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Genetic landscape in undiagnosed patients with syndromic hearing loss revealed by whole exome sequencing and phenotype similarity search.
Mutai H, Miya F, Nara K, Yamamoto N, Inoue S, Murakami H, Namba K, Shitara H, Minami S, Nakano A, Arimoto Y, Morimoto N, Kawasaki T, Wasano K, Fujioka M, Uchida Y, Kaga K, Yamazawa K, Kikkawa Y, Kosaki K, Tsunoda T, Matsunaga T. Mutai H, et al. Among authors: uchida y. Hum Genet. 2025 Jan 4. doi: 10.1007/s00439-024-02719-5. Online ahead of print. Hum Genet. 2025. PMID: 39755840
Association of interleukin-1 gene polymorphisms with sudden sensorineural hearing loss and Ménière's disease.
Furuta T, Teranishi M, Uchida Y, Nishio N, Kato K, Otake H, Yoshida T, Tagaya M, Suzuki H, Sugiura M, Sone M, Hiramatsu M, Sugiura S, Ando F, Shimokata H, Nakashima T. Furuta T, et al. Among authors: uchida y. Int J Immunogenet. 2011 Jun;38(3):249-54. doi: 10.1111/j.1744-313X.2011.01004.x. Epub 2011 Mar 9. Int J Immunogenet. 2011. PMID: 21385326
Polymorphisms in genes involved in oxidative stress response in patients with sudden sensorineural hearing loss and Ménière's disease in a Japanese population.
Teranishi M, Uchida Y, Nishio N, Kato K, Otake H, Yoshida T, Suzuki H, Sone M, Sugiura S, Ando F, Shimokata H, Nakashima T. Teranishi M, et al. Among authors: uchida y. DNA Cell Biol. 2012 Oct;31(10):1555-62. doi: 10.1089/dna.2012.1631. Epub 2012 Aug 9. DNA Cell Biol. 2012. PMID: 22877234 Free PMC article.
Endothelin-1 gene polymorphism in sudden sensorineural hearing loss.
Uchida Y, Teranishi M, Nishio N, Sugiura S, Hiramatsu M, Suzuki H, Kato K, Otake H, Yoshida T, Tagaya M, Suzuki H, Sone M, Ando F, Shimokata H, Nakashima T. Uchida Y, et al. Laryngoscope. 2013 Nov;123(11):E59-65. doi: 10.1002/lary.24298. Epub 2013 Aug 5. Laryngoscope. 2013. PMID: 23832707
2,769 results