Kiyoto Kurima - Concepedia

Author

Kiyoto Kurima

National Institute on Deafness and Other Communication Disorders

Also Known As

KIYOTO KURIMA, Kiyoto Kurima, Kurima, Kiyoto

Publications

3.8K

Citations

H-Index

Concepts

All Affiliations

National Institute on Deafness and Other Communication Disorders National Institutes of Health Boston Children's Hospital University of the Ryukyus The Ohio State University

About

Kiyoto Kurima is an author at National Institute on Deafness and Other Communication Disorders specializing in medicine, cell biology, and auditory physiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	16	2.1K
2	Health Sciences	5	5	1.2K
3	Arts	3	3	813
4	Natural Sciences	3	3	204
5	Engineering	2	2	239

Kiyoto Kurima

Publications

3.5K

Citations

H-Index

Page 1

	Year	Citations
Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function Kiyoto Kurima, Linda Peters, Yandan Yang, Nature Genetics Novel GeneGenetic DisorderGeneticsCochlear Hair-cell FunctionAudiology	2002	471
Mechanotransduction in mouse inner ear hair cells requires transmembrane channel–like genes Yoshiyuki Kawashima, Gwenaëlle S. G. Géléoc, Kiyoto Kurima, Journal of Clinical Investigation	2011	451
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, Neuron MechanobiologyHair CellsMammalian Inner EarPhysiologyAuditory Physiology	2013	438
TMC1 Forms the Pore of Mechanosensory Transduction Channels in Vertebrate Inner Ear Hair Cells Bifeng Pan, Nurunisa Akyuz, Xiaoping Liu, Neuron Cell PhysiologySignal TransductionMolecular PhysiologyPhysiologyIntercellular Communication	2018	361
Beethoven, a mouse model for dominant, progressive hearing loss DFNA36 Sarah Vreugde, Alexandra Erven, Corné J. Kros, Nature Genetics MusicAuditory ProcessingAuditory ModelingHealth SciencesAudiology	2002	287
TMC1 and TMC2 Localize at the Site of Mechanotransduction in Mammalian Inner Ear Hair Cell Stereocilia Kiyoto Kurima, Seham Ebrahim, Bifeng Pan, Cell Reports EngineeringStereocilia LocalizationMolecular BiologyCytoskeletonMechanotransduction	2015	209
A member of a family of sulfate-activating enzymes causes murine brachymorphism Kiyoto Kurima, Matthew L. Warman, Srinivasan Krishnan, Proceedings of the National Academy of Sciences Aldo-keto ReductaseGeneticsSulfate-activating EnzymesEnzymatic SynthesisMolecular Biology	1998	152
Characterization of the transmembrane channel-like (TMC) gene family: functional clues from hearing loss and epidermodysplasia verruciformis☆ Kiyoto Kurima, Yandan Yang, Katherine Sorber, Genomics Signal TransductionGeneticsIon ChannelsGene FamilyMolecular Genetics	2003	149
<i>NLRP3</i> mutation and cochlear autoinflammation cause syndromic and nonsyndromic hearing loss DFNA34 responsive to anakinra therapy Hiroshi Nakanishi, Yoshiyuki Kawashima, Kiyoto Kurima, Proceedings of the National Academy of Sciences	2017	148
Mouse model of enlarged vestibular aqueducts defines temporal requirement of Slc26a4 expression for hearing acquisition Byung Yoon Choi, Hyoung Mi Kim, Taku Ito, Journal of Clinical Investigation	2011	129

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