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Yasuhiro Takeshima

Showing results (141-150 of 317) with videos related to

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Human Mutation|November 19, 2011
Pathogenic orphan transduction created by a nonreference LINE-1 retrotransposonSzilvia Solyom, Adam D Ewing, Dustin C Hancks, et al.
Molecular Genetics and Metabolism|March 20, 2021
Analysis of daily energy, protein, fat, and carbohydrate intake in citrin-deficient patients: Towards prevention of adult-onset type II citrullinemiaYoshiyuki Okano, Miki Okamoto, Masahide Yazaki, et al.
Nucleic Acid Therapeutics|October 5, 2011
Antisense oligonucleotide induced dystrophin exon 45 skipping at a low half-maximal effective concentration in a cell-free splicing systemRusdy Ghazali Malueka, Mariko Yagi, Hiroyuki Awano, et al.
JIMD Reports|August 9, 2019
A Japanese case of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency who presented with severe metabolic acidosis and fatty liver without hypoglycemiaTomoko Lee, Yuichi Takami, Kenji Yamada, et al.
Brain & Development|March 20, 2018
Ambulatory capacity in Japanese patients with Duchenne muscular dystrophyHiroyuki Awano, Chieko Itoh, Yasuhiro Takeshima, et al.
Environmental Health and Preventive Medicine|September 28, 2022
Association of epidural analgesia during labor with neurodevelopment of children during the first three years: the Japan Environment and Children's StudyMasayuki Shima, Narumi Tokuda, Hideki Hasunuma, et al.
BMC Medical Genetics|March 31, 2010
Low incidence of limb-girdle muscular dystrophy type 2C revealed by a mutation study in Japanese patients clinically diagnosed with DMDYo Okizuka, Yasuhiro Takeshima, Kyoko Itoh, et al.
Journal of Human Genetics|October 12, 2002
Comparative study on deletions of the dystrophin gene in three Asian populationsPoh-San Lai, Yasuhiro Takeshima, Kayo Adachi, et al.
The Kobe Journal of Medical Sciences|March 26, 2002
Molecular genetics of spinal muscular atrophy: contribution of the NAIP gene to clinical severityTomoko Akutsu, Hisahide Nishio, Kimiaki Sumino, et al.
Brain Research|November 10, 2009
Enhanced cerebral ischemic lesions after two-vein occlusion in diabetic ratsDaisuke Wajima, Mitsutoshi Nakamura, Kaoru Horiuchi, et al.
Pageof 32

Showing results (141-150 of 317) with videos related to

Sort By:
Pageof 32
Human Mutation|November 19, 2011
Pathogenic orphan transduction created by a nonreference LINE-1 retrotransposonSzilvia Solyom, Adam D Ewing, Dustin C Hancks, et al.
Molecular Genetics and Metabolism|March 20, 2021
Analysis of daily energy, protein, fat, and carbohydrate intake in citrin-deficient patients: Towards prevention of adult-onset type II citrullinemiaYoshiyuki Okano, Miki Okamoto, Masahide Yazaki, et al.
Nucleic Acid Therapeutics|October 5, 2011
Antisense oligonucleotide induced dystrophin exon 45 skipping at a low half-maximal effective concentration in a cell-free splicing systemRusdy Ghazali Malueka, Mariko Yagi, Hiroyuki Awano, et al.
JIMD Reports|August 9, 2019
A Japanese case of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency who presented with severe metabolic acidosis and fatty liver without hypoglycemiaTomoko Lee, Yuichi Takami, Kenji Yamada, et al.
Brain & Development|March 20, 2018
Ambulatory capacity in Japanese patients with Duchenne muscular dystrophyHiroyuki Awano, Chieko Itoh, Yasuhiro Takeshima, et al.
Environmental Health and Preventive Medicine|September 28, 2022
Association of epidural analgesia during labor with neurodevelopment of children during the first three years: the Japan Environment and Children's StudyMasayuki Shima, Narumi Tokuda, Hideki Hasunuma, et al.
BMC Medical Genetics|March 31, 2010
Low incidence of limb-girdle muscular dystrophy type 2C revealed by a mutation study in Japanese patients clinically diagnosed with DMDYo Okizuka, Yasuhiro Takeshima, Kyoko Itoh, et al.
Journal of Human Genetics|October 12, 2002
Comparative study on deletions of the dystrophin gene in three Asian populationsPoh-San Lai, Yasuhiro Takeshima, Kayo Adachi, et al.
The Kobe Journal of Medical Sciences|March 26, 2002
Molecular genetics of spinal muscular atrophy: contribution of the NAIP gene to clinical severityTomoko Akutsu, Hisahide Nishio, Kimiaki Sumino, et al.
Brain Research|November 10, 2009
Enhanced cerebral ischemic lesions after two-vein occlusion in diabetic ratsDaisuke Wajima, Mitsutoshi Nakamura, Kaoru Horiuchi, et al.
Pageof 32