Zobrazeno 1 - 10
of 222
pro vyhledávání: '"Zhi-chao Wang"'
Autor:
Yi-Ni Bao, Qiao Yang, Xin-Lei Shen, Wen-Kai Yu, Li Zhou, Qing-Ru Zhu, Qi-Yuan Shan, Zhi-Chao Wang, Gang Cao
Publikováno v:
Cell Death and Disease, Vol 15, Iss 5, Pp 1-11 (2024)
Abstract Fibrosis is a reparative and progressive process characterized by abnormal extracellular matrix deposition, contributing to organ dysfunction in chronic diseases. The tumor suppressor p53 (p53), known for its regulatory roles in cell prolife
Externí odkaz:
https://doaj.org/article/8a4b1b78fe574be3b12cb3a2b6764232
Autor:
Zi-Zhen Guo, Zhi-Chao Wang, Dun Wang, Ling-Ling Ge, Yue-Hua Li, Yi-Hui Gu, Wei Wang, Cheng-Jiang Wei, Bin Gu, Min Yao, Ji-Ying Dong, Qing-Feng Li
Publikováno v:
European Journal of Medical Research, Vol 28, Iss 1, Pp 1-18 (2023)
Abstract Nowadays, laser is the mainstay treatment for cafe-au-lait macules (CALMs), but no systematic review has been published to demonstrate the overall efficacy and it’s still controversial which type of laser is optimal. Thus, we conduct the m
Externí odkaz:
https://doaj.org/article/13eeeee9a9f64b58a736309c0197ffdf
Publikováno v:
Guoji Yanke Zazhi, Vol 23, Iss 4, Pp 592-596 (2023)
Chorioretinal disease has become a significant problem affecting human vision. Abnormal expression of vascular endothelial growth factor(VEGF)leads to increased fundus permeability and neovascularization. Vitreous injection of anti-VEGF agents can ra
Externí odkaz:
https://doaj.org/article/28c7e63f5869495786ba7bfdb10aa311
Publikováno v:
The Journal of Pathology: Clinical Research, Vol 9, Iss 2, Pp 89-99 (2023)
Abstract Tropomyosin receptor kinase B (TrkB), a transmembrane receptor protein, has been found to play a pivotal role in neural development. This protein is encoded by the neurotrophic receptor tyrosine kinase 2 (NTRK2) gene, and its abnormal activa
Externí odkaz:
https://doaj.org/article/4d339d3492ca4d1eaf2224e1db79cb73
Autor:
Qiao-ling Ruan, Zhi-chao Wang, Cheng-jiang Wei, Wei Wang, Qing-luan Yang, Jing Wu, Yan-min Wan, Ling-ling Ge, Wen-hong Zhang, Qing-feng Li
Publikováno v:
Signal Transduction and Targeted Therapy, Vol 8, Iss 1, Pp 1-3 (2023)
Externí odkaz:
https://doaj.org/article/b16a8679feb047ea90f242810f0f6360
Publikováno v:
Chinese Journal of Magnetic Resonance, Vol 39, Iss 1, Pp 33-42 (2022)
Chemical exchange saturation transfer (CEST) imaging shows great potential in clinical applications. However, CEST imaging is challenging in abdomen due to the large B0 shift. Meanwhile, the nuclear Overhauser enhancement (NOE) effect contaminates am
Externí odkaz:
https://doaj.org/article/dbad05d99d274f6cb422c0e440272492
Autor:
Ye Xu, Zhi-Chao Wang
Publikováno v:
PLoS ONE, Vol 18, Iss 10, p e0289806 (2023)
Based on the data of 278 prefecture-level city panels in China from 2008 to 2020, this paper presents the policy of innovative pilot city as a quasi-natural experiment. It is found that (1) the implementation of innovative urban policy can significan
Externí odkaz:
https://doaj.org/article/c19490f8c4fa4806aa8cd2f40f9b9d18
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
Tuberous sclerosis complex (TSC) is an inherited disorder that typically presents with seizures, developmental delay, cutaneous lesions, and facial angiomas. Clinical diagnosis of TSC based on symptoms is sometimes challenging due to its clinical sim
Externí odkaz:
https://doaj.org/article/6db681d949da468c94421a3b2e754a8f
Autor:
Zhi-Chao Wang, Shu-Zhong Li, Xin-Fei Qu, Chu-Qiang Yin, Yuan-Liang Sun, Yue-Lei Wang, Jie Wang, Chen-Jing Liu, Zhen-Lu Cao, Ting Wang
Publikováno v:
BMC Surgery, Vol 21, Iss 1, Pp 1-8 (2021)
Abstract Background The open-door laminoplasty is an effective procedure for the treatment of cervical spondylotic myelopathy. However, little information is available about the surgical results of open-door laminoplasty in the treatment of intraspin
Externí odkaz:
https://doaj.org/article/bffbb4bd9d6a4fe8a80f211af24613bc
Autor:
Jun Liu, Jing-Ning Huang, Ming-Han Wang, Zhen-Yang Ni, Wei-Hao Jiang, Manhon Chung, Cheng-Jiang Wei, Zhi-Chao Wang
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
Neurofibromatosis type 1 (NF1) is a dominant hereditary disease characterized by the mutation of the NF1 gene, affecting 1/3000 individuals worldwide. Most NF1 patients are predisposed to benign peripheral nerve sheath tumors (PNSTs), including cutan
Externí odkaz:
https://doaj.org/article/6e3fff53308d48dc9f4c9a448456d443