Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4 (Q28119014)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7839145%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

title

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

2 references

4 January 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7839145%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

main subject

POU class 3 homeobox 4

1 reference

sensory perception of sound

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

1 reference

5

1 reference

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27 October 2019

author name string

Y J de Kok

1

1 reference

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27 October 2019

S M van der Maarel

2

1 reference

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27 October 2019

M Bitner-Glindzicz

3

1 reference

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27 October 2019

I Huber

4

1 reference

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27 October 2019

S Malcolm

6

1 reference

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27 October 2019

M E Pembrey

7

1 reference

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27 October 2019

H H Ropers

8

1 reference

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27 October 2019

F P Cremers

9

1 reference

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27 October 2019

language of work or name

English

0 references

publication date

1 February 1995

1 reference

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27 October 2019

2 references

4 January 2017

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27 October 2019

volume

267

2 references

4 January 2017

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27 October 2019

issue

5198

2 references

4 January 2017

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27 October 2019

page(s)

685-688

1 reference

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Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two families

27 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.7839145

Cloning of a gene that is rearranged in patients with choroideraemia

20 April 2017

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.7839145

The brain-specific POU-box gene Brn4 is a sex-linked transcription factor located on the human and mouse X chromosomes

20 April 2017

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.7839145

A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene

20 April 2017

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.7839145

Structure and evolution of four POU domain genes expressed in mouse brain

20 April 2017

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.7839145

Crystal structure of an engrailed homeodomain-DNA complex at 2.8 A resolution: a framework for understanding homeodomain-DNA interactions

20 April 2017

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.7839145

Crystal structure of the Oct-1 POU domain bound to an octamer site: DNA recognition with tethered DNA-binding modules

20 April 2017

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.7839145

RHS2, a POU domain-containing gene, and its expression in developing and adult rat

20 April 2017

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.7839145

The gene for an inherited form of deafness maps to chromosome 5q31

20 April 2017

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.7839145

Transcription factors: structural families and principles of DNA recognition

20 April 2017

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.7839145

Physical fine mapping of genes underlying X-linked deafness and non fra (X)-X-linked mental retardation at Xq21

20 April 2017

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.7839145

Close linkage of a gene for X linked deafness to three microsatellite repeats at Xq21 in radiologically normal and abnormal families

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.7839145

Assignment of human erythroid delta-aminolevulinate synthase (ALAS2) to a distal subregion of band Xp11.21 by PCR analysis of somatic cell hybrids containing X; autosome translocations

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.7839145

Physical fine mapping of the choroideremia locus using Xq21 deletions associated with complex syndromes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.7839145

A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.7839145

X-linked mixed deafness (DFN3): cloning and characterization of the critical region allows the identification of novel microdeletions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.7839145

Genetic epidemiology of hearing impairment

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.7839145

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.7839145

X-linked deafness, stapes gushers and a distinctive defect of the inner ear.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.7839145

Gene Expression in Narmal and Abnormal Inner Ears

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.7839145

Nucleotide sequence of mouse 5-aminolevulinic acid synthase cDNA and expression of its gene in hepatic and erythroid tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.7839145

X-linked mixed deafness with stapes fixation in a Mauritian kindred: linkage to Xq probe pDP34.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.7839145

21 January 2018

Identifiers

DOI

10.1126/SCIENCE.7839145

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7839145%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

2 references

4 January 2017