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Kiyoto Kurima

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Yoshiyuki Kawashima; Kiyoto Kurima; Valentina Labay; Andrea Lelli; Tomoko Makishima; Doris K Wu; Yukako Asai; Charles C Della Santina; Gwenaelle Geleoc; Jeffrey R Holt; Andrew J Griffith
Mechanotransduction in mouse inner ear hair cells requires transmembrane channel-like genes.
Byung Yoon Choi; Thomas B Friedman; Taku Ito; Hyoung-Mi Kim; Kiyoto Kurima; Kyu Yup Lee; Xiangming Li; Kelly Monahan; Ronald S Petralia; Thomas L Saunders; Philine Wangemann; Yaqing Wen; Elizabeth Wilson; Andrew J Griffith
Mouse model of enlarged vestibular aqueducts defines temporal requirement of Slc26a4 expression for hearing acquisition.
Ronna Hertzano; Kiyoto Kurima; Annie Morrisson; Michelle Sallin; Andrew Biedlingmaier; Siaw-Lin Chan; Douglas S Darling; David J Eisenman; Ran Elkon; Andrew J Griffith; Scott E Strome
Cell type-specific transcriptome analysis reveals a major role for Zeb1 and miR-200b in mouse inner ear morphogenesis.

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All Publications

2011: Yoshiyuki Kawashima; Kiyoto Kurima; Valentina Labay; Andrea Lelli; Tomoko Makishima; Doris K Wu; Yukako Asai; Charles C Della Santina; Gwenaelle Geleoc; Jeffrey R Holt; Andrew J Griffith
Mechanotransduction in mouse inner ear hair cells requires transmembrane channel-like genes.
The Journal of clinical investigation 2011;121(12):4796-809.
2011: Byung Yoon Choi; Thomas B Friedman; Taku Ito; Hyoung-Mi Kim; Kiyoto Kurima; Kyu Yup Lee; Xiangming Li; Kelly Monahan; Ronald S Petralia; Thomas L Saunders; Philine Wangemann; Yaqing Wen; Elizabeth Wilson; Andrew J Griffith
Mouse model of enlarged vestibular aqueducts defines temporal requirement of Slc26a4 expression for hearing acquisition.
The Journal of clinical investigation 2011;121(11):4516-25.
2011: Ronna Hertzano; Kiyoto Kurima; Annie Morrisson; Michelle Sallin; Andrew Biedlingmaier; Siaw-Lin Chan; Douglas S Darling; David J Eisenman; Ran Elkon; Andrew J Griffith; Scott E Strome
Cell type-specific transcriptome analysis reveals a major role for Zeb1 and miR-200b in mouse inner ear morphogenesis.
PLoS genetics 2011;7(9):e1002309.
2011: Kiyoto Kurima; Kyu Yup Lee; Kelly Monahan; Garani Nadaraja; Karl B Shpargel; Scott E Strome; Ronna Hertzano; Yujiro Higashi; Taku Ito; Yoshiyuki Kawashima; David J Eisenman; Oksana Gavrilova; Andrew J Griffith
A noncoding point mutation of Zeb1 causes multiple developmental malformations and obesity in Twirler mice.
PLoS genetics 2011;7(9):e1002307.
2009: Nele Hilgert; Kelly Monahan; Kiyoto Kurima; Cindy Li; Rick A Friedman; Andrew J Griffith; Guy Van Camp
Amino acid 572 in TMC1: hot spot or critical functional residue for dominant mutations causing hearing impairment.
Journal of human genetics 2009;54(3):188-90.
2006: Yoshihiro Noguchi; Kiyoto Kurima; Tomoko Makishima; Martin Hrabé De Angelis; Helmut Fuchs; Gregory I Frolenkov; Ken Kitamura; Andrew J Griffith
Multiple quantitative trait loci modify cochlear hair cell degeneration in the Beethoven (Tmc1Bth) mouse model of progressive hearing loss DFNA36.
Genetics 2006;173(4):2111-9.
2004: Tomoko Makishima; Kiyoto Kurima; Carmen C Brewer; Andrew J Griffith
Early onset and rapid progression of dominant nonsyndromic DFNA36 hearing loss.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2004;25(5):714-9.
2003: Kiyoto Kurima; Yandan Yang; Katherine Sorber; Andrew J Griffith
Characterization of the transmembrane channel-like (TMC) gene family: functional clues from hearing loss and epidermodysplasia verruciformis.
Genomics 2003;82(3):300-8.
2003: Yvonne M Szymko-Bennett; Kiyoto Kurima; Bjorn Olsen; Robert Seegmiller; Andrew J Griffith
Auditory function associated with Col11a1 haploinsufficiency in chondrodysplasia (cho) mice.
Hearing research 2003;175(1-2):178-82.
2002: Sarah Vreugde; Alexandra Erven; Corné J Kros; Walter Marcotti; Helmut Fuchs; Kiyoto Kurima; Edward R Wilcox; Thomas B Friedman; Andrew J Griffith; Rudi Balling; Martin Hrabé De Angelis; Karen B Avraham; Karen P Steel
Beethoven, a mouse model for dominant, progressive hearing loss DFNA36.
Nature genetics 2002;30(3):257-8.
2002: Kiyoto Kurima; Linda M Peters; Yandan Yang; Sheikh Amer Riazuddin; Zubair M Ahmed; Sadaf Naz; Deidre Arnaud; Stacy Drury; Jianhong Mo; Tomoko Makishima; Manju Ghosh; P S N Menon; Dilip Deshmukh; Carole Oddoux; Harry Ostrer; Shaheen Khan; Sheikh Riazuddin; Prescott L Deininger; Lori L Hampton; Susan L Sullivan; James F Battey; Bronya J B Keats; Edward R Wilcox; Thomas B Friedman; Andrew J Griffith
Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.
Nature genetics 2002;30(3):277-84.
2000: Andrew J Griffith; A A Chowdhry; Kiyoto Kurima; Linda J Hood; Bronya J B Keats; Charles I Berlin; Robert J Morell; Thomas B Friedman
Autosomal recessive nonsyndromic neurosensory deafness at DFNB1 not associated with the compound-heterozygous GJB2 (connexin 26) genotype M34T/167delT.
American journal of human genetics 2000;67(3):745-9.