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Acta Oto-Laryngologica|September 14, 2007
Clinical characteristics and genotype-phenotype correlation of hearing loss patients with SLC26A4 mutationsHiroaki Suzuki, Aki Oshima, Koji Tsukamoto, et al.Frontiers in Neurology|November 26, 2020
Congenital Membranous Stapes Footplate Producing Episodic Pressure-Induced Perilymphatic Fistula SymptomsHan Matsuda, Yasuhiko Tanzawa, Tatsuro Sekine, et al.European Journal of Human Genetics : EJHG|September 27, 2003
Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's diseaseShin-ichi Usami, Kentaro Takahashi, Isamu Yuge, et al.The Annals of Otology, Rhinology, and Laryngology|March 21, 2015
Mutations in the MYO15A gene are a significant cause of nonsyndromic hearing loss: massively parallel DNA sequencing-based analysisMaiko Miyagawa, Shin-Ya Nishio, Mitsuru Hattori, et al.Human Genome Variation|November 2, 2020
Correction to: Prevalence of the mitochondrial 1555 A>G and 1494 C>T mutations in a community-dwelling population in JapanYasunori Maeda, Akira Sasaki, Shuya Kasai, et al.Genes|February 26, 2025
Prevalence and Clinical Characteristics of OTOGL-Associated Hearing Loss Identified in a Cohort of 7065 Japanese Patients with Hearing LossKaruna Maekawa, Shin-Ya Nishio, Kotaro Ishikawa, et al.Human Genome Variation|October 5, 2020
Prevalence of the mitochondrial 1555 A>G and 1494 C>T mutations in a community-dwelling population in JapanYasunori Maeda, Akira Sasaki, Shuya Kasai, et al.Stem Cell Research|April 26, 2023
Generation and characterization of a human iPSC line (JUFMDOi007-A) from a patient with Usher syndrome due to mutation in USH2ATakao Ukaji, Mikako Takahashi-Shibata, Daisuke Arai, et al.International Journal of Molecular Sciences|March 13, 2024
Validation of RNA Extraction Methods and Suitable Reference Genes for Gene Expression Studies in Developing Fetal Human Inner Ear TissueClaudia Steinacher, Dietmar Rieder, Jasmin E Turner, et al.Acta Oto-Laryngologica|April 4, 2017
Epidemiological survey of acute low-tone sensorineural hearing lossHiroaki Sato, Shigeru Kuwashima, Shin-Ya Nishio, et al.Pageof 26