Immunogold electron microscopic evidence of in situ formation of homo- and heteromeric purinergic adenosine A(1 )and P2Y(2 )receptors in rat brain

Por Namba, Kazunori, Suzuki, Tokiko, Nakata, Hiroyasu
Publicado em 2010

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

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)