Increased E4 Activity in Mice Leads to Ubiquitin-containing Aggregates and Degeneration of Hypothalamic Neurons Resulting in Obesity

av Susaki, Etsuo, Kaneko-Oshikawa, Chie, Miyata, Keishi, Tabata, Mitsuhisa, Yamada, Tetsuya, Oike, Yuichi, Katagiri, Hideki, Nakayama, Keiichi I.
Publicerad 2010

Mammalian E4 Is Required for Cardiac Development and Maintenance of the Nervous System

av Kaneko-Oshikawa, Chie, Nakagawa, Tadashi, Yamada, Mitsunori, Yoshikawa, Hiroo, Matsumoto, Masaki, Yada, Masayoshi, Hatakeyama, Shigetsugu, Nakayama, Keiko, Nakayama, Keiichi I.
Publicerad 2005

Comprehensive Genetic Screening of KCNQ4 in a Large Autosomal Dominant Nonsyndromic Hearing Loss Cohort: Genotype-Phenotype Correlations and a Founder Mutation

av Naito, Takehiko, Nishio, Shin-ya, Iwasa, Yoh-ichiro, Yano, Takuya, Kumakawa, Kozo, Abe, Satoko, Ishikawa, Kotaro, Kojima, Hiromi, Namba, Atsushi, Oshikawa, Chie, Usami, Shin-ichi
Publicerad 2013

Massively Parallel DNA Sequencing Facilitates Diagnosis of Patients with Usher Syndrome Type 1

av Yoshimura, Hidekane, Iwasaki, Satoshi, Nishio, Shin-ya, Kumakawa, Kozo, Tono, Tetsuya, Kobayashi, Yumiko, Sato, Hiroaki, Nagai, Kyoko, Ishikawa, Kotaro, Ikezono, Tetsuo, Naito, Yasushi, Fukushima, Kunihiro, Oshikawa, Chie, Kimitsuki, Takashi, Nakanishi, Hiroshi, Usami, Shin-ichi
Publicerad 2014

Mutational Spectrum and Clinical Features of Patients with LOXHD1 Variants Identified in an 8074 Hearing Loss Patient Cohort

av Maekawa, Karuna, Nishio, Shin-ya, Abe, Satoko, Goto, Shin-ichi, Honkura, Yohei, Iwasaki, Satoshi, Kanda, Yukihiko, Kobayashi, Yumiko, Oka, Shin-ichiro, Okami, Mayuri, Oshikawa, Chie, Sakuma, Naoko, Sano, Hajime, Shirakura, Masayuki, Uehara, Natsumi, Usami, Shin-ichi
I publikationen Genes (Basel) (2019)

Clinical Characteristics and In Vitro Analysis of MYO6 Variants Causing Late-onset Progressive Hearing Loss

av Oka, Shin-ichiro, Day, Timothy F., Nishio, Shin-ya, Moteki, Hideaki, Miyagawa, Maiko, Morita, Shinya, Izumi, Shuji, Ikezono, Tetsuo, Abe, Satoko, Nakayama, Jun, Hyogo, Misako, Okamoto, Nobuhiko, Uehara, Natsumi, Oshikawa, Chie, Kitajiri, Shin-ichiro, Usami, Shin-ichi
I publikationen Genes (Basel) (2020)

Prevalence and clinical features of hearing loss caused by EYA4 variants

av 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
I publikationen Sci Rep (2020)

WFS1 mutation screening in a large series of Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis

av Kobayashi, Masafumi, Miyagawa, Maiko, Nishio, Shin-ya, Moteki, Hideaki, Fujikawa, Taro, Ohyama, Kenji, Sakaguchi, Hirofumi, Miyanohara, Ikuyo, Sugaya, Akiko, Naito, Yasushi, Morita, Shin-ya, Kanda, Yukihiko, Takahashi, Masahiro, Ishikawa, Kotaro, Nagano, Yuki, Tono, Tetsuya, Oshikawa, Chie, Kihara, Chiharu, Takahashi, Haruo, Noguchi, Yoshihiro, Usami, Shin-ichi
I publikationen PLoS One (2018)