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

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/..
 
?
2

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/..
 
?
3

Novel OTOF pathogenic variant segregating with non-syndromi..:

Kuchay, Raja A.H. ; Mir, Yaser Rafiq ; Zeng, Xue...
International Journal of Pediatric Otorhinolaryngology.  130 (2020)  - p. 109831 , 2020
Link: https://doi.org/10.1016/..
 
?
4

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/..
 
?
5

Prevalence of TECTA mutation in patients with mid-frequency..:

Yamamoto, Nobuko ; Mutai, Hideki ; Namba, Kazunori...
Orphanet Journal of Rare Diseases.  12 (2017)  1 - p. , 2017
Link: https://doi.org/10.1186/..
 
?
6

Clinical characteristics of a Japanese family with hearing ..:

Minami, Shujiro B. ; Mutai, Hideki ; Namba, Kazunori..
Auris Nasus Larynx.  43 (2016)  6 - p. 609-613 , 2016
Link: https://doi.org/10.1016/..
 
?
7

Frequency and specific characteristics of the incomplete pa..:

Kanno, Ayako ; Mutai, Hideki ; Namba, Kazunori...
The Laryngoscope.  127 (2016)  7 - p. 1663-1669 , 2016
Link: https://doi.org/10.1002/..
 
?
8

High prevalence of CDH23 mutations in patients with congeni..:

Mizutari, Kunio ; Mutai, Hideki ; Namba, Kazunori...
Orphanet Journal of Rare Diseases.  10 (2015)  1 - p. , 2015
Link: https://doi.org/10.1186/..
 
?
9

Chronic constipation recognized as a sign of a SOX10 mutati..:

Arimoto, Yukiko ; Namba, Kazunori ; Nakano, Atsuko.
Gene.  540 (2014)  2 - p. 258-262 , 2014
Link: https://doi.org/10.1016/..
 
?
10

A mutation in the heparin-binding site of noggin as a novel..:

Masuda, Sawako ; Namba, Kazunori ; Mutai, Hideki...
Biochemical and Biophysical Research Communications.  447 (2014)  3 - p. 496-502 , 2014
Link: https://doi.org/10.1016/..
 
?
11

Moderate hearing loss associated with a novel KCNQ4 non-tru..:

Watabe, Takahisa ; Matsunaga, Tatsuo ; Namba, Kazunori...
Biochemical and Biophysical Research Communications.  432 (2013)  3 - p. 475-479 , 2013
Link: https://doi.org/10.1016/..
 
?
12

Diverse spectrum of rare deafness genes underlies early-chi..:

Mutai, Hideki ; Suzuki, Naohiro ; Shimizu, Atsushi...
Orphanet Journal of Rare Diseases.  8 (2013)  1 - p. , 2013
Link: https://doi.org/10.1186/..
 
?
13

In silico modeling of the pore region of a KCNQ4 missense m..:

Namba, Kazunori ; Mutai, Hideki ; Kaneko, Hiroki..
BMC Research Notes.  5 (2012)  1 - p. , 2012
Link: https://doi.org/10.1186/..
 
?
14

Epha4 controls the midline crossing and contralateral axona..:

Hashimoto, Mitsuhiro ; Ito, Rie ; Kitamura, Naohito..
Journal of Comparative Neurology.  520 (2012)  8 - p. 1702-1720 , 2012
Link: https://doi.org/10.1002/..
 
?
15

Close correlation between the birth date of purkinje cells ..:

Namba, Kazunori ; Sugihara, Izumi ; Hashimoto, Mitsuhiro
Journal of Comparative Neurology.  519 (2011)  13 - p. 2594-2614 , 2011
Link: https://doi.org/10.1002/..
 
1-15