E-LIB Suche - Ergebnisse für: Mutai, Hideki

1

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

Hashimoto, Kosuke ; Miwa, Toru ; Ono, Chie...
Cureus. , 2024

Link: https://doi.org/10.7759/..

2

Generation of four induced pluripotent stem cell lines (KEI..:

Saegusa, Chika ; Mutai, Hideki ; Saeki, Tsubasa...
Stem Cell Research. 79 (2024) - p. 103489 , 2024

Link: https://doi.org/10.1016/..

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

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/..

5

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/..

6

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/..

7

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/..

8

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/..

9

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/..

10

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/..

11

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/..

12

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/..

13

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/..

14

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/..

15

Publisher Correction: IMSindel: An accurate intermediate-si..:

Shigemizu, Daichi ; Miya, Fuyuki ; Akiyama, Shintaro...
Scientific Reports. 8 (2018) 1 - p. , 2018

Link: https://doi.org/10.1038/..