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The Journal of Infectious Diseases|July 11, 2015
Multidrug-Resistance Transporter AbcA Secretes Staphylococcus aureus Cytolytic ToxinsHirono Yoshikai, Hayato Kizaki, Yuki Saito, et al.Scientific Reports|January 26, 2022
GWAS identifies candidate susceptibility loci and microRNA biomarkers for acute encephalopathy with biphasic seizures and late reduced diffusionMariko Kasai, Yosuke Omae, Yosuke Kawai, et al.Genes and Immunity|April 15, 2022
Protective association of HLA-DPB1*04:01:01 with acute encephalopathy with biphasic seizures and late reduced diffusion identified by HLA imputationMariko Kasai, Yosuke Omae, Seik-Soon Khor, et al.Human Genome Variation|August 29, 2024
Wilson disease (novel ATP7B variants) with concomitant FLNC-related cardiomyopathyTakeshi Imai, Satomi Mitsuhashi, Kenji Isahaya, et al.Plos One|December 17, 2008
A novel gene, fudoh, in the SCCmec region suppresses the colony spreading ability and virulence of Staphylococcus aureusChikara Kaito, Yosuke Omae, Yasuhiko Matsumoto, et al.Science Advances|January 24, 2024
Identification of region-specific gene isoforms in the human brain using long-read transcriptome sequencingMihoko Shimada, Yosuke Omae, Akiyoshi Kakita, et al.The Journal of Molecular Diagnostics : JMD|November 26, 2023
Cost-Effective Cas9-Mediated Targeted Sequencing of Spinocerebellar Ataxia Repeat ExpansionsKeiji Tachikawa, Takahiro Shimizu, Takeshi Imai, et al.Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|June 26, 2023
A case of hyperphosphatemic familial tumoral calcinosis due to maternal uniparental disomy of a <i>GALNT3</i> variantNaoko Nishimura-Kinoshita, Yasuhisa Ohata, Hiromi Sawai, et al.Journal of Human Genetics|July 17, 2024
Association study of GBA1 variants with MSA based on comprehensive sequence analysis -Pitfalls in short-read sequence analysis depending on the human reference genomeKenta Orimo, Jun Mitsui, Takashi Matsukawa, et al.BMC Neurology|April 11, 2024
A novel NODAL variant in a young embolic stroke patient with visceral heterotaxyKei Kaburagi, Yuta Hagiwara, Keiji Tachikawa, et al.Pageof 7