TMC and EVER genes belong to a larger novel family, the TMC gene family encoding transmembrane proteins

Por Mutai Hideki, Keresztes Gabor, Heller Stefan
Publicado em 2003-06-01

TMC and EVER genes belong to a larger novel family, the TMC gene family encoding transmembrane proteins

Por Keresztes, Gabor, Mutai, Hideki, Heller, Stefan
Publicado em 2003

In silico modeling of the pore region of a KCNQ4 missense mutant from a patient with hearing loss

Por Namba, Kazunori, Mutai, Hideki, Kaneko, Hiroki, Hashimoto, Sho, Matsunaga, Tatsuo
Publicado em 2012

Attenuation of Progressive Hearing Loss in DBA/2J Mice by Reagents that Affect Epigenetic Modifications Is Associated with Up-Regulation of the Zinc Importer Zip4

Por Mutai, Hideki, Miya, Fuyuki, Fujii, Masato, Tsunoda, Tatsuhiko, Matsunaga, Tatsuo
Publicado no PLoS One (2015)

Mitochondrial mutations in maternally inherited hearing loss

Por Mutai, Hideki, Watabe, Takahisa, Kosaki, Kenjiro, Ogawa, Kaoru, Matsunaga, Tatsuo
Publicado no BMC Med Genet (2017)

Characterization of the chicken inward rectifier K(+ )channel IRK1/Kir2.1 gene

Por Mutai, Hideki, Kenyon, Lawrence C, Locke, Emily, Kikuchi, Nami, Oberholtzer, John Carl
Publicado em 2004

Gene expression profiling of DBA/2J mice cochleae treated with l-methionine and valproic acid

Por Miya, Fuyuki, Mutai, Hideki, Fujii, Masato, Boroevich, Keith A., Matsunaga, Tatsuo, Tsunoda, Tatsuhiko
Publicado no Genom Data (2015)

A novel nonsense mutation in the NOG gene causes familial NOG-related symphalangism spectrum disorder

Por Takano, Kenichi, Ogasawara, Noriko, Matsunaga, Tatsuo, Mutai, Hideki, Sakurai, Akihiro, Ishikawa, Aki, Himi, Tetsuo
Publicado no Hum Genome Var (2016)

Systematic analysis of mitochondrial genes associated with hearing loss in the Japanese population: dHPLC reveals a new candidate mutation

Por Mutai, Hideki, Kouike, Hiroko, Teruya, Eiko, Takahashi-Kodomari, Ikuko, Kakishima, Hiroki, Taiji, Hidenobu, Usami, Shin-ichi, Okuyama, Torayuki, Matsunaga, Tatsuo
Publicado em 2011

Diverse spectrum of rare deafness genes underlies early-childhood hearing loss in Japanese patients: a cross-sectional, multi-center next-generation sequencing study

Por Mutai, Hideki, Suzuki, Naohiro, Shimizu, Atsushi, Torii, Chiharu, Namba, Kazunori, Morimoto, Noriko, Kudoh, Jun, Kaga, Kimitaka, Kosaki, Kenjiro, Matsunaga, Tatsuo
Publicado no Orphanet J Rare Dis (2013)

High prevalence of CDH23 mutations in patients with congenital high-frequency sporadic or recessively inherited hearing loss

Por Mizutari, Kunio, Mutai, Hideki, Namba, Kazunori, Miyanaga, Yuko, Nakano, Atsuko, Arimoto, Yukiko, Masuda, Sawako, Morimoto, Noriko, Sakamoto, Hirokazu, Kaga, Kimitaka, Matsunaga, Tatsuo
Publicado no Orphanet J Rare Dis (2015)

Prevalence of TECTA mutation in patients with mid-frequency sensorineural hearing loss

Por Yamamoto, Nobuko, Mutai, Hideki, Namba, Kazunori, Morita, Noriko, Masuda, Shin, Nishi, Yasuyuki, Nakano, Atsuko, Masuda, Sawako, Fujioka, Masato, Kaga, Kimitaka, Ogawa, Kaoru, Matsunaga, Tatsuo
Publicado no Orphanet J Rare Dis (2017)