Academic literature on the topic 'Xin ling cheng zhang'

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Journal articles on the topic "Xin ling cheng zhang"

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Zhang, Xin-Jian, Zhong-Cheng Liu, Kai-Kai Meng, Qiao-Ling Ding, Lei Wang, and Wen-Bo Liao. "Saxifraga luoxiaoensis (Saxifragaceae), a new species from Hunan and Jiangxi, China." Phytotaxa 350, no. 3 (2018): 291–96. https://doi.org/10.11646/phytotaxa.350.3.8.

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Zhang, Xin-Jian, Liu, Zhong-Cheng, Meng, Kai-Kai, Ding, Qiao-Ling, Wang, Lei, Liao, Wen-Bo (2018): Saxifraga luoxiaoensis (Saxifragaceae), a new species from Hunan and Jiangxi, China. Phytotaxa 350 (3): 291-296, DOI: 10.11646/phytotaxa.350.3.8, URL: http://dx.doi.org/10.11646/phytotaxa.350.3.8
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Liang, Meng, Ling-Ling Chang, Jia-Xin Wang, et al. "Dendrobium jizhuyeense (Orchidaceae; Epidendroideae) a new species from China: evidence from morphology and DNA." Phytotaxa 645, no. 1 (2024): 77–84. https://doi.org/10.11646/phytotaxa.645.1.7.

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Liang, Meng, Chang, Ling-Ling, Wang, Jia-Xin, Zhang, Yu, Liu, Lei, Zhang, Ze, Li, Zhen-Jian (2024): Dendrobium jizhuyeense (Orchidaceae; Epidendroideae) a new species from China: evidence from morphology and DNA. Phytotaxa 645 (1): 77-84, DOI: 10.11646/phytotaxa.645.1.7, URL: http://dx.doi.org/10.11646/phytotaxa.645.1.7
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Han, Yang, Tao Hou, Zi-Hui Zhang, et al. "Corybungines A K: Isoquinoline alkaloids from Corydalis bungeana with dopamine D2 receptor activity." Phytochemistry 199 (July 31, 2022): 1–10. https://doi.org/10.1016/j.phytochem.2022.113209.

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Han, Yang, Hou, Tao, Zhang, Zi-Hui, Zhu, Yun-Hui, Cheng, Jun-Xiang, Zhou, Han, Wang, Ji-Xia, Feng, Jia-Tao, Liu, Yan-Fang, Guo, Zhi-Mou, Liang, Xin-Miao (2022): Corybungines A K: Isoquinoline alkaloids from Corydalis bungeana with dopamine D2 receptor activity. Phytochemistry (113209) 199: 1-10, DOI: 10.1016/j.phytochem.2022.113209, URL: http://dx.doi.org/10.1016/j.phytochem.2022.113209
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Li, Yong-Fu, Min Zhang, Xian-Rong Wang, et al. "Revisiting the phylogeny and taxonomy of Osmanthus (Oleaceae) including description of the new genus Chengiodendron." Phytotaxa 436, no. 3 (2020): 283–92. https://doi.org/10.11646/phytotaxa.436.3.6.

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Li, Yong-Fu, Zhang, Min, Wang, Xian-Rong, Sylvester, Steven Paul, Xiang, Qi-Bai, Li, Xuan, Li, Meng, Zhu, Hong, Zhang, Cheng, Chen, Lin, Yi, Xian-Gui, Mao, Ling-Feng, Duan, Yi-Fan (2020): Revisiting the phylogeny and taxonomy of Osmanthus (Oleaceae) including description of the new genus Chengiodendron. Phytotaxa 436 (3): 283-292, DOI: 10.11646/phytotaxa.436.3.6, URL: http://dx.doi.org/10.11646/phytotaxa.436.3.6
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Chen, Yan-Ling, Xian-Guo Guo, Tian-Guang Ren, et al. "Infestation and distribution of chigger mites on Chevrieri's field mouse (Apodemus chevrieri) in Southwest China." International Journal for Parasitology: Parasites and Wildlife 17 (April 30, 2022): 74–82. https://doi.org/10.1016/j.ijppaw.2021.12.003.

