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Hearing Research|February 27, 2020
c.753A>G genome editing of a Cdh23ahl allele delays age-related hearing loss and degeneration of cochlear hair cells in C57BL/6J miceShumpei P Yasuda, Yuta Seki, Sari Suzuki, et al.Plos One|December 11, 2012
A 5-bp insertion in Mip causes recessive congenital cataract in KFRS4/Kyo ratsKei Watanabe, Kenta Wada, Tomoko Ohashi, et al.Scientific Reports|March 29, 2019
OHC-TRECK: A Novel System Using a Mouse Model for Investigation of the Molecular Mechanisms Associated with Outer Hair Cell Death in the Inner EarKunie Matsuoka, Kenta Wada, Yuki Miyasaka, et al.Genome Biology|February 28, 2018
i-GONAD: a robust method for in situ germline genome engineering using CRISPR nucleasesMasato Ohtsuka, Masahiro Sato, Hiromi Miura, et al.Poultry Science|August 11, 2022
Carcass traits and fat quality of breeding emu (Dromaius novaehollandiae) in Northern JapanYuichi Koshiishi, Michiko Murata-Okubo, Hinami Nakajyo, et al.Plos One|October 28, 2014
Expression of truncated PITX3 in the developing lens leads to microphthalmia and aphakia in miceKenta Wada, Yoshibumi Matsushima, Tomoki Tada, et al.Plos One|August 24, 2017
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 cellsYuta Seki, Yuki Miyasaka, Sari Suzuki, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|October 18, 2011
A deletion in a cis element of Foxe3 causes cataracts and microphthalmia in rct miceKenta Wada, Yukiko Y Maeda, Kei Watanabe, et al.Experimental Animals|March 13, 2010
Phenotypic and expression analysis of a novel spontaneous myosin VI null mutant mouseEiji Mochizuki, Kazuhiro Okumura, Masashi Ishikawa, et al.Pageof 3