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2025Cochlear gene therapy restores hearing and auditory processing in an atypical DFNB9 mouse model, Communications Medicine, 2025, 5 (1), pp.229. ⟨10.1038/s43856-025-00926-3⟩.
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2025Cell tropism of adeno-associated viruses within the mouse inner ear in vivo: from embryonic to adult stages., Sci Rep 2025 Apr; 15(1): 13479.
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2025MYO7A is required for the functional integrity of the mechanoelectrical transduction complex in hair cells of the adult cochlea., Proc Natl Acad Sci U S A 2025 Jan; 122(1): e2414707122.
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2024A free intravesicular C-terminal of otoferlin is essential for synaptic vesicle docking and fusion at auditory inner hair cell ribbon synapses., Prog Neurobiol 2024 Aug; 240(): 102658.
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2024In utero adeno-associated virus (AAV)-mediated gene delivery targeting sensory and supporting cells in the embryonic mouse inner ear., PLoS One 2024 ; 19(7): e0305742.
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2024Extended time frame for restoring inner ear function through gene therapy in Usher1G preclinical model, JCI Insight, 2024, 9 (3), pp.e169504. ⟨10.1172/jci.insight.169504⟩.
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2023Recent advances and future challenges in gene therapy for hearing loss., R Soc Open Sci 2023 Jun; 10(6): 230644.
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2023Deafness: from genetic architecture to gene therapy, Nature Reviews Genetics, 2023, ⟨10.1038/s41576-023-00597-7⟩.
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2023Towards the Clinical Application of Gene Therapy for Genetic Inner Ear Diseases., J Clin Med 2023 Jan; 12(3): .
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2022The SNARE protein SNAP-25 is required for normal exocytosis at auditory hair cell ribbon synapses., iScience 2022 Dec; 25(12): 105628.
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