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Chen, Yan-Ling, Guo, Xian-Guo, Ren, Tian-Guang, Zhang, Lei, Fan, Rong, Zhao, Cheng-Fu, Zhang, Zhi-Wei, Mao, Ke-Yu, Huang, Xiao-Bin, Qian, Ti-Jun (2022): Infestation and distribution of chigger mites on Chevrieri's field mouse (Apodemus chevrieri) in Southwest China. International Journal for Parasitology: Parasites and Wildlife 17: 74-82, DOI: 10.1016/j.ijppaw.2021.12.003, URL: http://dx.doi.org/10.1016/j.ijppaw.2021.12.003
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Zhou, Wei-Guo, De-Wen Ding, Qing-Song Yang, et al. "Marileptolyngbya sina gen. nov., sp. nov. and Salileptolyngbya diazotrophicum gen. nov., sp. nov. (Synechococcales, Cyanobacteria), species of cyanobacteria isolated from a marine ecosystem." Phytotaxa 383, no. 1 (2018): 75–92. https://doi.org/10.11646/phytotaxa.383.1.4.

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Zhou, Wei-Guo, Ding, De-Wen, Yang, Qing-Song, Ahmad, Manzoor, Zhang, Yuan-Zhou, Lin, Xian-Cheng, Zhang, Yan-Ying, Ling, Juan, Dong, Jun-De (2018): Marileptolyngbya sina gen. nov., sp. nov. and Salileptolyngbya diazotrophicum gen. nov., sp. nov. (Synechococcales, Cyanobacteria), species of cyanobacteria isolated from a marine ecosystem. Phytotaxa 383 (1): 75-92, DOI: 10.11646/phytotaxa.383.1.4, URL: http://dx.doi.org/10.11646/phytotaxa.383.1.4
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Cheng, Zhuo-Yang, Ding-Ding Zhang, Jing-Xian Ren, et al. "Stellerasespenes A-E: Sesquiterpenoids from Stellera chamaejasme and their anti-neuroinflammatory effects." Phytochemistry 201 (September 30, 2022): 1–9. https://doi.org/10.1016/j.phytochem.2022.113275.

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Cheng, Zhuo-Yang, Zhang, Ding-Ding, Ren, Jing-Xian, Li, Ya-Ling, Yao, Guo-Dong, Song, Shao-Jiang, Huang, Xiao-Xiao (2022): Stellerasespenes A-E: Sesquiterpenoids from Stellera chamaejasme and their anti-neuroinflammatory effects. Phytochemistry (113275) 201: 1-9, DOI: 10.1016/j.phytochem.2022.113275, URL: http://dx.doi.org/10.1016/j.phytochem.2022.113275
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Liang, Jia-Yuan, Cheng-Kang Zhang, Mei-Xia Chen, Wei Liu, Shi-Zhong Zheng, and Yu-Feng Hsu. "A new species of the genus Synanthedon Hübner [1819] (Lepidoptera Sesiidae) from Taiwan." Zootaxa 5133, no. 1 (2022): 133–42. https://doi.org/10.11646/zootaxa.5133.1.7.

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Liang, Jia-Yuan, Zhang, Cheng-Kang, Chen, Mei-Xia, Liu, Wei, Zheng, Shi-Zhong, Hsu, Yu-Feng (2022): A new species of the genus Synanthedon Hübner [1819] (Lepidoptera Sesiidae) from Taiwan. Zootaxa 5133 (1): 133-142, DOI: 10.11646/zootaxa.5133.1.7
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Liang, Yu, Yingyu Li, Yi Zhou, et al. "Abstract 6006: The discovery and development of a CD3 agonistic single domain antibody to accelerate the development of CD3 T cell engager multi-specific antibodies." Cancer Research 85, no. 8_Supplement_1 (2025): 6006. https://doi.org/10.1158/1538-7445.am2025-6006.

