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Yasuhiro Takeshima

Showing results (81-90 of 317) with videos related to

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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 mutationsMitsunori Ota, Yasuhiro Takeshima, Atsushi Nishida, 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.
British Journal of Neurosurgery|June 28, 2021
Embolic stroke induced by rotational persistent 1st intersegmental artery compressionYasuhiro Takeshima, Yasushi Motoyama, Ichiro Nakagawa, et al.
Journal of Psychiatric Research|June 11, 2021
Feelings about pregnancy and mother-infant bonding as predictors of persistent psychological distress in the perinatal period: The Japan Environment and Children's StudyNarumi Tokuda, Yoshiko Kobayashi, Hiroyuki Tanaka, 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.
Children (Basel, Switzerland)|May 27, 2023
A Pediatric Case of <i>COLQ</i>-Related Congenital Myasthenic Syndrome with Marked FatigueTakuya Horibe, Hideki Shimomura, Sachi Tokunaga, et al.
Brain & Development|November 17, 2021
Reply to letter to editor "Children with migraine and tension-type headache: Do they have behavioral and emotional issues?"Hideki Shimomura, Sachi Tokunaga, Naoko Taniguchi, et al.
Journal of Human Genetics|June 21, 2007
Identification of seven novel cryptic exons embedded in the dystrophin gene and characterization of 14 cryptic dystrophin exonsZhujun Zhang, Yasuaki Habara, Atsushi Nishiyama, et al.
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.
Pageof 32

Showing results (81-90 of 317) with videos related to

Sort By:
Pageof 32
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.
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.
British Journal of Neurosurgery|June 28, 2021
Embolic stroke induced by rotational persistent 1st intersegmental artery compressionYasuhiro Takeshima, Yasushi Motoyama, Ichiro Nakagawa, et al.
Journal of Psychiatric Research|June 11, 2021
Feelings about pregnancy and mother-infant bonding as predictors of persistent psychological distress in the perinatal period: The Japan Environment and Children's StudyNarumi Tokuda, Yoshiko Kobayashi, Hiroyuki Tanaka, 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.
Children (Basel, Switzerland)|May 27, 2023
A Pediatric Case of <i>COLQ</i>-Related Congenital Myasthenic Syndrome with Marked FatigueTakuya Horibe, Hideki Shimomura, Sachi Tokunaga, et al.
Brain & Development|November 17, 2021
Reply to letter to editor "Children with migraine and tension-type headache: Do they have behavioral and emotional issues?"Hideki Shimomura, Sachi Tokunaga, Naoko Taniguchi, et al.
Journal of Human Genetics|June 21, 2007
Identification of seven novel cryptic exons embedded in the dystrophin gene and characterization of 14 cryptic dystrophin exonsZhujun Zhang, Yasuaki Habara, Atsushi Nishiyama, et al.
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.
Pageof 32