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Cell Calcium|May 27, 2003
Vertebrate and invertebrate TRPV-like mechanoreceptorsHideki Mutai, Stefan HellerBMC Genomics|June 19, 2003
TMC and EVER genes belong to a larger novel family, the TMC gene family encoding transmembrane proteinsGabor Keresztes, Hideki Mutai, Stefan HellerBMC Research Notes|May 10, 2024
Structural basis for pathogenic variants of GJB2 and hearing levels of patients with hearing lossKazunori Namba, Hideki Mutai, Tatsuo Matsunaga, et al.Plos One|April 16, 2015
Attenuation of progressive hearing loss in DBA/2J mice by reagents that affect epigenetic modifications is associated with up-regulation of the zinc importer Zip4Hideki Mutai, Fuyuki Miya, Masato Fujii, et al.BMC Research Notes|March 17, 2012
In silico modeling of the pore region of a KCNQ4 missense mutant from a patient with hearing lossKazunori Namba, Hideki Mutai, Hiroki Kaneko, et al.Biochemical and Biophysical Research Communications|June 4, 2015
A novel frameshift mutation in KCNQ4 in a family with autosomal recessive non-syndromic hearing lossKoichiro Wasano, Hideki Mutai, Chie Obuchi, et al.Journal of Pharmacological Sciences|February 25, 2012
A novel animal model of hearing loss caused by acute endoplasmic reticulum stress in the cochleaYoshiaki Fujinami, Hideki Mutai, Kunio Mizutari, et al.BMC Medical Genetics|March 22, 2017
Mitochondrial mutations in maternally inherited hearing lossHideki Mutai, Takahisa Watabe, Kenjiro Kosaki, et al.Biochemical and Biophysical Research Communications|December 4, 2015
A novel frameshift variant of COCH supports the hypothesis that haploinsufficiency is not a cause of autosomal dominant nonsyndromic deafness 9Masatsugu Masuda, Hideki Mutai, Yukiko Arimoto, et al.Acta Oto-Laryngologica|November 21, 2012
Genetic analysis of PAX3 for diagnosis of Waardenburg syndrome type ITatsuo Matsunaga, Hideki Mutai, Kazunori Namba, et al.Pageof 7