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Abstract CD3 T cell engager (TCE) bispecific antibodies (BsAbs) is a clinically well validated and dominant therapeutic modality of approved bispecific antibodies, contributing to 10 out of 14 marketed BsAb drugs. To develop a TCE BsAb with desired potency and safety profile, a CD3 agonist Ab with appropriate potency and ideal developability is critical. Currently, all approved TCE BsAbs are based on a CD3 agonist Ab in the format of conventional monoclonal antibodies containing both light chain and heavy chain, which may limit the flexibility in multi-specific antibody construction and develo
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Qin, You, Rong-Rong Zhou, Jian Jin, et al. "Indole-based alkaloids from Ophiocordyceps xuefengensis." Phytochemistry 181 (January 31, 2021): 1–12. https://doi.org/10.1016/j.phytochem.2020.112536.

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Qin, You, Zhou, Rong-Rong, Jin, Jian, Cheng, Fei, Shen, Bing-Bing, Zeng, Hong-Liang, Wan, Dan, Zhong, Can, Xie, Jing, Shu, Jun, Shi, Shu-Yun, Zhang, Shui-Han (2021): Indole-based alkaloids from Ophiocordyceps xuefengensis. Phytochemistry (112536) 181: 1-12, DOI: 10.1016/j.phytochem.2020.112536, URL: http://dx.doi.org/10.1016/j.phytochem.2020.112536
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Dissertations / Theses on the topic "Xin ling cheng zhang"

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Lingenfelter, Andrea Diane. "A marked category : nine women of modern Chinese poetry, 1920-1997 /." Thesis, Connect to this title online; UW restricted, 1998. http://hdl.handle.net/1773/11129.

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Books on the topic "Xin ling cheng zhang"

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jie, Liu hong. Xin ling de cheng zhang. Ji lin ta xue chu ban she, 2009.

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Zhongguo qi ye ping jia xie hui. Guo yan, Sitanfu xiang mu ban gong shi, ed. Ba xin ling yi: Zhongguo qi ye xin ling xiu cheng zhang bao gao. Zhongguo fa zhan chu ban she, 2014.

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she, Zhi xin jie jie za zhi. Guan zhu hai zi xin ling de cheng zhang. Zhong guo shao nian er tong chu ban she, 2005.

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Li, Deng. Cheng zhang yang guang: Er tong xin ling shu. Er shi yi shi ji chu ban she, 2005.

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yong, Zhang xian. Ha fo nü hai cheng zhang zhen yan: Xin ling juan. Shi you gong ye chu ban she, 2008.

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yi, Zhang Dingqi, ed. Xin ling di tu: Zhui qiu ai he cheng zhang zhi lu. 5th ed. Tian xia yuan jian chu ban gong si, 2010.

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You, Han. Zheng jiu xin ling: Cong you shi jing li kan hou tian cheng zhang = Save souls. Xin shi jie chu ban she, 2007.

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qi, Feng. Zhong guo shi bai ling sheng cun shou ce. Zhong guo shui li shui dian chu ban she, 2009.

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sheng, Chen qi. Yi fen zhong ling ren gua mu xiang kan. Zhong guo fang zhi chu ban she, 2004.

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Hezhen, Xu, ed. Xin xi hua jin cheng zhong si ling ji guan jian she. Jie fang jun chu ban she, 2004.

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Book chapters on the topic "Xin ling cheng zhang"

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Taber, Douglass F. "C-O Ring Construction: The Theodorakis Synthesis of (-)-Englerin A." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0049.

