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Acta Oto-Laryngologica Volume 119, 1999 - Issue 7
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Research Article

Evaluation of Inner Ear Histology and Auditory Brainstem Response in Wriggle Mouse Sagami

Katsumasa Takahashi Department of Otolaryngology, Jichi Medical School, 3311-1 Yakushiji, Tochigi 329-0498, Japan
Pages 767-772 | Published online: 08 Jul 2009

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Hidenori Ozaki, Yoko Watanabe, Katsumasa Takahashi, Ken Kitamura, Akira Tanaka, Koko Urase, Takashi Momoi, Katsuko Sudo, Junko Sakagami, Masahide Asano, Yoichiro Iwakura & Kiyoshi Kawakami. (2001) Six4, a Putative myogeninGene Regulator, Is Not Essential for Mouse Embryonal Development. Molecular and Cellular Biology 21:10, pages 3343-3350.
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Articles from other publishers (7)

Keiji Honda, Yoshihiro Noguchi, Yoshiyuki Kawashima, Masatoki Takahashi, Ayako Nishio & Ken Kitamura. (2015) Ex Vivo Visualization of the Mouse Otoconial Layer Compared With Micro-Computed Tomography. Otology & Neurotology 36:2, pages 311-317.
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Ellen J. Hess & H.A. Jinnah. 2015. Movement Disorders. Movement Disorders 465 481 .
Björn Palmgren, Zhe Jin, Hongmin Ma, Yu Jiao & Petri Olivius. (2010) β-Bungarotoxin application to the round window: An in vivo deafferentation model of the inner ear. Hearing Research 265:1-2, pages 70-76.
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Sarah L. Spiden, Mario Bortolozzi, Francesca Di Leva, Martin Hrabé de Angelis, Helmut Fuchs, Dmitry Lim, Saida Ortolano, Neil J. Ingham, Marisa Brini, Ernesto Carafoli, Fabio Mammano & Karen P. Steel. (2008) The Novel Mouse Mutation Oblivion Inactivates the PMCA2 Pump and Causes Progressive Hearing Loss. PLoS Genetics 4:10, pages e1000238.
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ELLEN J. HESS & H.A. JINNAH. 2005. Animal Models of Movement Disorders. Animal Models of Movement Disorders 265 277 .
Brendan J. McCullough & Bruce L. Tempel. (2004) Haplo-insufficiency revealed in deafwaddler mice when tested for hearing loss and ataxia. Hearing Research 195:1-2, pages 90-102.
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Takeshi Ueno, Kohzoh Kameyama, Mihoko Hirata, Miyuki Ogawa, Hiromi Hatsuse, Yohtaroh Takagaki, Michio Ohmura, Nobutaka Osawa & Yoshihisa Kudo. (2002) A mouse with a point mutation in plasma membrane Ca2+-ATPase isoform 2 gene showed the reduced Ca2+ influx in cerebellar neurons. Neuroscience Research 42:4, pages 287-297.
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