Tricellular Tight Junctions in the Inner Ear

por Kitajiri, Shin-ichiro, Katsuno, Tatsuya
Publicado 2016

Deficiency of Angulin-2/ILDR1, a Tricellular Tight Junction-Associated Membrane Protein, Causes Deafness with Cochlear Hair Cell Degeneration in Mice

por Higashi, Tomohito, Katsuno, Tatsuya, Kitajiri, Shin-ichiro, Furuse, Mikio
Publicado 2015

Detailed Clinical Features of Deafness Caused by a Claudin-14 Variant

por Kitano, Tomohiro, Kitajiri, Shin-ichiro, Nishio, Shin-ya, Usami, Shin-ichi
Publicado 2019

Deafness in occludin-deficient mice with dislocation of tricellulin and progressive apoptosis of the hair cells

por Kitajiri, Shin-ichiro, Katsuno, Tatsuya, Sasaki, Hiroyuki, Ito, Juichi, Furuse, Mikio, Tsukita, Shoichiro
Publicado 2014

Prevalence and Clinical Characteristics of Hearing Loss Caused by MYH14 Variants

por Hiramatsu, Ken, Nishio, Shin-ya, Kitajiri, Shin-ichiro, Kitano, Tomohiro, Moteki, Hideaki, Usami, Shin-ichi
Publicado 2021

Radixin deficiency causes deafness associated with progressive degeneration of cochlear stereocilia

por Kitajiri, Shin-ichiro, Fukumoto, Kanehisa, Hata, Masaki, Sasaki, Hiroyuki, Katsuno, Tatsuya, Nakagawa, Takayuki, Ito, Juichi, Tsukita, Shoichiro, Tsukita, Sachiko
Publicado 2004

Carrier frequency of the GJB2 mutations that cause hereditary hearing loss in the Japanese population

por Taniguchi, Mirei, Matsuo, Hirotaka, Shimizu, Seiko, Nakayama, Akiyoshi, Suzuki, Koji, Hamajima, Nobuyuki, Shinomiya, Nariyoshi, Nishio, Shinya, Kosugi, Shinji, Usami, Shin-ichi, Ito, Juichi, Kitajiri, Shin-ichiro
Publicado 2015

Microarray analyses of otospheres derived from the cochlea in the inner ear identify putative transcription factors that regulate the characteristics of otospheres

por Iki, Takehiro, Tanaka, Michihiro, Kitajiri, Shin-ichiro, Kita, Tomoko, Kawasaki, Yuri, Mizukoshi, Akifumi, Fujibuchi, Wataru, Nakagawa, Takayuki, Nakahata, Tatsutoshi, Ito, Juichi, Omori, Koichi, Saito, Megumu K.
Publicado 2017

Unbalanced bidirectional radial stiffness gradients within the organ of Corti promoted by TRIOBP

por Babahosseini, Hesam, Belyantseva, Inna A., Yousaf, Rizwan, Tona, Risa, Hadi, Shadan, Inagaki, Sayaka, Wilson, Elizabeth, Kitajiri, Shin-ichiro, Frolenkov, Gregory I., Friedman, Thomas B., Cartagena-Rivera, Alexander X.
Publicado 2022

A novel splice site mutation of myosin VI in mice leads to stereociliary fusion caused by disruption of actin networks in the apical region of inner ear hair cells

por Seki, Yuta, Miyasaka, Yuki, Suzuki, Sari, Wada, Kenta, Yasuda, Shumpei P., Matsuoka, Kunie, Ohshiba, Yasuhiro, Endo, Kentaro, Ishii, Rie, Shitara, Hiroshi, Kitajiri, Shin-ichiro, Nakagata, Naomi, Takebayashi, Hirohide, Kikkawa, Yoshiaki
Publicado 2017

Constitutive activation of DIA1 (DIAPH1) via C‐terminal truncation causes human sensorineural hearing loss

por 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
Publicado 2016

Mid-Frequency Hearing Loss Is Characteristic Clinical Feature of OTOA-Associated Hearing Loss

por Sugiyama, Kenjiro, Moteki, Hideaki, Kitajiri, Shin-ichiro, Kitano, Tomohiro, Nishio, Shin-ya, Yamaguchi, Tomomi, Wakui, Keiko, Abe, Satoko, Ozaki, Akiko, Motegi, Remi, Matsui, Hirooki, Teraoka, Masato, Kobayashi, Yumiko, Kosho, Tomoki, Usami, Shin-ichi
Publicado 2019

Cochlear supporting cells function as macrophage-like cells and protect audiosensory receptor hair cells from pathogens

por Hayashi, Yushi, Suzuki, Hidenori, Nakajima, Wataru, Uehara, Ikuno, Tanimura, Atsuko, Himeda, Toshiki, Koike, Satoshi, Katsuno, Tatsuya, Kitajiri, Shin-ichiro, Koyanagi, Naoto, Kawaguchi, Yasushi, Onomoto, Koji, Kato, Hiroki, Yoneyama, Mitsutoshi, Fujita, Takashi, Tanaka, Nobuyuki
Publicado 2020

Novel ACTG1 mutations in patients identified by massively parallel DNA sequencing cause progressive hearing loss

por 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
Publicado 2020

Virus-infection in cochlear supporting cells induces audiosensory receptor hair cell death by TRAIL-induced necroptosis

por Hayashi, Yushi, Suzuki, Hidenori, Nakajima, Wataru, Uehara, Ikuno, Tanimura, Atsuko, Himeda, Toshiki, Koike, Satoshi, Katsuno, Tatsuya, Kitajiri, Shin-ichiro, Koyanagi, Naoto, Kawaguchi, Yasushi, Onomoto, Koji, Kato, Hiroki, Yoneyama, Mitsutoshi, Fujita, Takashi, Tanaka, Nobuyuki
Publicado 2021

Downsloping High-Frequency Hearing Loss Due to Inner Ear Tricellular Tight Junction Disruption by a Novel ILDR1 Mutation in the Ig-Like Domain

por Kim, Nayoung K. D., Higashi, Tomohito, Lee, Kyoung Yeul, Kim, Ah Reum, Kitajiri, Shin-ichiro, Kim, Min Young, Chang, Mun Young, Kim, Veronica, Oh, Seung-Ha, Kim, Dongsup, Furuse, Mikio, Park, Woong-Yang, Choi, Byung Yoon
Publicado 2015

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

por 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
Publicado 2020

Digenic inheritance of mutations in EPHA2 and SLC26A4 in Pendred syndrome

por 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
Publicado 2020