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Nara, Kiyomitsu
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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/..
 
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2

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/..
 
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3

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/..
 
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4

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/..
 
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5

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/..
 
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6

Investigation of the hearing levels of siblings affected by..:

Hosoya, Makoto ; Fujioka, Masato ; Nara, Kiyomitsu...
International Journal of Pediatric Otorhinolaryngology.  149 (2021)  - p. 110840 , 2021
Link: https://doi.org/10.1016/..
 
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7

Disease-specific ACMG/AMP guidelines improve sequence varia..:

Patel, Mayher J. ; DiStefano, Marina T. ; Oza, Andrea M....
Genetics in Medicine.  23 (2021)  11 - p. 2208-2212 , 2021
Link: https://doi.org/10.1038/..
 
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8

Differences in hearing levels between siblings with hearing..:

Fujioka, Masato ; Hosoya, Makoto ; Nara, Kiyomitsu...
Auris Nasus Larynx.  47 (2020)  6 - p. 938-942 , 2020
Link: https://doi.org/10.1016/..
 
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9

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/..
 
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10

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/..
 
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11

The first sporadic case of DFNA11 identified by next-genera..:

Kaneko, Yuka ; Nakano, Atsuko ; Arimoto, Yukiko...
International Journal of Pediatric Otorhinolaryngology.  100 (2017)  - p. 183-186 , 2017
Link: https://doi.org/10.1016/..
 
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12

A unique N-glycan on human transferrin in CSF: a possible b..:

Futakawa, Satoshi ; Nara, Kiyomitsu ; Miyajima, Masakazu...
Neurobiology of Aging.  33 (2012)  8 - p. 1807-1815 , 2012
Link: https://doi.org/10.1016/..
 
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13

High Throughput ELISAs to Measure a Unique Glycan on Transf..:

Shirotani, Keiro ; Futakawa, Satoshi ; Nara, Kiyomitsu...
International Journal of Alzheimer's Disease.  2011 (2011)  1 - p. , 2011
Link: https://doi.org/10.4061/..
 
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14

Inhibition of ganglioside synthesis reduces the neuronal su..:

Akasako, Yuko ; Nara, Kiyomitsu ; Nagai, Yoshitaka.
Neuroscience Letters.  488 (2011)  2 - p. 199-203 , 2011
Link: https://doi.org/10.1016/..
 
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15

Siglec-7 mediates nonapoptotic cell death independently of ..:

Mitsuki, Motoaki ; Nara, Kiyomitsu ; Yamaji, Toshiyuki...
Glycobiology.  20 (2009)  3 - p. 395-402 , 2009
Link: https://doi.org/10.1093/..
 
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