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Molecular Therapy : the Journal of the American Society of Gene Therapy|November 6, 2003
Improvement of skeletal lesions in mice with mucopolysaccharidosis type VII by neonatal adenoviral gene transferArihiko Kanaji, Motomichi Kosuga, Xiao Kang Li, et al.Molecular Genetics and Metabolism|June 2, 2016
Molecular diagnosis of 65 families with mucopolysaccharidosis type II (Hunter syndrome) characterized by 16 novel mutations in the IDS gene: Genetic, pathological, and structural studies on iduronate-2-sulfataseMotomichi Kosuga, Ryuichi Mashima, Asami Hirakiyama, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|February 28, 2002
Prolongation of transgene expression by coexpression of cytokine response modifier a in rodent liver after adenoviral gene transferXiao-Kang Li, Motomichi Kosuga, Keisuke Tokieda, et al.Journal of Gastroenterology and Hepatology|October 5, 2017
Fas-mediated apoptosis is involved in the elimination of gene-transduced hepatocytes with E1/E3-deleted adenoviral vectorsTorayuki Okuyama, Xiao-Kang Li, Naoko Funeshima, et al.Brain & Development|February 14, 2019
Early enzyme replacement therapy enables a successful hematopoietic stem cell transplantation in mucopolysaccharidosis type IH: Divergent clinical outcomes in two Japanese siblingsNarutoshi Yamazaki, Motomichi Kosuga, Kazuhiro Kida, et al.JIMD Reports|April 30, 2018
P-Tau and Subunit c Mitochondrial ATP Synthase Accumulation in the Central Nervous System of a Woman with Hurler-Scheie Syndrome Treated with Enzyme Replacement Therapy for 12 YearsHiroshi Kobayashi, Masamichi Ariga, Yohei Sato, et al.Journal of the Neurological Sciences|December 24, 2010
Cervical pachymeningeal hypertrophy as the initial and cardinal manifestation of mucopolysaccharidosis type I in monozygotic twins with a novel mutation in the alpha-L-iduronidase geneYutaka Furukawa, Ayumi Hamaguchi, Ichiro Nozaki, 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.Biological & Pharmaceutical Bulletin|September 1, 2022
Development of a Highly Sensitive and Rapid Liquid Chromatography-Tandem Mass Spectrometric Method Using a Basic Mobile Phase Additive to Determine the Characteristics of the Urinary Metabolites for Niemann-Pick Disease Type CMasamitsu Maekawa, Keitaro Miyoshi, Aya Narita, et al.International Journal of Neonatal Screening|July 24, 2026
Combined Intracerebroventricular Enzyme Replacement and Cord Blood Transplantation in Patients with Mucopolysaccharidosis Type II Diagnosed Through Newborn ScreeningYuki Ueda, Shinsuke Hirabayashi, Masayuki Miura, et al.Pageof 12