35,213 research outputs found

    Timomenus dilatatus Zhang et al. 1999

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    Timomenus dilatatus Zhang et al., 1999 Timomenus dilatatus Zhang et al., 1999: 77 –78. Measurements. Total body: ♂ 13.0, ♀ 13.0‒14.0; forceps: ♂ 4.0, ♀ 4.0‒5.0. Material. 1 ♂, Dazhulan, Huangkeng, Jianyang, Fujian, China, 1957. VIII. 9, collected by Fan Zi-De; 4 ♀♀, Tongmu, Chong’an, Fujian, China, elev. 790‒1150m, 1960. VI. 15‒26, collected by Jin Gen-Tao & Lin Yang-Ming; 1 ♀, Baishanzu, Qingyuan, Zhejiang, China, elev. 1050m, 1963. IV. 23, collected by Jin Gen-Tao. Distribution. China (Fujian, Zhejiang).Published as part of Sun, Meiling, Li, Kai & Liu, Xianwei, 2016, Three new species of the subfamily Opisthocosmiinae from China (Dermaptera, Forficulidae), with new synonymies and combinations, pp. 359-371 in Zootaxa 4109 (3) on page 364, DOI: 10.11646/zootaxa.4109.3.6, http://zenodo.org/record/26607

    Isopropyl 3-(3, 4-dihydroxyphenyl)-2-hydroxypropanoate protects lipopolysaccharide-induced acute lung injury in mice by attenuating pyroptosis- Supplemental Material

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    This dataset is supplemented to the manuscript entitled 'Mei-Ling Zhang1, Meng Wang1, Jian Chen1, Yan-Jie Liu1, Ya-Jie Yu, Li-Min Liu, Xiao-Hui Zheng, Ying-Chou Xiao, Jun-Ming Zhang, Meng-Xue Zhu, Xian Yue, Ye Zhao*, Wen Niu* and Zhi-Chao Li*, Isopropyl 3-(3, 4-dihydroxyphenyl)-2-hydroxypropanoate protects lipopolysaccharide-induced acute lung injury in mice by attenuating pyroptosis'.Appendix 1. Immunofluorescence staining analysis of Gsdmd expression (red stain) and the LPS-stimulated macrophages marker CD68 (green stain). The nuclei (blue stain) were counter-stained using DAPI staining solution. Appendix 2. Assays for apoptosis of THP-1 macrophages. (a) Control and (b) 180 μg/ml of IDHP administration.Appendix 3. Cell viability was measured by CCK8 assay.Appendix 4. Flow cytometry analyzed ROS production in THP-1 macrophages stimulated by LPS with or without IDHP pretreatment: (a) Control, (b) IDHP (180 μg/ml), (c) LPS (1 μg/ml), (d) IDHP (180 μg/ml) + LPS (1 μg/ml)

    sj-tif-1-onc-10.1177_11795549221092218 – Supplemental material for The Establishment and Experimental Verification of an lncRNA-Derived CD8+ T Cell Infiltration ceRNA Network in Colorectal Cancer

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    Supplemental material, sj-tif-1-onc-10.1177_11795549221092218 for The Establishment and Experimental Verification of an lncRNA-Derived CD8+ T Cell Infiltration ceRNA Network in Colorectal Cancer by Qi Wu, Zhiyuan Zhang, Meiling Ji, Tao Yan, Yudong Jiang, Yijiao Chen, Jiang Chang, Jicheng Zhang, Dong Tang, Dexiang Zhu and Ye Wei in Clinical Medicine Insights: Oncology</p

    sj-jpg-2-onc-10.1177_11795549221092218 – Supplemental material for The Establishment and Experimental Verification of an lncRNA-Derived CD8+ T Cell Infiltration ceRNA Network in Colorectal Cancer

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    Supplemental material, sj-jpg-2-onc-10.1177_11795549221092218 for The Establishment and Experimental Verification of an lncRNA-Derived CD8+ T Cell Infiltration ceRNA Network in Colorectal Cancer by Qi Wu, Zhiyuan Zhang, Meiling Ji, Tao Yan, Yudong Jiang, Yijiao Chen, Jiang Chang, Jicheng Zhang, Dong Tang, Dexiang Zhu and Ye Wei in Clinical Medicine Insights: Oncology</p

    Fig. 7. A in MAPKK2/4/5/7-MAPK3-JAZs modulate phenolic acid biosynthesis in Salvia miltiorrhiza

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    Fig. 7. A proposed model for the roles of SmMAPK3 in S. miltiorrhiza phenolic acid biosynthesis. Model illustrating the roles of SmMAPK3 in S. miltiorrhiza phenolic acid biosynthesis.Published as part of Xie, Yongfeng, Ding, Meiling, Yin, Xuecui, Wang, Guanfeng, Zhang, Bin, Chen, Lingxiang, Ma, Pengda & Dong, Juane, 2022, MAPKK2/4/5/7-MAPK3-JAZs modulate phenolic acid biosynthesis in Salvia miltiorrhiza, pp. 1-10 in Phytochemistry (113177) 199 on page 6, DOI: 10.1016/j.phytochem.2022.113177, http://zenodo.org/record/823567

