| Literature DB >> 31588229 |
Xiaoxiao Liu1,2,3, Yanyan Li4, Xiaodong Sun1, Yagmur Muftuoglu5, Bilan Wang3, Ting Yu1, Yuzhu Hu1, Lu Ma1, Mingli Xiang1, Gang Guo1, Chao You1, Xiang Gao1, Yuquan Wei1.
Abstract
[This corrects the article DOI: 10.7150/thno.24157.]. © The author(s).Entities:
Year: 2019 PMID: 31588229 PMCID: PMC6771235 DOI: 10.7150/thno.39082
Source DB: PubMed Journal: Theranostics ISSN: 1838-7640 Impact factor: 11.556
Figure A1(Figure 10C). Detection of cell apoptosis. Cell apoptosis was assessed by counting the number of TUNEL-positive cells in the field, and a greater level of apoptosis was observed in the DMA/pIL15 group compared to the other groups (mean ± SEM; five high power fields per slide; *, p < 0.01 DMA/pIL15 versus GS, DMA, DMA/pc3.1).
Figure A2(Supplementary Figure 5). Toxicity assessment in vivo with pathological sections. Histological examinations of H&E-stained sections of vital organs from mice in the different treatment groups: (A) heart, (B) liver, (C) lung, (D) kidney, and (E) spleen. No significant pathological changes were detected.