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Neuroscience Letters|November 25, 2010
Inhibition of ganglioside synthesis reduces the neuronal survival activity of astrocytesYuko Akasako, Kiyomitsu Nara, Yoshitaka Nagai, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 24, 2011
A large-scale analysis of odor coding in the olfactory epitheliumKiyomitsu Nara, Luis R Saraiva, Xiaolan Ye, et al.
International Journal of Pediatric Otorhinolaryngology|August 14, 2017
The first sporadic case of DFNA11 identified by next-generation sequencingYuka Kaneko, Atsuko Nakano, Yukiko Arimoto, et al.
International Journal of Pediatric Otorhinolaryngology|November 21, 2021
Clinical and genetic analysis of children with hearing loss and bilateral enlarged vestibular aqueductsAtsuko Nakano, Yukiko Arimoto, Hideki Mutai, et al.
Cureus|March 29, 2024
Gap Junction Beta-2 p.Val84Met Can Cause Autosomal Dominant Syndromic Hearing Loss With KeratodermaKosuke Hashimoto, Toru Miwa, Chie Ono, et al.
Gene|April 13, 2019
A clinical and genetic study of 16 Japanese families with Waardenburg syndromeShujiro B Minami, Kiyomitsu Nara, Hideki Mutai, et al.
Orphanet Journal of Rare Diseases|March 6, 2022
Whole exome analysis of patients in Japan with hearing loss reveals high heterogeneity among responsible and novel candidate genesHideki Mutai, Yukihide Momozawa, Yoichiro Kamatani, et al.
Glycobiology|December 25, 2009
Siglec-7 mediates nonapoptotic cell death independently of its immunoreceptor tyrosine-based inhibitory motifs in monocytic cell line U937Motoaki Mitsuki, Kiyomitsu Nara, Toshiyuki Yamaji, et al.
Auris, Nasus, Larynx|September 28, 2024
Detailed characterization of auditory neuropathy in perrault syndrome with TWNK variantsMarie N Shimanuki, Makoto Hosoya, Takanori Nishiyama, et al.
Scientific Reports|December 15, 2025
Clinical features of hearing loss and genotype-phenotype correlations in Alport syndrome caused by COL4A4 or COL4A5 variantsSaeko Matsuzaki, Kiyomitsu Nara, Hideki Mutai, et al.
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