3,537 research outputs found
“CAN'T HELP MYSELF”: BODY, SOUL, MACHINE. The art by Sun Yuan and Peng Yu as a form of obsessive-compulsive disorder.
No full textreservedAnalisi dell'opera “Can't Help Myself”, realizzata nel 2016 dalla coppia di artisti cinesi Sun Yuan e Peng Yu. Partendo da una panoramica sulla carriera dei due artisti, con qualche riferimento allo sviluppo dell'arte contemporanea cinese, viene descritta la storia dietro la costruzione dell'opera insieme alle dichiarazioni della coppia. In seguito, un approfondimento sul contesto intorno all'opera vede un confronto tra le due mostre a cui è stata esposta (Tales Of Our Time a New York nel 2016 e la Biennale d'arte di Venezia del 2019). In conclusione, uno sguardo alla ricezione e alla critica, analizzando le molteplici interpretazioni sul significato, il fenomeno mediatico che ha fatto diventare quest'opera virale online e collegamenti con temi di attualità
Eupholides A H, abietane diterpenoids from the roots of Euphorbia fischeriana, and their bioactivities
No full textLi, Da-Wei, Deng, Xiao-Peng, He, Xin, Han, Xiu-Yan, Ma, Yu-Fang, Huang, Hui-Lian, Yu, Zhen-Long, Feng, Lei, Wang, Chao, Ma, Xiao-Chi (2021): Eupholides A H, abietane diterpenoids from the roots of Euphorbia fischeriana, and their bioactivities. Phytochemistry (112593) 183: 1-8, DOI: 10.1016/j.phytochem.2020.112593, URL: http://dx.doi.org/10.1016/j.phytochem.2020.11259
Fig. 1 in Eupholides A H, abietane diterpenoids from the roots of Euphorbia fischeriana, and their bioactivities
No full textFig. 1. Structure of compounds 1–15.Published as part of Li, Da-Wei, Deng, Xiao-Peng, He, Xin, Han, Xiu-Yan, Ma, Yu-Fang, Huang, Hui-Lian, Yu, Zhen-Long, Feng, Lei, Wang, Chao & Ma, Xiao-Chi, 2021, Eupholides A H, abietane diterpenoids from the roots of Euphorbia fischeriana, and their bioactivities, pp. 1-8 in Phytochemistry (112593) 183 on page 2, DOI: 10.1016/j.phytochem.2020.112593, http://zenodo.org/record/829195
Fig. 2 in Eupholides A H, abietane diterpenoids from the roots of Euphorbia fischeriana, and their bioactivities
No full textFig. 2. The key HMBC (a), 1H–1H COSY (a), and NOESY (b) correlations of compound 1.Published as part of Li, Da-Wei, Deng, Xiao-Peng, He, Xin, Han, Xiu-Yan, Ma, Yu-Fang, Huang, Hui-Lian, Yu, Zhen-Long, Feng, Lei, Wang, Chao & Ma, Xiao-Chi, 2021, Eupholides A H, abietane diterpenoids from the roots of Euphorbia fischeriana, and their bioactivities, pp. 1-8 in Phytochemistry (112593) 183 on page 3, DOI: 10.1016/j.phytochem.2020.112593, http://zenodo.org/record/829195
Tinodes falcata Peng & Ge & Sun & Wang 2022, n. sp.
No full textTinodes falcata Peng & Sun, n. sp. (Figs 1a–1c) Description: Length of each forewing 3.4–3.5 mm (n = 1). Specimen in alcohol with compound eyes black, legs and thorax brown, abdomen dark brown dorsally, pale yellow ventrally, wings light brown. Male genitalia: In lateral view, sternum IX fan-shaped (Fig. 1c). Tergum IX covered with tiny villi; nearly triangular in dorsal view (Fig. 1b), boomerang-shaped in lateral view (Fig. 1c). Segment X originating from anterior one-third of dorsal edges of sternum IX; membranous, anterior margins straight, narrowly stalked in lateral view (Fig. 1c). Superior appendages originating from bases of segment X; clubbed, each with distal half setose in dorsal and lateral views (Figs 1b, 1c). Phallic sheath process originating from phallus, consisting of paired lateral branches (lat. pha. she. pro) and unpaired inner branch (inn. pha. she. pro.); paired lateral ones slightly sigmoid in lateral view (Fig. 1c), each with seven spurs scattered in middle and subterminally; unpaired inner one strongly sclerotized, slightly shorter than paired branches, distal third curved posterodorsad, with sharp tip having small fork in lateral and dorsal views (Figs 1b, 1c). Phallus slightly longer than phallic sheath process, with distal half inflated about twice width of lateral paired branches of phallic sheath process in lateral view (Fig. 1c). In lateral view, phallic guide (pha. gui.) with subapex widened and then divided into two branches, dorsal branch slender, curved downwards distally; ventral branch of phallic guide short, with one long bristle (Fig. 1c). Coxopodites (cox.) each broadly rounded dorsally in lateral view, divided apically into large glabrous dorsal branch and short ventral one (Figs. 1a, 1c); harpagones situated mesally between coxopodite branches, each nearly as long as dorsal branch, with numerous setae mostly mesal (Figs 1a, 