Results 41 to 50 of about 854 (148)
Mutations in the GJB2 gene [which encodes connexin 26 (Cx26)] are the most common causes of hereditary hearing loss in humans, and previous studies showed postnatal development arrest of the organ of Corti in different Cx26-null mouse models.
Sen Chen +7 more
doaj +1 more source
Porokeratotic Eccrine Nevus May Be Caused by Somatic Connexin26 Mutations [PDF]
Porokeratotic eccrine ostial and dermal duct nevus, or porokeratotic eccrine nevus (PEN), is a hyperkeratotic epidermal nevus. Several cases of widespread involvement have been reported, including one in association with the keratitis–ichthyosis–deafness
Kamps, Miriam A.F. +17 more
core +1 more source
Connexin26-mediated transfer of laterality cues in Xenopus
Summary A cilia-driven leftward flow of extracellular fluid breaks bilateral symmetry in the dorsal midline of the neurula stage vertebrate embryo.
Tina Beyer +3 more
doaj +1 more source
Aberrant Connexin26 Hemichannels Underlying Keratitis–Ichthyosis–Deafness Syndrome Are Potently Inhibited by Mefloquine [PDF]
Keratitis–ichthyosis–deafness (KID) syndrome is an ectodermal dysplasia caused by dominant mutations of connexin26 (Cx26). Loss of Cx26 function causes nonsyndromic sensorineural deafness, without consequence in the epidermis.
Li, Leping +6 more
core +1 more source
Connexins in Acquired Hearing Loss: Expanding Research Perspectives
Connexins, as key players in intercellular communication in the inner ear, are vital for maintaining normal hearing function. While numerous studies have explored their role in congenital hereditary hearing loss, the underlying mechanisms and therapeutic
Sihan Huang +7 more
doaj +1 more source
There is evidence that reactive oxygen species (ROS) are formed in the cochlea during acoustic injury. However, very little is known about the involvement of ROS signals in the spiral ligament (SL) during such injury.
Reiko Nagashima +3 more
doaj +1 more source
Prävalenzen von Mutationen auf dem kodierenden Exon2 des Connexin26 Genes in einem Patientenkollektiv einer mitteldeutschen Klinik [PDF]
Mutationen auf dem Connexin26 Gen – insbesondere die Mutation Gdel35 scheint in bestimmten Populationen für bis zu 50% sporadischer und familiärer frühkindlicher Schwerhörigkeit verantwortlich zu sein.
Wolf, Armin Hilmar
core
Chinese Clinical Practice Guidelines for Auditory Neuropathy (gCAN)
ABSTRACT Auditory neuropathy (AN) is an auditory disorder that affects the function of the auditory pathway. An increasing number of AN cases have been identified with the revelation of the underlying mechanisms, the advancements of diagnostic and detecting techniques.
Chinese Multi‐Center Research Collaborative Group on Clinical Diagnosis and Intervention of Auditory Neuropathy +5 more
wiley +1 more source
Connexins (Cxs) are critical for normal tissue development, differentiation, and cell proliferation. Normal expression and function of Cxs are considered to play a role in tumor suppression, but abnormal localization and abnormally increased expression of Cxs have been found in a variety of carcinomas.
Yusheng Han +6 more
wiley +1 more source
The Reconstruction of Peripheral Auditory Circuit: Recent Advances and Future Challenges
This paper summarizes the potential of biomaterials, stem cells, and gene editing technologies in the regeneration of inner ear hair cells, spiral ganglion neurons, and inner ear organoids. Challenges and potential developments are discussed and explored.
Zhe Li +3 more
wiley +1 more source

