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Supporting sensory transduction: cochlear fluid homeostasis and the endocochlear potential

The Journal of physiology, 2006-10, Vol.576 (1), p.11-21

Wangemann, Philine

2006

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Mouse Models for Pendrin-Associated Loss of Cochlear and Vestibular Function

Cellular physiology and biochemistry, 2013-01, Vol.32 (Suppl 1), p.157-165

Wangemann, Philine

2013

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The Role of Pendrin in the Development of the Murine Inner Ear

Cellular physiology and biochemistry, 2011-01, Vol.28 (3), p.527-534

Wangemann, Philine

2011

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Functional significance of channels and transporters expressed in the inner ear and kidney

American Journal of Physiology: Cell Physiology, 2007-10, Vol.293 (4), p.C1187-C1208

2007

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Failure of fluid absorption in the endolymphatic sac initiates cochlear enlargement that leads to deafness in mice lacking pendrin expression

PloS one, 2010-11, Vol.5 (11), p.e14041

2010

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Potassium Ion Movement in the Inner Ear: Insights from Genetic Disease and Mouse Models

Physiology (Bethesda, Md.), 2009-10, Vol.24 (5), p.307-316

2009

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Epithelial cell stretching and luminal acidification lead to a retarded development of stria vascularis and deafness in mice lacking pendrin

PloS one, 2011-03, Vol.6 (3), p.e17949-e17949

2011

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Molecular architecture underlying fluid absorption by the developing inner ear

eLife, 2017-10, Vol.6

2017

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Slc26a4 expression prevents fluctuation of hearing in a mouse model of large vestibular aqueduct syndrome

Neuroscience, 2016-08, Vol.329, p.74-82

2016

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Acute genetic ablation of pendrin lowers blood pressure in mice

Nephrology, dialysis, transplantation, 2017-07, Vol.32 (7), p.1137-1145

2017

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Tmc2 expression partially restores auditory function in a mouse model of DFNB7/B11 deafness caused by loss of Tmc1 function

Scientific reports, 2018-08, Vol.8 (1), p.12125-13, Article 12125

2018

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Slc26a4 -insufficiency causes fluctuating hearing loss and stria vascularis dysfunction

Neurobiology of disease, 2014-06, Vol.66, p.53-65

2014

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ILDR1 null mice, a model of human deafness DFNB42, show structural aberrations of tricellular tight junctions and degeneration of auditory hair cells

Human molecular genetics, 2015-02, Vol.24 (3), p.609-624

2015

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Gene therapy for hereditary hearing loss by SLC26A4 mutations in mice reveals distinct functional roles of pendrin in normal hearing

Theranostics, 2019-01, Vol.9 (24), p.7184-7199

2019

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SLC26A4 targeted to the endolymphatic sac rescues hearing and balance in Slc26a4 mutant mice

PLoS genetics, 2013-07, Vol.9 (7), p.e1003641-e1003641

2013

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Endolymphatic Na⁺ and K⁺ concentrations during cochlear growth and enlargement in mice lacking Slc26a4/pendrin

PloS one, 2013-05, Vol.8 (5), p.e65977-e65977

2013

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KCNJ10 (Kir4.1) potassium channel knockout abolishes endocochlear potential

American Journal of Physiology: Cell Physiology, 2002-02, Vol.282 (2), p.C403-C407

2002

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Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model

BMC medicine, 2004-08, Vol.2 (1), p.30-30, Article 30

2004

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K+ Cycling and Its Regulation in the Cochlea and the Vestibular Labyrinth

Audiology & neurotology, 2002-07, Vol.7 (4), p.199-205

Wangemann, Philine

2002

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NOS inhibition enhances myogenic tone by increasing rho-kinase mediated Ca2+ sensitivity in the male but not the female gerbil spiral modiolar artery

PloS one, 2013, Vol.8 (1), p.e53655-e53655

2013

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Targeted Ablation of Connexin26 in the Inner Ear Epithelial Gap Junction Network Causes Hearing Impairment and Cell Death

Current biology, 2002-07, Vol.12 (13), p.1106-1111

2002

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A claudin-9-based ion permeability barrier is essential for hearing

PLoS genetics, 2009-08, Vol.5 (8), p.e1000610

2009

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Lack of pendrin HCO3- transport elevates vestibular endolymphatic [Ca2+] by inhibition of acid-sensitive TRPV5 and TRPV6 channels

American journal of physiology. Renal physiology, 2007-05, Vol.292 (5), p.F1314-F1321

2007

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Gender differences in myogenic regulation along the vascular tree of the gerbil cochlea

PloS one, 2011-09, Vol.6 (9), p.e25659-e25659

2011

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Slc26a7 chloride channel activity and localization in mouse Reissner's membrane epithelium

PloS one, 2014-05, Vol.9 (5), p.e97191-e97191

2014

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Supporting sensory transduction: cochlear fluid homeostasis and the endocochlear potential

Mouse Models for Pendrin-Associated Loss of Cochlear and Vestibular Function

The Role of Pendrin in the Development of the Murine Inner Ear

Functional significance of channels and transporters expressed in the inner ear and kidney

Failure of fluid absorption in the endolymphatic sac initiates cochlear enlargement that leads to deafness in mice lacking pendrin expression

Potassium Ion Movement in the Inner Ear: Insights from Genetic Disease and Mouse Models

Epithelial cell stretching and luminal acidification lead to a retarded development of stria vascularis and deafness in mice lacking pendrin

Molecular architecture underlying fluid absorption by the developing inner ear

Slc26a4 expression prevents fluctuation of hearing in a mouse model of large vestibular aqueduct syndrome

Acute genetic ablation of pendrin lowers blood pressure in mice

Tmc2 expression partially restores auditory function in a mouse model of DFNB7/B11 deafness caused by loss of Tmc1 function

Slc26a4 -insufficiency causes fluctuating hearing loss and stria vascularis dysfunction

ILDR1 null mice, a model of human deafness DFNB42, show structural aberrations of tricellular tight junctions and degeneration of auditory hair cells

Gene therapy for hereditary hearing loss by SLC26A4 mutations in mice reveals distinct functional roles of pendrin in normal hearing

SLC26A4 targeted to the endolymphatic sac rescues hearing and balance in Slc26a4 mutant mice

Endolymphatic Na⁺ and K⁺ concentrations during cochlear growth and enlargement in mice lacking Slc26a4/pendrin

KCNJ10 (Kir4.1) potassium channel knockout abolishes endocochlear potential

Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model

K+ Cycling and Its Regulation in the Cochlea and the Vestibular Labyrinth

NOS inhibition enhances myogenic tone by increasing rho-kinase mediated Ca2+ sensitivity in the male but not the female gerbil spiral modiolar artery

Targeted Ablation of Connexin26 in the Inner Ear Epithelial Gap Junction Network Causes Hearing Impairment and Cell Death

A claudin-9-based ion permeability barrier is essential for hearing

Lack of pendrin HCO3- transport elevates vestibular endolymphatic [Ca2+] by inhibition of acid-sensitive TRPV5 and TRPV6 channels

Gender differences in myogenic regulation along the vascular tree of the gerbil cochlea

Slc26a7 chloride channel activity and localization in mouse Reissner's membrane epithelium

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