Search Results - "LUSTIG, Lawrence R"
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Restoration of Hearing in the VGLUT3 Knockout Mouse Using Virally Mediated Gene Therapy
Published in Neuron (Cambridge, Mass.) (26-07-2012)“…Mice lacking the vesicular glutamate transporter-3 (VGLUT3) are congenitally deaf due to loss of glutamate release at the inner hair cell afferent synapse…”
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Dual AAV-mediated gene therapy restores hearing in a DFNB9 mouse model
Published in Proceedings of the National Academy of Sciences - PNAS (05-03-2019)“…Autosomal recessive genetic forms (DFNB) account for most cases of profound congenital deafness. Adeno-associated virus (AAV)-based gene therapy is a promising…”
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A Large Genome-Wide Association Study of Age-Related Hearing Impairment Using Electronic Health Records
Published in PLoS genetics (20-10-2016)“…Age-related hearing impairment (ARHI), one of the most common sensory disorders, can be mitigated, but not cured or eliminated. To identify genetic influences…”
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Prevalence of adult unilateral hearing loss and hearing aid use in the United States
Published in The Laryngoscope (01-07-2018)“…Objective The prevalence of unilateral hearing loss (UHL) in adults has not been well characterized. The objectives of this study are to determine the…”
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Deletion of Tmtc4 activates the unfolded protein response and causes postnatal hearing loss
Published in The Journal of clinical investigation (01-11-2018)“…Hearing loss is a significant public health concern, affecting over 250 million people worldwide. Both genetic and environmental etiologies are linked to…”
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Sensorineural Deafness and Seizures in Mice Lacking Vesicular Glutamate Transporter 3
Published in Neuron (Cambridge, Mass.) (24-01-2008)“…The expression of unconventional vesicular glutamate transporter VGLUT3 by neurons known to release a different classical transmitter has suggested novel roles…”
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Modeling and Preventing Progressive Hearing Loss in Usher Syndrome III
Published in Scientific reports (18-10-2017)“…Usher syndrome type III (USH3) characterized by progressive loss of vision and hearing is caused by mutations in the clarin-1 gene ( CLRN1 ). Clrn1 knockout…”
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Spiral ganglion degeneration and hearing loss as a consequence of satellite cell death in saposin B-deficient mice
Published in The Journal of neuroscience (18-02-2015)“…Saposin B (Sap B) is an essential activator protein for arylsulfatase A in the hydrolysis of sulfatide, a lipid component of myelin. To study Sap B's role in…”
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Biological Therapies of the Inner Ear: What Otologists Need to Consider
Published in Otology & neurotology (01-02-2018)Get full text
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Disrupted bone remodeling leads to cochlear overgrowth and hearing loss in a mouse model of fibrous dysplasia
Published in PloS one (01-05-2014)“…Normal hearing requires exquisite cooperation between bony and sensorineural structures within the cochlea. For example, the inner ear secretes proteins such…”
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A Meta-analysis of the Complications Associated With Osseointegrated Hearing Aids
Published in Otology & neurotology (01-07-2013)“…OBJECTIVETo summarize available peer-reviewed literature to describe the range and rate of complications related to osseointegrated hearing aids in adult and…”
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Surgical method for virally mediated gene delivery to the mouse inner ear through the round window membrane
Published in Journal of visualized experiments (16-03-2015)“…Gene therapy, used to achieve functional recovery from sensorineural deafness, promises to grant better understanding of the underlying molecular and genetic…”
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Severe vestibular dysfunction and altered vestibular innervation in mice lacking prosaposin
Published in Neuroscience research (01-04-2012)“…► Prosaposin is expressed and localized in vestibular end-organs and Scarpa's ganglia. ► Prosaposin is important for the maintenance of normal vestibular…”
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Systematic and other reviews: Criteria and complexities
Published in Journal of otolaryngology-head and neck surgery (01-07-2021)Get full text
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Characterization of the human nicotinic acetylcholine receptor subunit alpha (α) 9 (CHRNA9) and alpha (α) 10 (CHRNA10) in lymphocytes
Published in Life sciences (1973) (03-12-2004)“…Though the nicotinic acetylcholine receptor (nAChR) subunits α9 and α 10 have been thoroughly characterized within hair cells of the organ of Corti in the…”
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Bell's Palsy and Its Semantic Change over Time
Published in Otology & neurotology (01-01-2023)“…From 1821 to 1829, Sir Charles Bell presented cases of facial paralysis from infection, trauma, and unknown causes. As such, "Bell's palsy" initially referred…”
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Otology and Neurotology in a Post-COVID-19 World
Published in Otology & neurotology (01-10-2020)Get full text
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Dehiscence of bone overlying the superior canal as a cause of apparent conductive hearing loss
Published in Otology & neurotology (01-03-2003)“…To identify patients with superior semicircular canal dehiscence and apparent conductive hearing loss and to define the cause of the air-bone gap. Prospective…”
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Venous malformations of the temporal bone are a common feature in CHARGE syndrome
Published in The Laryngoscope (01-04-2012)“…Objectives/Hypothesis: CHARGE (Coloboma of the eye, Heart defects, Atresia of the choanae, Retardation of growth and/or development, Genital and/or urinary…”
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Systematic and other reviews: Criteria and complexities
Published in World Journal of Otorhinolaryngology-Head and Neck Surgery (01-07-2021)Get full text
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