1c). Diagnosis: The species is unique in the genus Tinodes by its unpaired inner branch of the phallic sheath process (inn. pha. she. pro.). Holotype: Male, P. R. China, Zhe-jiang Province: An-ji city, Tian-huang-ping town, Da-xi village, Hengkeng-wu, 30.4706°N, 119.6619°E, alt. 290 m, 24 May 2017, light trap, leg. C. Sun & Y. Hu (NJAU). Distribution: China (Zhe-jiang). Etymology: The Latin adjective falcatus, -a, -um means “falcate, referring to the shape of the unpaired branch of the phallic sheath process in left lateral view.Published as part of Peng, Lang, Ge, Xin-Yu, Sun, Chang-Hai & Wang, Bei-Xin, 2022, Five new species of Tinodes (Trichoptera: Psychomyiidae) from China, pp. 280-290 in Zootaxa 5196 (2) on pages 281-283, DOI: 10.11646/zootaxa.5196.2.8, http://zenodo.org/record/722458
sj-docx-1-ini-10.1177_17534259221094559 - Supplemental material for Ursolic acid inhibits Th17 cell differentiation via STAT3/RORγt pathway and suppresses Schwann cell-mediated Th17 cell migration by reducing CXCL9/10 expression
No full textSupplemental material, sj-docx-1-ini-10.1177_17534259221094559 for Ursolic acid inhibits Th17 cell differentiation via STAT3/RORγt pathway and suppresses Schwann cell-mediated Th17 cell migration by reducing CXCL9/10 expression by Hua Xu, Ai-ling Yu, Da-peng Zhao, Guang-yuan Meng, Ling Wang, Min Shan, Nai-xia Hu and Yun-lin Liu in Innate Immunity</p
sj-xlsx-1-onc-10.1177_11795549221140781 – Supplemental material for TERT Mutations in Non–Small Cell Lung Cancer: Clinicopathologic Features and Prognostic Implications
No full textsj-xlsx-1-onc-10.1177_11795549221140781 for TERT Mutations in Non–Small Cell Lung Cancer: Clinicopathologic Features and Prognostic Implications by Liu Yang, Meng Wang, Na Li, Lu-Da Yan, Wen Zhou, Zhi-Qiong Yu, Xiao-Chun Peng, Jun Cai and Yong-Hua Yang in Clinical Medicine Insights: Oncology</p
Mycobacterium tuberculosis (Zopf, 1883) Lehmann & Neumann
No full text4.6. Inhibitory effects on Mycobacterium tuberculosis The inhibitory effects of isolated diterpenoids against M. tuberculosis were investigated using an Alamar blue cell viability assay (Thermo Fisher Scientific Inc.) in 96-well microplates. The test materials were dissolved in DMSO at an initial concentration of 50 mM. Ethambutol was used as the positive control antimicrobial agent. M. tuberculosis and the tested diterpenoids were coincubated in culture medium at 37 ◦ C. Then, the bacterial cells were determined by absorbance measurement at 595 nm. The detailed procedure about M. tuberculosis inhibitory assay was performed as previous work (Han et al., 2019).Published as part of Li, Da-Wei, Deng, Xiao-Peng, He, Xin, Han, Xiu-Yan, Ma, Yu-Fang, Huang, Hui-Lian, Yu, Zhen-Long, Feng, Lei, Wang, Chao & Ma, Xiao-Chi, 2021, Eupholides A H, abietane diterpenoids from the roots of Euphorbia fischeriana, and their bioactivities, pp. 1-8 in Phytochemistry (112593) (112593) 183 on page 7, DOI: 10.1016/j.phytochem.2020.112593, http://zenodo.org/record/829195
Mycobacterium tuberculosis (Zopf, 1883) Lehmann & Neumann
No full text2.2. Inhibitory effects of compounds 1–15 on Mycobacterium tuberculosis The inhibitory effect of isolated diterpenoids against M. tuberculosis H37Ra was evaluated using resazurin as the staining reagent. As a result, no M. tuberculosis bacterial cells were observed for co-incubation with compounds 6–8 at 50 μM, which indicated their MIC values. The other diterpenoids could not thoroughly inhibit the proliferation of M. tuberculosis at 100 μM.Published as part of Li, Da-Wei, Deng, Xiao-Peng, He, Xin, Han, Xiu-Yan, Ma, Yu-Fang, Huang, Hui-Lian, Yu, Zhen-Long, Feng, Lei, Wang, Chao & Ma, Xiao-Chi, 2021, Eupholides A H, abietane diterpenoids from the roots of Euphorbia fischeriana, and their bioactivities, pp. 1-8 in Phytochemistry (112593) (112593) 183 on page 5, DOI: 10.1016/j.phytochem.2020.112593, http://zenodo.org/record/829195
Supplemental material - The Association Between High-Sensitivity C-Reactive Protein/Albumin Ratio and Cardiovascular Prognosis in Patients Undergoing Percutaneous Coronary Intervention
No full textSupplementary material for The Association Between High-Sensitivity C-Reactive Protein/Albumin Ratio and Cardiovascular Prognosis in Patients Undergoing Percutaneous Coronary Intervention by Jie Yang, Chen Li, Yitian Zheng, Jun Gao, Yu Peng Liu, Jing jia Wang, Jing jing Song, Qing Zhou, Xiangbin Meng, Kuo Zhang, Wenyao Wang, Chunli Shao, and Yi-Da Tang in Angiology</p
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