Two pediatric cases of post-traumatic facial paralysis with delayed onset

by Taku Ito, Hiroki Watanabe, Motomu Honjo, Tomoaki Asamori
Published 2018-01-01

Genetic Hearing Loss Associated With Autoinflammation

by Hiroshi Nakanishi, Hiroshi Nakanishi, Pragya Prakash, Taku Ito, Taku Ito, H. Jeffrey Kim, Carmen C. Brewer, Danielle Harrow, Isabelle Roux, Seiji Hosokawa, Andrew J. Griffith
Published 2020-03-01

3-Tesla magnetic resonance imaging reveals vasculitis-caused otitis media in a patient with giant cell arteritis

by Natsuki Aoki, Taro Fujikawa, Natsuka Umezawa, Yoshiyuki Kawashima, Taku Ito, Keiji Honda, Takeshi Tsutsumi
Published 2021-01-01

Slc26a4-insufficiency causes fluctuating hearing loss and stria vascularis dysfunction

by Taku Ito, Xiangming Li, Kiyoto Kurima, Byung Yoon Choi, Philine Wangemann, Andrew J. Griffith
Published 2014-06-01

Increased expression of pendrin in eosinophilic chronic rhinosinusitis with nasal polyps

by Taku Ito, Satoshi Ikeda, Tomoaki Asamori, Keiji Honda, Yoshiyuki Kawashima, Ken Kitamura, Keiko Suzuki, Takeshi Tsutsumi
Published 2019-11-01

Production and Application of Stable Isotope-Labeled Internal Standards for RNA Modification Analysis

by Kayla Borland, Jan Diesend, Taku Ito-Kureha, Vigo Heissmeyer, Christian Hammann, Amy H. Buck, Stylianos Michalakis, Stefanie Kellner
Published 2019-01-01

SLC26A4 targeted to the endolymphatic sac rescues hearing and balance in Slc26a4 mutant mice.

by Xiangming Li, Joel D Sanneman, Donald G Harbidge, Fei Zhou, Taku Ito, Raoul Nelson, Nicolas Picard, Régine Chambrey, Dominique Eladari, Tracy Miesner, Andrew J Griffith, Daniel C Marcus, Philine Wangemann
Published 2013-01-01

The CCR4–NOT deadenylase complex safeguards thymic positive selection by down-regulating aberrant pro-apoptotic gene expression

by Taku Ito-Kureha, Takahisa Miyao, Saori Nishijima, Toru Suzuki, Shin-ichi Koizumi, Alejandro Villar-Briones, Akinori Takahashi, Nobuko Akiyama, Masahiro Morita, Isao Naguro, Hiroki Ishikawa, Hidenori Ichijo, Taishin Akiyama, Tadashi Yamamoto
Published 2020-12-01

A noncoding point mutation of Zeb1 causes multiple developmental malformations and obesity in Twirler mice.

by Kiyoto Kurima, Ronna Hertzano, Oksana Gavrilova, Kelly Monahan, Karl B Shpargel, Garani Nadaraja, Yoshiyuki Kawashima, Kyu Yup Lee, Taku Ito, Yujiro Higashi, David J Eisenman, Scott E Strome, Andrew J Griffith
Published 2011-09-01

Defining the RBPome of primary T helper cells to elucidate higher-order Roquin-mediated mRNA regulation

by Kai P. Hoefig, Alexander Reim, Christian Gallus, Elaine H. Wong, Gesine Behrens, Christine Conrad, Meng Xu, Lisa Kifinger, Taku Ito-Kureha, Kyra A. Y. Defourny, Arie Geerlof, Josef Mautner, Stefanie M. Hauck, Dirk Baumjohann, Regina Feederle, Matthias Mann, Michael Wierer, Elke Glasmacher, Vigo Heissmeyer
Published 2021-09-01