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Deafness

Mcph1-Deficient Mice Reveal a Role for MCPH1 in Otitis Media

Jing Chen, Neil Ingham, [ ... ], Karen P. Steel

The Reduced Cochlear Output and the Failure to Adapt the Central Auditory Response Causes Tinnitus in Noise Exposed Rats

Lukas Rüttiger, Wibke Singer, [ ... ], Marlies Knipper

Visual Word Recognition in Deaf Readers: Lexicality Is Modulated by Communication Mode

Laura Barca, Giovanni Pezzulo, [ ... ], Maria Cristina Caselli

Independent Validation of an Existing Model Enables Prediction of Hearing Loss after Childhood Bacterial Meningitis

Rogier C. J. de Jonge, Marieke S. Sanders, [ ... ], A. Marceline van Furth

Dual Sensory Impairment in Older Adults Increases the Risk of Mortality: A Population-Based Study

Bamini Gopinath, Julie Schneider, [ ... ], Paul Mitchell

A Rapid Method for Simultaneous Screening of Multi-Gene Mutations Associated with Hearing Loss in the Korean Population

Borum Sagong, Jeong-In Baek, [ ... ], Un-Kyung Kim

Availability and Readability of Emergency Preparedness Materials for Deaf and Hard-of-Hearing and Older Adult Populations: Issues and Assessments

Linda Neuhauser, Susan L. Ivey, [ ... ], Melissa Kealey

Application of Massively Parallel Sequencing to Genetic Diagnosis in Multiplex Families with Idiopathic Sensorineural Hearing Impairment

Chen-Chi Wu, Yin-Hung Lin, [ ... ], Pei-Lung Chen

Distinct Roles of Molecular Chaperones HSP90α and HSP90β in the Biogenesis of KCNQ4 Channels

Yanhong Gao, Sergey Yechikov, [ ... ], Liping Nie

Diaphanous homolog 3 (Diap3) Overexpression Causes Progressive Hearing Loss and Inner Hair Cell Defects in a Transgenic Mouse Model of Human Deafness

Cynthia J. Schoen, Margit Burmeister, Marci M. Lesperance

Headbobber: A Combined Morphogenetic and Cochleosaccular Mouse Model to Study 10qter Deletions in Human Deafness

Annalisa Buniello, Rachel E. Hardisty-Hughes, [ ... ], Karen P. Steel

Age-Related Hearing Loss in Rhesus Monkeys Is Correlated with Cochlear Histopathologies

James R. Engle, Steve Tinling, Gregg H. Recanzone

Identification and Functional Study of a New Missense Mutation in the Motor Head Domain of Myosin VIIA in a Family with Autosomal Dominant Hearing Impairment (DFNA11)

Qing Sang, Xukun Yan, [ ... ], Lei Wang

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