84,849 research outputs found
Huangdi nei jing su wen yi bian
No full textV.1-6. 重廣補註黃帝内經素問 -- v.7-10. 黃帝内經靈樞 -- v.10. 黃帝内經素問遺編.V.1-6. Chong guang bu zhu Huangdi nei jing Su wen -- v.7-10. Huangdi nei jing Ling shu -- v.10. Huangdi nei jing Su wen yi bian.啟玄子次註 ; 林億...[et al.]校正 ; 孫兆改誤. 黃帝内經靈樞 : 十二卷. 黃帝内經素問遺編 / 劉温舒原本.綫裝 .框21.1x15.7公分, 10行20字, 小字雙行同. 白口, 左右雙邊, 單黑魚尾. 版心中鐫"内經"及卷次, 下鐫葉次.書名頁刻"内經, 校對無訛, 京口文成堂摹刻宋本". 書名背頁牌記刻"光緖甲申年[1884]孟秋開雕, 文成".《中國中醫古籍總目》(00006)著錄.鈐"長沙李氏夢瑩藏本", "莊兆祥印", "莊兆祥".Xian zhuang .Kuang 21.1 x 15.7 gong fen, 10 hang 20 zi, xiao zi shuang hang tong. Bai kou, zuo you shuang bian, dan hei yu wei. Ban xin zhong juan "Nei jing" ji juan ci, xia juan ye ci.Detailed notes in vernacular field only.Detailed notes in vernacular field only.Qixuanzi ci zhu ; Lin Yi ...[et al.] jiao zheng ; Sun Zhao gai wu. Huangdi nei jing Ling shu : shi er juan. Huangdi nei jing Su wen yi bian / Liu Wenshu yuan ben.Qian "Changsha Li shi Mengying cang ben", "Zhuang Zhaoxiang yin", "zhuang zhao xiang"
A Study of the Old Men in Ching-Wen Cheng\ue2s Short Stories
No full textChing-Wen Cheng has been writing for more than 50 years. He uses easy Chinese and describes the deep side of human beings. He cares about the normal people in Taiwanese society. In this thesis, the author emphasizes on the old men, which few researchers notice. The first chapter is about the motivation of this research and the issues discussed in this study. The second chapter is about Ching-Wen Cheng\ue2s growing background,the history of his life, his litrature creating process and how these elements make him special.The third chapter is about the physical and psychological aging process of old men and how Ching-Wen Cheng depicts it in a sociological way. The fourth chapter analyzes old men in several ways. The author writes about controversial topics in traditional and modern societies and explores the meanings of life with past memories. The fifth chapter is the conclusion
Sun Protection Factor Analysis of Sunscreens Containing Titanium Dioxide Nanoparticles
No full textThe effect of micronization on sun protection factor SPF were tested on two types of titanium dioxide TiO2 with primary particle sizes of 20 nm and 170 nm. Oil/water creams with 5%, 10%, and 20% concentrations of each type of TiO2 were prepared, and SPF was measured using both in vitro and in vivo methods. In vitro analysis demonstrated that submicron-sized TiO2 cream had a lower SPF value than nanosized TiO2 formulations of the same concentration. In vivo experiments confirmed this result, and a strong correlation between in vitro and in vivo measurements was observed. Furthermore, the SPF values of nanosized TiO2 sunscreen were concentration -dependent in the range of 5% to 20%. Scanning electron microscopy results indicate that the higher SPF of nanosized TiO2 formulations may be due to the formation of multilayer agglomerates by small particles at nano- scales, leading to a reduced void space between particles and a more efficient barrier to protect skin from sunlight
An Interview with an Author and Editor: The View from Taiwan
No full textORCID Engagement Manager Asia-Pacific, Estelle Cheng, recently spoke with Wen-Yau Cathy Lin, an academic, author and scholarly journal editor about ORCID and its use in Taiwan
Fig. 19 in Recent studies on terpenoids in Aspergillus fungi: Chemical diversity, biosynthesis, and bioactivity
No full textFig. 19. Structures of meroterpenoids 223–243.Published as part of Zhao, Wen-Yu, Yi, Jing, Chang, Yi-Bo, Sun, Cheng-Peng & Ma, Xiao-Chi, 2022, Recent studies on terpenoids in Aspergillus fungi: Chemical diversity, biosynthesis, and bioactivity, pp. 1-25 in Phytochemistry (113011) 193 on page 13, DOI: 10.1016/j.phytochem.2021.113011, http://zenodo.org/record/823487
Fig. 23 in Recent studies on terpenoids in Aspergillus fungi: Chemical diversity, biosynthesis, and bioactivity
No full textFig. 23. Structures of meroterpenoids 244–268.Published as part of Zhao, Wen-Yu, Yi, Jing, Chang, Yi-Bo, Sun, Cheng-Peng & Ma, Xiao-Chi, 2022, Recent studies on terpenoids in Aspergillus fungi: Chemical diversity, biosynthesis, and bioactivity, pp. 1-25 in Phytochemistry (113011) 193 on page 16, DOI: 10.1016/j.phytochem.2021.113011, http://zenodo.org/record/823487
Fig. 6 in Recent studies on terpenoids in Aspergillus fungi: Chemical diversity, biosynthesis, and bioactivity
No full textFig. 6. Structures of protoilludane-type sesquiterpenoids 101–103.Published as part of Zhao, Wen-Yu, Yi, Jing, Chang, Yi-Bo, Sun, Cheng-Peng & Ma, Xiao-Chi, 2022, Recent studies on terpenoids in Aspergillus fungi: Chemical diversity, biosynthesis, and bioactivity, pp. 1-25 in Phytochemistry (113011) 193 on page 6, DOI: 10.1016/j.phytochem.2021.113011, http://zenodo.org/record/823487
sj-docx-1-evb-10.1177_11769343221134400 – Supplemental material for Distribution, Phylogeny and Evolution of Clinical and Environmental Vibrio vulnificus Antibiotic-Resistant Genes
No full textSupplemental material, sj-docx-1-evb-10.1177_11769343221134400 for Distribution, Phylogeny and Evolution of Clinical and Environmental Vibrio vulnificus Antibiotic-Resistant Genes by Nan Geng, Guojin Sun, Wen-Jia Liu, Bin-Cheng Gao, Cong Sun, Cundong Xu, Ertian Hua and Lin Xu in Evolutionary Bioinformatics</p
Fig. 30 in Recent studies on terpenoids in Aspergillus fungi: Chemical diversity, biosynthesis, and bioactivity
No full textFig. 30. Biogenetic pathway for austinol.Published as part of Zhao, Wen-Yu, Yi, Jing, Chang, Yi-Bo, Sun, Cheng-Peng & Ma, Xiao-Chi, 2022, Recent studies on terpenoids in Aspergillus fungi: Chemical diversity, biosynthesis, and bioactivity, pp. 1-25 in Phytochemistry (113011) 193 on page 19, DOI: 10.1016/j.phytochem.2021.113011, http://zenodo.org/record/823487
Fig. 4 in Recent studies on terpenoids in Aspergillus fungi: Chemical diversity, biosynthesis, and bioactivity
No full textFig. 4. Structures of cadinane-type sesquiterpenoids (83–91).Published as part of Zhao, Wen-Yu, Yi, Jing, Chang, Yi-Bo, Sun, Cheng-Peng & Ma, Xiao-Chi, 2022, Recent studies on terpenoids in Aspergillus fungi: Chemical diversity, biosynthesis, and bioactivity, pp. 1-25 in Phytochemistry (113011) 193 on page 5, DOI: 10.1016/j.phytochem.2021.113011, http://zenodo.org/record/823487
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