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Mariko Yagi

Showing results (21-30 of 76) with videos related to

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No to Hattatsu = Brain and Development|June 7, 2014
[Clinical manifestations of Menkes disease vary according to patient's genotype and the initiation time of treatment with copper-histidine injections]Mariko Yagi, Noriko Kusunoki, Tomoko Lee, et al.
Journal of Biochemistry|November 28, 2007
A strong exonic splicing enhancer in dystrophin exon 19 achieve proper splicing without an upstream polypyrimidine tractYasuaki Habara, Mari Doshita, Sadako Hirozawa, et al.
Journal of Human Genetics|November 15, 2013
Differences in carrier frequency between mothers of Duchenne and Becker muscular dystrophy patientsTomoko Lee, Yasuhiro Takeshima, Noriko Kusunoki, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|October 19, 2013
Childhood-onset hereditary pancreatitis with mutations in the CT gene and SPINK1 geneHiroyuki Awano, Tomoko Lee, Mariko Yagi, et al.
Molecular Genetics and Metabolism|June 28, 2005
A G-to-A transition at the fifth position of intron-32 of the dystrophin gene inactivates a splice-donor site both in vivo and in vitroHoai Thu Thi Tran, Yasuhiro Takeshima, Agus Surono, et al.
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 mutationsMitsunori Ota, Yasuhiro Takeshima, Atsushi Nishida, et al.
Human Genetics|June 29, 2004
Novel double-deletion mutations of the OFD1 gene creating multiple novel transcriptsTakeshi Morisawa, Mariko Yagi, Agus Surono, 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 dystrophyZhujun Zhang, Yasuhiro Takeshima, Hiroyuki Awano, et al.
Nucleic Acids Symposium Series (2004)|December 8, 2006
Design of 2'-O-Me RNA/ENA chimera oligonucleotides to induce exon skipping in dystrophin pre-mRNAMiho Takagi, Mariko Yagi, Kazuto Ishibashi, et al.
BMC Medical Genetics|April 13, 2007
Two novel missense mutations in the myostatin gene identified in Japanese patients with Duchenne muscular dystrophyAtsushi Nishiyama, Yasuhiro Takeshima, Kayoko Saiki, et al.
Pageof 8

Showing results (21-30 of 76) with videos related to

Sort By:
Pageof 8
No to Hattatsu = Brain and Development|June 7, 2014
[Clinical manifestations of Menkes disease vary according to patient's genotype and the initiation time of treatment with copper-histidine injections]Mariko Yagi, Noriko Kusunoki, Tomoko Lee, et al.
Journal of Biochemistry|November 28, 2007
A strong exonic splicing enhancer in dystrophin exon 19 achieve proper splicing without an upstream polypyrimidine tractYasuaki Habara, Mari Doshita, Sadako Hirozawa, et al.
Journal of Human Genetics|November 15, 2013
Differences in carrier frequency between mothers of Duchenne and Becker muscular dystrophy patientsTomoko Lee, Yasuhiro Takeshima, Noriko Kusunoki, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|October 19, 2013
Childhood-onset hereditary pancreatitis with mutations in the CT gene and SPINK1 geneHiroyuki Awano, Tomoko Lee, Mariko Yagi, et al.
Molecular Genetics and Metabolism|June 28, 2005
A G-to-A transition at the fifth position of intron-32 of the dystrophin gene inactivates a splice-donor site both in vivo and in vitroHoai Thu Thi Tran, Yasuhiro Takeshima, Agus Surono, et al.
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 mutationsMitsunori Ota, Yasuhiro Takeshima, Atsushi Nishida, et al.
Human Genetics|June 29, 2004
Novel double-deletion mutations of the OFD1 gene creating multiple novel transcriptsTakeshi Morisawa, Mariko Yagi, Agus Surono, 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 dystrophyZhujun Zhang, Yasuhiro Takeshima, Hiroyuki Awano, et al.
Nucleic Acids Symposium Series (2004)|December 8, 2006
Design of 2'-O-Me RNA/ENA chimera oligonucleotides to induce exon skipping in dystrophin pre-mRNAMiho Takagi, Mariko Yagi, Kazuto Ishibashi, et al.
BMC Medical Genetics|April 13, 2007
Two novel missense mutations in the myostatin gene identified in Japanese patients with Duchenne muscular dystrophyAtsushi Nishiyama, Yasuhiro Takeshima, Kayoko Saiki, et al.
Pageof 8