Michael Hoa

Michael Hoa

Auditory Development and Restoration Program, National Institutes of Health

Affiliated withNational Institutes of Health

Research Area

Biology

Biography

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JoVE Journal Publications

Article Total : 1	Year
Publication title	2023

Other Publications

Article	Year
Single-cell RNA-Seq resolves cellular complexity in sensory organs from the neonatal inner ear. Nature communications\| PubMed ID: 26469390	2015
mutation and cochlear autoinflammation cause syndromic and nonsyndromic hearing loss DFNA34 responsive to anakinra therapy. Proceedings of the National Academy of Sciences of the United States of America\| PubMed ID: 28847925	2017
Molecular architecture underlying fluid absorption by the developing inner ear. eLife\| PubMed ID: 28994389	2017
CDC14A phosphatase is essential for hearing and male fertility in mouse and human. Human molecular genetics\| PubMed ID: 29293958	2018
Deafness and loss of cochlear hair cells in the absence of thyroid hormone transporters Slc16a2 (Mct8) and Slc16a10 (Mct10). Scientific reports\| PubMed ID: 29535325	2018
Mutational and phenotypic spectra of KCNE1 deficiency in Jervell and Lange-Nielsen Syndrome and Romano-Ward Syndrome. Human mutation\| PubMed ID: 30461122	2019
Single Cell and Single Nucleus RNA-Seq Reveal Cellular Heterogeneity and Homeostatic Regulatory Networks in Adult Mouse Stria Vascularis. Frontiers in molecular neuroscience\| PubMed ID: 31920542	2019
Noncoding Microdeletion in Mouse Disrupts Neural Crest Migration into the Stria Vascularis, Reduces the Endocochlear Potential, and Suggests the Neuropathology for Human Nonsyndromic Deafne... The Journal of neuroscience : the official journal of the Society for Neuroscience\| PubMed ID: 32152201	2020
Applications of single-cell sequencing for the field of otolaryngology: A contemporary review. Laryngoscope investigative otolaryngology\| PubMed ID: 32596483	2020
Mouse Models of Human Pathogenic Variants of Associated with Non-Syndromic Deafness DFNB86 and DFNA65 and Syndromes Involving Deafness. Genes\| PubMed ID: 32987832	2020
Characterization of rare spindle and root cell transcriptional profiles in the stria vascularis of the adult mouse cochlea. Scientific reports\| PubMed ID: 33093630	2020
Identification of Potential Meniere's Disease Targets in the Adult Stria Vascularis. Frontiers in neurology\| PubMed ID: 33613436	2021
New insights into Perrault syndrome, a clinically and genetically heterogeneous disorder. Human genetics\| PubMed ID: 34338890	2022
Utilizing Single Cell RNA-Sequencing to Implicate Cell Types and Therapeutic Targets for SSNHL in the Adult Cochlea. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology\| PubMed ID: 34510123	2021
Single-Cell RNA-Seq of Cisplatin-Treated Adult Stria Vascularis Identifies Cell Type-Specific Regulatory Networks and Novel Therapeutic Gene Targets. Frontiers in molecular neuroscience\| PubMed ID: 34566577	2021
Repurposable Drugs That Interact with Steroid Responsive Gene Targets for Inner Ear Disease. Biomolecules\| PubMed ID: 36358991	2022
Editorial: Autoinflammation of the inner ear. Frontiers in neurology\| PubMed ID: 36388231	2022
The role of the stria vascularis in neglected otologic disease. Hearing research\| PubMed ID: 36584545	2023
Variants of LRP2, encoding a multifunctional cell-surface endocytic receptor, associated with hearing loss and retinal dystrophy. Clinical genetics\| PubMed ID: 36807241	2023