Prof. Shin-ichi Usami | HEARRING - Comprehensive Hearing Implant Centers

Abstracts

A large cohort study of GJB2 mutations in Japanese hearing loss patients
A new autosomal recessive form of Stickler syndrome is caused by a mutation in the COL9A1 gene
Application of deafness diagnostic screening panel based on deafness mutation/gene database using invader assay
Association of SLC26A4 mutations with clinical features and thyroid function in deaf infants with enlarged vestibular aqueduct
Audiological features and mitochondrial DNA sequence in a large family carrying mitochondrial A1555G mutation without use of ...
Chondrosarcoma of the nasal septum: A case report
Clinical characteristics and genotype-phenotype correlation of hearing loss patients with SLC26A4 mutations
Clinical course of hearing and language development in GJB2 and non-GJB2 deafness following habilitation with hearing aids
Clinical features of patients with GJB2 (connexin 26) mutations: severity of hearing loss is correlated with genotypes and ...
Construction and characterization of a vestibular-specific cDNA library using T7-based RNA amplification
CRYM mutations cause deafness through thyroid hormone binding properties in the fibrocytes of the cochlea
Deafness due to A1555G mitochondrial mutation without use of aminoglycoside
Differences in the expression of genes between normal tissue and squamous cell carcinomas of head and neck using cancer-rel. ...
Distribution and frequencies of CDH23 mutations in Japanese patients with non-syndromic hearing loss
Distribution and frequencies of PDS (SLC26A4) mutations in Pendred syndrome and nonsyndromic hearing loss associated with ...
Effect of single-drug treatment on idiopathic sudden sensorineural hearing loss
Endolymphatic hydrops and therapeutic effects are visualized in 'atypical' Meniere's disease
Factors that affect hearing level in individuals with the mitochondrial 1555A.G mutation
GABA-induced response in spiral ganglion cells acutely isolated from guinea pig cochlea
Genetic background of candidates for EAS (Electric-Acoustic Stimulation)
Genetic features, clinical phenotypes, and prevalence of sensorineural hearing loss associated with the 961de lT mitochondrial..
GJB2 deafness gene shows a specific spectrum of mutations in Japan, including a frequent founder mutation
Hybrid carcinoma of the parotid gland: report of a case (epithelial-myoepithelial carcinoma and salivary duct carcinoma) and ...
Identification of 605ins46, a novel GJB2 mutation in a Japanese family
Identification of CRYM as a candidate responsible for nonsyndromic deafness, through cDNA microarray analysis of human ...
Identification of differentially expressed genes in salivary gland tumors with cDNA microarray
Immunocytochemical localization of ubiquitin A-52 protein in the mouse inner ear
Malignant peripheral nerve sheath tumor of the parotid gland
Meningioma of the paranasal sinus: a case report
Micro-Crystallin as an intracellular 3,5,3'-triiodothyronine holder in vivo
Mutation analysis of COL9A3, a gene highly expressed in the cochlea, in hearing loss patients
Mutation profile of the CDH23 gene in 56 probands with Usher syndrome type I
Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of ...
Mutations in the WFS1 gene are a frequent cause of autosomal dominant nonsyndromic low-frequency hearing loss in Japanese
Neurotological findings in a family with episodic ataxia
Origins and frequencies of SLC26A4(PDS) mutations in east and south Asians: global implications for the epidemiology of deafness
Phenotypic consequences in a Japanese family having branchio-oto-renal syndrome with a novel frameshift mutation in the geneEYA1
Pivotal Advance: Eosinophilia in the MES rat strain is caused by a loss-of-function mutation in the gene for cytochrome ...
Polysialic acid and HNK-1 are expressed in the adult rat vestibular endorgans
Pre-Baha operation three dimensional computed tomography with markers for determining optimal implant site
Semi-quantitative evaluation of endolymphatic hydrops by bilateral intratympanic gadolinium-based contrast agent (GBCA) ...
The effect of hypergravity on the inner ear: CREB and syntaxin are up-regulated
The localization of proteins encoded by CRYM, KIAA1199, UBA52, COL9A3, and COL9A1, genes highly expressed in the cochlea
The responsible genes in Japanese deafness patients and clinical application using Invader assay
Transplanted human amniotic epithelial cells express connexin 26 and Na-K-adenosine triphosphatase in the inner ear
Type IX collagen is crucial for normal hearing
Type IX collagen knock-out mouse shows progressive hearing loss