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Molecular Genetics and Metabolism|October 4, 2011
Newborn screening for Pompe disease in JapanEri Oda, Toju Tanaka, Ohsuke Migita, et al.
Molecular Genetics and Metabolism Reports|December 6, 2023
Enhanced osteoblastic differentiation of parietal bone in a novel murine model of mucopolysaccharidosis type IINarutoshi Yamazaki, Mari Ohira, Shuji Takada, et al.
Human Genome Variation|April 8, 2020
Novel HADHB mutations in a patient with mitochondrial trifunctional protein deficiencyMina Nakama, Hideo Sasai, Mitsuru Kubota, et al.
Human Genome Variation|September 26, 2025
Juvenile/adult-type galactosialidosis with a homozygous CTSA variant without consanguinityMachiko Toki, Kazushige Tsunoda, Tetsumin So, et al.
American Journal of Medical Genetics. Part A|July 17, 2008
The CASK gene harbored in a deletion detected by array-CGH as a potential candidate for a gene causative of X-linked dominant mental retardationShin Hayashi, Seiji Mizuno, Ohsuke Migita, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms|September 4, 2021
Production of therapeutic iduronate-2-sulfatase enzyme with a novel single-stranded RNA virus vectorMari Ohira, Emika Kikuchi, Shiori Mizuta, et al.
Liver Transplantation : Official Publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society|July 29, 2003
Prolonged survival of rat liver allograft with adenoviral gene transfection of human immunodeficiency virus type 1 nefMasayuki Fujino, Kensuke Adachi, Mikiko Kawasaki, et al.
American Journal of Medical Genetics. Part A|March 9, 2007
Clinical and molecular cytogenetic characterization of two patients with non-mutational aberrations of the FMR2 geneShozo Honda, Shin Hayashi, Mitsuhiro Kato, et al.
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