|
🦁
|
Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function
25 auth.
Kiyoto Kurima,
Linda M. Peters,
Yandan Yang,
S. Riazuddin,
Zubair M. Ahmed,
S. Naz,
D. Arnaud,
S. Drury,
J. Mo,
T. Makishima,
M. Ghosh,
P. Menon,
D. Deshmukh,
C. Oddoux,
H. Ostrer,
...
Shaheen N. Khan,
S. Riazuddin,
P. Deininger,
L. Hampton,
S. L. Sullivan,
J. Battey,
B. Keats,
E. Wilcox,
T. Friedman,
A. Griffith
|
8 |
2002 |
8
🦁
|
|
🐜
|
TMC1 and TMC2 Are Components of the Mechanotransduction Channel in Hair Cells of the Mammalian Inner Ear
9 auth.
B. Pan,
G. Géléoc,
Y. Asai,
Geoffrey C. Horwitz,
Kiyoto Kurima,
Kotaro Ishikawa,
...
Yoshiyuki Kawashima,
A. Griffith,
J. R. Holt
|
8 |
2013 |
8
🐜
|
|
🐜
|
Mechanotransduction in mouse inner ear hair cells requires transmembrane channel-like genes.
11 auth.
Yoshiyuki Kawashima,
G. Géléoc,
Kiyoto Kurima,
V. Labay,
A. Lelli,
Y. Asai,
...
T. Makishima,
Doris K. Wu,
C. D. Della Santina,
J. R. Holt,
A. Griffith
|
8 |
2011 |
8
🐜
|
|
🐜
|
TMC1 Forms the Pore of Mechanosensory Transduction Channels in Vertebrate Inner Ear Hair Cells
14 auth.
B. Pan,
Nurunisa Akyuz,
Xiao-ping Liu,
Y. Asai,
Carl Nist-Lund,
Kiyoto Kurima,
B. Derfler,
B. György,
W. Limapichat,
Sanket Walujkar,
...
Lahiru N. Wimalasena,
M. Sotomayor,
D. Corey,
J. R. Holt
|
8 |
2018 |
8
🐜
|
|
🐜
|
Beethoven, a mouse model for dominant, progressive hearing loss DFNA36
13 auth.
S. Vreugde,
A. Erven,
C. Kros,
W. Marcotti,
H. Fuchs,
Kiyoto Kurima,
E. Wilcox,
T. Friedman,
A. Griffith,
R. Balling,
...
M. H. Angelis,
K. Avraham,
K. Steel
|
8 |
2002 |
8
🐜
|
|
🦁
|
TMC1 and TMC2 Localize at the Site of Mechanotransduction in Mammalian Inner Ear Hair Cell Stereocilia.
15 auth.
Kiyoto Kurima,
Seham Ebrahim,
B. Pan,
M. Sedlacek,
P. Sengupta,
Bryan A. Millis,
Runjia Cui,
H. Nakanishi,
T. Fujikawa,
Yoshiyuki Kawashima,
...
B. Choi,
Kelly Monahan,
J. R. Holt,
A. Griffith,
B. Kachar
|
7 |
2015 |
7
🦁
|
|
🦁
|
Characterization of the transmembrane channel-like (TMC) gene family: functional clues from hearing loss and epidermodysplasia verruciformis.
Kiyoto Kurima,
Yandan Yang,
Katherine Sorber,
A. Griffith
|
7 |
2003 |
7
🦁
|
|
🐜
|
NLRP3 mutation and cochlear autoinflammation cause syndromic and nonsyndromic hearing loss DFNA34 responsive to anakinra therapy
22 auth.
H. Nakanishi,
Yoshiyuki Kawashima,
Kiyoto Kurima,
J. Chae,
Astin M. Ross,
G. Pinto-Patarroyo,
Seema K. Patel,
Julie A. Muskett,
Jessica S. Ratay,
Parna Chattaraj,
...
Yong Hwan Park,
S. Grevich,
Carmen C. Brewer,
M. Hoa,
H. J. Kim,
J. Butman,
L. Broderick,
H. Hoffman,
I. Aksentijevich,
Daniel L. Kastner,
R. Goldbach-Mansky,
Andrew J. Griffith
|
6 |
2017 |
6
🐜
|
|
🐜
|
Mouse model of enlarged vestibular aqueducts defines temporal requirement of Slc26a4 expression for hearing acquisition.
14 auth.
B. Choi,
Hyoung-Mi Kim,
Taku Ito,
K. Lee,
Xiangming Li,
Kelly Monahan,
Yaqing Wen,
Elizabeth Wilson,
Kiyoto Kurima,
T. Saunders,
...
R. Petralia,
P. Wangemann,
T. Friedman,
A. Griffith
|
6 |
2011 |
6
🐜
|
|
🐬
|
Transmembrane channel-like (TMC) genes are required for auditory and vestibular mechanosensation
Yoshiyuki Kawashima,
Kiyoto Kurima,
B. Pan,
A. Griffith,
J. R. Holt
|
6 |
2014 |
6
🐬
|
|
🐜
|
Cell Type–Specific Transcriptome Analysis Reveals a Major Role for Zeb1 and miR-200b in Mouse Inner Ear Morphogenesis
11 auth.
R. Hertzano,
Ran Elkon,
Kiyoto Kurima,
Annie Morrisson,
S. Chan,
Michelle A Sallin,
...
Andrew Biedlingmaier,
D. Darling,
A. Griffith,
D. Eisenman,
S. Strome
|
6 |
2011 |
6
🐜
|
