Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Zhipeng, Nie"'
Publikováno v:
Advances in Civil Engineering, Vol 2021 (2021)
For improving the toughness and long-term strength of the fractured rock mass reinforced with epoxy resin and reducing the opening displacement of the crack tip, three types of converging cracks are established according to the deformation and failur
Externí odkaz:
https://doaj.org/article/ee6b67d233204c7f8a1828e0e6c4e092
Publikováno v:
Energies, Vol 15, Iss 11, p 3862 (2022)
In view of the nonlinear mechanical characteristics of rock foundation creep fracture and its influence on the stability of wind turbine under wind load, based on the influence of wind load, this paper proposed the elastoplastic creep fracture and ro
Externí odkaz:
https://doaj.org/article/5d43150e724049199d127ed884efd3a5
Autor:
Hezuo Liu, Xiaorong Chen, Minhui Huang, Xiaomin Yu, Ye Gan, Ji Wang, Qiujin Chen, Zhipeng Nie, Haijing Ge
Publikováno v:
Reviews on Environmental Health.
Objectives The association between screen time and attention deficit hyperactivity disorder (ADHD) has been controversial. This study sheds light on the contentious correlation between screen time and ADHD. Content Until August 2022, electronic searc
In order to analyze the adverse effect of flood effect on slope stability, the analytical expressions of buoyancy force and capillary force, hydrodynamic pressure and impact force, and scour erosion were proposed based on the aging characteristics of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee995d8fbf89d03ceae5195ea186cb37
https://doi.org/10.21203/rs.3.rs-2446384/v1
https://doi.org/10.21203/rs.3.rs-2446384/v1
Autor:
Zhipeng Nie, Chenghui Wang, Jiarong Chen, Yanchun Ji, Hongxing Zhang, Fuxin Zhao, Xiangtian Zhou, Min-Xin Guan
Publikováno v:
Human molecular genetics.
Leber’s hereditary optic neuropathy (LHON) is a maternally inherited eye disease that results from degeneration of retinal ganglion cells (RGC). Mitochondrial ND4 11778G > A mutation, which affects structural components of complex I, is the most pr
Publikováno v:
IEEE Transactions on Computational Imaging. 5:262-273
Multifocus image fusion is an important technique that aims to generate a single clean image by fusing multiple input images. In this paper, we propose a novel multilevel features convolutional neural network (MLFCNN) architecture for image fusion. I
Autor:
Yanchun, Ji, Zhipeng, Nie, Feilong, Meng, Cuifang, Hu, Hui, Chen, Lihao, Jin, Mengquan, Chen, Minglian, Zhang, Juanjuan, Zhang, Min, Liang, Meng, Wang, Min-Xin, Guan
Publikováno v:
The Journal of Biological Chemistry
Mitochondrial tRNA 3’-end metabolism is critical for the formation of functional tRNAs. Deficient mitochondrial tRNA 3’-end metabolism is linked to an array of human diseases, including optic neuropathy, but their pathophysiology remains poorly u
Publikováno v:
Sensors, Vol 16, Iss 9, p 1532 (2016)
To obtain efficient data gathering methods for wireless sensor networks (WSNs), a novel graph based transform regularized (GBTR) matrix completion algorithm is proposed. The graph based transform sparsity of the sensed data is explored, which is also
Externí odkaz:
https://doaj.org/article/0f711c57ea93445aba2a02d4ce7813d2
Autor:
Lihao Jin, Juanjuan Zhang, Min Liang, Zhipeng Nie, Hui Chen, Feilong Meng, Min-Xin Guan, Mengquan Chen, Meng Wang, Yanchun Ji, Cuifang Hu, Minglian Zhang
Publikováno v:
Journal of Biological Chemistry. 297:100816
Mitochondrial tRNA 3'-end metabolism is critical for the formation of functional tRNAs. Deficient mitochondrial tRNA 3'-end metabolism is linked to an array of human diseases, including optic neuropathy, but their pathophysiology remains poorly under
Autor:
Zengming Zhang, Mengquan Chen, Chenghui Wang, Zhipeng Nie, Min-Xin Guan, Qiuzi Yi, Jian Zou, Xiaofen Jin, Pingping Jiang, Feilong Meng, Jiji Sun
Publikováno v:
The Journal of Biological Chemistry
Mitochondria maintain a distinct pool of ribosomal machinery, including tRNAs and tRNAs activating enzymes, such as mitochondrial tyrosyl-tRNA synthetase (YARS2). Mutations in YARS2, which typically lead to the impairment of mitochondrial protein syn