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Genes|March 8, 2020
Clinical Characteristics and In Vitro Analysis of <i>MYO6</i> Variants Causing Late-Onset Progressive Hearing LossShin-Ichiro Oka, Timothy F Day, Shin-Ya Nishio, et al.Human Mutation|January 17, 2020
POLD1 variants leading to reduced polymerase activity can cause hearing loss without syndromic featuresDoo-Yi Oh, Yoshihiro Matsumoto, Shin-Ichiro Kitajiri, et al.Journal of Medical Genetics|September 2, 2019
Differential disruption of autoinhibition and defect in assembly of cytoskeleton during cell division decide the fate of human <i>DIAPH1</i>-related cytoskeletopathyBong Jik Kim, Takehiko Ueyama, Takushi Miyoshi, et al.Cell|June 1, 2010
Actin-bundling protein TRIOBP forms resilient rootlets of hair cell stereocilia essential for hearingShin-ichiro Kitajiri, Takeshi Sakamoto, Inna A Belyantseva, et al.Nature Communications|March 14, 2020
Digenic inheritance of mutations in EPHA2 and SLC26A4 in Pendred syndromeMengnan Li, Shin-Ya Nishio, Chie Naruse, et al.JCI Insight|June 21, 2019
TRIOBP-5 sculpts stereocilia rootlets and stiffens supporting cells enabling hearingTatsuya Katsuno, Inna A Belyantseva, Alexander X Cartagena-Rivera, et al.Pageof 5