The role of Pax2 in mouse inner ear development (Q28595027)

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1 February 2017

Laura K. Cole

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1 February 2017

Michael Mulheisen

3

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1 February 2017

Weise Chang

4

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1 February 2017

Doris K. Wu

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

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1 February 2017

language of work or name

English

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publication date

1 August 2004

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1 February 2017

Developmental Biology

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1 February 2017

272

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1 February 2017

1

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1 February 2017

161–175

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1 February 2017

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https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.04.024

The motor and tail regions of myosin XV are critical for normal structure and function of auditory and vestibular hair cells

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.04.024

Patterning of the mammalian cochlea

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.04.024

Hearing loss in athyroid pax8 knockout mice and effects of thyroxine substitution

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.04.024

Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.04.024

Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.04.024

The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.04.024

Hair cells and supporting cells share a common progenitor in the avian inner ear.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.04.024

Lack of pendrin expression leads to deafness and expansion of the endolymphatic compartment in inner ears of Foxi1 null mutant mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.04.024

Eya1 expression in the developing ear and kidney: towards the understanding of the pathogenesis of Branchio-Oto-Renal (BOR) syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.04.024

Transcription factor GATA-3 alters pathway selection of olivocochlear neurons and affects morphogenesis of the ear

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.04.024

Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.04.024

Expression of the transcription factors GATA3 and Pax2 during development of the mammalian inner ear.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.04.024

Essential role of BETA2/NeuroD1 in development of the vestibular and auditory systems

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.04.024

neurogenin1 is essential for the determination of neuronal precursors for proximal cranial sensory ganglia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.04.024

Expression of Delta1 and Serrate1 (Jagged1) in the mouse inner ear

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.04.024

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.04.024

Six1 controls patterning of the mouse otic vesicle

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.04.024

Comparative analysis of Pax-2 protein distributions during neurulation in mice and zebrafish.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.04.024

Specification of the mammalian cochlea is dependent on Sonic hedgehog

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.04.024

Distinct temporal expression of mouse Nkx-5.1 and Nkx-5.2 homeobox genes during brain and ear development.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.04.024

Regionalized expression of Nkx5-1, Nkx5-2, Pax2 and sek genes during mouse inner ear development.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.04.024

Specific expression of the retinoic acid-synthesizing enzyme RALDH2 during mouse inner ear development

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.04.024

Localization and functional studies of pendrin in the mouse inner ear provide insight about the etiology of deafness in pendred syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.04.024

Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.04.024

GATA3 haplo-insufficiency causes human HDR syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.04.024

Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.04.024

Six1 is required for the early organogenesis of mammalian kidney

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.04.024

Molecular identification of a major retinoic-acid-synthesizing enzyme, a retinaldehyde-specific dehydrogenase

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.04.024

The role of Six1 in mammalian auditory system development

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.04.024