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Author/Creator Miyoshi, Takushi

2. Constitutive activation of DIA1 (DIAPH1) via C‐terminal truncation causes human sensorineural hearing loss. Issue 11 (5th October 2016)

Authors:
Ueyama, Takehiko; Ninoyu, Yuzuru; Nishio, Shin‐ya; Miyoshi, Takushi; Torii, Hiroko; Nishimura, Koji; Sugahara, Kazuma; Sakata, Hideaki; Thumkeo, Dean; Sakaguchi, Hirofumi; Watanabe, Naoki; Usami, Shin‐ichi; Saito, Naoaki; Kitajiri, Shin‐ichiro
Journal:
EMBO molecular medicine
Issue:
Volume 8:Issue 11(2016)
Page Start:
1310
Record Type:
Journal Article
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3. Differential disruption of autoinhibition and defect in assembly of cytoskeleton during cell division decide the fate of human DIAPH1-related cytoskeletopathy. Issue 12 (31st August 2019)

Authors:
Kim, Bong Jik; Ueyama, Takehiko; Miyoshi, Takushi; Lee, Seungmin; Han, Jin Hee; Park, Hye-Rim; Kim, Ah Reum; Oh, Jayoung; Kim, Min Young; Kang, Yong Seok; Oh, Doo Yi; Yun, Jiwon; Hwang, Sang Mee; Kim, Nayoung K D; Park, Woong-Yang; Kitajiri, Shin-ichiro; Choi, Byung Yoon
Journal:
Journal of medical genetics
Issue:
Volume 56:Issue 12(2019)
Page Start:
818
Record Type:
Journal Article
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5. The phenotypic landscape of a Tbc1d24 mutant mouse includes convulsive seizures resembling human early infantile epileptic encephalopathy. (2nd January 2019)

Authors:
Tona, Risa; Chen, Wenqian; Nakano, Yoko; Reyes, Laura D; Petralia, Ronald S; Wang, Ya-Xian; Starost, Matthew F; Wafa, Talah T; Morell, Robert J; Cravedi, Kevin D; du Hoffmann, Johann; Miyoshi, Takushi; Munasinghe, Jeeva P; Fitzgerald, Tracy S; Chudasama, Yogita; Omori, Koichi; Pierpaoli, Carlo; B...
Journal:
Human molecular genetics
Issue:
Volume 28:Number 9(2019)
Page Start:
1530
Record Type:
Journal Article
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