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Human Genetics|July 7, 2021
Human deafness-associated variants alter the dynamics of key molecules in hair cell stereocilia F-actin coresTakushi Miyoshi, Inna A Belyantseva, Shin-Ichiro Kitajiri, et al.Plos One|August 24, 2017
A novel splice site mutation of myosin VI in mice leads to stereociliary fusion caused by disruption of actin networks in the apical region of inner ear hair cellsYuta Seki, Yuki Miyasaka, Sari Suzuki, et al.EMBO Molecular Medicine|October 7, 2016
Constitutive activation of DIA1 (DIAPH1) via C-terminal truncation causes human sensorineural hearing lossTakehiko Ueyama, Yuzuru Ninoyu, Shin-Ya Nishio, et al.Scientific Reports|April 23, 2020
Cochlear supporting cells function as macrophage-like cells and protect audiosensory receptor hair cells from pathogensYushi Hayashi, Hidenori Suzuki, Wataru Nakajima, et al.Scientific Reports|April 29, 2020
Novel ACTG1 mutations in patients identified by massively parallel DNA sequencing cause progressive hearing lossHiroki Miyajima, Hideaki Moteki, Timothy Day, et al.Genes|September 19, 2019
Mid-Frequency Hearing Loss Is Characteristic Clinical Feature of <i>OTOA</i>-Associated Hearing LossKenjiro Sugiyama, Hideaki Moteki, Shin-Ichiro Kitajiri, et al.Plos One|November 29, 2021
Virus-infection in cochlear supporting cells induces audiosensory receptor hair cell death by TRAIL-induced necroptosisYushi Hayashi, Hidenori Suzuki, Wataru Nakajima, et al.Plos One|February 11, 2015
Downsloping high-frequency hearing loss due to inner ear tricellular tight junction disruption by a novel ILDR1 mutation in the Ig-like domainNayoung K D Kim, Tomohito Higashi, Kyoung Yeul Lee, et al.Human Mutation|January 18, 2007
Mutations of the RDX gene cause nonsyndromic hearing loss at the DFNB24 locusShahid Y Khan, Zubair M Ahmed, Muhammad I Shabbir, et al.American Journal of Human Genetics|December 23, 2006
Tricellulin is a tight-junction protein necessary for hearingSaima Riazuddin, Zubair M Ahmed, Alan S Fanning, et al.Pageof 5