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Genetic Testing and Molecular Biomarkers
|
August 23, 2011
A G-to-T transversion at the splice acceptor site of dystrophin exon 14 shows multiple splicing outcomes that are not exemplified by transition mutations
Mitsunori Ota, Yasuhiro Takeshima, Atsushi Nishida, et al.
Scientific Reports
|
September 15, 2019
Strain-induced switching of heat current direction generated by magneto-thermoelectric effects
Shinya Ota, Ken-Ichi Uchida, Ryo Iguchi, et al.
Journal of Human Genetics
|
December 28, 2007
Tandem duplications of two separate fragments of the dystrophin gene in a patient with Duchenne muscular dystrophy
Zhujun Zhang, Yasuhiro Takeshima, Hiroyuki Awano, et al.
Journal of Cardiology
|
July 22, 2023
Electrocardiographic R wave amplitude in V6 lead as a predictive marker of cardiac dysfunction in Duchenne muscular dystrophy
Tetsushi Yamamoto, Yoshinori Nambu, Ryosuke Bo, et al.
Scientific Reports
|
March 4, 2026
Reconfigurable magneto-optical diffractive neural network with enhanced optical phase modulation
Hotaka Sakaguchi, Kanata Watanabe, Juri Ikeda, et al.
Journal of Human Genetics
|
May 21, 2010
Mutation spectrum of the dystrophin gene in 442 Duchenne/Becker muscular dystrophy cases from one Japanese referral center
Yasuhiro Takeshima, Mariko Yagi, Yo Okizuka, et al.
Biochemistry and Biophysics Reports
|
November 19, 2019
Schwann cell-specific Dp116 is expressed in glioblastoma cells, revealing two novel <i>DMD</i> gene splicing patterns
Abdul Qawee Mahyoob Rani, Kazuhiro Maeta, Tatsuya Kawaguchi, et al.
Life (Basel, Switzerland)
|
September 28, 2021
Dystrophin Dp71 Subisoforms Localize to the Mitochondria of Human Cells
Emma Tabe Eko Niba, Hiroyuki Awano, Tomoko Lee, et al.
No to Hattatsu = Brain and Development
|
March 14, 2014
[Clinical manifestations of three neonates with family histories of Menkes disease]
Mariko Yagi, Noriko Kusunoki, Tomoko Lee, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society
|
May 15, 2009
Two Japanese infants with congenital generalized lipodystrophy due to BSCL2 mutations
Atsushi Nishiyama, Mariko Yagi, Hiroyuki Awano, et al.
Page
of 16
Search research articles
Search
Showing results (41-50 of 152) with videos related to
Sort By:
Page
of 16
Genetic Testing and Molecular Biomarkers
|
August 23, 2011
A G-to-T transversion at the splice acceptor site of dystrophin exon 14 shows multiple splicing outcomes that are not exemplified by transition mutations
Mitsunori Ota, Yasuhiro Takeshima, Atsushi Nishida, et al.
Scientific Reports
|
September 15, 2019
Strain-induced switching of heat current direction generated by magneto-thermoelectric effects
Shinya Ota, Ken-Ichi Uchida, Ryo Iguchi, et al.
Journal of Human Genetics
|
December 28, 2007
Tandem duplications of two separate fragments of the dystrophin gene in a patient with Duchenne muscular dystrophy
Zhujun Zhang, Yasuhiro Takeshima, Hiroyuki Awano, et al.
Journal of Cardiology
|
July 22, 2023
Electrocardiographic R wave amplitude in V6 lead as a predictive marker of cardiac dysfunction in Duchenne muscular dystrophy
Tetsushi Yamamoto, Yoshinori Nambu, Ryosuke Bo, et al.
Scientific Reports
|
March 4, 2026
Reconfigurable magneto-optical diffractive neural network with enhanced optical phase modulation
Hotaka Sakaguchi, Kanata Watanabe, Juri Ikeda, et al.
Journal of Human Genetics
|
May 21, 2010
Mutation spectrum of the dystrophin gene in 442 Duchenne/Becker muscular dystrophy cases from one Japanese referral center
Yasuhiro Takeshima, Mariko Yagi, Yo Okizuka, et al.
Biochemistry and Biophysics Reports
|
November 19, 2019
Schwann cell-specific Dp116 is expressed in glioblastoma cells, revealing two novel <i>DMD</i> gene splicing patterns
Abdul Qawee Mahyoob Rani, Kazuhiro Maeta, Tatsuya Kawaguchi, et al.
Life (Basel, Switzerland)
|
September 28, 2021
Dystrophin Dp71 Subisoforms Localize to the Mitochondria of Human Cells
Emma Tabe Eko Niba, Hiroyuki Awano, Tomoko Lee, et al.
No to Hattatsu = Brain and Development
|
March 14, 2014
[Clinical manifestations of three neonates with family histories of Menkes disease]
Mariko Yagi, Noriko Kusunoki, Tomoko Lee, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society
|
May 15, 2009
Two Japanese infants with congenital generalized lipodystrophy due to BSCL2 mutations
Atsushi Nishiyama, Mariko Yagi, Hiroyuki Awano, et al.
Page
of 16