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Last Updated: 10/31/2025
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Found 875 publications
The TECTB-C225Y Variant Causing Autosomal Dominant Deafness in a Nicaraguan Family Enhances Sensitivity to Noise-Induced Hearing Loss in Mice.
Journal: medRxiv : the preprint server for health sciences
Published: August 20, 2025
Establishing a comprehensive national auditory implant registry in Japan: Trends and demographics from the first two years (2023-2024).
Journal: Auris, nasus, larynx
Published: August 04, 2025
TMC1 and TMC2 are cholesterol-dependent scramblases that regulate membrane homeostasis in auditory hair cells.
Journal: bioRxiv : the preprint server for biology
Published: July 09, 2025
Hyperkinetic Movement Disorder in KARS1-Related Disease: An Illustrative Video-Recorded Case and Narrative Literature Review.
Journal: Neurology international
Published: June 28, 2025
Adeno-associated virus-based rescue of Myo7a expression restores hair-cell function and improves hearing thresholds in a USH1B mouse strain.
Journal: The Journal of physiology
Published: June 18, 2025
The predawn dilemma in adeno-associated virus-based gene therapies for hereditary deafness.
Journal: American journal of stem cells
Published: June 07, 2025
Cochlear inflammation in AAV-mediated gene therapy: serotype-dependent macrophage activation and promoter-driven immunogenicity.
Journal: Acta oto-laryngologica
Published: May 03, 2025
Promotion of new expression of connexin gene Cx46 ( GJA3 ) in the cochlea after Cx26 ( GJB2 ) deficiency.
Journal: bioRxiv : the preprint server for biology
Published: April 16, 2025
GJB2 promotes ovarian cancer progression and cisplatin resistance by upregulating TNC expression.
Journal: Biochimica et biophysica acta. Molecular cell research
Published: April 08, 2025
Exploring the binding sites of VRT534 at Cx26 as a putative chemical chaperone for targeted treatment of hereditary hearing disorders.
Journal: Frontiers in medicine
Published: April 07, 2025
Partial loss of FITM2 function causes hereditary spastic paraplegia.
Journal: medRxiv : the preprint server for health sciences
Published: February 20, 2025
Genetic and clinical phenotypic analysis of Usher syndrome-associated gene variants
Journal: Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery
Published: February 18, 2025
Last Updated: 10/31/2025