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The Prevalence and Clinical Characteristics of TECTA-Associated Autosomal Dominant Hearing Loss.
Yasukawa R, Moteki H, Nishio SY, Ishikawa K, Abe S, Honkura Y, Hyogo M, Mihashi R, Ikezono T, Shintani T, Ogasawara N, Shirai K, Yoshihashi H, Ishino T, Otsuki K, Ito T, Sugahara K, Usami SI. Yasukawa R, et al. Among authors: shirai k. Genes (Basel). 2019 Sep 24;10(10):744. doi: 10.3390/genes10100744. Genes (Basel). 2019. PMID: 31554319 Free PMC article.
Cochlear implantation in a patient with a POU4F3 mutation.
Miyake K, Shirai K, Nishiyama N, Kawaguchi S, Ohta Y, Kawano A, Usami SI, Kitano T, Tsukahara K. Miyake K, et al. Among authors: shirai k. Clin Case Rep. 2020 Nov 11;9(1):298-303. doi: 10.1002/ccr3.3520. eCollection 2021 Jan. Clin Case Rep. 2020. PMID: 33489177 Free PMC article.
Generation of two induced pluripotent stem cell lines from PBMCs of siblings carrying c.235delC mutation in the GJB2 gene associated with sensorineural hearing loss.
Fukunaga I, Shirai K, Oe Y, Danzaki K, Ohta S, Shiga T, Chen C, Ikeda K, Akamatsu W, Kawano A, Kamiya K. Fukunaga I, et al. Among authors: shirai k. Stem Cell Res. 2020 Jul 19;47:101910. doi: 10.1016/j.scr.2020.101910. Online ahead of print. Stem Cell Res. 2020. PMID: 32745712 Free article.
Modeling gap junction beta 2 gene-related deafness with human iPSC.
Fukunaga I, Oe Y, Danzaki K, Ohta S, Chen C, Shirai K, Kawano A, Ikeda K, Kamiya K. Fukunaga I, et al. Among authors: shirai k. Hum Mol Genet. 2021 Jul 9;30(15):1429-1442. doi: 10.1093/hmg/ddab097. Hum Mol Genet. 2021. PMID: 33997905
1,213 results