Development of the cochlea

EC Driver, MW Kelley - Development, 2020 - journals.biologists.com
The cochlea, a coiled structure located in the ventral region of the inner ear, acts as the
primary structure for the perception of sound. Along the length of the cochlear spiral is the …

DNA methylation biomarkers in asthma and rhinitis: are we there yet?

E Legaki, C Arsenis, S Taka… - Clinical and …, 2022 - Wiley Online Library
The study of epigenetics has improved our understanding of mechanisms underpinning
gene‐environment interactions and is providing new insights in the pathophysiology of …

Single-cell transcriptomic landscapes of the otic neuronal lineage at multiple early embryonic ages

Y Sun, L Wang, T Zhu, B Wu, G Wang, Z Luo, C Li… - Cell Reports, 2022 - cell.com
Inner ear vestibular and spiral ganglion neurons (VGNs and SGNs) are known to play
pivotal roles in balance control and sound detection. However, the molecular mechanisms …

Age-related transcriptome changes in Sox2+ supporting cells in the mouse cochlea

C Cheng, Y Wang, L Guo, X Lu, W Zhu… - Stem cell research & …, 2019 - Springer
Background Inner ear supporting cells (SCs) in the neonatal mouse cochlea are a potential
source for hair cell (HC) regeneration, but several studies have shown that the regeneration …

Early steps towards hearing: placodes and sensory development

A Zine, B Fritzsch - International journal of molecular sciences, 2023 - mdpi.com
Sensorineural hearing loss is the most prevalent sensory deficit in humans. Most cases of
hearing loss are due to the degeneration of key structures of the sensory pathway in the …

Nasal DNA methylation differentiates corticosteroid treatment response in pediatric asthma: A pilot study

X Zhang, JM Biagini Myers, VK Yadagiri, A Ulm… - PloS one, 2017 - journals.plos.org
Background Treatment response to systemic corticosteroid in asthmatic children is
heterogeneous and may be mediated by epigenetic mechanism (s). We aim to identify DNA …

ESRP1 mutations cause hearing loss due to defects in alternative splicing that disrupt cochlear development

AM Rohacek, TW Bebee, RK Tilton, CM Radens… - Developmental cell, 2017 - cell.com
Alternative splicing contributes to gene expression dynamics in many tissues, yet its role in
auditory development remains unclear. We performed whole-exome sequencing in …

Lineage tracing of Sox2-expressing progenitor cells in the mouse inner ear reveals a broad contribution to non-sensory tissues and insights into the origin of the organ …

R Gu, RM Brown II, CW Hsu, T Cai, AL Crowder… - Developmental …, 2016 - Elsevier
The transcription factor Sox2 is both necessary and sufficient for the generation of sensory
regions of the inner ear. It regulates expression of the Notch ligand Jag1 in prosensory …

CHD7 and SOX2 act in a common gene regulatory network during mammalian semicircular canal and cochlear development

J Gao, JM Skidmore, J Cimerman… - Proceedings of the …, 2024 - National Acad Sciences
Inner ear morphogenesis requires tightly regulated epigenetic and transcriptional control of
gene expression. CHD7, an ATP-dependent chromodomain helicase DNA-binding protein …

Mapping the regulatory landscape of auditory hair cells from single-cell multi-omics data

S Wang, MP Lee, S Jones, J Liu… - Genome Research, 2021 - genome.cshlp.org
Auditory hair cells transduce sound to the brain, and in mammals, these cells reside together
with supporting cells in the sensory epithelium of the cochlea, called the organ of Corti. To …