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Liming Zhang of the University of California, Santa Barbara, described (J. Am. Chem. Soc. 2010, 132, 8550) the remarkable transformation of a propargyl alcohol 1 into the oxetanone 2. The transformation proceeded without loss of ee, as did the ring expansion of 3 to 5 reported (J. Org. Chem. 2010, 75, 6229) by Peter R. Schreiner of Justus-Liebig University, Giessen, and Andrey A. Fokin of the Kiev Polytechnic Institute. Takeo Taguchi of the Tokyo University of Pharmacy and Life Sciences developed (Chem. Commun. 2010, 46, 8728) a catalyst for the stereoselective conjugate addition of 7 to 6. Mitsuru Shindo of Kyushu University devised (Org. Lett. 2010, 12, 5346) the thioester 10, which condensed smoothly with an α-hydroxy ketone 9 to deliver the lactone 11. Zili Chen of the Renmin University of China and Lin Guo of the Beijing University of Aeronautics and Astronautics developed (Org. Lett. 2010, 12, 3468) the diastereoselective double addition of propargyl alcohol 13 to 12 to give 14. Jian-Wu Xie of Zhejiang Normal University uncovered (J. Org. Chem. 2010, 75, 8716) the catalyzed enantioselective addition of 16 to 15 to give the dihydrofuran 17. James S. Panek of Boston University extended (Org. Lett. 2010, 12, 4624) the utility of the enantiomerically pure allenic nucleophile 19, adding it to the acceptor 18 to give 20 with both ring and sidechain stereocontrol. Biswanath Das of the Indian Institute of Chemical Technology, Hyderabad, showed (Tetrahedron Lett. 2010, 51, 6011) that the epoxide of the tartrate-derived acetonide 21 could be rearranged to the fully substituted, differentially protected tetrahydrofuran 22. Paul E. Floreancig of the University of Pittsburgh uncovered (Angew. Chem. Int. Ed. 2010, 49, 5894) the highly stereocontrolled oxidative cyclization of 22 to 23. Dirk Menche of the University of Heidelberg found (Angew. Chem. Int. Ed. 2010, 49, 9270) that the Pd-mediated addition of 24 to 25 also proceeded with high diastereocontrol. Dipolar cycloaddition to a furan is of increasing importance in target-directed synthesis. Emmanuel A. Theodorakis of the University of California, San Diego, added (Org. Lett. 2010, 12, 3708) the diazo ester 27, prepared from the inexpensive chiral auxiliary pantolactone, to the furan 28.
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Liu, Hong, Chang-Lin Feng, Xiao-Qing Xie, et al. "12. Impacts of Extreme Weather Spells on Flowering Phenology of Wild Orchids in Guangxi, Southwestern China - Hong Liu, Chang-Lin Feng, Xiao-Qing Xie, Wuying Lin, Zheng-Hai Deng, Xin-Lian Wei, Shi-Yong Liu, and Yi-Bo Luo." In Darwin's Orchids. University of Chicago Press, 2014. http://dx.doi.org/10.7208/chicago/9780226173641.003.0012.

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Conference papers on the topic "Xin ling cheng zhang"

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Xiaozhi Wang and Neil Pegg, ISSC 2022 Editors. "Proceedings of the 21st International Ship and Offshore Structures Congress VOLUME 3 Discussions." In 21st International Ship and Offshore Structures Congress Volume 3 Discussions. SNAME, 2022. http://dx.doi.org/10.5957/issc-2022-discussion-vol-3.

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Committee I.1: Environment Alexander Babanin (Chair); Mariana Bernardino; Franz von Bock und Polach; Ricardo Campos,; Jun Ding; Sanne van Essen; Tomaso Gaggero; Maryam Haroutunian; Vanessa Katsardi; Alexander Nilva; Arttu Polojarvi; Erik Vanem; Jungyong Wang; Huidong Zhang; Tingyao Zhu Floor Discussers: Florian Sprenger; Carlos Guedes Soares; Henk den Besten Committee I.2: Loads Ole Andreas Hermundstad (Chair); Shuhong Chai; Guillaume de Hauteclocque; Sheng Dong; Chih-Chung Fang; Thomas B. Johannessen; Celso Morooka; Masayoshi Oka; Jasna Prpić-Oršić; Alessandro Sacchet; Mahmud Sazidy; Bahadir
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