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Journal of Human Genetics
|
September 1, 2005
A novel cryptic exon identified in the 3' region of intron 2 of the human dystrophin gene
Van Khanh Tran, Zhujun Zhang, Mariko Yagi, et al.
Journal of Medical Genetics
|
June 2, 2006
Splicing analysis disclosed a determinant single nucleotide for exon skipping caused by a novel intraexonic four-nucleotide deletion in the dystrophin gene
Van Khanh Tran, Yasuhiro Takeshima, Zhujun Zhang, 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.
No to Hattatsu = Brain and Development
|
September 18, 2002
[Dystrophin gene analysis on 76 families with dystrophinopathy]
Kayo Adachi, Mariko Yagi, Toshiyuki Ito, 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.
Disability and Rehabilitation. Assistive Technology
|
February 8, 2019
Application of a wearable switch to perform a mouse left click for a child with mix type of cerebral palsy: a single case study
Akio Yamamoto, Kenji Kihara, Mariko Yagi, et al.
Human Gene Therapy
|
August 21, 2004
Chimeric RNA/ethylene-bridged nucleic acids promote dystrophin expression in myocytes of duchenne muscular dystrophy by inducing skipping of the nonsense mutation-encoding exon
Agus Surono, Tran Van Khanh, Yasuhiro Takeshima, et al.
Human Genetics
|
October 7, 2006
A nonsense mutation-created intraexonic splice site is active in the lymphocytes, but not in the skeletal muscle of a DMD patient
Van Khanh Tran, Yasuhiro Takeshima, Zhujun Zhang, et al.
Journal of Trace Elements in Medicine and Biology : Organ of the Society for Minerals and Trace Elements (GMS)
|
August 24, 2014
Changes in body weight and height in survivors of Menkes disease
Yan-Hong Gu, Hiroko Kodama, Eishin Ogawa, et al.
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of 8
Search research articles
Search
Showing results (31-40 of 76) with videos related to
Sort By:
Page
of 8
Journal of Human Genetics
|
September 1, 2005
A novel cryptic exon identified in the 3' region of intron 2 of the human dystrophin gene
Van Khanh Tran, Zhujun Zhang, Mariko Yagi, et al.
Journal of Medical Genetics
|
June 2, 2006
Splicing analysis disclosed a determinant single nucleotide for exon skipping caused by a novel intraexonic four-nucleotide deletion in the dystrophin gene
Van Khanh Tran, Yasuhiro Takeshima, Zhujun Zhang, 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.
No to Hattatsu = Brain and Development
|
September 18, 2002
[Dystrophin gene analysis on 76 families with dystrophinopathy]
Kayo Adachi, Mariko Yagi, Toshiyuki Ito, 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.
Disability and Rehabilitation. Assistive Technology
|
February 8, 2019
Application of a wearable switch to perform a mouse left click for a child with mix type of cerebral palsy: a single case study
Akio Yamamoto, Kenji Kihara, Mariko Yagi, et al.
Human Gene Therapy
|
August 21, 2004
Chimeric RNA/ethylene-bridged nucleic acids promote dystrophin expression in myocytes of duchenne muscular dystrophy by inducing skipping of the nonsense mutation-encoding exon
Agus Surono, Tran Van Khanh, Yasuhiro Takeshima, et al.
Human Genetics
|
October 7, 2006
A nonsense mutation-created intraexonic splice site is active in the lymphocytes, but not in the skeletal muscle of a DMD patient
Van Khanh Tran, Yasuhiro Takeshima, Zhujun Zhang, et al.
Journal of Trace Elements in Medicine and Biology : Organ of the Society for Minerals and Trace Elements (GMS)
|
August 24, 2014
Changes in body weight and height in survivors of Menkes disease
Yan-Hong Gu, Hiroko Kodama, Eishin Ogawa, et al.
Page
of 8