Kiyoto Kurima

Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function

Kiyoto Kurima, Linda Peters, Yandan Yang et al. · Nature Genetics · 2002 · 471 citations · Full text

Novel Gene, Genetic Disorder, Genetics +15

Mechanotransduction in mouse inner ear hair cells requires transmembrane channel–like genes

Yoshiyuki Kawashima, Gwenaëlle S. G. Géléoc, Kiyoto Kurima et al. · Journal of Clinical Investigation · 2011 · 451 citations · Full text

TMC1 and TMC2 Are Components of the Mechanotransduction Channel in Hair Cells of the Mammalian Inner Ear

Bifeng Pan, Gwenaëlle S. G. Géléoc, Yukako Asai et al. · Neuron · 2013 · 438 citations · Full text

Mechanobiology, Hair Cells, Mammalian Inner Ear +10

TMC1 Forms the Pore of Mechanosensory Transduction Channels in Vertebrate Inner Ear Hair Cells

Bifeng Pan, Nurunisa Akyuz, Xiaoping Liu et al. · Neuron · 2018 · 361 citations · Full text

Cell Physiology, Signal Transduction, Molecular Physiology +12

Beethoven, a mouse model for dominant, progressive hearing loss DFNA36

Sarah Vreugde, Alexandra Erven, Corné J. Kros et al. · Nature Genetics · 2002 · 287 citations

Music, Auditory Processing, Auditory Modeling +12