I agree that this site is using cookies. You can find further informations here.
X
Mutai, Hideki
88  results:
Search for persons X
?
1

Loss of Pax3 causes reduction of melanocytes in the develop..:

Udagawa, Tomokatsu ; Takahashi, Erisa ; Tatsumi, Norifumi...
Scientific Reports.  14 (2024)  1 - p. , 2024
Link: https://doi.org/10.1038/..
 
?
2

Gap Junction Beta-2 p.Val84Met Can Cause Autosomal Dominant..:

Hashimoto, Kosuke ; Miwa, Toru ; Ono, Chie...
Cureus.  , 2024
Link: https://doi.org/10.7759/..
 
?
3

Structural basis for pathogenic variants of GJB2 and hearin..:

Namba, Kazunori ; Mutai, Hideki ; Matsunaga, Tatsuo.
BMC Research Notes.  17 (2024)  1 - p. , 2024
Link: https://doi.org/10.1186/..
 
?
4

Correlation between genotype and phenotype with special att..:

Oishi, Naoki ; Noguchi, Masaru ; Fujioka, Masato...
Scientific Reports.  13 (2023)  1 - p. , 2023
Link: https://doi.org/10.1038/..
 
?
5

Molecular basis of carotid body tumor and associated clinic..:

Yoshihama, Keisuke ; Mutai, Hideki ; Sekimizu, Mariko...
Clinical Genetics.  103 (2023)  4 - p. 466-471 , 2023
Link: https://doi.org/10.1111/..
 
?
6

Apoptosis of type I spiral ganglion neuron cells in Otof-mu..:

Tsuzuki, Nobuyoshi ; Namba, Kazunori ; Saegusa, Chika...
Neuroscience Letters.  803 (2023)  - p. 137178 , 2023
Link: https://doi.org/10.1016/..
 
?
7

Phenotype–genotype correlation in patients with typical and..:

Masuda, Masatsugu ; Kanno, Ayako ; Nara, Kiyomitsu...
Scientific Reports.  12 (2022)  1 - p. , 2022
Link: https://doi.org/10.1038/..
 
?
8

Whole exome analysis of patients in Japan with hearing loss..:

Mutai, Hideki ; Momozawa, Yukihide ; Kamatani, Yoichiro...
Orphanet Journal of Rare Diseases.  17 (2022)  1 - p. , 2022
Link: https://doi.org/10.1186/..
 
?
9

Clinical and genetic analysis of children with hearing loss..:

Nakano, Atsuko ; Arimoto, Yukiko ; Mutai, Hideki...
International Journal of Pediatric Otorhinolaryngology.  152 (2022)  - p. 110975 , 2022
Link: https://doi.org/10.1016/..
 
?
10

Variants encoding a restricted carboxy-terminal domain of S..:

Mutai, Hideki ; Wasano, Koichiro ; Momozawa, Yukihide...
PLOS Genetics.  16 (2020)  4 - p. e1008643 , 2020
Link: https://doi.org/10.1371/..
 
?
11

Systematic quantification of the anion transport function o..:

Wasano, Koichiro ; Takahashi, Satoe ; Rosenberg, Samuel K....
Human Mutation.  41 (2019)  1 - p. 316-331 , 2019
Link: https://doi.org/10.1002/..
 
?
12

A clinical and genetic study of 16 Japanese families with W..:

Minami, Shujiro B. ; Nara, Kiyomitsu ; Mutai, Hideki...
Gene.  704 (2019)  - p. 86-90 , 2019
Link: https://doi.org/10.1016/..
 
?
13

Homozygous EDNRB mutation in a patient with Waardenburg syn..:

Morimoto, Noriko ; Mutai, Hideki ; Namba, Kazunori...
Auris Nasus Larynx.  45 (2018)  2 - p. 222-226 , 2018
Link: https://doi.org/10.1016/..
 
?
14

High-level heteroplasmy for the m.7445A>G mitochondrial DNA..:

Matsushima, Kana ; Nakano, Atsuko ; Arimoto, Yukiko...
International Journal of Pediatric Otorhinolaryngology.  108 (2018)  - p. 125-131 , 2018
Link: https://doi.org/10.1016/..
 
?
15

A case report of reversible generalized seizures in a patie..:

Suzuki, Noriomi ; Mutai, Hideki ; Miya, Fuyuki...
BMC Pediatrics.  18 (2018)  1 - p. , 2018
Link: https://doi.org/10.1186/..
 
1-15