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Frontiers in Genetics|January 30, 2023
Gene therapy for lysosomal storage diseases: Current clinical trial prospectsJun Kido, Keishin Sugawara, Kimitoshi NakamuraDiagnostics (Basel, Switzerland)|October 23, 2021
High-Risk Screening for Fabry Disease: A Nationwide Study in Japan and Literature ReviewTakaaki Sawada, Jun Kido, Keishin Sugawara, et al.World Journal of Hepatology|August 8, 2019
Wilson disease developing osteoarthritic pain in severe acute liver failure: A case reportJun Kido, Shirou Matsumoto, Keishin Sugawara, et al.Frontiers in Genetics|October 28, 2022
Pathogenic variants of ornithine transcarbamylase deficiency: Nation-wide study in Japan and literature reviewJun Kido, Keishin Sugawara, Takaaki Sawada, et al.Human Genome Variation|July 21, 2021
Hyperprolinemia type I caused by homozygous p.T466M mutation in PRODHRina Hama, Jun Kido, Keishin Sugawara, et al.Journal of Structural Biology|March 4, 2008
Zernike phase contrast electron microscopy of ice-embedded influenza A virusMasashi Yamaguchi, Radostin Danev, Kiyoto Nishiyama, et al.American Journal of Medical Genetics. Part A|April 14, 2021
Variants associated with urea cycle disorders in Japanese patients: Nationwide study and literature reviewJun Kido, Shirou Matsumoto, Keishin Sugawara, et al.Molecular Genetics and Metabolism Reports|September 16, 2024
Rapid genotyping of inversion variants in Mucopolysaccharidosis type II using long-range PCR: A case reportYusuke Hattori, Jun Kido, Keishin Sugawara, et al.Molecular Genetics and Metabolism|May 18, 2026
Riboflavin-responsive hyperprolinemia type I with a PRODH p.Thr466Met variant: Clinical and fibroblast-based evidenceJun Kido, Keishin Sugawara, Ikuko Egashira, et al.Journal of Bioscience and Bioengineering|November 13, 2008
Large-scale production of major house dust mite allergen der f 2 mutant (C8/119S) in Escherichia coliSatoshi Koyanagi, Toshihiro Maeda, Toshio Murakami, et al.Pageof 5