Developing sensory circuits exhibit different patterns of spontaneous activity, patterns that
are related to the construction and refinement of functional networks. During the …

Hearing loss is the most common congenital sensory impairment. Mutations or deficiencies
of the GJB2 gene are the most common genetic cause of congenital non-syndromic …

In mammals, hearing loss is irreversible due to the lack of regenerative potential of non-
sensory cochlear cells. Neonatal cochlear cells, however, can grow into organoids that …

The mammalian cochlea is the sensory organ of hearing with a delicate, highly organised
structure that supports unique operating mechanisms. ATP release from the secretory …

Wiring an animal brain is a complex process involving a staggering number of cell-types
born at different times and locations in the developing brain. Incorporation of these cells into …

In mammals, the sense of hearing arises through a complex sequence of morphogenetic
events that drive the sculpting of the auditory sensory epithelium into its terminally functional …

Hearing loss is a common and disabling condition, yet our understanding of the physiologic
workings of the inner ear has been limited by longstanding difficulty characterizing the …

Programmed cell death (PCD) plays a critical role in the development and maturation of the
cochlea. Significant remodeling occurs among cells of the greater epithelial ridge (GER) of …

ATP, as a paracrine signalling molecule, induces intracellular Ca2+ elevation via the
activation of purinergic receptors on the surface of glia-like cochlear supporting cells. These …

Structured Abstract Background Eponyms have historically been used in different fields like
literature, law, and various sciences including medicine. The continued use of eponyms in …