Zobrazeno 1 - 10
of 54
pro vyhledávání: '"CHENG Jiang-wei"'
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
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 Convalescent Medicine / Zhongguo Liaoyang Yixue; nov2024, Vol. 33 Issue 11, p11-15, 5p
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:
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
Autor:
Wei Wang, Cheng-Jiang Wei, Xi-Wei Cui, Yue-Hua Li, Yi-Hui Gu, Bin Gu, Qing-Feng Li, Zhi-Chao Wang
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Neurofibromatosis type 1 (NF1) is a tumor predisposition genetic disorder that directly affects more than 1 in 3,000 individuals worldwide. It results from mutations of the NF1 gene and shows almost complete penetrance. NF1 patients show high phenoty
Externí odkaz:
https://doaj.org/article/258fb9ca4e534ebb8fcb1543b59ad807
Autor:
Yi-Hui Gu, Xi-Wei Cui, Jie-Yi Ren, Man-Mei Long, Wei Wang, Cheng-Jiang Wei, Rehanguli Aimaier, Yue-Hua Li, Man-Hon Chung, Bin Gu, Qing-Feng Li, Zhi-Chao Wang
Publikováno v:
PLoS ONE, Vol 16, Iss 2, p e0241821 (2021)
Real-time quantitative PCR (RT-qPCR) has been widely applied in uncovering disease mechanisms and screening potential biomarkers. Internal reference gene selection determines the accuracy and reproducibility of data analyses. The aim of this study wa
Externí odkaz:
https://doaj.org/article/0d46e7e3a6b74bc39e5cd1badff99d64
Akademický článek
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Autor:
Jie-Yi Ren, Yi-Hui Gu, Xi-Wei Cui, Man-Mei Long, Wei Wang, Cheng-Jiang Wei, Bin Gu, Hai-Bing Zhang, Qing-Feng Li, Zhi-Chao Wang
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 8 (2020)
Malignant peripheral nerve sheath tumors (MPNST) are aggressive sarcomas with over half of cases developed in the context of neurofibromatosis type 1. Surgical resection is the only effective therapy for MPNST. The prognosis is very dismal once recur
Externí odkaz:
https://doaj.org/article/3e9cb67ee8804f5ca00e32195c1f51c9
Autor:
Cheng-Jiang Wei, Cheng Yan, Yan Tang, Wei Wang, Yi-Hui Gu, Jie-Yi Ren, Xi-Wei Cui, Xiang Lian, Jin Liu, Hui-Jing Wang, Bin Gu, Tao Zan, Qing-Feng Li, Zhi-Chao Wang
Publikováno v:
Frontiers in Oncology, Vol 10 (2020)
Background: Because neurofibromatosis type I (NF1) is a cancer predisposition disease, it is important to distinguish between benign and malignant lesions, especially in the craniofacial area.Purpose: The purpose of this study is to improve effective
Externí odkaz:
https://doaj.org/article/13c30535126c401daf6b10391b78d21c