Published December 31, 2014 | Version v1
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Fig. 10 in Abstrαct

  • 1. . Department of Neuropathology, Medical Research Institute and Center for Brain Integrative Research, Tokyo Medical and Dental University, Yushima, Bunkyo-ku, Tokyo, Japan,
  • 2. . Department of Biomolecular Science, Faculty of Science, Toho University, Miyama, Funabashi, Chiba, Japan

Description

Fig. 10. The effect of SP600125 on the viability of the HD and SCA1 models. The viability was calculated as described in the ''Materials and Methods'' section. The concentrations are presented on the X-axis, and the viability is presented on the Y-axis. Three HD models (A–C) and 3 SCA1 models (D–F) were employed. The genotypes are described within each graph. Each bar represents the mean ¡ SE. The number of vials tested is indicated on the shoulder of each bar. Single and double asterisks indicate significant differences (p,0.05 and 0.01, respectively). The results of the statistical analyses are listed in S6 Table. doi:10.1371/journal.pone.0116567.g010

Notes

Published as part of Shiraishi, Risa, Tamura, Takuya, Sone, Masaki & Okazawa, Hitoshi, 2014, Abstrαct, pp. 1-25 in PLoS ONE (e116567) 9 (12) on page 21, DOI: 10.1371/journal.pone.0116567, http://zenodo.org/record/12802403

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Journal article: 10.1371/journal.pone.0116567 (DOI)
Journal article: urn:lsid:plazi.org:pub:FFA3FFD0FFE09009FFFE7275FFD84C1B (LSID)
Journal article: https://zenodo.org/record/12802403 (URL)