagenesis of the POU-domain gene Brn4/Pou3f4 causes developmental defects in the inner ear.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2939330

28 October 2018

POU domain family values: flexibility, partnerships, and developmental codes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2939330

28 October 2018

A duplication/paracentric inversion associated with familial X-linked deafness (DFN3) suggests the presence of a regulatory element more than 400 kb upstream of the POU3F4 gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2939330

28 October 2018

XIPOU 2, a noggin-inducible gene, has direct neuralizing activity.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2939330

28 October 2018

Zebrafish enhancer detection (ZED) vector: A new tool to facilitate transgenesis and the functional analysis ofcis-regulatory regions in zebrafish

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2939330

28 October 2018

A family with X-linked deafness showing linkage to the proximal Xq region of the X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/20668882

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a hot spot for microdeletions in patients with X- linked deafness type 3 (DFN3) 900 kb proximal to the DFN3 gene POU3F4

1 reference

https://pubmed.ncbi.nlm.nih.gov/20668882

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00439-010-0864-X

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20668882%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

Dimensions Publication ID

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1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20668882%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20668882%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

ResearchGate publication ID

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