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

Mutations of KCNJ10 Together with Mutations of SLC26A4 Cause Digenic Nonsyndromic Hearing Loss Associated with Enlarged Vestibular Aqueduct Syndrome

(2009) Tao Yang et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Prestin's Anion Transport and Voltage-Sensing Capabilities Are Independent

(2009) Jun-Ping Bai et al.   BIOPHYSICAL JOURNAL

NKCC1-Dependent GABAergic Excitation Drives Synaptic Network Maturation during Early Hippocampal Development

(2009) C. K. Pfeffer et al.   JOURNAL OF NEUROSCIENCE

Deafness and Permanently Reduced Potassium Channel Gene Expression and Function in Hypothyroid Pit1dw Mutants

(2009) M. Mustapha et al.   JOURNAL OF NEUROSCIENCE

Epilepsy, Ataxia, Sensorineural Deafness, Tubulopathy, andKCNJ10Mutations

(2009) Detlef Bockenhauer et al.   NEW ENGLAND JOURNAL OF MEDICINE

Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10

(2009) U. I. Scholl et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Cochlear amplification, outer hair cells and prestin

(2008) Peter Dallos   CURRENT OPINION IN NEUROBIOLOGY

Gap junctions and connexins in the inner ear: their roles in homeostasis and deafness

(2008) Regina Nickel et al.   Current Opinion in Otolaryngology & Head and Neck Surgery

Endocochlear potential depends on Cl− channels: mechanism underlying deafness in Bartter syndrome IV

(2008) Gesa Rickheit et al.   EMBO JOURNAL

Cochlear Outer Hair Cell Motility

(2008) Jonathan Ashmore   PHYSIOLOGICAL REVIEWS

The endocochlear potential depends on two K+ diffusion potentials and an electrical barrier in the stria vascularis of the inner ear

(2008) F. Nin et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA