(Q50500477)

14 March 2018

title

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

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14 March 2018

author name string

Phippard D

1

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14 March 2018

Lu L

2

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14 March 2018

Lee D

3

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14 March 2018

Saunders JC

4

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14 March 2018

Crenshaw EB 3rd

5

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14 March 2018

language of work or name

English

0 references

publication date

1 July 1999

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14 March 2018

published in

Journal of Neuroscience

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14 March 2018

volume

19

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14 March 2018

issue

14

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14 March 2018

page(s)

5980-5989

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14 March 2018

Genetic analyses of mammalian ear development

cites work

1 reference

12 December 2020

The embryonic and postnatal development of the inner ear of the mouse

1 reference

12 December 2020

Expression of a large family of POU-domain regulatory genes in mammalian brain development

1 reference

12 December 2020

Model of forebrain regionalization based on spatiotemporal patterns of POU-III homeobox gene expression, birthdates, and morphological features

1 reference

12 December 2020

Anatomic and physiologic aging: a behavioral neuroscience perspective

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Epithelial control of periotic mesenchyme chondrogenesis.

1 reference

12 December 2020

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

1 reference

12 December 2020

Development of the mouse inner ear and origin of its sensory organs.

1 reference

12 December 2020

Pit-1-dependent expression of the receptor for growth hormone releasing factor mediates pituitary cell growth

1 reference

12 December 2020

Dwarf locus mutants lacking three pituitary cell types result from mutations in the POU-domain gene pit-1.

1 reference

12 December 2020

Essential role of POU-domain factor Brn-3c in auditory and vestibular hair cell development

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

X-linked progressive mixed deafness: a new microdeletion that involves a more proximal region in Xq21.

1 reference

12 December 2020

The POU domain transcription factor Brn-2 is required for the determination of specific neuronal lineages in the hypothalamus of the mouse

1 reference

12 December 2020

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

12 December 2020

The POU domain: versatility in transcriptional regulation by a flexible two-in-one DNA-binding domain.

1 reference

12 December 2020

Development and survival of the endocrine hypothalamus and posterior pituitary gland requires the neuronal POU domain factor Brn-2

1 reference

12 December 2020

Role of transcription factors Brn-3.1 and Brn-3.2 in auditory and visual system development

1 reference

12 December 2020

Scarpa's ganglion in the rat and guinea pig.

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12 December 2020

Overview of genetic auditory syndromes.

1 reference

12 December 2020

Influence of the Neural Tube on the Differentiation of the Inner Ear in the Mammalian Embryo

1 reference

12 December 2020

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

1 reference

12 December 2020

Brain 4: a novel mammalian POU domain transcription factor exhibiting restricted brain-specific expression

1 reference

12 December 2020

Tst-1/Oct-6/SCIP regulates a unique step in peripheral myelination and is required for normal respiration

1 reference

12 December 2020

Epithelial-mesenchymal tissue interactions guiding otic capsule formation: the role of the otocyst

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12 December 2020

Cell fate specification in the inner ear.

1 reference

12 December 2020

Development of hearing. Part II. Embryology.

1 reference

12 December 2020

Targeted deletion of the mouse POU domain gene Brn-3a causes selective loss of neurons in the brainstem and trigeminal ganglion, uncoordinated limb movement, and impaired suckling

1 reference

12 December 2020

Identifiers

PubMed ID

10407036

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14 March 2018