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Molecular Genetics and Metabolism|May 8, 2007
Arrhythmia induced by spatiotemporal overexpression of calreticulin in the heartKiyoko Hattori, Kimitoshi Nakamura, Yuichiro Hisatomi, et al.
Cloning and Stem Cells|June 21, 2007
Isolation of tissue progenitor cells from duct-ligated salivary glands of swineShirou Matsumoto, Kenji Okumura, Akira Ogata, et al.
Molecular Genetics and Metabolism Reports|January 21, 2020
Newborn screening for Fabry disease in the western region of JapanTakaaki Sawada, Jun Kido, Shinichiro Yoshida, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|February 12, 2016
Clinical and genetic features of lysinuric protein intolerance in JapanAtsuko Noguchi, Kimitoshi Nakamura, Kei Murayama, et al.
Journal of Inherited Metabolic Disease|December 15, 2011
Long-term outcome and intervention of urea cycle disorders in JapanJun Kido, Kimitoshi Nakamura, Hiroshi Mitsubuchi, et al.
Pediatric Transplantation|February 25, 2015
Living donor liver transplantation from a heterozygous parent for classical maple syrup urine diseaseMasashi Kadohisa, Shirou Matsumoto, Hirotake Sawada, et al.
Orphanet Journal of Rare Diseases|December 19, 2021
Current status of newborn screening for Pompe disease in JapanTakaaki Sawada, Jun Kido, Keishin Sugawara, et al.
Pediatric Transplantation|July 21, 2016
Antibody-mediated rejection after ABO-incompatible pediatric living donor liver transplantation for propionic acidemia: A case reportMasaki Honda, Seisuke Sakamoto, Rieko Sakamoto, et al.
Stem Cells (Dayton, Ohio)|December 19, 2014
HPGCD outperforms HPBCD as a potential treatment for Niemann-Pick disease type C during disease modeling with iPS cellsMinami Soga, Yoichi Ishitsuka, Makoto Hamasaki, et al.
Molecular Genetics and Metabolism|February 16, 2011
Improved assay for differential diagnosis between Pompe disease and acid α-glucosidase pseudodeficiency on dried blood spotsShohei Shigeto, Tatsuya Katafuchi, Yuya Okada, et al.
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