Inner hair cell dysfunction in Klhl18 mutant mice leads to low frequency progressive hearing loss

Characterization of the development of the mouse cochlear epithelium at the single cell level

(2020) Likhitha Kolla et al.   Nature Communications

Auditory Neuropathy Spectrum Disorders: From Diagnosis to Treatment: Literature Review and Case Reports

(2020) Romolo Daniele De Siati et al.   Journal of Clinical Medicine

Insights into the Biology of Hearing and Deafness Revealed by Single-Cell RNA Sequencing

(2019) Paul T. Ranum et al.   Cell Reports

Sodium-activated potassium channels shape peripheral auditory function and activity of the primary auditory neurons in mice

(2019) Daniël O. J. Reijntjes et al.   Scientific Reports

Hair Cell and Neural Contributions to the Cochlear Summating Potential

(2019) Andrew K Pappa et al.   JOURNAL OF NEUROPHYSIOLOGY

Mouse screen reveals multiple new genes underlying mouse and human hearing loss

(2019) Neil J. Ingham et al.   PLOS BIOLOGY

Cul3‐Klhl18 ubiquitin ligase modulates rod transducin translocation during light‐dark adaptation

(2019) Taro Chaya et al.   EMBO JOURNAL

Transient auditory nerve demyelination as a new mechanism for hidden hearing loss

(2017) Guoqiang Wan et al.   Nature Communications

A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction

(2017) Michael R. Bowl et al.   Nature Communications

Auditory neuropathy — neural and synaptic mechanisms

(2016) Tobias Moser et al.   Nature Reviews Neurology

Hair cells use active zones with different voltage dependence of Ca2+influx to decompose sounds into complementary neural codes

(2016) Tzu-Lun Ohn et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Stereocilia-staircase spacing is influenced by myosin III motors and their cargos espin-1 and espin-like

(2016) Seham Ebrahim et al.   Nature Communications

Absence of plastin 1 causes abnormal maintenance of hair cell stereocilia and a moderate form of hearing loss in mice

(2014) Ruth Taylor et al.   HUMAN MOLECULAR GENETICS

Genome-wide Generation and Systematic Phenotyping of Knockout Mice Reveals New Roles for Many Genes

(2013) Jacqueline K. White et al.   CELL

Progressive hearing loss and gradual deterioration of sensory hair bundles in the ears of mice lacking the actin-binding protein Eps8L2

(2013) David N. Furness et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Identification of two novel missense WFS1 mutations, H696Y and R703H, in patients with non-syndromic low-frequency sensorineural hearing loss

(2011) Yi Sun et al.   Journal of Genetics and Genomics

A conditional knockout resource for the genome-wide study of mouse gene function

(2011) William C. Skarnes et al.   NATURE

Roles of the Espin Actin-Bundling Proteins in the Morphogenesis and Stabilization of Hair Cell Stereocilia Revealed in CBA/CaJ Congenic Jerker Mice

(2011) Gabriella Sekerková et al.   PLoS Genetics

The CUL3-KLHL18 ligase regulates mitotic entry and ubiquitylates Aurora-A

(2011) S. Moghe et al.   Biology Open

Adding Insult to Injury: Cochlear Nerve Degeneration after "Temporary" Noise-Induced Hearing Loss

(2009) S. G. Kujawa et al.   JOURNAL OF NEUROSCIENCE

Hearing loss in a mouse model of Muenke syndrome

(2008) Suzanne L. Mansour et al.   HUMAN MOLECULAR GENETICS