スポンサーリンク
Department Of Otorhinolaryngology Shinshu University School Of Medicine | 論文
- Clinical features of patients with GJB2 (connexin 26) mutations : severity of hearing loss is correlated with genotypes and protein expression patterns
- Type IX collagen knock-out mouse shows progressive hearing loss
- Ferromagnetic Resonance in Single Crystals of Fe-Ni Ferrite System
- Mutations in the gene encoding KIAA1199 protein, an inner-ear protein expressed in Deiters' cells and the fibrocytes, as the cause of nonsyndromic hearing loss
- Construction and characterization of a vestibular-specific cDNA library using T7-based RNA amplification
- Neurotransmission in the vestibular endorgans : Glutamatergic transmission in the afferent synapses of hair cells
- Genetic features of hearing loss associated with ear anomalies : PDS and EYA1 mutation analysis
- Clinical and genetic features of nonsyndromic autosomal dominant sensorineural hearing loss : KCNQ4 is a gene responsible in Japanese
- Rapid mass screening method and counseling for the 1555A'G mitochondrial mutation
- EYA1 nonsense mutation in a Japanese branchio-oto-renal syndrome family
- GABA-induced response in spiral ganglion cells acutely isolated from guinea pig cochlea
- New trends with cochlear implant electrodes
- Genetic analysis of hearing impairment(I. Genetics and comprehensive care of hearing disorders)
- Novel USH2A mutations in Japanese Usher syndrome type 2 patients : marked differences in the mutation spectrum between the Japanese and other populations
- TECTA mutations in Japanese with mid-frequency hearing loss affected by zona pellucida domain protein secretion