Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Ze-yu Zhu"'
Publikováno v:
Case Studies in Thermal Engineering, Vol 63, Iss , Pp 105393- (2024)
Functionally graded materials have found extensive applications in the aerospace industry and solar energy systems due to their excellent performance in enhancing heat transfer/insulation. Developing corresponding theoretical frameworks for the coupl
Externí odkaz:
https://doaj.org/article/074b42fced4c41e78e57f2a42e1a4a0a
Autor:
Zhi-Yue Wang, Guang-Yu Zhang, Jian Wang, Zhe Geng, Ze-Yu Zhu, Ming-Hao Jia, Qian Zhang, Zhen-Hao Zheng, Kun Ge, Jia-Yao Gu, Lu-Cheng Zhu, Hong-Fei Zhang
Publikováno v:
Frontiers in Astronomy and Space Sciences, Vol 10 (2023)
Externí odkaz:
https://doaj.org/article/225265fda6914bc9a41e148c94e48803
Autor:
Zhi-Yue Wang, Guang-Yu Zhang, Jian Wang, Zhe Geng, Ze-Yu Zhu, Ming-Hao Jia, Qian Zhang, Zhen-Hao Zheng, Kun Ge, Jia-Yao Gu, Lu-Cheng Zhu, Hong-Fei Zhang
Publikováno v:
Frontiers in Astronomy and Space Sciences, Vol 10 (2023)
With the increasing demand for astronomical observations, telescope systems are becoming increasingly complex. Thus, the observatory control software needs to be more intelligent. It has to control each instrument inside the observatory, finish the o
Externí odkaz:
https://doaj.org/article/2997c17eac4b40cea93a3d7919d15251
Autor:
Wo‐Tu Tian, Li‐Hua Liu, Hai‐Yan Zhou, Chao Zhang, Fei‐Xia Zhan, Ze‐Yu Zhu, Sheng‐Di Chen, Xing‐Hua Luan, Li Cao
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 7, Iss 2, Pp 200-209 (2020)
Abstract Objective To describe the clinical and genetic features of two patients with different phenotypes due to various Dynactin 1 (DCTN1) gene mutations and further explore the phenotype–genotype relationship. Methods Patient 1 is a 23‐year‐
Externí odkaz:
https://doaj.org/article/c8a501542dd34c1592f93086f4c43977
Publikováno v:
Renewable Energy. 211:140-154
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c8262c97246aad3a889a1aae493d8f31
https://doi.org/10.1016/j.renene.2023.04.130
https://doi.org/10.1016/j.renene.2023.04.130
Autor:
Wo-Tu Tian, Fei-Xia Zhan, Qing Liu, Xing-Hua Luan, Chao Zhang, Liang Shang, Ben-Yan Zhang, Si-Jian Pan, Fei Miao, Jiong Hu, Ping Zhong, Shi-Hua Liu, Ze-Yu Zhu, Hai-Yan Zhou, Suya Sun, Xiao-Li Liu, Xiao-Jun Huang, Jing-Wen Jiang, Jian-Fang Ma, Ying Wang, Shu-Fen Chen, Hui-Dong Tang, Sheng-Di Chen, Li Cao
Publikováno v:
Translational Neurodegeneration, Vol 8, Iss 1, Pp 1-13 (2019)
Abstract Background CSF1R-related leukoencephalopathy, also known as hereditary diffuse leukoencephalopathy with spheroids (HDLS), is a rare white-matter encephalopathy characterized by motor and neuropsychiatric symptoms due to colony-stimulating fa
Externí odkaz:
https://doaj.org/article/36f4bf5ce79e46218c24661b65904989
Autor:
Wo‐Tu Tian, Hai‐Yan Zhou, Fei‐Xia Zhan, Ze‐Yu Zhu, Jie Yang, Sheng‐Di Chen, Xing‐Hua Luan, Li Cao
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 6, Iss 6, Pp 1062-1071 (2019)
Abstract Objective GDP‐mannose pyrophosphorylase B (GMPPB) related phenotype spectrum ranges widely from congenital myasthenic syndrome (CMS), limb‐girdle muscular dystrophy type 2T (LGMD 2T) to severe congenital muscle‐eye‐brain syndrome. Ou
Externí odkaz:
https://doaj.org/article/79e2925189b54aec91f071fc77d17247
Autor:
Zhen-hao Zheng, Hong-fei Zhang, Zhi-yue Wang, Qian Zhang, Ze-yu Zhu, Hui Wang, Cheng Chen, Lu-cheng Zhu, Kun Ge, Hao Liu, Jian Wang
Publikováno v:
X-Ray, Optical, and Infrared Detectors for Astronomy X.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f7cf4585188fd057664e4088af0a4fea
https://doi.org/10.1117/12.2629188
https://doi.org/10.1117/12.2629188
Autor:
Zhe Geng, Zhi-yue Wang, Qian Zhang, Ze-yu Zhu, Jia-yao Gu, Zhen-hao Zheng, Lu-cheng Zhu, Kun Ge, Hao Liu, Hong-fei Zhang, Jian Wang
Publikováno v:
Software and Cyberinfrastructure for Astronomy VII.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::afd8e41da022ff54035ad1a7b79f89c7
https://doi.org/10.1117/12.2628783
https://doi.org/10.1117/12.2628783
Autor:
Li Cao, Hui-Dong Tang, Guang Chen, Ze-Yu Zhu, Xiaoxuan Song, Xiao-ying Liu, Jingying Wu, Xiao-Hang Qian, Shi-Ge Wang
Publikováno v:
Seizure. 84:47-52
Background Mutations in the IRF2BPL gene can cause neurodevelopmental disorders. We describe the clinical and genetic characteristics of a Chinese patient with a novel abnormality in this gene, explore the potential pathogenic mechanism and summarize
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17df8c6b15ae138b0cda8c90f4dd3289
https://doi.org/10.1016/j.seizure.2020.11.006
https://doi.org/10.1016/j.seizure.2020.11.006