Current status and molecular biology of human papillomavirus‐independent gastric‐type adenocarcinoma of the cervix von Nishio, Shin

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The genetic etiology of hearing loss in Japan revealed by the social health insurance-based genetic testing of 10K patients von Usami, Shin-ichi, Nishio, Shin-ya

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Variants in CDH23 cause a broad spectrum of hearing loss: from non-syndromic to syndromic hearing loss as well as from congenital to age-related hearing loss von Usami, Shin-ichi, Isaka, Yuichi, Miyagawa, Maiko, Nishio, Shin-ya

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Frequency of the STRC-CATSPER2 deletion in STRC-associated hearing loss patients von Nishio, Shin-ya, Usami, Shin-ichi

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Prevalence and clinical features of autosomal dominant and recessive TMC1-associated hearing loss von Nishio, Shin-ya, Usami, Shin-ichi

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Cochlear Implantation From the Perspective of Genetic Background von Usami, Shin‐ichi, Nishio, Shin‐ya, Moteki, Hideaki, Miyagawa, Maiko, Yoshimura, Hidekane

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Genetic background in late-onset sensorineural hearing loss patients von Uehara, Natsumi, Fujita, Takeshi, Yamashita, Daisuke, Yokoi, Jun, Katsunuma, Sayaka, Kakigi, Akinobu, Nishio, Shin-Ya, Nibu, Ken-Ichi, Usami, Shin-Ichi

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Comparison of vestibular function in hereditary hearing loss patients with GJB2, CDH23, and SLC26A4 variants von Tsukada, Keita, Nishio, Shin-ya, Takumi, Yutaka, Usami, Shin-ichi

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Digenic inheritance of mutations in EPHA2 and SLC26A4 in Pendred syndrome von Li, Mengnan, Nishio, Shin-ya, Naruse, Chie, Riddell, Meghan, Sapski, Sabrina, Katsuno, Tatsuya, Hikita, Takao, Mizapourshafiyi, Fatemeh, Smith, Fiona M., Cooper, Leanne T., Lee, Min Goo, Asano, Masahide, Boettger, Thomas, Krueger, Marcus, Wietelmann, Astrid, Graumann, Johannes, Day, Bryan W., Boyd, Andrew W., Offermanns, Stefan, Kitajiri, Shin-ichiro, Usami, Shin-ichi, Nakayama, Masanori

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Human deafness-associated variants alter the dynamics of key molecules in hair cell stereocilia F-actin cores von Miyoshi, Takushi, Belyantseva, Inna A., Kitajiri, Shin-ichiro, Miyajima, Hiroki, Nishio, Shin-ya, Usami, Shin-ichi, Kim, Bong Jik, Choi, Byung Yoon, Omori, Koichi, Shroff, Hari, Friedman, Thomas B.

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Clinical significance of primary debulking surgery and neoadjuvant chemotherapy-interval debulking surgery in advanced ovarian cancer von Nishio, Shin, Ushijima, Kimio

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Epidemiology, aetiology and diagnosis of congenital hearing loss via hearing screening of 153 913 newborns von Yoshimura, Hidekane, Okubo, Takuya, Shinagawa, Jun, Nishio, Shin-Ya, Takumi, Yutaka, Usami, Shin-Ichi

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Mutation spectrum and genotype-phenotype correlation of hearing loss patients caused by SLC26A4 mutations in the Japanese: a large cohort study von Miyagawa, Maiko, Nishio, Shin-Ya, Usami, Shin-Ichi

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Constitutive activation of DIA1 (DIAPH1) via C‐terminal truncation causes human sensorineural hearing loss von Ueyama, Takehiko, Ninoyu, Yuzuru, Nishio, Shin‐ya, Miyoshi, Takushi, Torii, Hiroko, Nishimura, Koji, Sugahara, Kazuma, Sakata, Hideaki, Thumkeo, Dean, Sakaguchi, Hirofumi, Watanabe, Naoki, Usami, Shin‐ichi, Saito, Naoaki, Kitajiri, Shin‐ichiro

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Prevalence and clinical features of hearing loss caused by EYA4 variants von Shinagawa, Jun, Moteki, Hideaki, Nishio, Shin-ya, Ohyama, Kenji, Otsuki, Koshi, Iwasaki, Satoshi, Masuda, Shin, Oshikawa, Chie, Ohta, Yumi, Arai, Yasuhiro, Takahashi, Masahiro, Sakuma, Naoko, Abe, Satoko, Sakurai, Yuika, Sakaguchi, Hirofumi, Ishino, Takashi, Uehara, Natsumi, Usami, Shin-ichi

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Milestones toward cochlear gene therapy for patients with hereditary hearing loss von Yoshimura, Hidekane, Nishio, Shin‐Ya, Usami, Shin‐Ichi

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The Clinical Next‐Generation Sequencing Database: A Tool for the Unified Management of Clinical Information and Genetic Variants to Accelerate Variant Pathogenicity Classification... von Nishio, Shin‐ya, Usami, Shin‐ichi

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Novel ACTG1 mutations in patients identified by massively parallel DNA sequencing cause progressive hearing loss von Miyajima, Hiroki, Moteki, Hideaki, Day, Timothy, Nishio, Shin-ya, Murata, Takaaki, Ikezono, Tetsuo, Takeda, Hidehiko, Abe, Satoko, Iwasaki, Satoshi, Takahashi, Masahiro, Naito, Yasushi, Yamazaki, Hiroshi, Kanda, Yukihiko, Kitajiri, Shin-ichiro, Usami, Shin-ichi

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Targeted exon sequencing successfully discovers rare causative genes and clarifies the molecular epidemiology of Japanese deafness patients von Miyagawa, Maiko, Naito, Takehiko, Nishio, Shin-ya, Kamatani, Naoyuki, Usami, Shin-ichi

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Frequency and clinical features of hearing loss caused by STRC deletions von Yokota, Yoh, Moteki, Hideaki, Nishio, Shin-ya, Yamaguchi, Tomomi, Wakui, Keiko, Kobayashi, Yumiko, Ohyama, Kenji, Miyazaki, Hiromitsu, Matsuoka, Rina, Abe, Satoko, Kumakawa, Kozo, Takahashi, Masahiro, Sakaguchi, Hirofumi, Uehara, Natsumi, Ishino, Takashi, Kosho, Tomoki, Fukushima, Yoshimitsu, Usami, Shin-ichi

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