    Mesolabia Shiraki 1906

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    Key to species of genus Mesolabia Shiraki, 1906 1 Elytra as long as pronotum; wings completely absent.................................. M. niitakaensis Shiraki, 1906 - Elytra about twice as long as pronotum; wings completely developed............. M. ramosa (Zhang, Ma & Chen, 1992)Published as part of Sun, Meiling, Li, Kai & Liu, Xianwei, 2016, Three new species of the subfamily Opisthocosmiinae from China (Dermaptera, Forficulidae), with new synonymies and combinations, pp. 359-371 in Zootaxa 4109 (3) on page 368, DOI: 10.11646/zootaxa.4109.3.6, http://zenodo.org/record/26607

    Fig. 6 in MAPKK2/4/5/7-MAPK3-JAZs modulate phenolic acid biosynthesis in Salvia miltiorrhiza

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    Fig. 6. Protein–protein interaction of SmMAPK3 with JA signaling members. Y2H (A) and LCI (B–C) assays to detect the interactions of SmMAPK3 with JAZs.Published as part of Xie, Yongfeng, Ding, Meiling, Yin, Xuecui, Wang, Guanfeng, Zhang, Bin, Chen, Lingxiang, Ma, Pengda & Dong, Juane, 2022, MAPKK2/4/5/7-MAPK3-JAZs modulate phenolic acid biosynthesis in Salvia miltiorrhiza, pp. 1-10 in Phytochemistry (113177) 199 on page 5, DOI: 10.1016/j.phytochem.2022.113177, http://zenodo.org/record/823567

    Fig. 3 in MAPKK2/4/5/7-MAPK3-JAZs modulate phenolic acid biosynthesis in Salvia miltiorrhiza

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    Fig. 3. Tissue-specific expression analysis and elicitors-induced analysis of SmMAPK3 in S. miltiorrhiza. (A) Tissue-specific expression of SmMAPK3; the expression levels were normalized to values from roots. (B) SA-induced analysis of SmMAPK3. (C) MeJA-induced analysis of SmMAPK3.Published as part of Xie, Yongfeng, Ding, Meiling, Yin, Xuecui, Wang, Guanfeng, Zhang, Bin, Chen, Lingxiang, Ma, Pengda & Dong, Juane, 2022, MAPKK2/4/5/7-MAPK3-JAZs modulate phenolic acid biosynthesis in Salvia miltiorrhiza, pp. 1-10 in Phytochemistry (113177) 199 on page 4, DOI: 10.1016/j.phytochem.2022.113177, http://zenodo.org/record/823567

    Adenine DNA methylation is involved in regulating ethanol and osmotic stress responses in Lacticaseibacillus paracasei Zhang

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    Abstract As an important feature of epigenetics, DNA methylation is a critical way to regulate gene expression and thus bacterial growth and metabolism. Lacticaseibacillus paracasei Zhang is a probiotic strain originated from koumiss. This study hypothesized that adenine methylation was involved in bacterial regulation of physiological adaptations when grown under environmental stress. Thus, this study compared the growth of an adenine methyltransferase‐inactivated mutant (ΔpglX) and the wild‐type L. paracasei Zhang when cultured under ethanol and osmotic stress. Transcriptomic and proteomic analyses were implemented to identify their differentially expressed genes/proteins (DEGs/DEPs) when grown under the stressed environments. The membrane fatty acid composition was also determined. Comparing with the wild‐type, the viable counts of the mutant under ethanol and osmotic stress increased by 2.6 times and decreased by half, respectively (ethanol stress: mutant, 4.30 ± 0.0038 × 108 CFU/mL; wild‐type, 1.64 ± 0.010 × 108 CFU/mL; osmotic stress: mutant, 2.21 ± 0.029 × 108 CFU/mL; wild‐type, 4.30 ± 0.13 × 108 CFU/mL). Common to both conditions, many identified DEGs and DEPs were involved in carbohydrate metabolism and fatty acid biosynthesis, generally, with more carbohydrate metabolism pathways but fewer fatty acid biosynthesis pathways, accompanied by increases in the membrane fatty acids. Our observations suggested that L. paracasei Zhang maximizes its energy metabolism by enhancing carbohydrate metabolism and improves its membrane strength via increasing the fatty acid content under environmental stress. This is the first report analyzing the epigenetic‐level stress responsive mechanism of L. paracasei Zhang, providing insights into methylation‐based regulation of bacterial adaptive responses

    †Chuchinolepididae Zhang 1978

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    Family †Chuchinolepididae Zhang 1978, spelling in prevailing recent practice †Chuchinolepidae Zhang 1978a: 296 (family) † Chuchinolepis Zhang 1978 [family name also seen as †Chuchinolepididae; author also seen as Chang] †Qujinolepidae Zhang 1978b: 173 (family) † Qujinolepis Zhang 1978 [family name sometimes seen as † Qujinolepididae] †Procondylolepidae Zhang 1984: 82 (family) † Procondylolepis Zhang 1984Published as part of Laan, Richard Van Der, 2018, Family-group names of fossil fishes, pp. 1-167 in European Journal of Taxonomy 466 on page 27, DOI: 10.5852/ejt.2018.466, http://zenodo.org/record/555755
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