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Plant & Cell Physiology|May 22, 2012
Loss of XRN4 function can trigger cosuppression in a sequence-dependent mannerMakoto Hayashi, Chieko Nanba, Miyuki Saito, et al.Immunomethods|February 1, 1994
Soluble Fc epsilon RII/CD23 in patients with autoimmune diseases and Epstein-Barr virus-related disorders: analysis by ELISA for soluble Fc epsilon RII/CD23T Yoshikawa, T Nanba, H Kato, et al.Journal of Human Genetics|October 3, 2022
Challenges of secondary finding disclosure in genomic medicine in rare diseases: A nation-wide survey of Japanese facilities outsourcing comprehensive genetic testingKana Hiromoto, Takahiro Yamada, Mio Tsuchiya, et al.Annals of Surgical Oncology|May 20, 2024
Liver Resection Under Total Hepatic Vascular Exclusion with In Situ Hypothermic Isolated Hepatic Perfusion for Advanced Liver TumorsHiroshi Sadamori, Kazuteru Monden, Masayoshi Hioki, et al.Experimental Dermatology|September 20, 2023
Single-cell analysis of human dermal fibroblasts isolated from a single male donor over 35 yearsEriko Itai, Toru Atsugi, Ken Inomata, et al.Journal of Environmental Radioactivity|September 17, 2016
Morphological abnormalities in Japanese red pine (Pinus densiflora) at the territories contaminated as a result of the accident at Fukushima Dai-Ichi Nuclear Power PlantVasyl Yoschenko, Kenji Nanba, Satoshi Yoshida, et al.Bioscience, Biotechnology, and Biochemistry|February 4, 2015
Production of CoQ10 in fission yeast by expression of genes responsible for CoQ10 biosynthesisDaisuke Moriyama, Kouji Hosono, Makoto Fujii, et al.Journal of Pharmaceutical Sciences|April 1, 1986
Enhancement of bioavailability of cinnarizine from its beta-cyclodextrin complex on oral administration with DL-phenylalanine as a competing agentT Tokumura, M Nanba, Y Tsushima, et al.Brain, Behavior, and Immunity|January 7, 1998
Abnormal expansion of peripheral gamma delta T cells in patients with neurologic disordersT Yamamoto, T Hara, E Nanba, et al.Congenital Anomalies|March 26, 2024
Difficulties in disclosing secondary findings by facilities performing comprehensive germline genetic testing for rare diseases in JapanKana Hiromoto, Takahiro Yamada, Mio Tsuchiya, et al.Pageof 91