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Matsunaga, Tatsuo
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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/..
 
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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/..
 
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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/..
 
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4

Generation of an induced pluripotent stem cell line (KEIUi0..:

Masano, Yusuke ; Saegusa, Chika ; Ishikawa, Mitsuru...
Stem Cell Research.  78 (2024)  - p. 103452 , 2024
Link: https://doi.org/10.1016/..
 
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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/..
 
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6

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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7

The pathogenic role of the BRCA2 c.7847C>T (p.Ser2616Phe) v..:

Yamazawa, Kazuki ; Sugano, Kokichi ; Tanakaya, Kohji...
Cancer Science.  114 (2023)  7 - p. 2993-3002 , 2023
Link: https://doi.org/10.1111/..
 
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8

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/..
 
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9

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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10

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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11

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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12

A Japanese boy with double diagnoses of 2p15p16.1 microdele..:

Yamazawa, Kazuki ; Shimizu, Kenji ; Ohashi, Hirofumi...
Human Genome Variation.  8 (2021)  1 - p. , 2021
Link: https://doi.org/10.1038/..
 
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13

Clinical genetics, practice, and research of deafblindness:..:

Matsunaga, Tatsuo
Auris Nasus Larynx.  48 (2021)  2 - p. 185-193 , 2021
Link: https://doi.org/10.1016/..
 
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14

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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15

A High Risk of Missing Congenital Cytomegalovirus-Associate..:

Minami, Shujiro Bando ; Yamanobe, Yoshiharu ; Nakano, Atsuko...
Journal of Clinical Medicine.  10 (2021)  21 - p. 5056 , 2021
Link: https://doi.org/10.3390/..
 
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